Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Danish Cancer Society, Copenhagen, Denmark.
Acta Oncol. 2023 Apr;62(4):364-371. doi: 10.1080/0284186X.2023.2197124. Epub 2023 Apr 12.
Insulin resistance is a critical cause of metabolic dysfunctions. Metabolic dysfunction is common in patients with cancer and is associated with higher cancer recurrence rates and reduced overall survival. Yet, insulin resistance is rarely considered in the clinic and thus it is uncertain how frequently this condition occurs in patients with cancer.
To address this knowledge gap, we performed a systematic review and a meta-analysis guided by the Preferred Items for Systematic Review and Meta-Analyses (PRISMA) statement. We included studies assessing insulin resistance in patients with various cancer diagnoses, using the gold-standard hyperinsulinemic-euglycemic clamp method. Studies eligible for inclusion were as follows: (1) included cancer patients older than 18 years of age; (2) included an age-matched control group consisting of individuals without cancer or other types of neoplasms; (3) measured insulin sensitivity using the hyperinsulinemic-euglycemic clamp method. We searched the databases MEDLINE, Embase, and Cochrane Central Register of Controlled Trials for articles published from database inception through March 2023 with no language restriction, supplemented by backward and forward citation searching. Bias was assessed using funnel plot.
Fifteen studies satisfied the criteria. The mean insulin-stimulated rate of glucose disposal (Rd) was 7.5 mg/kg/min in control subjects ( = 154), and 4.7 mg/kg/min in patients with a cancer diagnosis ( = 187). Thus, the Rd mean difference was -2.61 mg/kg/min [95% confidence interval, -3.04; -2.19], <.01). Heterogeneity among the included studies was insignificant (=.24).
These findings suggest that patients with a cancer diagnosis are markedly insulin resistant. As metabolic dysfunction in patients with cancer associates with increased recurrence and reduced overall survival, future studies should address if ameliorating insulin resistance in this population can improve these outcomes thereby improving patient care.Key pointsMetabolic dysfunction increases cancer recurrence rates and reduces survival for patients with cancer.Insulin resistance is a critical cause of metabolic dysfunctions.To date, no comprehensive compilation of research investigating insulin resistance in cancer patients has been produced.In this meta-analysis, we found that patients with various cancers were markedly insulin-resistant.
胰岛素抵抗是代谢功能障碍的一个关键原因。代谢功能障碍在癌症患者中很常见,与更高的癌症复发率和降低的总生存率相关。然而,临床上很少考虑到胰岛素抵抗,因此不确定这种情况在癌症患者中发生的频率如何。
为了解决这一知识空白,我们按照系统评价和荟萃分析的首选项目 (PRISMA) 声明进行了系统评价和荟萃分析。我们纳入了使用金标准高胰岛素-正常血糖钳夹法评估各种癌症诊断患者胰岛素抵抗的研究。符合纳入标准的研究如下:(1)纳入年龄大于 18 岁的癌症患者;(2)纳入由无癌症或其他类型肿瘤的个体组成的年龄匹配对照组;(3)使用高胰岛素-正常血糖钳夹法测量胰岛素敏感性。我们在数据库 MEDLINE、Embase 和 Cochrane 对照试验中心注册库中进行了检索,检索时间从数据库建立开始到 2023 年 3 月,没有语言限制,并通过回溯和前向引文搜索进行了补充。使用漏斗图评估偏倚。
15 项研究符合标准。对照组(n=154)的胰岛素刺激葡萄糖处置率(Rd)平均为 7.5mg/kg/min,而癌症诊断患者(n=187)的 Rd 平均为 4.7mg/kg/min。因此,Rd 平均差值为-2.61mg/kg/min[95%置信区间,-3.04;-2.19],<.01)。纳入研究的异质性不显著(=.24)。
这些发现表明,癌症诊断患者明显存在胰岛素抵抗。由于癌症患者的代谢功能障碍与增加的复发率和降低的总生存率相关,因此未来的研究应该解决在这一人群中改善胰岛素抵抗是否可以改善这些结果,从而改善患者的治疗。
代谢功能障碍增加癌症复发率并降低癌症患者的生存率。胰岛素抵抗是代谢功能障碍的一个关键原因。迄今为止,尚无关于研究癌症患者胰岛素抵抗的综合研究。在这项荟萃分析中,我们发现患有各种癌症的患者明显存在胰岛素抵抗。