Lee Seung Hwan, Rhee Marie, Kwon Hyuk Sang, Park Yong Moon, Yoon Kun Ho
Division of Endocrinology and Metabolism, Department of Internal Medicine, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Division of Endocrinology and Metabolism, Department of Internal Medicine, Yeouido St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Diabetes Metab J. 2018 Feb;42(1):53-62. doi: 10.4093/dmj.2018.42.1.53. Epub 2017 Nov 3.
Betatrophin is a newly identified hormone derived from the liver and adipose tissue, which has been suggested to regulate glucose and lipid metabolism. Circulating levels of betatrophin are altered in various metabolic diseases, although the results are inconsistent. We aimed to examine whether betatrophin is a useful biomarker in predicting the development of diabetes.
A nested case-control study was performed using a prospective Chungju Metabolic disease Cohort Study. During a 4-year follow-up period, we analyzed 167 individuals who converted to diabetes and 167 non-converters, who were matched by age, sex, and body mass index. Serum betatrophin levels were measured by an ELISA (enzyme-linked immunosorbent assay).
Baseline serum betatrophin levels were significantly higher in the converter group compared to the non-converter group (1,315±598 pg/mL vs. 1,072±446 pg/mL, P<0.001). After adjusting for age, sex, body mass index, fasting plasma glucose, systolic blood pressure, total cholesterol, and family history of diabetes, the risk of developing diabetes showed a stepwise increase across the betatrophin quartile groups. Subjects in the highest baseline quartile of betatrophin levels had more than a threefold higher risk of incident diabetes than the subjects in the lowest quartile (relative risk, 3.275; 95% confidence interval, 1.574 to 6.814; P=0.010). However, no significant relationships were observed between serum betatrophin levels and indices of insulin resistance or β-cell function.
Circulating levels of betatrophin could be a potential biomarker for predicting new-onset diabetes. Further studies are needed to understand the underlying mechanism of this association.
β-促胰岛素释放肽是一种新发现的由肝脏和脂肪组织产生的激素,有人认为它可调节葡萄糖和脂质代谢。尽管结果并不一致,但在各种代谢性疾病中,β-促胰岛素释放肽的循环水平都会发生改变。我们旨在研究β-促胰岛素释放肽是否是预测糖尿病发生的有用生物标志物。
采用前瞻性忠州代谢疾病队列研究进行巢式病例对照研究。在4年的随访期内,我们分析了167例转变为糖尿病的个体和167例未转变者,这些个体按年龄、性别和体重指数进行匹配。通过酶联免疫吸附测定(ELISA)测量血清β-促胰岛素释放肽水平。
转变者组的基线血清β-促胰岛素释放肽水平显著高于未转变者组(1315±598 pg/mL对1072±446 pg/mL,P<0.001)。在调整年龄、性别、体重指数、空腹血糖、收缩压、总胆固醇和糖尿病家族史后,糖尿病发生风险在β-促胰岛素释放肽四分位数组中呈逐步增加。β-促胰岛素释放肽水平处于最高基线四分位数的受试者发生糖尿病的风险比处于最低四分位数的受试者高出三倍多(相对风险,3.275;95%置信区间,1.574至6.814;P=0.010)。然而,未观察到血清β-促胰岛素释放肽水平与胰岛素抵抗或β细胞功能指标之间存在显著关系。
β-促胰岛素释放肽的循环水平可能是预测新发糖尿病的潜在生物标志物。需要进一步研究以了解这种关联的潜在机制。