Akasaka Hiroshi, Ohnishi Hirofumi, Narita Yoshifumi, Kameda Masami, Miki Takayuki, Takahashi Hiroki, Yamamoto Wari, Sohma Hitoshi, Masumori Naoya, Miura Tetsuji
Clinical Training Center, Sapporo Medical University Hospital, Japan.
Department of Cardiovascular, Renal and Metabolic Medicine, Japan.
Intern Med. 2017 Nov 15;56(22):3009-3018. doi: 10.2169/internalmedicine.8716-16. Epub 2017 Sep 25.
Objective Inflammatory cytokines generated in visceral fat have been shown to contribute to the development of insulin resistance. The involvement of pulmonary inflammation in insulin resistance remains unclear, but smoking is known to be a risk factor for diabetes as well as chronic obstructive pulmonary disease. We herein examined the hypothesis that increased serum levels of lung interstitial injury biomarkers [surfactant protein (SP)-A, SP-D and Krebs von den Lungen (KL)-6] are associated with the risk of diabetes development. Methods For cross-sectional and longitudinal analyses, we enrolled 750 apparently healthy non-diabetic subjects who received annual examinations in 2011 or 2012 in the Tanno-Sobetsu cohort. Results A cross-sectional analysis showed that distinct clinical parameters were associated with SP-A, SP-D and KL-6. In a multiple regression analysis, independent explanatory variables were Brinkman index and brain natriuretic peptide (BNP) for SP-A, sex (women), BNP and body mass index (BMI) for SP-D, and age and BMI for KL-6. A longitudinal analysis of 415 subjects who received annual examinations in both 2011 and 2014 showed that 13 (3.1%) of the patients developed type 2 diabetes during the 3-year follow-up. A multiple logistic regression analysis showed the KL-6 levels, systolic blood pressure and homeostasis model assessment of insulin resistance (HOMA-IR) in 2011 to be independently associated with new-onset diabetes. In a multiple regression analysis for HOMA-IR in 2014, the KL-6 level and BMI in 2011 were selected as explanatory variables. Conclusion A modest elevation of the serum KL-6 level is therefore considered to be associated with the risk for insulin resistance development and new-onset diabetes mellitus in a general population.
目的 内脏脂肪中产生的炎性细胞因子已被证明与胰岛素抵抗的发生有关。肺部炎症与胰岛素抵抗之间的关系尚不清楚,但吸烟是糖尿病以及慢性阻塞性肺疾病的危险因素。我们在此检验了以下假设:血清肺间质损伤生物标志物[表面活性蛋白(SP)-A、SP-D和克雷伯斯冯登龙根(KL)-6]水平升高与糖尿病发生风险相关。方法 为进行横断面和纵向分析,我们纳入了750名在2011年或2012年接受年度检查的表面健康的非糖尿病受试者,他们来自胆野-小越队列。结果 横断面分析显示,不同的临床参数与SP-A、SP-D和KL-6相关。在多元回归分析中,SP-A的独立解释变量是布林克曼指数和脑钠肽(BNP),SP-D的是性别(女性)、BNP和体重指数(BMI),KL-6的是年龄和BMI。对415名在2011年和2014年都接受年度检查 的受试者进行的纵向分析显示,在3年随访期间有13名(3.1%)患者患2型糖尿病。多元逻辑回归分析显示,2011年的KL-6水平、收缩压和胰岛素抵抗稳态模型评估(HOMA-IR)与新发糖尿病独立相关。在对2014年HOMA-IR的多元回归分析中,选择2011年的KL-6水平和BMI作为解释变量。结论 因此,血清KL-6水平的适度升高被认为与普通人群中胰岛素抵抗发生风险和新发糖尿病有关。