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Advanced glycation end-products in senile diabetic and non-diabetic patients with cardiovascular complications

机译:老年糖尿病和非糖尿病合并心血管疾病患者的晚期糖基化终产物

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摘要

Advanced glycation end products (AGEs) have been reported to contribute to aging and cardiovascular complications. In the present study, the immunoreactivity of AGEs in human serum samples of healthy older subjects (n = 31), senile diabetic patients without cardiovascular complications (n = 33), senile diabetic patients with cardiovascular complications (n = 32), senile non-diabetic patients with cardiovascular complications (n = 30) ,and healthy young subjects (n = 31) were investigated. The patients were selected on clinical grounds from the National Institute of Cardiovascular Disease, Karachi and the Jinnah Postgraduate Medical Centre, Karachi, Pakistan. Fasting blood glucose, HbA1C and serum fructosamine levels were significantly (P < 0.001) increased in senile diabetic patients with and without cardiovascular complications as compared to non-diabetic senile patients with cardiovascular complications and healthy older subjects. Additionally, serum AGEs were found to be significantly (P < 0.001) increased in senile diabetic patients with cardiovascular complications and senile non-diabetic patients with cardiovascular complications, followed by diabetic patients without cardiovascular complications as compared to healthy older subjects and young control subjects. However, no significant difference was found in the senile diabetic patients without cardiovascular complications and senile non-diabetic patients with cardiovascular complications. In contrast to all four senile groups, serum AGEs were significantly (P < 0.001) lower in young control subjects. The AGEs distribution in the senile groups corroborates the hypothesis that the advanced glycation process might play a role in the development of cardiovascular complications, which are more severe in diabetic patients compared with non-diabetic patients with cardiovascular complications.
机译:据报道,晚期糖基化终末产物(AGEs)会导致衰老和心血管并发症。在本研究中,AGEs在健康老年人(n = 31),无心血管并发症的老年糖尿病患者(n = 33),老年糖尿病(心血管并发症)(n = 32),老年非糖尿病患者的血清样品中的免疫反应性对患有心血管并发症的糖尿病患者(n = 30)和健康的年轻受试者(n = 31)进行了调查。这些患者是根据临床依据从卡拉奇国家心血管疾病研究所和巴基斯坦卡拉奇的Jinnah研究生医学中心选出的。与具有心血管并发症的非糖尿病老年患者和健康的老年受试者相比,患有和不患有心血管并发症的老年糖尿病患者的空腹血糖,HbA1C和血清果糖胺水平显着增加(P <0.001)。此外,与健康的老年受试者和年轻的对照受试者相比,发现患有心血管并发症的老年糖尿病患者和患有心血管并发症的老年非糖尿病患者的血清AGEs显着增加(P <0.001),其次是没有心血管并发症的糖尿病患者。但是,在没有心血管并发症的老年糖尿病患者和有心血管并发症的老年非糖尿病患者中,没有发现显着差异。与所有四个老年组相比,年轻对照组的血清AGEs显着降低(P <0.001)。老年组中的AGEs分布证实了以下假设:晚期糖基化过程可能在心血管并发症的发生中起作用,与非糖尿病合并心血管疾病的患者相比,糖尿病合并糖尿病的情况更为严重。

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