The impact of anti-TNFα agents on weight-related changes: new insights from a real-world pharmacovigilance study using the FDA adverse event reporting system (FAERS) database

被引:25
|
作者
Mazhar, Faizan [1 ]
Battini, Vera [1 ]
Gringeri, Michele [1 ]
Pozzi, Marco [2 ]
Mosini, Giulia [1 ]
Marran, Albaraa Mohammed N. [3 ]
Akram, Shahzad [4 ,5 ]
van Manen, Robbert P. [5 ]
Radice, Sonia [1 ]
Clementi, Emilio [1 ,2 ]
Carnovale, Carla [1 ]
机构
[1] Luigi Sacco Univ Hosp, Univ Milano, Milan, Italy
[2] IRCCS Medea, Sci Inst, Bosisio Parini, Italy
[3] Prince Mohammed Bin Nasser Hosp, Dept Pharmaceut Care, Jizan, Saudi Arabia
[4] King Abdullah Specialist Children Hosp, Natl Guard Hlth Affairs, King Abdul Aziz Med City, Pharmaceut Care Dept, Riyadh, Saudi Arabia
[5] Oracle Hlth Sci, Kattendijke, Netherlands
关键词
Body weight; pharmacovigilance; anti-TNF-alpha agents; immune-mediated inflammatory diseases; ANTITUMOR NECROSIS FACTOR; RHEUMATOID-ARTHRITIS; INSULIN-RESISTANCE; FAT MASS; DISEASE; THERAPY; INFLIXIMAB; OBESITY; GAIN; ETANERCEPT;
D O I
10.1080/14712598.2021.1948529
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction Studies in patients with immune-mediated inflammatory diseases (IMIDs) have inconsistently suggested that anti-TNF alpha therapy may be associated with excessive weight gain. Areas covered We performed a nested case/non-case analysis to investigate the anti-TNF-alpha inhibitor-associated body-changes in the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database. The risk was expressed as a measure of disproportionality using the reporting odds ratio (ROR) while adjusting for sex, drugs known to cause weight gain and reporter type. We also performed a time-to-onset (TTO) analysis of body weight-related events. Results Infliximab was the most commonly involved TNF-alpha inhibitor in body weight-related changes, reaching an aROR of 1.42 (95%CI:1. 26; 1.59). An increased risk was especially found in patients affected by rheumatic disorders, both in the adult and pediatric population. The median TTO after the start of anti- TNF alpha therapy was about 6-7 months for both children and adults. Conclusions Given the potential effect of these agents on the excess weight gain in IMIDs patients, continuous attention for this side effect with appropriate counseling regarding lifestyle modifications are warranted, especially in those at high risk for obesity.
引用
收藏
页码:1281 / 1290
页数:10
相关论文
共 50 条
  • [41] The Antidepressant Effects of Hypoglycaemic Agents: New Insights from an Analysis of the FDA Adverse Event Reporting System (FAERS) Database
    Carnovale, C.
    Battini, V.
    Gringeri, M.
    Mosini, G.
    Guarnieri, G.
    Radice, S.
    Clementi, E.
    Manen, R. P. V.
    [J]. DRUG SAFETY, 2022, 45 (10) : 1285 - 1285
  • [42] Adverse events of epidiolex: A real-world drug safety surveillance study based on the FDA adverse event reporting system (FAERS) database
    Zhou, Qin
    Du, Zhiqiang
    Qu, Kankan
    Shen, Yuan
    Jiang, Ying
    Zhu, Haohao
    Zhang, Xiuhong
    [J]. ASIAN JOURNAL OF PSYCHIATRY, 2023, 90
  • [43] A real-world pharmacovigilance analysis for transthyretin inhibitors: findings from the FDA adverse event reporting database
    Liu, Yuan
    Li, Hao
    Hu, Cheng
    Tan, Li
    Yin, Ping
    Li, Zhihao
    Zhou, Shuangshan
    Su, Li
    [J]. FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [44] A real-world analysis of safety profile of selexipag by using FDA adverse Event Reporting System (FAERS)
    Zhao, Jie
    Wang, Mei
    Yu, Qing
    Yang, Yi
    Zhang, Bin
    Zhan, Sanhua
    [J]. EXPERT OPINION ON DRUG SAFETY, 2024, 23 (07) : 937 - 948
  • [45] A real-world pharmacovigilance study of cardiac adverse events induced by sugammadex in the FDA adverse event reporting system
    Lin, Xiao-Na
    Zeng, You-Jie
    Cao, Si
    Jing, Xi-Bo
    [J]. EXPERT OPINION ON DRUG SAFETY, 2024,
  • [46] Pancreatitis with use of new diabetic medications: a real-world data study using the post-marketing FDA adverse event reporting system (FAERS) database
    Alenzi, Khalidah A.
    Alsuhaibani, Deemah
    Batarfi, Bader
    Alshammari, Thamir M.
    [J]. FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [47] Statin-related neurocognitive disorder: a real-world pharmacovigilance study based on the FDA adverse event reporting system
    Xiao, Min
    Li, Li
    Zhu, Weiwei
    Wu, Fengbo
    Wu, Bin
    [J]. EXPERT REVIEW OF CLINICAL PHARMACOLOGY, 2024, 17 (03) : 255 - 261
  • [48] Gender differences in adverse events related to Osimertinib: a real-world pharmacovigilance analysis of FDA adverse event reporting system
    Li, Zhiping
    Zou, Wenbin
    Yuan, Jiao
    Zhong, Yunxiang
    Fu, Zhiwen
    [J]. EXPERT OPINION ON DRUG SAFETY, 2023,
  • [49] Safety of TNF-α inhibitors: A real-world study based on the US FDA Adverse Event Reporting System Database
    Zheng, Bohui
    Liu, Manting
    Dai, Dandan
    Shang, Yifan
    Dou, Xiangyun
    Liu, Bingshuo
    Zhong, Zilan
    Huang, Shulan
    Luo, Dongqiang
    [J]. MEDICINE, 2024, 103 (29)
  • [50] Assessment of adverse events related to anti-interleukin-6 receptor monoclonal antibodies using the FDA adverse event reporting system: a real-world pharmacovigilance study
    Hu, Jing
    Sun, Yao
    Zuo, Xiangrong
    Zou, Ying
    [J]. EXPERT OPINION ON DRUG SAFETY, 2024,