Alameddine Zakaria, Abi Melhem Racha, Dimachkie Reem, Rabah Hussein, Chehab Hamed, El Khoury Michel, Qaqish Faris, Stefanov Dimitre, El-Sayegh Suzanne
Department of Internal Medicine, Staten Island University Hospital, 475 Seaview Avenue, Staten Island, NY 10305, USA.
Biostatistics Unit, Feinstein Institutes for Medical Research, 350 Community Dr, Manhasset, NY 11030, USA.
J Clin Med. 2023 Sep 22;12(19):6114. doi: 10.3390/jcm12196114.
Inflammatory bowel disease is a chronic inflammatory disorder of the gastrointestinal tract. Biologic drugs target specific molecules in the body's immune system to control inflammation. Recent studies have suggested a potential link between their use and an increased risk of nephrolithiasis. We conducted a study to further investigate this association.
The study used multiple logistic regression analysis to assess the association between the use of biologic drugs and nephrolithiasis. A -value of <0.05 was considered statistically significant. SAS 9.4 was used for statistical analysis.
The final sample consisted of 22,895 cases, among which 5603 (24.51%) were receiving at least one biologic drug. The biologic drugs received were as follows: Adalimumab 2437 (10.66%), Infliximab 1996 (8.73%), Vedolizumab 1397 (6.11%), Ustekinumab 1304 (5.70%); Tofacitinib, 308 (1.35%); Certolizumab, 248 (1.08%); and Golimumab, 121 (0.53%). There were 1780 (7.74%) patients with Nephrolithiasis: 438 (8.0%) patients were receiving biologic treatment. We found that the use of Vedolizumab (OR = 1.307, 95% CI 1.076-1.588, = 0.0071) increased the odds of Nephrolithiasis by 31%.
Vedolizumab use was associated with an increased risk of nephrolithiasis. The use of two or more biologic drugs also increased the risk compared to no biologic treatment.
炎症性肠病是一种胃肠道慢性炎症性疾病。生物药物靶向人体免疫系统中的特定分子以控制炎症。最近的研究表明,使用这些药物与肾结石风险增加之间可能存在联系。我们进行了一项研究以进一步调查这种关联。
该研究使用多元逻辑回归分析来评估生物药物使用与肾结石之间的关联。P值<0.05被认为具有统计学意义。使用SAS 9.4进行统计分析。
最终样本包括22895例病例,其中5603例(24.51%)正在接受至少一种生物药物治疗。所接受的生物药物如下:阿达木单抗2437例(10.66%),英夫利昔单抗1996例(8.73%),维得利珠单抗1397例(6.11%),乌司奴单抗1304例(5.70%);托法替布308例(1.35%);赛妥珠单抗248例(1.08%);戈利木单抗121例(0.53%)。有1780例(7.74%)患者患有肾结石:438例(8.0%)患者正在接受生物治疗。我们发现,使用维得利珠单抗(OR = 1.307,95%CI 1.076 - 1.588,P = 0.0071)使肾结石的几率增加了31%。
使用维得利珠单抗与肾结石风险增加相关。与未接受生物治疗相比,使用两种或更多种生物药物也增加了风险。