Barton James C, Barton Jackson Clayborn, Acton Ronald T
1 Southern Iron Disorders Center , Birmingham, Alabama.
2 Department of Medicine, University of Alabama at Birmingham , Birmingham, Alabama.
Metab Syndr Relat Disord. 2018 Aug;16(6):267-273. doi: 10.1089/met.2018.0036. Epub 2018 May 31.
We sought to determine associations with insulin resistance (IR) and metabolic syndrome (MetS) in African Americans.
We studied African American adults without diabetes in a postscreening examination. Participants included Cases: transferrin saturation (TS) >50% and serum ferritin (SF) >300 μg/L (M), and TS >45% and SF >200 μg/L (F), regardless of HFE genotype; and Controls: TS/SF 25th to 75th percentiles and HFE wt/wt (wild type). We excluded participants with fasting <8 h; fasting glucose >126 mg/dL; hepatitis B or C; cirrhosis; pregnancy; or incomplete datasets. We analyzed age; sex; Case/Control; body mass index (BMI); systolic and diastolic blood pressures; neutrophils; lymphocytes; alanine aminotransferase; aspartate aminotransferase; elevated C-reactive protein (CRP >0.5 mg/L); TS; and SF. We computed homeostasis model assessment of insulin resistance (HOMA-IR) using fasting serum glucose and insulin, and defined IR as HOMA-IR fourth quartile (≥2.42).
There were 312 Cases and 86 Controls (56.3% men). Ninety-one percent had HFE wt/wt. None had HFE p.C282Y. A significant increasing trend across HOMA-IR quartiles was observed for BMI only. Multivariable regression on HOMA-IR revealed significant positive associations: age; BMI; lymphocytes; SF; and CRP >0.5 mg/L; and significant negative associations: neutrophils and TS. Logistic regression on IR revealed BMI [odds ratio (OR) 1.3 (95% confidence interval 1.2-1.4)] and CRP >0.5 mg/L [OR 2.7 (1.2-6.3)]. Fourteen participants (3.5%) had MetS. Logistic regression on MetS revealed one association: IR [OR 7.4 (2.1-25.2)].
In African Americans without diabetes, IR was associated with BMI and CRP >0.5 mg/L, after adjustment for other variables. MetS was associated with IR alone.
我们试图确定非裔美国人中胰岛素抵抗(IR)和代谢综合征(MetS)之间的关联。
我们在一次筛查后检查中研究了无糖尿病的非裔美国成年人。参与者包括病例组:转铁蛋白饱和度(TS)>50%且血清铁蛋白(SF)>300μg/L(男性),以及TS>45%且SF>200μg/L(女性),无论HFE基因型如何;对照组:TS/SF处于第25至75百分位数且HFE为野生型(wt/wt)。我们排除了空腹时间<8小时、空腹血糖>126mg/dL、患有乙型或丙型肝炎、肝硬化、怀孕或数据集不完整的参与者。我们分析了年龄、性别、病例/对照、体重指数(BMI)、收缩压和舒张压、中性粒细胞、淋巴细胞、丙氨酸转氨酶、天冬氨酸转氨酶、C反应蛋白升高(CRP>0.5mg/L)、TS和SF。我们使用空腹血清葡萄糖和胰岛素计算胰岛素抵抗的稳态模型评估(HOMA-IR),并将IR定义为HOMA-IR处于第四四分位数(≥2.42)。
有312例病例和86例对照(56.3%为男性)。91%的人HFE为wt/wt。无人携带HFE p.C282Y突变。仅观察到BMI在HOMA-IR四分位数之间有显著的上升趋势。对HOMA-IR进行多变量回归分析发现显著的正相关因素:年龄、BMI、淋巴细胞、SF和CRP>0.5mg/L;以及显著的负相关因素:中性粒细胞和TS。对IR进行逻辑回归分析发现BMI[比值比(OR)1.3(95%置信区间1.2-1.4)]和CRP>