Liatis S, Sfikakis P P, Tsiakou A, Stathi C, Terpos E, Katsilambros N, Makrilakis K
First Department of Propaedeutic Medicine & Diabetes Center, Athens University Medical School, Laiko General Hospital, 17 Ag. Thoma str, 11527 Athens, Greece.
First Department of Propaedeutic Medicine & Diabetes Center, Athens University Medical School, Laiko General Hospital, 17 Ag. Thoma str, 11527 Athens, Greece.
Diabetes Metab. 2014 Jun;40(3):198-203. doi: 10.1016/j.diabet.2014.01.001. Epub 2014 Feb 12.
Experimental evidence suggests that osteocalcin is a key messenger that affects both adipocytes and insulin-producing β cells. Epidemiological cross-sectional studies have shown a negative association between plasma levels of osteocalcin and glucose. For this reason, the hypothesis that lower baseline osteocalcin plasma levels are associated with diabetes was prospectively tested.
The study population consisted of individuals at high risk for type 2 diabetes who were screened for participation in the Greek arm of a European type 2 diabetes prevention study (the DE-PLAN study). All participants were free of diabetes at baseline and underwent a second evaluation 3 years later. Diabetes status was defined according to an oral glucose tolerance test.
A total of 307 subjects were included in the present analysis. The population, including 154 men (50.3%), was middle-aged (54.4 ± 10.2 years) and overweight (BMI: 29.5 ± 4.9 kg/m(2)). At baseline, mean total plasma osteocalcin was lower in those with impaired fasting glucose and/or impaired glucose tolerance compared with those with normal glucose tolerance (6.0 ± 3.1 ng/mL vs. 7.3 ± 4.0 ng/mL, respectively; P = 0.01). After 3 years, 36 subjects had developed diabetes. In the prospective evaluation, there was no association between baseline osteocalcin levels and diabetes (OR: 1.04 per 1 ng/mL, 95% CI: 0.93-1.15; P = 0.49) on multivariable logistic regression analysis, nor was there any correlation with changes in plasma glucose after 3 years (r = 0.09, P = 0.38).
Our prospective results show that lower levels of circulating osteocalcin do not predict future diabetes development and, in contrast to most cross-sectional published data so far, suggest that this molecule may not be playing a major role in glucose homoeostasis in humans.
实验证据表明骨钙素是影响脂肪细胞和胰岛素分泌β细胞的关键信使。流行病学横断面研究显示骨钙素血浆水平与血糖之间呈负相关。因此,我们前瞻性地检验了较低的基线骨钙素血浆水平与糖尿病相关的假说。
研究人群包括2型糖尿病高危个体,这些个体经过筛查参与了一项欧洲2型糖尿病预防研究的希腊分支(DE-PLAN研究)。所有参与者在基线时均无糖尿病,并在3年后接受了第二次评估。糖尿病状态根据口服葡萄糖耐量试验确定。
本分析共纳入307名受试者。该人群包括154名男性(50.3%),为中年人群(54.4±10.2岁)且超重(BMI:29.5±4.9kg/m²)。在基线时,空腹血糖受损和/或糖耐量受损者的平均总血浆骨钙素水平低于糖耐量正常者(分别为6.0±3.1ng/mL和7.3±4.0ng/mL;P = 0.01)。3年后,36名受试者患上了糖尿病。在前瞻性评估中,多变量逻辑回归分析显示基线骨钙素水平与糖尿病之间无关联(每1ng/mL的OR为1.04,95%CI:0.93 - 1.15;P = 0.49),与3年后血浆葡萄糖变化也无相关性(r = 0.09,P = 0.38)。
我们的前瞻性结果表明,循环骨钙素水平较低并不能预测未来糖尿病的发生,并且与目前大多数已发表的横断面数据相反,提示该分子可能在人类血糖稳态中不发挥主要作用。