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Age‐related changes of proinsulin processing in diabetic and non‐diabetic Japanese individuals

机译:糖尿病和非糖尿病日本人的年龄相关变化

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摘要

Aim The present study was carried out to examine whether the insulin secretory mechanism deteriorates during the aging process using the new intact proinsulin assay system in non‐diabetic and diabetic individuals. Methods A total of 172 participants were separated into four groups according to their age (64?years and 65?years) and an association of type?2 diabetes; that is, 46 older diabetics (mean age 74.5?±?6.2?years, glycated hemoglobin [National Glycohemoglobin Standardization Program] 7.5?±?1.3%), 27 older non‐diabetics (mean age 76.9?±?7.5?years), 48 middle‐aged diabetics (mean age 50.8?±?10.4, glycated hemoglobin 7.8?±?1.5%) and 51 middle aged non‐diabetics (mean age 46.6?±?13.0?years) participants were enrolled. Results The proinsulin/insulin (PI/I) ratio of the diabetic group was higher than that of the non‐diabetic group in the older group (0.19?±?0.12 vs 0.11?±?0.06, P =?0.002). In the middle‐aged groups, the PI/I ratio of the diabetic group was higher than that of the non‐diabetic group (0.16?±?0.15 vs 0.09?±?0.09, P =?0.003). Simple regression analysis showed that male sex (95% CI 0.02–0.01, P =?0.004), age (95% CI 0.00–0.002, P =?0.03), lower body mass index (95% CI ?0.06 to 0.00, P =?0.02) and the presence of diabetes mellitus (95% CI 0.04–0.012, P ?0.0001) were significantly associated with the increase in the PI/I ratio. Multivariate regression analysis showed that male sex and age were the independent factors determining the increase in the PI/I ratio in the non‐diabetic group. After adjusted for body mass index, the PI/I ratio correlated significantly with age only in the non‐diabetic group ( r =?0.5, P =?0.004). Conclusions The proinsulin processing system might deteriorate not only in diabetics, but also in non‐diabetic Japanese individuals with age. Also, sex‐related hormones can be protective for the proinsulin processing system. Geriatr Gerontol Int 2018; 18: 1046–1050 .
机译:目的,进行本研究以检查胰岛素分泌机制是否在非糖尿病和糖尿病个体中使用新的完整胰岛素测定系统在老化过程中劣化。方法根据其年龄(& 64岁及65岁)和类型的糖尿病协会,共172名参与者分为四组。也就是说,46名较旧的糖尿病患者(平均年龄74.5?±6.2?年,糖化血红蛋白[National Glycohemoglobin标准化程序] 7.5?±1.3%),27名更老的非糖尿病(平均年龄76.9?±7.5岁), 48个中年糖尿病患者(平均年龄为50.8〜±10.4,糖化血红蛋白7.8?±1.5%)和51名中年非糖尿病(平均年龄46.6?±13.0岁)参与者进行了注册。结果糖尿病组的胰岛素/胰岛素(PI / I)比率高于较旧组中非糖尿病基团的比例(0.19≤α±0.12 Vs 0.11?±0.06,P = 0.002)。在中年基团中,糖尿病组的PI / I比率高于非糖尿病基团(0.16〜±0.10.15 Vs 0.09?±0.09,P = 0.003)。简单的回归分析表明,男性(95%CI 0.02-0.01,P = 0.004),年龄(95%CI 0.00-002,P = 0.03),低体重指数(95%CI〜0.06至0.00,P =?0.02)和糖尿病的存在(95%CI 0.04-0.012,P <0.0001)与PI / I比的增加显着相关。多元回归分析表明,男性性和年龄是确定非糖尿病组中PI / I比增加的独立因素。调整体质量指数后,PI / I比仅在非糖尿病基团中的年龄显着相关(R = 0.5,P = 0.004)。结论胰岛素加工系统不仅可以在糖尿病患者中恶化,也可能在具有年龄的非糖尿病日本人身上恶化。此外,性交相关的激素可以保护胰岛素加工系统。 GeriaTr Gerontol int 2018; 18:1046-1050。

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