Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
PLoS One. 2022 May 24;17(5):e0268927. doi: 10.1371/journal.pone.0268927. eCollection 2022.
We sought association between serum Lipoprotein(a) and C-Peptide levels as two predictors with cardiometabolic biomarkers in patients with type 2 diabetes mellitus. This nested case-control study was conducted on 253 participants with type 2 diabetes mellitus and control from the second phase of the KERCADR cohort study. The participants were randomly allocated into case and control groups. The quantitative levels of Lipoprotein(a) and C-Peptide were measured by ELISA. Atherogenic indices of plasma were measured. The plasma Atherogenic Index of Plasma significantly decreased (P = 0.002) in case-male participants, and plasma Castelli Risk Index II level significantly increased (P = 0.008) in control-male participants with the highest dichotomy of Lipoprotein(a). The plasma Atherogenic Index of Plasma level in case-female participants significantly increased (P = 0.023) with the highest dichotomy of C-Peptide. Serum C-Peptide level significantly increased (P = 0.010 and P = 0.002, respectively) in control-male participants with the highest dichotomies of Atherogenic Index of Plasma and Castelli Risk Index I. There was a significant association between the highest quartile of C-Peptide and higher anthropometric values in case participants; and higher atherogenic indices of plasma and anthropometric values in control participants. Raised serum C-peptide than raised Lipoprotein(a) can be a prior predictor for cardiometabolic disease risk in healthy participants and patients with type 2 diabetes mellitus with increased cardiometabolic biomarkers. Case and control males with general and visceral obesity and case and control females with visceral obesity are exposure to increased C-peptide, respectively. Lipoprotein(a) may be risk independent biomarker for type 2 diabetes mellitus. Reducing raised Lipoprotein(a) levels to less than 30ng/ml with strict control of low density lipoprotein cholesterol would be the best approach to prevent coronary artery disease consequences. It is suggested that a screening system be set up to measure the Lp(a) levels in the community for seemingly healthy people or individuals with one or more cardiometabolic biomarkers.
我们寻求血清脂蛋白(a)和 C-肽水平作为两种预测因子与 2 型糖尿病患者的代谢生物标志物之间的关联。这项嵌套病例对照研究在 KERCADR 队列研究的第二阶段对 253 名 2 型糖尿病患者和对照组进行了研究。参与者被随机分配到病例组和对照组。通过 ELISA 测量脂蛋白(a)和 C-肽的定量水平。测量血浆致动脉粥样硬化指数。病例组男性中血浆致动脉粥样硬化指数显著降低(P = 0.002),对照组男性中血浆 Castelli 风险指数 II 水平显著升高(P = 0.008),脂蛋白(a)的最高二分位数。病例组女性中血浆致动脉粥样硬化指数水平显著升高(P = 0.023),C-肽的最高二分位数。对照组男性中血浆致动脉粥样硬化指数和 Castelli 风险指数 I 的最高二分位数中血清 C-肽水平显著升高(P = 0.010 和 P = 0.002)。最高四分位数的 C-肽与病例组的更高的人体测量值之间存在显著相关性;对照组中更高的致动脉粥样硬化指数和人体测量值。与升高的脂蛋白(a)相比,升高的血清 C-肽可作为健康参与者和伴有代谢性心血管疾病标志物升高的 2 型糖尿病患者发生代谢性心血管疾病风险的早期预测因子。普通和内脏肥胖的病例和对照组男性,以及内脏肥胖的病例和对照组女性,分别接触到更高的 C-肽。脂蛋白(a)可能是 2 型糖尿病的独立风险标志物。通过严格控制低密度脂蛋白胆固醇,将升高的脂蛋白(a)水平降低到 30ng/ml 以下,将是预防冠心病后果的最佳方法。建议在社区中建立一个筛查系统,以测量看似健康的人群或具有一个或多个代谢性心血管标志物的个体的 Lp(a)水平。