Iron Status Correlates Strongly to Insulin Resistance Among US Adults: A Nationwide Population-Based Study

Author:

Liu Xue12,Zhang Yuhao3,Chai Yuwei12,Li Yuchen12,Yuan Jie4,Zhang Li5,Zhang Haiqing1267ORCID

Affiliation:

1. Department of Endocrinology, Shandong Provincial Hospital, Shandong University , Jinan, Shandong, 250021 , China

2. Department of Endocrinology, Shandong Provincial Hospital Affiliated to Shandong First Medical University , Jinan, Shandong, 250021 , China

3. Department of Urology, Linyi Central Hospital , Linyi, Shandong 276400 , China

4. Department of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University , Jinan, Shandong, 250021 , China

5. Department of Vascular Surgery, Shandong Provincial Hospital Affiliated to Shandong First Medical University , Jinan, Shandong, 250021 , China

6. Shandong Clinical Medical Center of Endocrinology and Metabolism , Jinan, 250021 , China

7. Institute of Endocrinology and Metabolism, Shandong Academy of Clinical Medicine , Jinan, 250021 , China

Abstract

Abstract Context Evidence on the link between iron status markers and insulin resistance (IR) is limited. Objective We aimed to explore the relationship between iron status and IR among US adults. Methods This study involved 2993 participants from the National Health and Nutrition Examination Survey (NHANES) 2003-2006, 2017-2020. IR is characterized by a homeostatic model assessment (HOMA)-IR value of ≥2.5. Weighted linear and multivariable logistic regression analyses were used to examine the linear relationships between iron status and IR. Furthermore, restricted cubic splines (RCS) were used to identify the nonlinear dose–response associations. Stratified analyses by age, sex, body mass index, and physical activity were also performed. Last, a receiver operating characteristic (ROC) curve was used to evaluate the predictive value of iron status in IR. Results In weighted linear analyses, serum iron (SI) exhibited a negative correlation with HOMA-IR (β −0.03, 95% CI −0.05, −0.01, P = .01). In weighted multivariate logistic analyses, iron intake and the serum transferrin receptor (sTfR) were positively correlated with IR (OR 1.02, 95% CI 1.00-1.04, P = .04; OR 1.07, 95% CI 1.02-1.13, P = .01). Also, SI and transferrin saturation (TSAT) were negatively correlated with IR (OR 0.96, 95% CI 0.94-0.98, P < .0001; OR 0.98, 95% CI 0.97-0.99, P < .001) after adjusting for confounding factors. RCS depicted a nonlinear dose–response relationship between sTfR and TSAT and IR. This correlation remained consistent across various population subgroups. The ROC curve showed that TSAT performed better than iron intake, SI and sTfR in ROC analyses for IR prediction. Conclusion All biomarkers demonstrated significantly lower risk of IR with increasing iron levels, which will contribute to a more comprehensive and in-depth understanding of the relationship between the 2 and provide a solid foundation for future exploration of the mechanisms underlying their relationship.

Funder

National Natural Science Foundation of China

Publisher

The Endocrine Society

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