Department of Clinical Pharmacy and Pharmacy Administration, School of Pharmacy, Fujian Medical University, Fuzhou, China.
Department of Endocrinology, Fujian Medical University Union Hospital, Fuzhou, China.
Drug Saf. 2022 Sep;45(9):951-959. doi: 10.1007/s40264-022-01210-2. Epub 2022 Jul 20.
An association between tumor necrosis factor (TNF)-α inhibitors and hypoglycemia has been detected in a few case reports and small case series; however, no relevant pharmacovigilance data have been published yet.
The objective of this study was to detect and characterize relevant safety signals between hypoglycemia and TNF-α inhibitor use.
Indication-focused disproportionality analysis was conducted to detect increased reporting of TNF-α-associated hypoglycemia compared with all other reports with the same indication during the same time period. Reporting odds ratios (RORs) with 95% confidence intervals (CIs) were calculated to determine disproportionality. To reduce potential confounding factors, adjusted RORs were further calculated by logistic regression to control for age, sex, diabetes status, and concomitant drugs that potentially affect blood glucose levels.
In all, 1086 adverse drug reactions related to TNF-α inhibitors were reported as 'hypoglycemia'. There were no disproportionality signals of hypoglycemia in TNF-α inhibitor users with indication of inflammatory bowel disease. When TNF-α inhibitors were considered as a class, disproportion for hypoglycemia only emerged in indication of psoriasis (n = 267, ROR 1.20, 95% CI 1.02-1.41). In further analyses of specific TNF-α inhibitor type, significant RORs for hypoglycemia were found in indication of rheumatic disease, including adalimumab in ankylosing spondylitis (n = 37, ROR 1.97, 95% CI 1.28-3.04), psoriasis (n = 160, ROR 1.64, 95% CI 1.37-1.97), and rheumatoid arthritis (n = 230, ROR 1.35, 95% CI 1.16-1.56) and infliximab in psoriasis (n = 18, ROR 2.14, 95% CI 1.33-3.42). After adjusting for confounding factors, only the signals of adalimumab were stable.
Our study identified some potential pharmacovigilance signals between hypoglycemia and TNF-α inhibitors, which warrants further validation.
已有少数病例报告和小病例系列研究发现肿瘤坏死因子(TNF)-α抑制剂与低血糖之间存在关联;然而,尚未发表相关的药物警戒数据。
本研究旨在检测和描述 TNF-α抑制剂使用与低血糖之间相关的安全性信号。
进行了针对适应证的不比例性分析,以检测在同一时期内,与同一适应证的所有其他报告相比,TNF-α相关低血糖的报告是否增加。计算报告比值比(ROR)及其 95%置信区间(CI)以确定不比例性。为了减少潜在的混杂因素,通过逻辑回归进一步计算调整后的 ROR,以控制年龄、性别、糖尿病状态和可能影响血糖水平的伴随药物。
共有 1086 例与 TNF-α抑制剂相关的不良反应报告为“低血糖”。在炎症性肠病适应证的 TNF-α抑制剂使用者中,没有低血糖的不比例性信号。当将 TNF-α抑制剂视为一类药物时,仅在银屑病适应证中出现低血糖的比例失调(n=267,ROR 1.20,95%CI 1.02-1.41)。在对特定 TNF-α抑制剂类型的进一步分析中,在风湿性疾病适应证中发现了低血糖的显著 ROR,包括在强直性脊柱炎(n=37,ROR 1.97,95%CI 1.28-3.04)、银屑病(n=160,ROR 1.64,95%CI 1.37-1.97)和类风湿关节炎(n=230,ROR 1.35,95%CI 1.16-1.56)中使用阿达木单抗,以及在银屑病中使用英夫利昔单抗(n=18,ROR 2.14,95%CI 1.33-3.42)。在调整混杂因素后,只有阿达木单抗的信号是稳定的。
本研究确定了低血糖与 TNF-α抑制剂之间的一些潜在药物警戒信号,这需要进一步验证。