Childhood Social Isolation as a Predictor of Retinal Neuronal Thickness in Middle Age: A Lifecourse Birth Cohort Study.


Journal

Psychosomatic medicine
ISSN: 1534-7796
Titre abrégé: Psychosom Med
Pays: United States
ID NLM: 0376505

Informations de publication

Date de publication:
01 04 2023
Historique:
pmc-release: 01 04 2024
medline: 5 4 2023
pubmed: 18 2 2023
entrez: 17 2 2023
Statut: ppublish

Résumé

We investigated whether childhood social isolation was associated with retinal neural layer changes in adulthood, and whether this association was independent of other childhood or adulthood risk factors, including adult social isolation. Participants were members of the Dunedin Multidisciplinary Health and Development Study, a longitudinal population-based birth cohort from Aotearoa New Zealand ( n = 1037), born 1972 to 1973 and followed until age 45 years, with 94% of the living cohort still participating. Social isolation was recorded prospectively at ages 5, 7, 9, and 11 years, from teacher and parent report. Retinal nerve fiber layer (RNFL) and ganglion cell-inner plexiform layer thicknesses were measured via optical coherence tomography at age 45 years. Childhood social isolation was associated with thinner average RNFL ( B = -0.739, p = .02), nasal RNFL ( B = -1.118, p = .005), and inferior RNFL ( B = -1.524, p = .007), although only nasal RNFL remained significant after adjustment. These associations were not fully explained by other psychosocial or physical health risk factors in childhood or adulthood, nor were they mediated by adult loneliness or social support. Childhood social isolation was an independent predictor of RNFL thickness in middle age. Highlighting prospective links between childhood psychosocial adversity and retinal neuronal measures will help to inform future research into the utility of retinal neuronal thickness as a biomarker for neurodegeneration.

Identifiants

pubmed: 36800261
doi: 10.1097/PSY.0000000000001177
pii: 00006842-202304000-00005
pmc: PMC10073287
mid: NIHMS1869698
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

238-249

Subventions

Organisme : NIA NIH HHS
ID : R01 AG032282
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG049789
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG069939
Pays : United States
Organisme : Medical Research Council
ID : MR/P005918/1
Pays : United Kingdom

Informations de copyright

Copyright © 2023 by the American Psychosomatic Society.

Références

Cacioppo JT, Cacioppo S, Capitanio JP, Cole SW. The neuroendocrinology of social isolation. Annu Rev Psychol 2015;66:733–67.
Caspi A, Harrington H, Moffitt TE, Milne BJ, Poulton R. Socially isolated children 20 years later: risk of cardiovascular disease. Arch Pediatr Adolesc Med 2006;160:805–11.
Holt-Lunstad J, Smith TB, Layton JB. Social relationships and mortality risk: a meta-analytic review. PLoS Med 2010;7:e1000316.
Pantell M, Rehkopf D, Jutte D, Syme SL, Balmes J, Adler N. Social isolation: a predictor of mortality comparable to traditional clinical risk factors. Am J Public Health 2013;103:2056–62.
Hawton A, Green C, Dickens AP, Richards SH, Taylor RS, Edwards R, et al. The impact of social isolation on the health status and health-related quality of life of older people. Qual Life Res 2011;20:57–67.
Hjalmarsson S, Mood C. Do poorer youth have fewer friends? The role of household and child economic resources in adolescent school-class friendships. Child Youth Serv Rev 2015;57:201–11.
Holt-Lunstad J, Steptoe A. Social isolation: an underappreciated determinant of physical health. Curr Opin Psychol 2022;43:232–7.
Cacioppo JT, Hawkley LC, Norman GJ, Berntson GG. Social isolation. Ann N Y Acad Sci 2011;1231:17–22.
National Academies of Sciences, Engineering, and Medicine, Division of Behavioral and Social Sciences and Education, Health and Medicine Division, Board on Behavioral, Cognitive, and Sensory Sciences, Board on Health Sciences Policy, Committee on the Health and Medical Dimensions of Social Isolation and Loneliness in Older Adults. Health Impacts of Social Isolation and Loneliness on Morbidity and Quality of Life. In: Social Isolation and Loneliness in Older Adults: Opportunities for the Health Care System [Internet]. Washington, DC: National Academies Press (US); 2020. Available at: https://www.ncbi.nlm.nih.gov/books/NBK557983/ . Accessed September 28, 2022.
Wigfield A, Turner R, Alden S, Green M, Karania VK. Developing a new conceptual framework of meaningful interaction for understanding social isolation and loneliness. Soc Policy Soc 2022;21:172–93.
Qualter P, Brown SL, Rotenberg KJ, Vanhalst J, Harris RA, Goossens L, et al. Trajectories of loneliness during childhood and adolescence: predictors and health outcomes. J Adolesc 2013;36:1283–93.
Asher SR, Paquette JA. Loneliness and peer relations in childhood. Curr Dir Psychol Sci 2003;12:75–8.
Cassidy J, Asher SR. Loneliness and peer relations in young children. Child Dev 1992;63:350–65.
Gunnar M, Quevedo K. The neurobiology of stress and development. Annu Rev Psychol 2007;58:145–73.
Boyce WT, Levitt P, Martinez FD, McEwen BS, Shonkoff JP. Genes, environments, and time: the biology of adversity and resilience. Pediatrics 2021;147:e20201651.
Hertzman C. The biological embedding of early experience and its effects on health in adulthood. Ann N Y Acad Sci 1999;896:85–95.
Lupien SJ, McEwen BS, Gunnar MR, Heim C. Effects of stress throughout the lifespan on the brain, behaviour and cognition. Nat Rev Neurosci 2009;10:434–45.
Danese A, McEwen BS. Adverse childhood experiences, allostasis, allostatic load, and age-related disease. Physiol Behav 2012;106:29–39.
Farrell AK, Simpson JA, Carlson EA, Englund MM, Sung S. The impact of stress at different life stages on physical health and the buffering effects of maternal sensitivity. Health Psychol 2017;36:35–44.
Cross D, Fani N, Powers A, Bradley B. Neurobiological development in the context of childhood trauma. Clin Psychol Sci Pract 2017;24:111–24.
Hughes K, Bellis MA, Hardcastle KA, Sethi D, Butchart A, Mikton C, et al. The effect of multiple adverse childhood experiences on health: a systematic review and meta-analysis. Lancet Public Health 2017;2:e356–66.
Shonkoff JP, Slopen N, Williams DR. Early childhood adversity, toxic stress, and the impacts of racism on the foundations of health. Annu Rev Public Health 2021;42:115–34.
Danese A, Moffitt TE, Harrington H, Milne BJ, Polanczyk G, Pariante CM, et al. Adverse childhood experiences and adult risk factors for age-related disease. Arch Pediatr Adolesc Med 2009;163:1135–43.
Castillo-Gómez E, Pérez-Rando M, Bellés M, Gilabert-Juan J, Llorens JV, Carceller H, et al. Early social isolation stress and perinatal NMDA receptor antagonist treatment induce changes in the structure and neurochemistry of inhibitory neurons of the adult amygdala and prefrontal cortex. eNeuro 2017;4:e0034–17.
Calvin CM, Batty GD, Brett CE, Deary IJ. Childhood club participation and all-cause mortality in adulthood: a 65-year follow-up study of a population-representative sample in Scotland. Psychosom Med 2015;77:712–20.
Gehred MZ, Knodt AR, Ambler A, Bourassa KJ, Danese A, Elliott ML, et al. Long-term neural embedding of childhood adversity in a population-representative birth cohort followed for 5 decades. Biol Psychiatry 2021;90:182–93.
Evans GW, Li D, Whipple SS. Cumulative risk and child development. Psychol Bull 2013;139:1342–96.
D’Amico D, Amestoy ME, Fiocco AJ. The association between allostatic load and cognitive function: a systematic and meta-analytic review. Psychoneuroendocrinology 2020;121:104849.
Peavy GM, Salmon DP, Jacobson MW, Hervey A, Gamst AC, Wolfson T, et al. Effects of chronic stress on memory decline in cognitively normal and mildly impaired older adults. Am J Psychiatry 2009;166:1384–91.
Rothman SM, Mattson MP. Adverse stress, hippocampal networks, and Alzheimer’s disease. Neuromolecular Med 2010;12:56–70.
Hoeijmakers L, Lesuis SL, Krugers H, Lucassen PJ, Korosi A. A preclinical perspective on the enhanced vulnerability to Alzheimer’s disease after early-life stress. Neurobiol Stress 2018;8:172–85.
Song H, Sieurin J, Wirdefeldt K, Pedersen NL, Almqvist C, Larsson H, et al. Association of stress-related disorders with subsequent neurodegenerative diseases. JAMA Neurol 2020;77:700–9.
Lesuis SL, Hoeijmakers L, Korosi A, de Rooij SR, Swaab DF, Kessels HW, et al. Vulnerability and resilience to Alzheimer’s disease: early life conditions modulate neuropathology and determine cognitive reserve. Alzheimers Res Ther 2018;10:95.
Conde-Sala JL, Garre-Olmo J. Early parental death and psychosocial risk factors for dementia: a case–control study in Europe. Int J Geriatr Psychiatry 2020;35:1051–9.
Epel ES, Blackburn EH, Lin J, Dhabhar FS, Adler NE, Morrow JD, et al. Accelerated telomere shortening in response to life stress. Proc Natl Acad Sci 2004;101:17312–5.
London A, Benhar I, Schwartz M. The retina as a window to the brain—from eye research to CNS disorders. Nat Rev Neurol 2013;9:44–53.
Alber J, Goldfarb D, Thompson LI, Arthur E, Hernandez K, Cheng D, et al. Developing retinal biomarkers for the earliest stages of Alzheimer’s disease: what we know, what we don’t, and how to move forward. Alzheimers Dement 2020;16:229–43.
Cheung CY, Ikram MK, Chen C, Wong TY. Imaging retina to study dementia and stroke. Prog Retin Eye Res 2017;57:89–107.
Cheung CY, Mok V, Foster PJ, Trucco E, Chen C, Wong TY. Retinal imaging in Alzheimer’s disease. J Neurol Neurosurg Psychiatry 2021;92:983–94.
Ong YT, Hilal S, Cheung CY, Venketasubramanian N, Niessen WJ, Vrooman H, et al. Retinal neurodegeneration on optical coherence tomography and cerebral atrophy. Neurosci Lett 2015;584:12–6.
Liu S, Ong YT, Hilal S, Loke YM, Wong TY, Chen CLH, et al. The association between retinal neuronal layer and brain structure is disrupted in patients with cognitive impairment and Alzheimer’s disease. J Alzheimers Dis 2016;54:585–95.
Zhang Y, Wang Y, Shi C, Shen M, Lu F. Advances in retina imaging as potential biomarkers for early diagnosis of Alzheimer’s disease. Transl Neurodegener 2021;10:6.
den Haan J, Verbraak FD, Visser PJ, Bouwman FH. Retinal thickness in Alzheimer’s disease: a systematic review and meta-analysis. Alzheimers Dement (Amst) 2017;6:162–70.
Cheung CY, Chan VTT, Mok VC, Chen C, Wong TY. Potential retinal biomarkers for dementia: what is new? Curr Opin Neurol 2019;32:82–91.
Chan VTT, Tso THK, Tang F, Tham C, Mok V, Chen C, et al. Using retinal imaging to study dementia. J Vis Exp 2017;129:56137.
Cheung CY, Ong YT, Hilal S, Ikram MK, Low S, Ong YL, et al. Retinal ganglion cell analysis using high-definition optical coherence tomography in patients with mild cognitive impairment and Alzheimer’s disease. J Alzheimers Dis 2015;45:45–56.
Barrett-Young A, Ambler A, Cheyne K, Guiney H, Kokaua J, Steptoe B, et al. Associations between retinal nerve fiber layer and ganglion cell layer in middle age and cognition from childhood to adulthood. JAMA Ophthalmol 2022;140:262–8.
Chrysou A, Jansonius NM, van Laar T. Retinal layers in Parkinson’s disease: a meta-analysis of spectral-domain optical coherence tomography studies. Parkinsonism Relat Disord 2019;64:40–9.
Bougea A, Anagnostouli M, Angelopoulou E, Spanou I, Chrousos G. Psychosocial and trauma-related stress and risk of dementia: a meta-analytic systematic review of longitudinal studies. J Geriatr Psychiatry Neurol 2022;35:24–37.
Djamshidian A, Lees AJ. Can stress trigger Parkinson’s disease? J Neurol Neurosurg Psychiatry 2014;85:878–81.
Steptoe A, Hamer M, Chida Y. The effects of acute psychological stress on circulating inflammatory factors in humans: a review and meta-analysis. Brain Behav Immun 2007;21:901–12.
Rasmussen LJH, Moffitt TE, Eugen-Olsen J, Belsky DW, Danese A, Harrington H, et al. Cumulative childhood risk is associated with a new measure of chronic inflammation in adulthood. J Child Psychol Psychiatry 2019;60:199–208.
Steinle JJ, Sharma S, Smith CP, McFayden-Ketchum LS. Normal aging involves modulation of specific inflammatory markers in the rat retina and choroid. J Gerontol A Biol Sci Med Sci 2009;64A:325–31.
Sun C, Wang JJ, Mackey DA, Wong TY. Retinal vascular caliber: systemic, environmental, and genetic associations. Surv Ophthalmol 2009;54:74–95.
Whitcup SM, Nussenblatt RB, Lightman SL, Hollander DA. Inflammation in retinal disease. Int J Inflamm 2013;2013:724648.
Jensen RA, Shea S, Ranjit N, Diez-Roux A, Wong TY, Klein R, et al. Psychosocial risk factors and retinal microvascular signs: the Multi-Ethnic Study of Atherosclerosis. Am J Epidemiol 2010;171:522–31.
Li LJ, Ikram MK, Broekman L, Cheung CYL, Chen H, Gooley JJ, et al. Antenatal mental health and retinal vascular caliber in pregnant women. Transl Vis Sci Technol [Internet] 2013;2(2):2. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763888/ . Accessed March 22, 2021.
Nguyen TT, Wong TY, Islam FMA, Hubbard L, Ajilore O, Haroon E, et al. Evidence of early retinal microvascular changes in patients with type 2 diabetes and depression. Psychosom Med 2010;72:535–8.
O’Neill RA, Maxwell AP, Kee F, Young I, Hogg RE, Cruise S, et al. Association of reduced retinal arteriolar tortuosity with depression in older participants from the Northern Ireland Cohort for the Longitudinal Study of Ageing. BMC Geriatr 2021;21:62.
Malan L, Hamer M, von Känel R, Schlaich MP, Reimann M, Frasure-Smith N, et al. Chronic depression symptoms and salivary NOx are associated with retinal vascular dysregulation: the SABPA study. Nitric Oxide 2016;55–56:10–7.
Caspi A, Houts RM, Belsky DW, Goldman-Mellor SJ, Harrington H, Israel S, et al. The p factor: one general psychopathology factor in the structure of psychiatric disorders? Clin Psychol Sci 2014;2:119–37.
Gopinath B, Liew G, Burlutsky G, Baur LA, Mitchell P. Health-related quality of life in adolescents and the retinal microvascular structure. Sci Rep 2018;8:3068.
Cheung N, Rogers S, Mosley TH, Klein R, Couper D, Wong TY. Vital exhaustion and retinal microvascular changes in cardiovascular disease: Atherosclerosis Risk in Communities Study. Psychosom Med 2009;71:308–12.
Gerber M, Endes K, Herrmann C, Colledge F, Brand S, Donath L, et al. Does physical fitness buffer the relationship between psychosocial stress, retinal vessel diameters, and blood pressure among primary schoolchildren? Biomed Res Int 2016;2016:e6340431.
Sun C, Tikellis G, Klein R, Steffens DC, Larsen EKM, Siscovick DS, et al. Are microvascular abnormalities in the retina associated with depression symptoms? The Cardiovascular Health Study. Am J Geriatr Psychiatry 2007;15:335–43.
Meier MH, Shalev I, Moffitt TE, Kapur S, Keefe RSE, Wong TY, et al. Microvascular abnormality in schizophrenia as shown by retinal imaging. Am J Psychiatry 2013;170:1451–9.
Van Aart CJC, Nawrot TS, Sioen I, De Boever P, Zaqout M, De Henauw S, et al. Longitudinal association between psychosocial stress and retinal microvasculature in children and adolescents. Psychoneuroendocrinology 2018;92:50–6.
Malan NT, von Känel R, Smith W, Lambert GW, Vilser W, Eikelis N, et al. A challenged sympathetic system is associated with retinal vascular calibre in a Black male cohort: the SABPA Study. In: Lenasi H, editor. Microcirculation Revisited—From Molecules to Clinical Practice [Internet]. InTech; 2016. Available at: http://www.intechopen.com/books/microcirculation-revisited-from-molecules-to-clinical-practice/a-challenged-sympathetic-system-is-associated-with-retinal-vascular-calibre-in-a-black-male-cohort-t . Accessed March 24, 2021.
Lee SSY, Sanfilippo PG, Yazar S, Pennell CE, Hewitt AW, Wang CA, et al. Do levels of stress markers influence the retinal nerve fiber layer thickness in young adults? J Glaucoma 2020;29:587–92.
Jacobs J, Agho K, Stevens G, Raphael B. Do childhood adversities cluster in predictable ways? A systematic review. Vulnerable Child Youth Stud 2012;7:103–15.
Bussemakers C, Kraaykamp G, Tolsma J. Co-occurrence of adverse childhood experiences and its association with family characteristics. A latent class analysis with Dutch population data. Child Abuse Negl 2019;98:104185.
Poulton R, Moffitt TE, Silva PA. The Dunedin Multidisciplinary Health and Development Study: overview of the first 40 years, with an eye to the future. Soc Psychiatry Psychiatr Epidemiol 2015;50:679–93.
Poulton R, Guiney H, Ramrakha S, Moffitt TE. The Dunedin study after half a century: reflections on the past, and course for the future. J R Soc N Z 2022;0:1–20.
Rutter M. A children’s behaviour questionnaire for completion by teachers: preliminary findings. J Child Psychol Psychiatry 1967;8:1–11.
Qualter P, Brown SL, Munn P, Rotenberg KJ. Childhood loneliness as a predictor of adolescent depressive symptoms: an 8-year longitudinal study. Eur Child Adolesc Psychiatry 2010;19:493–501.
Lay-Yee R, Matthews T, Moffitt T, Poulton R, Caspi A, Milne B. Do socially isolated children become socially isolated adults? [published online December 2021]. Adv Life Course Res 2021;50. doi:10.1016/j.alcr.2021.100419.
doi: 10.1016/j.alcr.2021.100419
Elley WB, Irving JC. A socio-economic index for New Zealand based on levels of education and income from the 1966 Census. N Z J Educ Stud 1972;7:153–67.
Poulton R, Caspi A, Milne BJ, Thomson WM, Taylor A, Sears MR, et al. Association between children’s experience of socioeconomic disadvantage and adult health: a life-course study. Lancet 2002;360:1640–5.
Caspi A, McClay J, Moffitt TE, Mill J, Martin J, Craig IW, et al. Role of genotype in the cycle of violence in maltreated children. Science 2002;297:851–4.
Russell DW. UCLA Loneliness Scale (Version 3): reliability, validity, and factor structure. J Pers Assess 2010;66:20–40.
Radloff LS. The CES-D scale: a self-report depression scale for research in the general population. Appl Psychol Measur 1977;1:385–401.
Zimet GD, Dahlem NW, Zimet SG, Farley GK. The Multidimensional Scale of Perceived Social Support. J Pers Assess 1988;52:30–41.
Hayes AF. Introduction to Mediation, Moderation, and Conditional Process Analysis: A Regression-Based Approach. 2nd ed. New York, NY: Guilford Press; 2018. 692 p. (Methodology in the Social Sciences).
Lacey RE, Kumari M, Bartley M. Social isolation in childhood and adult inflammation: evidence from the National Child Development Study. Psychoneuroendocrinology 2014;50:85–94.
Echevarria FD, Formichella CR, Sappington RM. Interleukin-6 deficiency attenuates retinal ganglion cell axonopathy and glaucoma-related vision loss. Front Neurosci [Internet] 2017;11:318. Available at: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5450377/ . Accessed June 15, 2021.
Wang CY, Liang CY, Feng SC, Lin KH, Lee HN, Shen YC, et al. Analysis of the interleukin-6 (−174) locus polymorphism and serum IL-6 levels with the severity of normal tension glaucoma. Ophthalmic Res 2017;57:224–9.
Loades ME, Chatburn E, Higson-Sweeney N, Reynolds S, Shafran R, Brigden A, et al. Rapid systematic review: the impact of social isolation and loneliness on the mental health of children and adolescents in the context of COVID-19. J Am Acad Child Adolesc Psychiatry 2020;59:1218–1239.e3.
Krause-Parello CA. Loneliness in the school setting. J Sch Nurs 2008;24:66–70.
Eccles AM, Qualter P. Review: alleviating loneliness in young people—a meta-analysis of interventions. Child Adolesc Ment Health 2021;26:17–33.
Giletta M, Slavich GM, Rudolph KD, Hastings PD, Nock MK, Prinstein MJ. Peer victimization predicts heightened inflammatory reactivity to social stress in cognitively vulnerable adolescents. J Child Psychol Psychiatry 2018;59:129–39.
Harris RA, Qualter P, Robinson SJ. Loneliness trajectories from middle childhood to pre-adolescence: impact on perceived health and sleep disturbance. J Adolesc 2013;36:1295–304.
Matthews T, Danese A, Gregory AM, Caspi A, Moffitt TE, Arseneault L. Sleeping with one eye open: loneliness and sleep quality in young adults. Psychol Med 2017;47:2177–86.
Matthews T, Danese A, Caspi A, Fisher HL, Goldman-Mellor S, Kepa A, et al. Lonely young adults in modern Britain: findings from an epidemiological cohort study. Psychol Med 2019;49:268–77.
Asher SR, Hymel S, Renshaw PD. Loneliness in children. Child Dev 1984;55:1456–64.
Wertz J, Caspi A, Ambler A, Broadbent J, Hancox RJ, Harrington H, et al. Association of history of psychopathology with accelerated aging at midlife. JAMA Psychiat 2021;78:530–9.
Matthews T, Danese A, Wertz J, Ambler A, Kelly M, Diver A, et al. Social isolation and mental health at primary and secondary school entry: a longitudinal cohort study. J Am Acad Child Adolesc Psychiatry 2015;54:225–32.
Kalenderoglu A, Çelik M, Sevgi-Karadag A, Egilmez OB. Optic coherence tomography shows inflammation and degeneration in major depressive disorder patients correlated with disease severity. J Affect Disord 2016;204:159–65.
van der Heide FCT, Steens ILM, Geraets AFJ, Foreman YD, Henry RMA, Kroon AA, et al. Association of retinal nerve fiber layer thickness, an index of neurodegeneration, with depressive symptoms over time. JAMA Netw Open 2021;4:e2134753.
Gladstone BM, Boydell KM, Seeman MV, McKeever PD. Children’s experiences of parental mental illness: a literature review. Early Interv Psychiatry 2011;5:271–89.
Chen G, Kong Y, Deater-Deckard K, Zhang W. Bullying victimization heightens cortisol response to psychosocial stress in Chinese children. J Abnorm Child Psychol 2018;46:1051–9.
Afifi TO, MacMillan HL. Resilience following child maltreatment: a review of protective factors. Can J Psychiatry 2011;56:266–72.
Jaffee SR, Bowes L, Ouellet-Morin I, Fisher HL, Moffitt TE, Merrick MT, et al. Safe, stable, nurturing relationships break the intergenerational cycle of abuse: a prospective nationally representative cohort of children in the United Kingdom. J Adolesc Health 2013;53(Suppl 4):S4–10.
Giocanti-Aurégan A, Gazeau G, Hrarat L, Lévy V, Amari F, Bodaghi B, et al. Ethnic differences in normal retinal capillary density and foveal avascular zone measurements. Int Ophthalmol 2020;40:3043–8.
Wylęgała A, Wang L, Zhang S, Liu Z, Teper S, Wylęgała E. Comparison of foveal avascular zone and retinal vascular density in healthy Chinese and Caucasian adults. Acta Ophthalmol 2020;98:e464–9.
Wagner-Schuman M, Dubis AM, Nordgren RN, Lei Y, Odell D, Chiao H, et al. Race- and sex-related differences in retinal thickness and foveal pit morphology. Invest Ophthalmol Vis Sci 2011;52:625–34.
Roberts SO, Bareket-Shavit C, Dollins FA, Goldie PD, Mortenson E. Racial inequality in psychological research: trends of the past and recommendations for the future. Perspect Psychol Sci 2020;15:1295–309.

Auteurs

Ashleigh Barrett-Young (A)

From the Dunedin Multidisciplinary Health and Development Research Unit (Barrett-Young, Cheyne, Guiney, Kokaua, Poulton); Department of Psychology (Barrett-Young, Cheyne, Guiney, Poulton), University of Otago, Dunedin, New Zealand; Social, Genetic and Developmental Psychiatry Centre, Institute of Psychiatry, Psychology and Neuroscience (Ambler), King's College London, London, United Kingdom; Va'a O Tautai-Centre for Pacific Health (Kokaua), University of Otago, Dunedin, New Zealand; Singapore Eye Research Institute (Tham, Wong), Singapore National Eye Centre, Singapore; Duke-NUS Medical School (Tham, Wong), Singapore; and Department of Medicine, Otago Medical School (Williams, Wilson), University of Otago, Dunedin, New Zealand.

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