Glycated serum proteins and albumin but not glycated albumin show negative correlation with BMI in an overweight/obese, diabetic population from the United States

IF 2.5 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinical biochemistry Pub Date : 2023-10-01 DOI:10.1016/j.clinbiochem.2023.110654
Jennifer Powers Carson , Jyoti Arora
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Abstract

Background and aims

Multiple previously published studies have shown a weak to medium, negative correlation between BMI and glycated albumin (GA). However, many of these studies were in populations with a narrow range of BMI. It is unknown whether this trend exists if a wider BMI range is used. This is an important question for proper interpretation of GA levels in obese populations.

Materials and methods:

A retrospective analysis of clinical trial data (NCT02519309) was performed. After appropriate exclusions, 334 subjects remained. These included 73.7% with type 2 diabetes (T2D) diagnosis and 26.3% with prediabetes. BMI ranged from 24.8–86.9 kg/m2. Laboratory data were measured in a CLIA-certified laboratory using commercially available, automated methods.

Results:

No significant, negative correlation was seen between GA and BMI. However, individual components (glycated serum proteins and albumin) as well as the GA/HbA1c ratio show a weak, negative correlation with BMI for all subjects and those with T2D. The strongest negative correlation was with albumin. Examination by traditional BMI subgroups also showed statistically significant differences for those with T2D, but not for the prediabetic cohort. Correlations between BMI and C-reactive protein were similar in those with diabetes and prediabetes; however, correlation between BMI and insulin was stronger in those with diabetes.

Conclusion:

Negative correlations between BMI and albumin or BMI and glycated serum proteins persist in diabetic populations that are obese and overweight, even when a statistically significant negative correlation is not observed between BMI and GA. Inflammation or insulin-mediated changes in protein synthesis could be contributors to these negative correlations, but BMI-related changes to the glomerulus could also affect clearance of albumin or glycated proteins and should be examined.

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在美国超重/肥胖糖尿病人群中,糖化血清蛋白和白蛋白(而非糖化白蛋白)与BMI呈负相关。
背景和目的:先前发表的多项研究表明,BMI和糖化白蛋白(GA)之间存在弱到中等的负相关性。然而,这些研究中的许多都是针对BMI范围较窄的人群。如果使用更宽的BMI范围,这种趋势是否存在还不得而知。这是正确解释肥胖人群GA水平的一个重要问题。材料和方法:对NCT02519309临床试验数据进行回顾性分析。在适当排除后,仍有334名受试者。其中73.7%诊断为2型糖尿病(T2D),26.3%诊断为糖尿病前期。BMI范围为24.8-86.9 kg/m2。实验室数据在CLIA认证的实验室中使用商业上可获得的自动化方法进行测量。结果:GA与BMI之间无显著负相关。然而,所有受试者和T2D患者的个体成分(糖化血清蛋白和白蛋白)以及GA/HbA1c比率与BMI呈弱负相关。与白蛋白呈最强负相关。传统BMI亚组的检查也显示T2D患者的统计学显著差异,但糖尿病前期队列没有。糖尿病和糖尿病前期患者的BMI和C反应蛋白之间的相关性相似;然而,在糖尿病患者中,BMI和胰岛素之间的相关性更强。结论:在肥胖和超重的糖尿病人群中,BMI与白蛋白或BMI与糖化血清蛋白之间的负相关性仍然存在,即使BMI与GA之间没有观察到统计学上显著的负相关性。炎症或胰岛素介导的蛋白质合成变化可能是这些负相关性的原因,但与BMI相关的肾小球变化也可能影响白蛋白或糖化蛋白的清除,应进行检查。
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来源期刊
Clinical biochemistry
Clinical biochemistry 医学-医学实验技术
CiteScore
5.10
自引率
0.00%
发文量
151
审稿时长
25 days
期刊介绍: Clinical Biochemistry publishes articles relating to clinical chemistry, molecular biology and genetics, therapeutic drug monitoring and toxicology, laboratory immunology and laboratory medicine in general, with the focus on analytical and clinical investigation of laboratory tests in humans used for diagnosis, prognosis, treatment and therapy, and monitoring of disease.
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