Chen Xue, Li Xiaosheng, Kang Sheng, Duan Wenbiao
Department of Pathology and Pathophysiology, Zhaoqing Medical College, Zhaoqing City, Guangdong Province 526020, China.
Emergency Department, Dinghu District People's Hospital, Zhaoqing City, Guangdong Province 526070, China.
Evid Based Complement Alternat Med. 2022 Apr 21;2022:7707875. doi: 10.1155/2022/7707875. eCollection 2022.
Diabetes mellitus is a common chronic disease. This study aimed to investigate the correlation between serum insulin-like growth factor 1 receptor (IGF-1R), vascular endothelial growth factor (VEGF), endothelin (ET) levels, and bone mineral density (BMD) in type 2 diabetic mellitus (T2DM) patients treated with metformin plus -glucosidase inhibitors and evaluate the predictive value of serum factors in the prognosis of osteoporosis in these patients. It was a prospective study that enrolled 142 patients with T2DM treated in Dinghu District People's Hospital from March 2019 to May 2020. All enrollments were randomized (1 : 1) to receive either metformin (control group) or metformin plus -glucosidase inhibitors (study group). After 12 weeks of treatment, metformin plus -glucosidase inhibitors were associated with significantly lower levels of 2 hPG, FPG, HbA1c, and HOMA-IR versus metformin alone ( < 0.05). After treatment, the BMD was positively correlated with IGF-1R and negatively correlated with VEGF and ET. Alpha-glucosidase inhibitors plus metformin for primary T2DM can effectively manage blood glucose and reduce insulin resistance in patients, but the prediction of osteoporosis development remains to be further explored in large sample studies.
糖尿病是一种常见的慢性疾病。本研究旨在探讨二甲双胍联合α-葡萄糖苷酶抑制剂治疗的2型糖尿病(T2DM)患者血清胰岛素样生长因子1受体(IGF-1R)、血管内皮生长因子(VEGF)、内皮素(ET)水平与骨密度(BMD)之间的相关性,并评估血清学因素对这些患者骨质疏松症预后的预测价值。这是一项前瞻性研究,纳入了2019年3月至2020年5月在鼎湖区人民医院接受治疗的142例T2DM患者。所有入组患者均随机(1∶1)分为接受二甲双胍治疗的对照组和接受二甲双胍联合α-葡萄糖苷酶抑制剂治疗的研究组。治疗12周后,与单用二甲双胍相比,二甲双胍联合α-葡萄糖苷酶抑制剂治疗使2 hPG、FPG、HbA1c和HOMA-IR水平显著降低(P<0.05)。治疗后,BMD与IGF-1R呈正相关,与VEGF和ET呈负相关。α-葡萄糖苷酶抑制剂联合二甲双胍治疗初发T2DM可有效控制血糖并降低患者胰岛素抵抗,但骨质疏松症发生发展的预测仍有待大样本研究进一步探索。