| Literature DB >> 34673080 |
Kimberly D Martin1, Gloria L Beckles2, Chengyi Wu3, Leslie A McClure3, April P Carson4, Aleena Bennett5, Kai McKeever Bullard2, M Maria Glymour6, Fred Unverzagt7, Solveig Cunningham8, Giuseppina Imperatore2, Virginia J Howard4.
Abstract
Low socioeconomic position (SEP) across the lifecourse is associated with Type 2 diabetes (T2DM). We examined whether these economic disparities differ by race and sex. We included 5448 African American (AA) and white participants aged ≥45 years from the national (United States) REasons for Geographic and Racial Differences in Stroke (REGARDS) cohort without T2DM at baseline (2003-07). Incident T2DM was defined by fasting glucose ≥126 mg/dL, random glucose ≥200 mg/dL, or using T2DM medications at follow-up (2013-16). Derived SEP scores in childhood (CSEP) and adulthood (ASEP) were used to calculate a cumulative (CumSEP) score. Social mobility was defined as change in SEP. We fitted race-stratified logistic regression models to estimate the association between each lifecourse SEP indicator and T2DM, adjusting for covariates; additionally, we tested SEP-sex interactions. Over a median of 9.0 (range 7-14) years of follow-up, T2DM incidence was 167.1 per 1000 persons among AA and 89.9 per 1000 persons among white participants. Low CSEP was associated with T2DM incidence among AA (OR = 1.61; 95%CI 1.05-2.46) but not white (1.06; 0.74-2.33) participants; this was attenuated after adjustment for ASEP. In contrast, low CumSEP was associated with T2DM incidence for both racial groups. T2DM risk was similar for stable low SEP and increased for downward mobility when compared with stable high SEP in both groups, whereas upward mobility increased T2DM risk among AAs only. No differences by sex were observed. Among AAs, low CSEP was not independently associated with T2DM, but CSEP may shape later-life experiences and health risks.Entities:
Keywords: African American; Lifecourse socioeconomic position; Social mobility; Type 2 diabetes mellitus
Mesh:
Year: 2021 PMID: 34673080 PMCID: PMC8658048 DOI: 10.1016/j.ypmed.2021.106848
Source DB: PubMed Journal: Prev Med ISSN: 0091-7435 Impact factor: 4.018