Institute for Community Medicine, University Medicine Greifswald, Greifswald, Germany.
Institute for Community Medicine, University Medicine Greifswald, Greifswald, Germany.
Diabetes Res Clin Pract. 2020 May;163:108149. doi: 10.1016/j.diabres.2020.108149. Epub 2020 Apr 15.
To assess the role of serum ferritin and transferrin with prevalent and incident type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) and whether these associations are independent of inflammatory markers and hepatic enzymes.
We analyzed data from 3,232 participants aged 20-81 years of the population-based Study of Health in Pomerania (SHIP) from Northeast Germany with a median follow-up time of 10.6 years. Logistic and Cox regression analyses were performed.
Serum ferritin concentrations were associated with a higher prevalence of T2DM (total population OR: 1.16 [95% CI: 1.07, 1.26]; men OR: 1.18 [95% CI: 1.08, 1.30) and MetS (total population OR: 1.27 [95% CI: 1.16, 1.38]; men OR: 1.26 [95% CI: 1.15, 1.38]) in the total population and men independently of inflammatory markers and hepatic enzymes. In longitudinal analyses, baseline ferritin concentrations were associated with a higher risk of incident T2DM in women (HR: 1.38 [95% CI: 1.10, 1.71]), but not in men or in the total population and also with a higher risk of incident MetS (HR: 1.09 [95% CI: 1.01, 1.17]) in the total population. These longitudinal associations attenuated considerably after adjustment for hepatic enzymes but not inflammatory markers. Transferrin was not associated with any of the outcomes.
Our results suggest a link between ferritin and T2DM and MetS, which might be partially explained by hepatic dysfunction.
评估血清铁蛋白和转铁蛋白与 2 型糖尿病(T2DM)和代谢综合征(MetS)的现患和新发情况,以及这些关联是否独立于炎症标志物和肝酶。
我们分析了来自德国东北部波罗的海健康研究(SHIP)的 3232 名年龄在 20-81 岁的人群数据,中位随访时间为 10.6 年。进行了逻辑和 Cox 回归分析。
血清铁蛋白浓度与 T2DM(总人群 OR:1.16 [95% CI:1.07, 1.26];男性 OR:1.18 [95% CI:1.08, 1.30])和 MetS(总人群 OR:1.27 [95% CI:1.16, 1.38];男性 OR:1.26 [95% CI:1.15, 1.38])的现患率升高相关,且独立于炎症标志物和肝酶。在纵向分析中,基线铁蛋白浓度与女性发生 T2DM 的风险升高相关(HR:1.38 [95% CI:1.10, 1.71]),但与男性或总人群无关,且与总人群发生 MetS 的风险升高相关(HR:1.09 [95% CI:1.01, 1.17])。这些纵向关联在调整肝酶后显著减弱,但调整炎症标志物后则无显著变化。转铁蛋白与任何结局均无关联。
我们的结果表明铁蛋白与 T2DM 和 MetS 之间存在关联,这种关联可能部分归因于肝功能障碍。