Abstract

ObjectivesTo examine the associations of iron status with metabolic health outcomes in women of reproductive age (WRA), as part of a population-based biomarker survey in Southern India. MethodsParticipants were WRA (15–40 y; n = 980) who were not pregnant or lactating (2017–2018). Blood samples were analyzed for hemoglobin (Hb; Coulter Counter) and glycated hemoglobin (HbA1c; nephelometry). Serum ferritin (SF) was measured by electrochemiluminescence; soluble transferrin receptor, C-reactive protein, and alpha-1 acid glycoprotein were analyzed via immuno-based assays (Roche). Anthropometric and blood pressure measurements were collected in triplicate. Bioelectrical impedance analysis (BC-418 MA) was used to estimate whole body (WF%) and trunk (TF%) fat in women ≥ 18y. Anemia was defined as Hb < 12.0 g/dL. SF was adjusted for inflammation using Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) methods; iron deficiency (ID) was defined as SF < 15.0 μg/L. Linear and binomial regression were used to examine associations of iron status with metabolic outcomes. ResultsA total of 41.5% of WRA had anemia, and 46.3% had ID (61.5%; BRINDA-adjusted). A total of 23.3% of adults were overweight (BMI: 25.0-<30.0 kg/m2) and 9.6% had obesity (BMI ≥ 30.0 kg/m2). Waist circumference (WC; ≥88.9 cm) and waist-hip ratio (WHR; ≥0.85) were elevated in 13.4% and 20.8% of women, and 25.0% had elevated HbA1c (≥6.5%: 5.0%; ≥5.7-<6.5%: 20.0%). Higher Hb concentrations were associated with increased BMI (β: 0.42 [SE: 0.09]; p < 0.01), WC (0.77 [0.21]; p < 0.01), and WF% (0.89 [0.17]; p < 0.01). Higher SF levels were associated with higher WF% (β: 0.79 [SE: 0.32]; p = 0.01) and TF% (0.92 [0.39]; p = 0.02), and elevated WC (RR: 1.20 [95% CI: 1.02–1.42]). Iron status was not significantly associated with HbA1c or blood pressure. ConclusionsThe burden of adverse metabolic outcomes was substantial in this population. Higher iron status was associated with higher BMI and central adiposity. Evaluating iron status and metabolic outcomes in future studies could help inform screening and interventions to improve the health of WRA. Funding SourcesCenters for Disease Control and Prevention (5U01DD001007), University of South Carolina Disability Research and Dissemination Center; Consejo Nacional de Ciencia y Tecnología (CEGL); NIH 5T32HD087137 (AF); NIH T32DK007158 (HMG).

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