Análisis de los niveles de metilación del ADN relacionados con la exposición a la violencia y su impacto en medidas de salud cerebral en una muestra de adultos colombianos

dc.contributor.advisorSantamaría García, Hernando
dc.contributor.authorÁvila Rincón, Cristian David
dc.coverage.countryColombia
dc.coverage.tgnhttp://vocab.getty.edu/page/tgn/1000050
dc.date.accessioned2026-02-12T22:32:37Z
dc.date.available2026-02-12T22:32:37Z
dc.date.issued2025-11-25
dc.descriptionilustraciones a color, diagramasspa
dc.description.abstractLa exposición crónica a violencia puede inducir alteraciones epigenéticas con repercusiones sobre la salud cerebral. El presente estudio examinó la relación entre exposición a violencia, aceleración de la edad epigenética (AEE) y medidas de salud cerebral en adultos afectados por el conflicto armado colombiano, incluyendo excombatientes y víctimas civiles. Se analizaron 54 participantes (35 expuestos y 19 controles) mediante pruebas de cognición (MoCA), funciones ejecutivas (IFS) y funcionalidad (FAST), junto con cinco relojes epigenéticos (Horvath1, Horvath2, Hannum, PhenoAge y GrimAge) y dos marcadores complementarios (DNAmTL y DunedinPACE). La AEE estimada por GrimAge fue significativamente mayor en personas expuestas a violencia (p < 0.05; d = –0.573) y en quienes presentaron menor desempeño ejecutivo (p < 0.01). En los análisis estratificados por nivel educativo, PhenoAge mostró una asociación significativa entre menor escolaridad y mayor aceleración epigenética en participantes con bajo rendimiento ejecutivo (β = 1.306; IC95%: 0.186–2.426; p < 0.05 ). Aunque los modelos de mediación no revelaron efectos indirectos consistentes, los resultados evidencian vínculos biológicos diferenciados entre violencia, envejecimiento epigenético y función cognitiva, y sugieren que la educación podría modular los efectos del estrés crónico sobre el envejecimiento cerebral. (Texto tomado de la fuente)spa
dc.description.abstractChronic exposure to violence can induce epigenetic alterations with repercussions for brain health. The present study examined the relationship between exposure to violence, epigenetic age acceleration (EAA), and measures of brain health in adults affected by the Colombian armed conflict, including former combatants and civilian victims. A total of 54 participants (35 exposed and 19 controls) were assessed through cognitive tests (MoCA), executive function (IFS), and functionality (FAST), along with five epigenetic clocks (Horvath1, Horvath2, Hannum, PhenoAge, and GrimAge) and two complementary markers (DNAmTL and DunedinPACE). EAA estimated by GrimAge was significantly higher in individuals exposed to violence (p < 0.05; d = –0.573) and in those with poorer executive performance (p < 0.01). In analyses stratified by educational level, PhenoAge showed a significant association between lower schooling and greater epigenetic acceleration among participants with low executive performance (β = 1.306; 95% CI: 0.186–2.426; p < 0.05). Although mediation models did not reveal consistent indirect effects, the results indicate differentiated biological links between violence, epigenetic aging, and cognitive function, suggesting that education may modulate the impact of chronic stress on brain aging.eng
dc.description.degreelevelMaestría
dc.description.degreenameMagíster en Neurociencias
dc.description.researchareaComportamiento humano
dc.format.extentxi, 75 páginas
dc.format.mimetypeapplication/pdf
dc.identifier.instnameUniversidad Nacional de Colombiaspa
dc.identifier.reponameRepositorio Institucional Universidad Nacional de Colombiaspa
dc.identifier.repourlhttps://repositorio.unal.edu.co/spa
dc.identifier.urihttps://repositorio.unal.edu.co/handle/unal/89534
dc.publisherUniversidad Nacional de Colombia
dc.publisher.branchUniversidad Nacional de Colombia - Sede Bogotá
dc.publisher.facultyFacultad de Medicina
dc.publisher.placeBogotá, Colombia
dc.publisher.programBogotá - Medicina - Maestría en Neurociencias
dc.relation.indexedBireme
dc.relation.referencesItzhaky L, Gelkopf M, Levin Y, Stein JY, Solomon Z. Psychiatric reactions to continuous traumatic stress: A Latent Profile Analysis of two Israeli samples. J Anxiety Disord. octubre de 2017;51:94-100.
dc.relation.referencesKakaje A, Al Zohbi R, Hosam Aldeen O, Makki L, Alyousbashi A, Alhaffar MBA. Mental disorder and PTSD in Syria during wartime: a nationwide crisis. BMC Psychiatry. 2 de enero de 2021;21(1):2.
dc.relation.referencesGros DF, Szafranski DD, Brady KT, Back SE. Relations between pain, PTSD symptoms, and substance use in veterans. Psychiatry: Interpersonal and Biological Processes. 2015;78:277-87
dc.relation.referencesMlouki I, Naimi A, Sioud I, Bouanene I, El Mhamdi S. Adverse childhood experiences and sleep disorders among Tunisian adolescents: The mediating role of internet addiction. Child Abuse Negl. 16 de enero de 2023;136:106028.
dc.relation.referencesSuglia SF, Sapra KJ, Koenen KC. Violence and Cardiovascular Health. Am J Prev Med. febrero de 2015;48(2):205-12.
dc.relation.referencesWeitzman A, Goosby BJ. Intimate partner violence, circulating glucose, and non-communicable Disease: Adding insult to injury? SSM Popul Health. 25 de noviembre de 2020;13:100701.
dc.relation.referencesWexler J, Ajibewa TA, Lee J, Toledo-Corral C, Hasson RE. Community violence exposure and cortisol awakening responses in adolescents who are overweight/obese. Psychoneuroendocrinology. 1 de noviembre de 2020;121:104842.
dc.relation.referencesWuest J, O’Donnell S, Scott-Storey K, Malcolm J, Vincent CD, Taylor P. Cumulative Lifetime Violence Severity and Chronic Pain in a Community Sample of Canadian Men. Pain Med. 4 de junio de 2021;22(6):1387-98.
dc.relation.referencesXu T, Magnusson Hanson LL, Lange T, Starkopf L, Westerlund H, Madsen IEH, et al. Workplace bullying and violence as risk factors for type 2 diabetes: a multicohort study and meta-analysis. Diabetologia. enero de 2018;61(1):75-83.
dc.relation.referencesBush NR, Aschbacher K. Immune Biomarkers of Early-Life Adversity and Exposure to Stress and Violence—Searching Outside the Streetlight. JAMA Pediatrics. 1 de enero de 2020;174(1):17-9.
dc.relation.referencesFinegood ED, Chen E, Kish J, Vause K, Leigh AKK, Hoffer L, et al. Community violence and cellular and cytokine indicators of inflammation in adolescents. Psychoneuroendocrinology. mayo de 2020;115:104628.
dc.relation.referencesPeckins MK, Roberts AG, Hein TC, Hyde LW, Mitchell C, Brooks-Gunn J, et al. Violence exposure and social deprivation is associated with cortisol reactivity in urban adolescents. Psychoneuroendocrinology. enero de 2020;111:104426.
dc.relation.referencesRasmussen LJH, Moffitt TE, Arseneault L, Danese A, Eugen-Olsen J, Fisher HL, et al. Association of Adverse Experiences and Exposure to Violence in Childhood and Adolescence With Inflammatory Burden in Young People. JAMA Pediatr. 1 de enero de 2020;174(1):38-47.
dc.relation.referencesShalev I, Moffitt TE, Sugden K, Williams B, Houts RM, Danese A, et al. Exposure to violence during childhood is associated with telomere erosion from 5 to 10 years of age: a longitudinal study. Mol Psychiatry. mayo de 2013;18(5):576-81.
dc.relation.referencesBerger SL, Kouzarides T, Shiekhattar R, Shilatifard A. An operational definition of epigenetics. Genes Dev. 1 de abril de 2009;23(7):781-3.
dc.relation.referencesCavalli G, Heard E. Advances in epigenetics link genetics to the environment and disease. Nature. julio de 2019;571(7766):489-99.
dc.relation.referencesLi Y. Modern epigenetics methods in biological research. Methods. marzo de 2021;187:104-13.
dc.relation.referencesMulligan CJ, Quinn EB, Hamadmad D, Dutton CL, Nevell L, Binder AM, et al. Epigenetic signatures of intergenerational exposure to violence in three generations of Syrian refugees. Sci Rep. 27 de febrero de 2025;15(1):5945.
dc.relation.referencesJovanovic T, Vance LA, Cross D, Knight AK, Kilaru V, Michopoulos V, et al. Exposure to Violence Accelerates Epigenetic Aging in Children. Sci Rep. 21 de agosto de 2017;7(1):8962
dc.relation.referencesBrunst KJ, Tignor N, Just A, Liu Z, Lin X, Hacker MR, et al. Cumulative lifetime maternal stress and epigenome-wide placental DNA methylation in the PRISM cohort. Epigenetics. 3 de junio de 2018;13(6):665-81.
dc.relation.referencesParade SH, Huffhines L, Daniels TE, Stroud LR, Nugent NR, Tyrka AR. A systematic review of childhood maltreatment and DNA methylation: candidate gene and epigenome-wide approaches. Transl Psychiatry. 19 de febrero de 2021;11(1):1-33.
dc.relation.referencesMoore LD, Le T, Fan G. DNA Methylation and Its Basic Function. Neuropsychopharmacol. enero de 2013;38(1):23-38.
dc.relation.referencesEspín-Pérez A, Brennan K, Ediriwickrema AS, Gevaert O, Lossos IS, Gentles AJ. Peripheral blood DNA methylation profiles predict future development of B-cell Non-Hodgkin Lymphoma. npj Precis Onc. 21 de julio de 2022;6(1):1-9
dc.relation.referencesGilbert TM, Zürcher NR, Catanese MC, Tseng CEJ, Di Biase MA, Lyall AE, et al. Neuroepigenetic signatures of age and sex in the living human brain. Nat Commun. 3 de julio de 2019;10(1):2945.
dc.relation.referencesZhang Y, Sun Z, Jia J, Du T, Zhang N, Tang Y, et al. Overview of Histone Modification. Adv Exp Med Biol. 2021;1283:1-16.
dc.relation.referencesGarber K. Epigenetics comes to RNA. Science. 5 de julio de 2019;365(6448):16-7.
dc.relation.referencesHoloch D, Moazed D. RNA-mediated epigenetic regulation of gene expression. Nat Rev Genet. febrero de 2015;16(2):71-84.
dc.relation.referencesTeschendorff AE, Horvath S. Epigenetic ageing clocks: statistical methods and emerging computational challenges. Nat Rev Genet. mayo de 2025;26(5):350-68.
dc.relation.referencesHorvath S, Raj K. DNA methylation-based biomarkers and the epigenetic clock theory of ageing. Nat Rev Genet. junio de 2018;19(6):371-84
dc.relation.referencesVermeulen R, Schymanski EL, Barabási AL, Miller GW. The exposome and health: Where chemistry meets biology. Science. 24 de enero de 2020;367(6476):392-6.
dc.relation.referencesVineis P, Robinson O, Chadeau-Hyam M, Dehghan A, Mudway I, Dagnino S. What is new in the exposome? Environ Int. octubre de 2020;143:105887
dc.relation.referencesRider CF, Carlsten C. Air pollution and DNA methylation: effects of exposure in humans. Clinical Epigenetics. 3 de septiembre de 2019;11(1):131.
dc.relation.referencesMancilla VJ, Peeri NC, Silzer T, Basha R, Felini M, Jones HP, et al. Understanding the Interplay Between Health Disparities and Epigenomics. Frontiers in Genetics [Internet]. 2020 [citado 5 de febrero de 2023];11. Disponible en: https://www.frontiersin.org/articles/10.3389/fgene.2020.00903
dc.relation.referencesMartin CL, Ghastine L, Lodge EK, Dhingra R, Ward-Caviness CK. Understanding Health Inequalities Through the Lens of Social Epigenetics. Annual Review of Public Health. 2022;43(1):235-54.
dc.relation.referencesMerrill SM, Gladish N, Kobor MS. Social Environment and Epigenetics. Curr Top Behav Neurosci. 2019;42:83-126.
dc.relation.referencesCerutti J, Lussier AA, Zhu Y, Liu J, Dunn EC. Associations between indicators of socioeconomic position and DNA methylation: a scoping review. Clinical Epigenetics. 14 de diciembre de 2021;13(1):221.
dc.relation.referencesCoker ES, Gunier R, Huen K, Holland N, Eskenazi B. DNA methylation and socioeconomic status in a Mexican-American birth cohort. Clinical Epigenetics. 8 de mayo de 2018;10(1):61.
dc.relation.referencesSchmitz LL, Zhao W, Ratliff SM, Goodwin J, Miao J, Lu Q, et al. The Socioeconomic Gradient in Epigenetic Ageing Clocks: Evidence from the Multi-Ethnic Study of Atherosclerosis and the Health and Retirement Study. Epigenetics. junio de 2022;17(6):589-611.
dc.relation.referencesSimons RL, Lei MK, Klopach E, Berg M, Zhang Y, Beach SSR. Re(Setting) Epigenetic Clocks: An Important Avenue Whereby Social Conditions Become Biologically Embedded across the Life Course. J Health Soc Behav. septiembre de 2021;62(3):436-53.
dc.relation.referencesChen Y, Demnitz N, Yamamoto S, Yaffe K, Lawlor B, Leroi I. Defining brain health: A concept analysis. International Journal of Geriatric Psychiatry [Internet]. 2022 [citado 31 de enero de 2023];37(1). Disponible en: https://onlinelibrary.wiley.com/doi/abs/10.1002/gps.5564
dc.relation.referencesGardener H, Wright CB, Rundek T, Sacco RL. Brain health and shared risk factors for dementia and stroke. Nat Rev Neurol. noviembre de 2015;11(11):651-7.
dc.relation.referencesSherwin E, Dinan TG, Cryan JF. Recent developments in understanding the role of the gut microbiota in brain health and disease. Annals of the New York Academy of Sciences. 2018;1420(1):5-25.
dc.relation.referencesAvan A, Hachinski V, the Brain Health Learn and Act Group. Brain health: Key to health, productivity, and well-being. Alzheimer’s & Dementia. 2022;18(7):1396-407.
dc.relation.referencesMehta UM, Bhagyavathi HD, Thirthalli J, Kumar KJ, Gangadhar BN. Neurocognitive predictors of social cognition in remitted schizophrenia. Psychiatry Research. 30 de octubre de 2014;219(2):268-74.
dc.relation.referencesSpreng RN. Examining the role of memory in social cognition. Frontiers in Psychology [Internet]. 2013 [citado 9 de marzo de 2023];4. Disponible en: https://www.frontiersin.org/articles/10.3389/fpsyg.2013.00437
dc.relation.referencesLean RE, Constantino-Pettit A, Gorham LS, Herzberg MP, Anaya B, Rogers CE, et al. Social Determinants of Health, the developing brain, and risk and resilience for psychopathology. Neuropsychopharmacol. 16 de julio de 2025;1-18.
dc.relation.referencesVaidya N, Marquand AF, Nees F, Siehl S, Schumann G. The impact of psychosocial adversity on brain and behaviour: an overview of existing knowledge and directions for future research. Mol Psychiatry. octubre de 2024;29(10):3245-67.
dc.relation.referencesRost NS, Salinas J, Jordan JT, Banwell B, Correa DJ, Said RR, et al. The Brain Health Imperative in the 21st Century—A Call to Action. Neurology. 26 de septiembre de 2023;101(13):570-9.
dc.relation.referencesCaviedes A, Orellana P, Ávila-Rincón Cristian, Ibañez A, Corley M, Santamaria-Garcia H, et al. Epigenetics of dementia remains unraveled in Latin American and Caribbean populations: A call for collaborative efforts. Alzheimer’s & Dementia
dc.relation.referencesBell V, Méndez F, Martínez C, Palma PP, Bosch M. Characteristics of the Colombian armed conflict and the mental health of civilians living in active conflict zones. Conflict and Health. 21 de noviembre de 2012;6(1):10.
dc.relation.referencesBell CG, Lowe R, Adams PD, Baccarelli AA, Beck S, Bell JT, et al. DNA methylation aging clocks: challenges and recommendations. Genome Biol. 25 de noviembre de 2019;20:249.
dc.relation.referencesMarroquín Rivera A, Rincón Rodríguez CJ, Padilla-Muñoz A, Gómez-Restrepo C. Mental health in adolescents displaced by the armed conflict: findings from the Colombian national mental health survey. Child and Adolescent Psychiatry and Mental Health. 19 de mayo de 2020;14(1):23.
dc.relation.referencesTamayo-Agudelo W, Bell V. Armed conflict and mental health in Colombia. BJPsych Int. mayo de 2019;16(2):40-2.
dc.relation.referencesAl Aboud NM, Tupper C, Jialal I. Genetics, Epigenetic Mechanism. En: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 [citado 7 de febrero de 2023]. Disponible en: http://www.ncbi.nlm.nih.gov/books/NBK532999/
dc.relation.referencesLoyfer N, Magenheim J, Peretz A, Cann G, Bredno J, Klochendler A, et al. A DNA methylation atlas of normal human cell types. Nature. enero de 2023;613(7943):355-64.
dc.relation.referencesBollati V, Baccarelli A. Environmental epigenetics. Heredity. julio de 2010;105(1):105-12.
dc.relation.referencesFischle W. Molecular mechanisms of histone modification function. Biochim Biophys Acta. agosto de 2014;1839(8):621-2.
dc.relation.referencesWei JW, Huang K, Yang C, Kang CS. Non-coding RNAs as regulators in epigenetics (Review). Oncol Rep. enero de 2017;37(1):3-9.
dc.relation.referencesChervova O, Panteleeva K, Chernysheva E, Widayati TA, Baronik ŽF, Hrbková N, et al. Breaking new ground on human health and well-being with epigenetic clocks: A systematic review and meta-analysis of epigenetic age acceleration associations. Ageing Research Reviews. 1 de diciembre de 2024;102:102552.
dc.relation.referencesZhang L, Lu Q, Chang C. Epigenetics in Health and Disease. Adv Exp Med Biol. 2020;1253:3-55.
dc.relation.referencesEvans L, Engelman M, Mikulas A, Malecki K. How are social determinants of health integrated into epigenetic research? A systematic review. Social Science & Medicine. 1 de marzo de 2021;273:113738.
dc.relation.referencesLancet T. Brain health and its social determinants. The Lancet. 18 de septiembre de 2021;398(10305):1021.
dc.relation.referencesMarmot, Wilkinson. Social Determinants of Health | Oxford Academic [Internet]. 2005 [citado 9 de marzo de 2023]. Disponible en: https://academic.oup.com/book/9987
dc.relation.referencesNotterman DA, Mitchell C. Epigenetics and Understanding the Impact of Social Determinants of Health. Pediatr Clin North Am. octubre de 2015;62(5):1227-40.
dc.relation.referencesMcCrory C, Fiorito G, O’Halloran AM, Polidoro S, Vineis P, Kenny RA. Early life adversity and age acceleration at mid-life and older ages indexed using the next-generation GrimAge and Pace of Aging epigenetic clocks. Psychoneuroendocrinology. marzo de 2022;137:105643.
dc.relation.referencesSumner JA, Gambazza S, Gao X, Baccarelli AA, Uddin M, McLaughlin KA. Epigenetics of early-life adversity in youth: cross-sectional and longitudinal associations. Clinical Epigenetics. 8 de abril de 2022;14(1):48.
dc.relation.referencesCrimmins EM, Thyagarajan B, Levine ME, Weir DR, Faul J. Associations of Age, Sex, Race/Ethnicity, and Education With 13 Epigenetic Clocks in a Nationally Representative U.S. Sample: The Health and Retirement Study. J Gerontol A Biol Sci Med Sci. 22 de mayo de 2021;76(6):1117-23.
dc.relation.referencesMcDade TW, Ryan CP, Jones MJ, Hoke MK, Borja J, Miller GE, et al. Genome-wide analysis of DNA methylation in relation to socioeconomic status during development and early adulthood. Am J Phys Anthropol. mayo de 2019;169(1):3-11.
dc.relation.referencesFiorito G, Polidoro S, Dugué PA, Kivimaki M, Ponzi E, Matullo G, et al. Social adversity and epigenetic aging: a multi-cohort study on socioeconomic differences in peripheral blood DNA methylation. Sci Rep. 24 de noviembre de 2017;7(1):16266.
dc.relation.referencesJanusek LW, Tell D, Gaylord-Harden N, Mathews HL. Relationship of childhood adversity and neighborhood violence to a proinflammatory phenotype in emerging adult African American men: An epigenetic link. Brain, Behavior, and Immunity. 1 de febrero de 2017;60:126-35.
dc.relation.referencesMulligan CJ, Quinn EB, Hamadmad D, Dutton CL, Nevell L, Binder AM, et al. Epigenetic signatures of intergenerational exposure to violence in three generations of Syrian refugees. Sci Rep. 27 de febrero de 2025;15(1):5945.
dc.relation.referencesdos Santos Oliveira NC, Katrinli S, de Assis SG, Smith AK, Serpeloni F. Community and domestic violence are associated with DNA methylation GrimAge acceleration and heart rate variability in adolescents. Eur J Psychotraumatol. 2023;14(2):2202054.
dc.relation.referencesKatrinli S, Smith AK, Drury SS, Covault J, Ford JD, Singh V, et al. Cumulative stress, PTSD, and emotion dysregulation during pregnancy and epigenetic age acceleration in Hispanic mothers and their newborn infants. Epigenetics. 31 de diciembre de 2023;18(1):2231722.
dc.relation.referencesDauncey MJ. Recent advances in nutrition, genes and brain health. Proc Nutr Soc. noviembre de 2012;71(4):581-91.
dc.relation.referencesDelgado-Gallén S, Soler MD, Albu S, Pachón-García C, Alviárez-Schulze V, Solana-Sánchez J, et al. Cognitive Reserve as a Protective Factor of Mental Health in Middle-Aged Adults Affected by Chronic Pain. Front Psychol. 2021;12:752623.
dc.relation.referencesSteinbusch. Epigenetic changes and brainstem dysfunction in neuropsychiatric disorders – AD/PD/Anx | Neurology Conferences 2017 | Neuroscience Conferences | Neurology Congress 2017 [Internet]. 2017 [citado 4 de abril de 2023]. Disponible en: https://neurologycongress.com/program/scientific-program/2017/epigenetic-changes-and-brainstem-dysfunction-in-neuropsychiatric-disorders-ad-pd-anx
dc.relation.referencesTeschendorff AE, Horvath S. Epigenetic ageing clocks: statistical methods and emerging computational challenges. Nat Rev Genet. mayo de 2025;26(5):350-68.
dc.relation.referencesLu AT, Seeboth A, Tsai PC, Sun D, Quach A, Reiner AP, et al. DNA methylation-based estimator of telomere length. Aging (Albany NY). 18 de agosto de 2019;11(16):5895-923.
dc.relation.referencesGaragnani P, Bacalini MG, Pirazzini C, Gori D, Giuliani C, Mari D, et al. Methylation of ELOVL2 gene as a new epigenetic marker of age. Aging Cell. 2012;11(6):1132-4.
dc.relation.referencesHorvath S. DNA methylation age of human tissues and cell types. Genome Biol. 2013;14(10):R115.
dc.relation.referencesHorvath S, Levine AJ. HIV-1 Infection Accelerates Age According to the Epigenetic Clock. The Journal of Infectious Diseases. 15 de noviembre de 2015;212(10):1563-73.
dc.relation.referencesMcCartney DL, Hillary RF, Stevenson AJ, Ritchie SJ, Walker RM, Zhang Q, et al. Epigenetic prediction of complex traits and death. Genome Biology. 27 de septiembre de 2018;19(1):136.
dc.relation.referencesOblak L, van der Zaag J, Higgins-Chen AT, Levine ME, Boks MP. A systematic review of biological, social and environmental factors associated with epigenetic clock acceleration. Ageing Research Reviews. 1 de agosto de 2021;69:101348.
dc.relation.referencesHarris KM, Levitt B, Gaydosh L, Martin C, Meyer JM, Mishra AA, et al. Sociodemographic and Lifestyle Factors and Epigenetic Aging in US Young Adults: NIMHD Social Epigenomics Program. JAMA Network Open. 29 de julio de 2024;7(7):e2427889.
dc.relation.referencesHorvath S, Oshima J, Martin GM, Lu AT, Quach A, Cohen H, et al. Epigenetic clock for skin and blood cells applied to Hutchinson Gilford Progeria Syndrome and ex vivo studies. Aging (Albany NY). 26 de julio de 2018;10(7):1758-75.
dc.relation.referencesHannum G, Guinney J, Zhao L, Zhang L, Hughes G, Sadda S, et al. Genome-wide Methylation Profiles Reveal Quantitative Views of Human Aging Rates. Mol Cell. 24 de enero de 2013;49(2):359-67.
dc.relation.referencesLei MK, Simons RL, Beach SRH, Philibert RA. Neighborhood Disadvantage and Biological Aging: Using Marginal Structural Models to Assess the Link Between Neighborhood Census Variables and Epigenetic Aging. J Gerontol B Psychol Sci Soc Sci. septiembre de 2019;74(7):e50-9.
dc.relation.referencesSimons RL, Lei MK, Beach SRH, Philibert RA, Cutrona CE, Gibbons FX, et al. Economic Hardship and Biological Weathering: The Epigenetics of Aging in a U.S. Sample of Black Women. Soc Sci Med. febrero de 2016;150:192-200.
dc.relation.referencesLevine ME, Lu AT, Quach A, Chen BH, Assimes TL, Bandinelli S, et al. An epigenetic biomarker of aging for lifespan and healthspan. Aging (Albany NY). 17 de abril de 2018;10(4):573-91.
dc.relation.referencesCao X, Li W, Wang T, Ran D, Davalos V, Planas-Serra L, et al. Accelerated biological aging in COVID-19 patients. Nat Commun. 19 de abril de 2022;13(1):2135.
dc.relation.referencesMartin CL, Ward-Caviness CK, Dhingra R, Zikry TM, Galea S, Wildman DE, et al. Neighborhood environment, social cohesion, and epigenetic aging. Aging (Albany NY). 14 de marzo de 2021;13(6):7883-99.
dc.relation.referencesLu AT, Quach A, Wilson JG, Reiner AP, Aviv A, Raj K, et al. DNA methylation GrimAge strongly predicts lifespan and healthspan. Aging (Albany NY). 21 de enero de 2019;11(2):303-27.
dc.relation.referencesPrigerson HG, Russell D, Maciejewski PK. Associations between positive and negative social experiences and epigenetic aging. Sci Rep. 1 de julio de 2025;15:22284.
dc.relation.referencesBelsky DW, Caspi A, Corcoran DL, Sugden K, Poulton R, Arseneault L, et al. DunedinPACE, a DNA methylation biomarker of the pace of aging. Deelen J, Tyler JK, Suderman M, Deelen J, editores. eLife. 14 de enero de 2022;11:e73420
dc.relation.referencesCuevas AG, Cole SW, Belsky DW, McSorley AM, Shon JM, Chang VW. Multi-discrimination exposure and biological aging: Results from the midlife in the United States study. Brain, Behavior, & Immunity - Health. 1 de agosto de 2024;39:100774.
dc.relation.referencesBourassa KJ, Halverson TF, Garrett ME, Hair L, Dennis M, Ashley-Koch AE, et al. Demographic characteristics and epigenetic biological aging among post-9/11 veterans: Associations of DunedinPACE with sex, race, and age. Psychiatry Research. 1 de junio de 2024;336:115908.
dc.relation.referencesOMS. Brain health [Internet]. 2025 [citado 23 de octubre de 2025]. Disponible en: https://www.who.int/health-topics/brain-health
dc.relation.referencesWang Y, Pan Y, Li H. What is brain health and why is it important? BMJ. 9 de octubre de 2020;371:m3683.
dc.relation.referencesIbanez A, Zimmer ER. Time to synergize mental health with brain health. Nat Ment Health. julio de 2023;1(7):441-3.
dc.relation.referencesWang Y, Pan Y, Li H. What is brain health and why is it important? BMJ. 9 de octubre de 2020;371:m3683.
dc.relation.referencesBoa Sorte Silva NC, Barha CK, Erickson KI, Kramer AF, Liu-Ambrose T. Physical exercise, cognition, and brain health in aging. Trends Neurosci. junio de 2024;47(6):402-17.
dc.relation.referencesFarina FR, Bridgeman K, Gregory S, Crivelli L, Foote IF, Jutila OEI, et al. Next generation brain health: transforming global research and public health to promote prevention of dementia and reduce its risk in young adult populations. The Lancet Healthy Longevity [Internet]. 1 de diciembre de 2024 [citado 5 de julio de 2025];5(12). Disponible en: https://www.thelancet.com/journals/lanhl/article/PIIS2666-7568(24)00191-0/fulltext
dc.relation.referencesBekdash RA. Methyl Donors, Epigenetic Alterations, and Brain Health: Understanding the Connection. Int J Mol Sci. 25 de enero de 2023;24(3):2346.
dc.relation.referencesMarshall P, Bredy TW. Cognitive neuroepigenetics: the next evolution in our understanding of the molecular mechanisms underlying learning and memory? npj Science Learn. 20 de julio de 2016;1(1):1-8.
dc.relation.referencesBarter JD, Foster TC. Aging in the Brain: New Roles of Epigenetics in Cognitive Decline. Neuroscientist. 1 de octubre de 2018;24(5):516-25.
dc.relation.referencesDay JJ, Sweatt JD. Epigenetic Mechanisms in Cognition. Neuron. junio de 2011;70(5):813-29.
dc.relation.referencesMiller G. A Role for Epigenetics in Cognition. Science. 2 de julio de 2010;329(5987):27-27.
dc.relation.referencesTang L, Liu J, Zhu Y, Duan J, Chen Y, Wei Y, et al. ANK3 Gene Polymorphism Rs10994336 Influences Executive Functions by Modulating Methylation in Patients With Bipolar Disorder. Frontiers in Neuroscience [Internet]. 2021 [citado 18 de abril de 2023];15. Disponible en: https://www.frontiersin.org/articles/10.3389/fnins.2021.682873
dc.relation.referencesShelton AL, Cornish KM, Kolbe S, Clough M, Slater HR, Li X, et al. Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females. Transl Psychiatry. diciembre de 2016;6(12):e984-e984.
dc.relation.referencesFelt JM, Yusupov N, Harrington KD, Fietz J, Zhang Z “Zach”, Sliwinski MJ, et al. Epigenetic age acceleration as a biomarker for impaired cognitive abilities in adulthood following early life adversity and psychiatric disorders. Neurobiology of Stress. 1 de noviembre de 2023;27:100577.
dc.relation.referencesBeydoun MA, Shaked D, Tajuddin SM, Weiss J, Evans MK, Zonderman AB. Accelerated epigenetic age and cognitive decline among urban-dwelling adults. Neurology. 11 de febrero de 2020;94(6):e613-25.
dc.relation.referencesRubin LH, Connelly JJ, Reilly JL, Carter CS, Drogos LL, Pournajafi-Nazarloo H, et al. Sex and diagnosis specific associations between DNA methylation of the oxytocin receptor gene with emotion processing and temporal-limbic and prefrontal brain volumes in psychotic disorders. Biol Psychiatry Cogn Neurosci Neuroimaging. 1 de marzo de 2016;1(2):141-51.
dc.relation.referencesReuter M, Felten A, Zamoscik V, Bravo R, Ugartemendia L, Kirsch P, et al. Genetic and epigenetic serotonergic markers predict the ability to recognize mental states. Physiol Behav. 1 de diciembre de 2020;227:113143.
dc.relation.referencesOchiai K, Nishitani S, Yao A, Hiraoka D, Kawata NYS, Suzuki S, et al. Behavioral and emotional difficulties in maltreated children: Associations with epigenetic clock changes and visual attention to social cues. PLOS ONE. 30 de mayo de 2025;20(5):e0321952.
dc.relation.referencesXiao L, Cheng H, Cai H, Wei Y, Zan G, Feng X, et al. Associations of Heavy Metals with Activities of Daily Living Disability: An Epigenome-Wide View of DNA Methylation and Mediation Analysis. Environ Health Perspect. 29 de agosto de 2022;130(8):087009.
dc.relation.referencesGuintivano J, Kaminsky ZA. Role of epigenetic factors in the development of mental illness throughout life. Neuroscience Research. 1 de enero de 2016;102:56-66.
dc.relation.referencesNestler EJ, Peña CJ, Kundakovic M, Mitchell A, Akbarian S. Epigenetic Basis of Mental Illness. Neuroscientist. octubre de 2016;22(5):447-63.
dc.relation.referencesNöthling J, Malan-Müller S, Abrahams N, Hemmings SMJ, Seedat S. Epigenetic alterations associated with childhood trauma and adult mental health outcomes: A systematic review. The World Journal of Biological Psychiatry. 8 de agosto de 2020;21(7):493-512.
dc.relation.referencesYusupov N, Dieckmann L, Erhart M, Sauer S, Rex-Haffner M, Kopf-Beck J, et al. Transdiagnostic evaluation of epigenetic age acceleration and burden of psychiatric disorders. Neuropsychopharmacol. agosto de 2023;48(9):1409-17.
dc.relation.referencesHaas BW, Filkowski MM, Cochran RN, Denison L, Ishak A, Nishitani S, et al. Epigenetic modification of OXT and human sociability. Proceedings of the National Academy of Sciences. 5 de julio de 2016;113(27):E3816-23.
dc.relation.referencesLam F, Chu J, Choi JS, Cao C, Hitchens TK, Silverman SK, et al. Epigenetic MRI: Noninvasive imaging of DNA methylation in the brain. Proceedings of the National Academy of Sciences. 8 de marzo de 2022;119(10):e2119891119.
dc.relation.referencesLancaster K, Morris JP, Connelly JJ. Neuroimaging Epigenetics: Challenges and Recommendations for Best Practices. Neuroscience. 1 de febrero de 2018;370:88-100.
dc.relation.referencesWheater ENW, Stoye DQ, Cox SR, Wardlaw JM, Drake AJ, Bastin ME, et al. DNA methylation and brain structure and function across the life course: A systematic review. Neuroscience & Biobehavioral Reviews. 1 de junio de 2020;113:133-56.
dc.relation.referencesSwartz JR, Hariri AR, Williamson DE. An epigenetic mechanism links socioeconomic status to changes in depression-related brain function in high-risk adolescents. Mol Psychiatry. febrero de 2017;22(2):209-14.
dc.relation.referencesGraves AJ, Danoff JS, Kim M, Brindley SR, Skyberg AM, Giamberardino SN, et al. Accelerated epigenetic age is associated with whole-brain functional connectivity and impaired cognitive performance in older adults. Sci Rep. 26 de abril de 2024;14(1):9646.
dc.relation.referencesRöhr S, Pabst A, Baber R, Engel C, Glaesmer H, Hinz A, et al. Social determinants and lifestyle factors for brain health: implications for risk reduction of cognitive decline and dementia. Sci Rep. 28 de julio de 2022;12(1):12965.
dc.relation.referencesBorçoi AR, Mendes SO, Gasparini dos Santos J, Mota de Oliveira M, Moreno IAA, Freitas FV, et al. Risk factors for depression in adults: NR3C1 DNA methylation and lifestyle association. Journal of Psychiatric Research. 1 de febrero de 2020;121:24-30.
dc.relation.referencesLiu L, Wu J, Qing L, Li J, Yang H, Ji A, et al. DNA Methylation Analysis of the NR3C1 Gene in Patients with Schizophrenia. J Mol Neurosci. 1 de agosto de 2020;70(8):1177-85.
dc.relation.referencesMiller O, Shakespeare-Finch J, Bruenig D, Mehta D. DNA methylation of NR3C1 and FKBP5 is associated with posttraumatic stress disorder, posttraumatic growth, and resilience. Psychological Trauma: Theory, Research, Practice, and Policy. 2020;12:750-5.
dc.relation.referencesFiorito G, Pedron S, Ochoa-Rosales C, McCrory C, Polidoro S, Zhang Y, et al. The Role of Epigenetic Clocks in Explaining Educational Inequalities in Mortality: A Multicohort Study and Meta-analysis. The Journals of Gerontology: Series A. 1 de septiembre de 2022;77(9):1750-9.
dc.relation.referencesMariani Wigley ILC, Mascheroni E, Peruzzo D, Giorda R, Bonichini S, Montirosso R. Neuroimaging and DNA Methylation: An Innovative Approach to Study the Effects of Early Life Stress on Developmental Plasticity. Front Psychol. 17 de mayo de 2021;12:672786.
dc.relation.referencesFujisawa TX, Nishitani S, Takiguchi S, Shimada K, Smith AK, Tomoda A. Oxytocin receptor DNA methylation and alterations of brain volumes in maltreated children. Neuropsychopharmacol. noviembre de 2019;44(12):2045-53.
dc.relation.referencesRaza Z, Hussain SF, Foster VS, Wall J, Coffey PJ, Martin JF, et al. Exposure to war and conflict: The individual and inherited epigenetic effects on health, with a focus on post-traumatic stress disorder. Frontiers in Epidemiology [Internet]. 2023 [citado 12 de abril de 2023];3. Disponible en: https://www.frontiersin.org/articles/10.3389/fepid.2023.1066158
dc.relation.referencesKertes DA, Bhatt SS, Kamin HS, Hughes DA, Rodney NC, Mulligan CJ. BNDF methylation in mothers and newborns is associated with maternal exposure to war trauma. Clinical Epigenetics. 30 de junio de 2017;9(1):68.
dc.relation.referencesKim TY, Kim SJ, Chung HG, Choi JH, Kim SH, Kang JI. Epigenetic alterations of the BDNF gene in combat-related post-traumatic stress disorder. Acta Psychiatrica Scandinavica. 2017;135(2):170-9.
dc.relation.referencesSmeeth D, Ecker S, Chervova O, McEwen F, Karam E, Beck S, et al. War Exposure and DNA Methylation in Syrian Refugee Children and Adolescents. JAMA Psychiatry. 1 de febrero de 2025;82(2):191-200.
dc.relation.referencesMcDONALD CC, Richmond TR. The relationship between community violence exposure and mental health symptoms in urban adolescents. Journal of Psychiatric and Mental Health Nursing. 2008;15(10):833-49.
dc.relation.referencesPerkins S, Graham-Bermann S. Violence exposure and the development of school-related functioning: Mental health, neurocognition, and learning. Aggression and Violent Behavior. 1 de enero de 2012;17(1):89-98.
dc.relation.referencesScoglio AAJ, Salhi C. Violence Exposure and Mental Health Among Resettled Refugees: A Systematic Review. Trauma Violence Abuse. diciembre de 2021;22(5):1192-208.
dc.relation.referencesButler O, Yang X, Laube C, Kühn S, Immordino‐Yang MH. Community violence exposure correlates with smaller gray matter volume and lower IQ in urban adolescents. Hum Brain Mapp. 15 de febrero de 2018;39(5):2088-97
dc.relation.referencesBogliacino F, Grimalda G, Ortoleva P, Ring P. Exposure to and recall of violence reduce short-term memory and cognitive control. Proceedings of the National Academy of Sciences. 8 de agosto de 2017;114(32):8505-10.
dc.relation.referencesOberth C, Goulter N, McMahon RJ. The comparative and cumulative impact of different forms of violence exposure during childhood and adolescence on long-term adult outcomes. Dev Psychopathol. octubre de 2022;34(4):1313-28.
dc.relation.referencesLöfving-Gupta S, Willebrand M, Koposov R, Blatný M, Hrdlička M, Schwab-Stone M, et al. Community violence exposure and substance use: cross-cultural and gender perspectives. Eur Child Adolesc Psychiatry. 2018;27(4):493-500.
dc.relation.referencesDaniels JP. Mental health in post-conflict Colombia. The Lancet Psychiatry. 1 de marzo de 2018;5(3):199.
dc.relation.referencesTrujillo S, Giraldo LS, López JD, Acosta A, Trujillo N. Mental health outcomes in communities exposed to Armed Conflict Experiences. BMC Psychology. 27 de agosto de 2021;9(1):127.
dc.relation.referencesTobón C, Aguirre-Acevedo DC, Velilla L, Duque J, Ramos CP, Pineda D. [Psychiatric, Cognitive and Emotional Profile in Ex-combatants of Illegal Armed Groups in Colombia]. Rev Colomb Psiquiatr. 2016;45(1):28-36
dc.relation.referencesTrujillo SP, Valencia S, Trujillo N, Ugarriza JE, Rodríguez MV, Rendón J, et al. Atypical Modulations of N170 Component during Emotional Processing and Their Links to Social Behaviors in Ex-combatants. Frontiers in Human Neuroscience [Internet]. 2017 [citado 13 de abril de 2023];11. Disponible en: https://www.frontiersin.org/articles/10.3389/fnhum.2017.00244
dc.relation.referencesTrujillo SP, Trujillo N, Ugarriza JE, Uribe LH, Pineda DA, Aguirre-Acevedo DC, et al. How empathic are war veterans? An examination of the psychological impacts of combat exposure. Peace and Conflict: Journal of Peace Psychology. 2017;23:422-6.
dc.relation.referencesGarcia-Barrera MA, Karr JE, Trujillo-Orrego N, Trujillo-Orrego S, Pineda DA. Evaluating empathy in Colombian ex-combatants: Examination of the internal structure of the Interpersonal Reactivity Index (IRI) in Spanish. Psychol Assess. enero de 2017;29(1):116-22.
dc.relation.referencesPalacios-Perdomo H, Acosta-Ramírez N. Perceptions of adolescent pregnancy in the rural context and the Colombian armed conflict: a qualitative approach based on social determination of health. Int J Equity Health. 20 de octubre de 2021;20(1):232.
dc.relation.referencesBaez S, Santamaría-García H, Ibáñez A. Disarming Ex-Combatants’ Minds: Toward Situated Reintegration Process in Post-conflict Colombia. Frontiers in Psychology [Internet]. 2019 [citado 14 de abril de 2023];10. Disponible en: https://www.frontiersin.org/articles/10.3389/fpsyg.2019.00073
dc.relation.referencesSantamaría-García H, Baez S, Aponte-Canencio DM, Pasciarello GO, Donnelly-Kehoe PA, Maggiotti G, et al. Uncovering social-contextual and individual mental health factors associated with violence via computational inference. Patterns. 12 de febrero de 2021;2(2):100176.
dc.relation.referencesSmeeth D, McEwen FS, Popham CM, Karam EG, Fayyad J, Saab D, et al. War exposure, post-traumatic stress symptoms and hair cortisol concentrations in Syrian refugee children. Mol Psychiatry. febrero de 2023;28(2):647-56.
dc.relation.referencesvon Majewski K, Kraus O, Rhein C, Lieb M, Erim Y, Rohleder N. Acute stress responses of autonomous nervous system, HPA axis, and inflammatory system in posttraumatic stress disorder. Transl Psychiatry. 3 de febrero de 2023;13(1):36.
dc.relation.referencesDunlavey CJ. Introduction to the Hypothalamic-Pituitary-Adrenal Axis: Healthy and Dysregulated Stress Responses, Developmental Stress and Neurodegeneration. J Undergrad Neurosci Educ. 15 de junio de 2018;16(2):R59-60.
dc.relation.referencesGądek-Michalska A, Spyrka J, Rachwalska P, Tadeusz J, Bugajski J. Influence of chronic stress on brain corticosteroid receptors and HPA axis activity. Pharmacological Reports. 1 de septiembre de 2013;65(5):1163-75.
dc.relation.referencesKatrinli S, Oliveira NCS, Felger JC, Michopoulos V, Smith AK. The role of the immune system in posttraumatic stress disorder. Transl Psychiatry. 4 de agosto de 2022;12:313.
dc.relation.referencesMuhie S, Gautam A, Yang R, Misganaw B, Daigle BJ, Mellon SH, et al. Molecular signatures of post-traumatic stress disorder in war-zone-exposed veteran and active-duty soldiers. CR Med [Internet]. 16 de mayo de 2023 [citado 2 de julio de 2025];4(5). Disponible en: https://www.cell.com/cell-reports-medicine/abstract/S2666-3791(23)00159-3
dc.relation.referencesYitshak-Sade M, Mendelson N, Novack V, Codish S, Liberty IF. The association between an increase in glucose levels and armed conflict-related stress: A population-based study. Sci Rep. 3 de febrero de 2020;10(1):1710.
dc.relation.referencesSuglia SF, Koenen KC, Boynton-Jarrett R, Chan PS, Clark CJ, Danese A, et al. Childhood and Adolescent Adversity and Cardiometabolic Outcomes: A Scientific Statement From the American Heart Association. Circulation. 30 de enero de 2018;137(5):e15-28.
dc.relation.referencesAmsalem D, Haim-Nachum S, Lazarov A, Levi-Belz Y, Markowitz JC, Bergman M, et al. The effects of war-related experiences on mental health symptoms of individuals living in conflict zones: a longitudinal study. Sci Rep. 6 de enero de 2025;15(1):889.
dc.relation.referencesBogic M, Njoku A, Priebe S. Long-term mental health of war-refugees: a systematic literature review. BMC Int Health Hum Rights. 28 de octubre de 2015;15(1):29.
dc.relation.referencesKoen N, Jones MJ, Nhapi RT, Lake MT, Donald KA, Barnett W, et al. Maternal psychosocial risk factors and child gestational epigenetic age in a South African birth cohort study. Transl Psychiatry. 2 de julio de 2021;11:358.
dc.relation.referencesHammamieh R, Chakraborty N, Gautam A, Muhie S, Yang R, Donohue D, et al. Whole-genome DNA methylation status associated with clinical PTSD measures of OIF/OEF veterans. Transl Psychiatry. 11 de julio de 2017;7(7):e1169.
dc.relation.referencesWang Z, Wilson CM, Ge Y, Nemes J, LaValle C, Boutté A, et al. DNA Methylation Patterns of Chronic Explosive Breaching in U.S. Military Warfighters. Front Neurol [Internet]. 23 de octubre de 2020 [citado 14 de julio de 2025];11. Disponible en: https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2020.01010/full
dc.relation.referencesWang Z, Wilson CM, Mendelev N, Ge Y, Galfalvy H, Elder G, et al. Acute and Chronic Molecular Signatures and Associated Symptoms of Blast Exposure in Military Breachers. J Neurotrauma. 15 de mayo de 2020;37(10):1221-32.
dc.relation.referencesYang R, Gautam A, Getnet D, Daigle BJ, Miller S, Misganaw B, et al. Epigenetic biotypes of post-traumatic stress disorder in war-zone exposed veteran and active duty males. Mol Psychiatry. agosto de 2021;26(8):4300-14.
dc.relation.referencesMehta D, Bruenig D, Pierce J, Sathyanarayanan A, Stringfellow R, Miller O, et al. Recalibrating the epigenetic clock after exposure to trauma: The role of risk and protective psychosocial factors. Journal of Psychiatric Research. 1 de mayo de 2022;149:374-81.
dc.relation.referencesNasreddine ZS, Phillips NA, Bédirian V, Charbonneau S, Whitehead V, Collin I, et al. The Montreal Cognitive Assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. abril de 2005;53(4):695-9.
dc.relation.referencesPedraza OL, Salazar AM, Sierra FA, Soler D, Castro J, Castillo P, et al. Contabilidad, validez de criterio y discriminante del Montreal Cognitive Assessment (MoCA) test, en un grupo de adultos de Bogotá. Acta Medica Colombiana. diciembre de 2016;41(4):221-8.
dc.relation.referencesNicotra A, Maestri G, Salvadori E, Pantoni L. Brain health assessment. An exploratory review of tools related to its cognitive dimension. Cerebral Circulation - Cognition and Behavior. 1 de enero de 2024;6:100188.
dc.relation.referencesLee A, Shah S, Atha K, Indoe P, Mahmoud N, Niblett G, et al. Brain health measurement: a scoping review. BMJ Open. 10 de febrero de 2024;14(2):e080334.
dc.relation.referencesMuñoz E, Hyun J, Diaz JA, Scott SB, Sliwinski MJ. Exposure to neighborhood violence, and laboratory-based and ambulatory cognitive task performance in adulthood. Soc Sci Med. mayo de 2024;348:116807.
dc.relation.referencesChicoine AX, Chertkow H, Tardif JC, Busseuil D, D’Antono B. Childhood maltreatment, cognitive performance, and cognitive decline in middle-aged and older adults with chronic disease: A prospective study. Journal of Psychosomatic Research. 1 de diciembre de 2024;187:111965.
dc.relation.referencesSaadi A, Cruz-Gonzalez M, Hwang A, Cohen L, Alegria M. Associations between Trauma, Sleep and Cognitive Impairment among Latino and Asian Older Adults. J Am Geriatr Soc. abril de 2021;69(4):1019-26.
dc.relation.referencesTorralva T, Roca M, Gleichgerrcht E, Bekinschtein T, Manes F. A neuropsychological battery to detect specific executive and social cognitive impairments in early frontotemporal dementia. Brain. mayo de 2009;132(Pt 5):1299-309.
dc.relation.referencesTorralva T, Roca M, Gleichgerrcht E, López P, Manes F. INECO Frontal Screening (IFS): a brief, sensitive, and specific tool to assess executive functions in dementia. J Int Neuropsychol Soc. septiembre de 2009;15(5):777-86.
dc.relation.referencesBaez S, Ibanez A, Gleichgerrcht E, Perez A, Roca M, Manes F, et al. The utility of IFS (INECO Frontal Screening) for the detection of executive dysfunction in adults with bipolar disorder and ADHD. Psychiatry Res. 15 de mayo de 2014;216(2):269-76.
dc.relation.referencesSatarian F, Mehri A, Jalaie S. Correlation of INECO Frontal Screening With Verbal Fluency Tasks and MMSE in Persian Healthy Population | Journal of Modern Rehabilitation. 2024 [citado 28 de octubre de 2025]; Disponible en: https://jmr.tums.ac.ir/index.php/jmr/article/view/147
dc.relation.referencesBaez S, Ibanez A, Gleichgerrcht E, Perez A, Roca M, Manes F, et al. The utility of IFS (INECO Frontal Screening) for the detection of executive dysfunction in adults with bipolar disorder and ADHD. Psychiatry Research. 15 de mayo de 2014;216(2):269-76.
dc.relation.referencesMoreira HS, Costa AS, Machado Á, Castro SL, Lima CF, Vicente SG. Distinguishing mild cognitive impairment from healthy aging and Alzheimer’s Disease: The contribution of the INECO Frontal Screening (IFS). PLOS ONE. 10 de septiembre de 2019;14(9):e0221873.
dc.relation.referencesReisberg B. Functional Assessment Staging (FAST). Psychopharmacology Bulletin. 1988;24(4):653-9.
dc.relation.referencesReisberg B, Ferris SH, de Leon MJ, Crook T. The Global Deterioration Scale for assessment of primary degenerative dementia. Am J Psychiatry. septiembre de 1982;139(9):1136-9.
dc.relation.referencesOlde Rikkert MGM, Tona KD, Janssen L, Burns A, Lobo A, Robert P, et al. Validity, Reliability, and Feasibility of Clinical Staging Scales in Dementia: A Systematic Review. Am J Alzheimers Dis Other Demen. 1 de agosto de 2011;26(5):357-65.
dc.relation.referencesGiebel CM, Sutcliffe C, Challis D. Activities of daily living and quality of life across different stages of dementia: a UK study. Aging & Mental Health. 2 de enero de 2015;19(1):63-71.
dc.relation.referencesKoçak FOK, Kumral E. The relationship between dementia staging scales, cognitive-behavioral scales and functionality in patients with cognitive impairment. PLOS ONE. 2 de mayo de 2025;20(5):e0322572.
dc.relation.referencesForman T, Williams D, Jackson D, Gardner C. Race, Place, and Discrimination. En: In Perspectives on Social Problems. JAI Press; 1997. p. 231-61.
dc.relation.referencesWilliams DR, Mohammed SA. Discrimination and racial disparities in health: evidence and needed research. J Behav Med. 1 de febrero de 2009;32(1):20-47.
dc.relation.referencesClark R, Coleman AP, Novak JD. Brief report: Initial psychometric properties of the everyday discrimination scale in black adolescents. Journal of Adolescence. 1 de junio de 2004;27(3):363-8.
dc.relation.referencesLawrence JA, Kawachi I, White K, Bassett MT, Priest N, Masunga JG, et al. A systematic review and meta-analysis of the Everyday Discrimination Scale and biomarker outcomes. Psychoneuroendocrinology. 1 de agosto de 2022;142:105772
dc.relation.referencesKrueger F, Kreck B, Franke A, Andrews SR. DNA methylome analysis using short bisulfite sequencing data. Nat Methods. febrero de 2012;9(2):145-51.
dc.relation.referencesBaron RM, Kenny DA. The moderator-mediator variable distinction in social psychological research: conceptual, strategic, and statistical considerations. J Pers Soc Psychol. diciembre de 1986;51(6):1173-82.
dc.relation.referencesChang OD, Meier HCS, Maguire-Jack K, Davis-Kean P, Mitchell C. Childhood Maltreatment and Longitudinal Epigenetic Aging. [citado 19 de septiembre de 2025]; Disponible en: https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2821614
dc.relation.referencesFinegood ED, Chen E, Kish J, Vause K, Leigh AKK, Hoffer L, et al. Community Violence and Cellular and Cytokine Indicators of Inflammation In Adolescents. Psychoneuroendocrinology. mayo de 2020;115:104628.
dc.relation.referencesCarter JR, Goldstein DS. Sympathoneural and Adrenomedullary Responses to Mental Stress. Compr Physiol. enero de 2015;5(1):119-46.
dc.relation.referencesKanczkowski W, Alexaki VI, Tran N, Großklaus S, Zacharowski K, Martinez A, et al. Hypothalamo-pituitary and immune-dependent adrenal regulation during systemic inflammation. Proceedings of the National Academy of Sciences. 3 de septiembre de 2013;110(36):14801-6.
dc.relation.referencesBellavance MA, Rivest S. The HPA – Immune Axis and the Immunomodulatory Actions of Glucocorticoids in the Brain. Front Immunol. 31 de marzo de 2014;5:136.
dc.relation.referencesRing M. An Integrative Approach to HPA Axis Dysfunction: From Recognition to Recovery. The American Journal of Medicine. 1 de octubre de 2025;138(10):1451-63.
dc.relation.referencesDeng X, Liu D, Li M, He J, Fu Y. Association between systemic immune-inflammation index and insulin resistance and mortality. Sci Rep. 23 de enero de 2024;14(1):2013.
dc.relation.referencesHillary RF, Stevenson AJ, Cox SR, McCartney DL, Harris SE, Seeboth A, et al. An epigenetic predictor of death captures multi-modal measures of brain health. Mol Psychiatry. agosto de 2021;26(8):3806-16.
dc.relation.referencesFriedman NP, Robbins TW. The role of prefrontal cortex in cognitive control and executive function. Neuropsychopharmacol. enero de 2022;47(1):72-89.
dc.relation.referencesHarvanek ZM, Kudinova AY, Wong SA, Xu K, Brick L, Daniels T, et al. Childhood Adversity, Accelerated GrimAge, and Associated Health Consequences. J Behav Med. octubre de 2024;47(5):913-26
dc.relation.referencesChang OD, Meier HCS, Maguire-Jack K, Davis-Kean P, Mitchell C. Childhood Maltreatment and Longitudinal Epigenetic Aging: NIMHD Social Epigenomics Program. JAMA Network Open. 29 de julio de 2024;7(7):e2421877.
dc.relation.referencesBalaj M, Henson CA, Aronsson A, Aravkin A, Beck K, Degail C, et al. Effects of education on adult mortality: a global systematic review and meta-analysis. The Lancet Public Health. 1 de marzo de 2024;9(3):e155-65.
dc.relation.referencesMaurel M, Castagné R, Berger E, Bochud M, Chadeau-Hyam M, Fraga S, et al. Patterning of educational attainment across inflammatory markers: Findings from a multi-cohort study. Brain Behav Immun. noviembre de 2020;90:303-10.
dc.relation.referencesStevenson AJ, McCartney DL, Hillary RF, Redmond P, Taylor AM, Zhang Q, et al. Childhood intelligence attenuates the association between biological ageing and health outcomes in later life. Transl Psychiatry. 28 de noviembre de 2019;9(1):323.
dc.relation.referencesKorous KM, Surachman A, Rogers CR, Cuevas AG. Parental Education and Epigenetic Aging in Middle-Aged and Older Adults in the United States: A Life Course Perspective. Soc Sci Med. septiembre de 2023;333:116173.
dc.relation.referencesGomez-Verjan JC, Esparza-Aguilar M, Martín-Martín V, Salazar-Perez C, Cadena-Trejo C, Gutierrez-Robledo LM, et al. Years of Schooling Could Reduce Epigenetic Aging: A Study of a Mexican Cohort. Genes. septiembre de 2021;12(9):1408
dc.relation.referencesO’Shea D, Tremont G, Drake JD. DNA methylation «GrimAge» acceleration mediates sex differences in verbal learning and memory: Findings from the health and retirement study. Alzheimer’s & Dementia. 2021;17(S5):e058373.
dc.relation.referencesWare EB, Higgins Tejera C, Wang H, Harris S, Fisher JD, Bakulski KM. Interplay of education and DNA methylation age on cognitive impairment: insights from the Health and Retirement Study. Geroscience. junio de 2025;47(3):3177-90
dc.relation.referencesMagnus MC, Lee Y, Carlsen EØ, Arge LA, Jugessur A, Kvalvik LG, et al. Parental epigenetic age acceleration and risk of adverse birth outcomes: the Norwegian mother, father and child cohort study. BMC Med. 25 de noviembre de 2024;22(1):554.
dc.relation.referencesMartínez JH, López ME, Ariza P, Chavez M, Pineda-Pardo JA, López-Sanz D, et al. Functional brain networks reveal the existence of cognitive reserve and the interplay between network topology and dynamics. Sci Rep. 12 de julio de 2018;8(1):10525.
dc.relation.referencesTemp AGM, Tarakdjian GN, Kasper E, Machts J, Kaufmann J, Vielhaber S, et al. The role of cognitive and brain reserve in the clinical presentation and progression of amyotrophic lateral sclerosis. Sci Rep. 20 de junio de 2025;15(1):20232.
dc.relation.referencesGarcía-Moreno JA, Cañadas F, García-García J, Roldan-Tapia MD. Cognitive reserve as a protective variable against psychological stress in individuals with high anxiety. International Journal of Stress Management. 2024;31(3):302-12.
dc.relation.referencesPorricelli D, Tecilla M, Pucci V, Di Rosa E, Mondini S, Cappelletti M. Cognitive reserve modulates mental health in adulthood. Aging Clin Exp Res. 2024;36(1):139
dc.relation.referencesSclan SG, Reisberg B. Functional Assessment Staging (FAST) in Alzheimer’s Disease: Reliability, Validity, and Ordinality. International Psychogeriatrics. 1 de abril de 1992;4(3):55-69.
dc.relation.referencesRoyall DR, Lauterbach EC, Cummings JL, Reeve A, Rummans TA, Kaufer DI, et al. Executive control function: a review of its promise and challenges for clinical research. A report from the Committee on Research of the American Neuropsychiatric Association. J Neuropsychiatry Clin Neurosci. 2002;14(4):377-405.
dc.relation.referencesChen SW, Keglovits M, Devine M, Stark S. Sociodemographic Differences in Respondent Preferences for Survey Formats: Sampling Bias and Potential Threats to External Validity. Arch Rehabil Res Clin Transl. 13 de diciembre de 2021;4(1):100175.
dc.relation.referencesMunafò MR, Tilling K, Taylor AE, Evans DM, Davey Smith G. Collider scope: when selection bias can substantially influence observed associations. Int J Epidemiol. 1 de febrero de 2018;47(1):226-35.
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.rights.licenseAtribución-CompartirIgual 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-sa/4.0/
dc.subject.ddc610 - Medicina y salud::616 - Enfermedades
dc.subject.decsFunción Ejecutivaspa
dc.subject.decsExecutive Functioneng
dc.subject.decsEstudios Transversalesspa
dc.subject.decsCross-Sectional Studieseng
dc.subject.decsEpigénesis Genéticaspa
dc.subject.decsEpigenesis, Geneticeng
dc.subject.proposalEpigenetic ageeng
dc.subject.proposalRelojes epigeneticosspa
dc.subject.proposalEpigenetic clockseng
dc.subject.proposalMetilación del ADNspa
dc.subject.proposalDNA methylationeng
dc.subject.proposalConflicto armadospa
dc.subject.proposalArmed clonflicteng
dc.subject.proposalSalud cerebralspa
dc.subject.proposalBrain healtheng
dc.subject.proposalCogniciónspa
dc.subject.proposalCognitioneng
dc.titleAnálisis de los niveles de metilación del ADN relacionados con la exposición a la violencia y su impacto en medidas de salud cerebral en una muestra de adultos colombianosspa
dc.title.translatedAnalysis of DNA methylation levels associated with exposure to violence and their impact on brain health measures in a sample of Colombian adultseng
dc.typeTrabajo de grado - Maestría
dc.type.coarhttp://purl.org/coar/resource_type/c_bdcc
dc.type.coarversionhttp://purl.org/coar/version/c_ab4af688f83e57aa
dc.type.contentText
dc.type.driverinfo:eu-repo/semantics/masterThesis
dc.type.redcolhttp://purl.org/redcol/resource_type/TM
dc.type.versioninfo:eu-repo/semantics/acceptedVersion
dcterms.audience.professionaldevelopmentEstudiantes
dcterms.audience.professionaldevelopmentInvestigadores
oaire.accessrightshttp://purl.org/coar/access_right/c_abf2

Archivos

Bloque original

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
Tesis cristian avila.pdf
Tamaño:
756.1 KB
Formato:
Adobe Portable Document Format
Descripción:
Tesis de Maestría en Neurociencias

Bloque de licencias

Mostrando 1 - 1 de 1
Cargando...
Miniatura
Nombre:
license.txt
Tamaño:
5.74 KB
Formato:
Item-specific license agreed upon to submission
Descripción: