Background: Current literature on the association between mobility in socioeconomic position (SEP) and depression demonstrates mixed findings, with variation in the benefits of upward SEP by racial group and ethnic background. No study has examined life-course SEP mobility and depressive symptoms among Black women in the United States. Methods: Our cohort included 1,612 Black women enrolled in the Study of Environment, Lifestyle and Fibroids between 2010 and 2012 and followed for 5 years. We used data on socioeconomic indicators at childhood and adulthood and used latent class analysis to create a life-course SEP mobility measure (persistently low, downward, upward, and persistently high). Using the 11-item Center for Epidemiologic Studies Depression Scale (CES-D), we assessed high (>= 9) versus low depressive symptoms. Multivariable log risk models were used to produce risk ratios (RRs) and 95% confidence intervals (CIs). Results: Of the participants, 37% had high depressive symptoms. Persistently low (RR, 1.56; 95% CI, 1.31-1.86) and downward (RR, 1.36; 95% CI, 1.14-1.63) SEP mobility was associated with high depressive symptoms after adjustment for age, adult social support, and marital status. There was evidence of an effect measure modification by adult social support, with a stronger association among those who reported high adult social support compared with low adult social support. Conclusions: These findings suggest directing mental health resources to people experiencing low SEP at any stage in life, especially those with low SEP in adulthood, to aid in the management of depressive symptoms. (c) 2022 Jacobs Institute of Women's Health, George Washington University. Published by Elsevier Inc. All rights reserved.
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Univ Bristol, Sch Social & Community Med, Oakfield House, Bristol BS8 2BN, Avon, EnglandUniv Bristol, Sch Social & Community Med, Oakfield House, Bristol BS8 2BN, Avon, England
Joinson, Carol
Kounali, Daphne
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Univ Bristol, Sch Social & Community Med, Oakfield House, Bristol BS8 2BN, Avon, EnglandUniv Bristol, Sch Social & Community Med, Oakfield House, Bristol BS8 2BN, Avon, England
Kounali, Daphne
Lewis, Glyn
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UCL, Div Psychiat, 67-73 Riding House St, London W1W 7EJ, EnglandUniv Bristol, Sch Social & Community Med, Oakfield House, Bristol BS8 2BN, Avon, England
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Karolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, SwedenKarolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
Ericsson, Malin
Pedersen, Nancy L.
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Karolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, SwedenKarolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
Pedersen, Nancy L.
Johansson, Anna L., V
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Karolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
Canc Registry Norway, Oslo, NorwayKarolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
Johansson, Anna L., V
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Fors, Stefan
Aslan, Anna K. Dahl
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Karolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
Jonkoping Univ, Sch Hlth & Welf, Inst Gerontol & Aging Res Network Jonkoping ARN J, Jonkoping, SwedenKarolinska Inst, Dept Med Epidemiol & Biostat, POB 281, SE-17177 Stockholm, Sweden
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Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USAUniv Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA
Matthews, Karen A.
Schwartz, Joseph E.
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SUNY Stony Brook, Dept Psychiat & Behav Sci, Stony Brook, NY 11794 USA
Columbia Univ, Med Ctr, Dept Med, New York, NY USAUniv Pittsburgh, Dept Psychiat, Pittsburgh, PA 15213 USA