Plasma Fetuin-A Levels and Risk of Type 2 Diabetes Mellitus in A Chinese Population: A Nested Case-Control Study
- Author:
Yeli WANG
1
;
Woon Puay KOH
;
Majken K JENSEN
;
Jian Min YUAN
;
An PAN
Author Information
- Publication Type:Original Article
- Keywords: Alpha-2-HS-glycoprotein; Association; Case-control studies; Diabetes mellitus, type 2; Epidemiology
- MeSH: African Americans; alpha-2-HS-Glycoprotein; Asian Continental Ancestry Group; Case-Control Studies; Cohort Studies; Diabetes Mellitus, Type 2; Epidemiologic Studies; Epidemiology; Follow-Up Studies; Humans; Insulin Resistance; Logistic Models; Odds Ratio; Plasma; Prospective Studies; Retrospective Studies; Singapore
- From:Diabetes & Metabolism Journal 2019;43(4):474-486
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Fetuin-A is a hepatokine that involved in the pathogenesis of insulin resistance. Previous epidemiological studies have found a positive association between blood fetuin-A and type 2 diabetes mellitus (T2DM) risk among Caucasians and African Americans. We aimed to investigate the prospective relationship between fetuin-A and T2DM in an Asian population for the first time. METHODS: A nested case-control study was established within a prospective cohort of Chinese living in Singapore. At blood collection (1999 to 2004), all participants were free of diagnosed T2DM and aged 50 to 79 years. At subsequent follow-up (2006 to 2010), 558 people reported to have T2DM and were classified as incident cases, and 558 controls were randomly chosen from the participants who did not develop T2DM to match with cases on age, sex, dialect group, and date of blood collection. Plasma fetuin-A levels were measured retrospectively in cases and controls using samples collected at baseline. Conditional logistic regression models were used to compute the odds ratio (OR) and 95% confidence interval (CI). Restricted cubic spline analysis was used to examine a potential non-linear association between fetuin-A levels and T2DM risk. RESULTS: Compared with those in the lowest fetuin-A quintile, participants in the highest quintile had a two-fold increased risk of developing T2DM (OR, 2.06; 95% CI, 1.21 to 3.51). A non-linear association was observed (P nonlinearity=0.005), where the association between fetuin-A levels and T2DM risk plateaued at plasma concentrations around 830 µg/mL. CONCLUSION: There is a positive association between plasma fetuin-A levels and risk of developing T2DM in this Chinese population.
