Pham Tan, Cornea Anna, Blick Kenneth E, Jenkins Alicia, Scofield R Hal
Endocrinology Division, Department of Medicine, University of Oklahoma Health Science Center, Oklahoma City, Oklahoma, USA.
Am J Med Sci. 2007 Jun;333(6):333-9. doi: 10.1097/MAJ.0b013e318065bdbe.
Glucosamine is used to treat osteoarthritis. In animals, the compound is known to cause insulin resistance, the underlying abnormality in type 2 diabetes mellitus. Insulin resistance in humans taking oral glucosamine in doses used for osteoarthritis has not been studied.
Volunteer human subjects (n = 38) without known abnormality of glucose homeostasis had fasting serum glucose, insulin, and lipids determined before and after taking 1500 mg glucosamine by mouth every day for 6 weeks. Fasting insulin and glucose were used to calculate homeostasis model assessment (HOMA-IR) and quantitative insulin sensitivity check index (QUICKI). Vascular elasticity was measured by pulse wave analysis. The paired Student's t test was used to compare baseline with posttreatment values. Pearson's correlation was used to determine the relation of baseline HOMA-IR with changes in other variables.
We found a rise in HOMA-IR after 6 weeks of glucosamine (2.8 versus 3.2, P < 0.04). The fall in HOMA-IR among the subjects was statistically related to a higher baseline HOMA-IR by Pearson's correlation(P < 0.01). A rise in serum triglycerides and a rise in LDL cholesterol were statistically related to baseline HOMA-IR. Small artery elasticity fell, and the decrease was higher in those with the highest baseline HOMA-IR.
Notwithstanding its efficacy remaining in question, glucosamine is widely used as treatment for osteoarthritis, which is a condition associated with both obesity and type 2 diabetes mellitus. Our data indicate that persons with underlying poorer insulin sensitivity are at risk for worsening insulin resistance and vascular function with the use of glucosamine in doses used to treat osteoarthritis.
氨基葡萄糖用于治疗骨关节炎。在动物中,已知该化合物会导致胰岛素抵抗,这是2型糖尿病的潜在异常情况。尚未对服用用于骨关节炎剂量的口服氨基葡萄糖的人类的胰岛素抵抗进行研究。
38名无已知葡萄糖稳态异常的志愿者在每天口服1500毫克氨基葡萄糖6周前后测定空腹血清葡萄糖、胰岛素和血脂。空腹胰岛素和葡萄糖用于计算稳态模型评估(HOMA-IR)和定量胰岛素敏感性检查指数(QUICKI)。通过脉搏波分析测量血管弹性。采用配对t检验比较基线值与治疗后的值。使用Pearson相关性分析来确定基线HOMA-IR与其他变量变化之间的关系。
我们发现服用氨基葡萄糖6周后HOMA-IR升高(从2.8升至3.2,P<0.04)。通过Pearson相关性分析,受试者中HOMA-IR的下降与较高的基线HOMA-IR在统计学上相关(P<0.01)。血清甘油三酯升高和低密度脂蛋白胆固醇升高与基线HOMA-IR在统计学上相关。小动脉弹性下降,且基线HOMA-IR最高者下降幅度更大。
尽管其疗效仍存在疑问,但氨基葡萄糖被广泛用作骨关节炎的治疗药物,而骨关节炎是一种与肥胖和2型糖尿病相关的疾病。我们的数据表明,胰岛素敏感性较差的人在使用用于治疗骨关节炎剂量的氨基葡萄糖时,有胰岛素抵抗和血管功能恶化的风险。