Systematic review and meta-analysis: dipeptidyl peptidase-4 inhibitors and rheumatoid arthritis risk

被引:5
作者
Wang, Miao [1 ]
Li, Muqin [1 ]
Xie, Ying [1 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Suzhou 215004, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Diabetes; Dipeptidyl peptidase-4 inhibitors; Rheumatoid arthritis; Meta-analysis; Systematic review; ARTHRALGIA; CD26; IV;
D O I
10.1507/endocrj.EJ20-0647
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This review evaluated the risk of rheumatoid arthritis in patients with type 2 diabetes treated with dipeptidyl peptidase-4 inhibitors (Dpp-4i). The MEDLINE (via PubMed), Embase, the Cochrane Library databases and web of science were used to search the effects of Dpp-4i on rheumatoid arthritis in patients with type 2 diabetes from inception to 7 September, 2020. We included studies that met the following criteria:(i) A randomized controlled trial (RCT), prospective or retrospective cohort study examining the relationship between Dpp-4i and rheumatoid arthritis. Exclusion criteria included the following: Reviews and researches related to other diseases or subjects-, and studies without data on the prevalence of rheumatoid arthritis were excluded. Risk of Bias table contained in Review Manager 5.3 and Newcastle-Ottawa scale (NOS) were used for quality assessment of included RCT and observational studies separately. Meta-analysis was used to estimate the risk of disease. We conducted a subgroup analysis of duration of follow-up, adjusted (adjusted RR or unadjusted RR), sample size and study design. A total of 10 independent studies assessing 1,420,414 patients were included in this analysis. In this meta-analysis, we found that there was nonsignificant increase of rheumatoid arthritis with Dpp-4 inhibitor exposure (RR 0.96, 95%CI (0.69.1 .32)). Our results revealed that Dpp-4 inhibitors do not seem to increase the risk of rheumatoid arthritis. Long-term follow-up monitoring is necessary.
引用
收藏
页码:729 / 738
页数:10
相关论文
共 35 条
[1]  
[Anonymous], 2015, FDA Drug Safety Communication: FDA has reviewed possible risks of pain medicine use durng pregnancy
[2]  
Aytac Ugur, 2004, Current Drug Targets - Immune Endocrine and Metabolic Disorders, V4, P11, DOI 10.2174/1568008043340035
[3]  
Boehringer I, 2010, EFFICACY SAFETY BI 1
[4]  
Bristol-Myers S., 2013, DOES SAXAGLIPTIN RED
[5]   Circulating CD26 is negatively associated with inflammation in human and experimental arthritis [J].
Busso, N ;
Wagtmann, N ;
Herling, C ;
Chobaz-Péclat, V ;
Bischof-Delaloye, A ;
So, A ;
Grouzmann, E .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 166 (02) :433-442
[6]   The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes [J].
Drucker, Daniel J. ;
Nauck, Michael A. .
LANCET, 2006, 368 (9548) :1696-1705
[7]   EXPRESSION OF THE RAT CD26 ANTIGEN (DIPEPTIDYL PEPTIDASE-IV) ON SUBPOPULATIONS OF RAT LYMPHOCYTES [J].
GORRELL, MD ;
WICKSON, J ;
MCCAUGHAN, GW .
CELLULAR IMMUNOLOGY, 1991, 134 (01) :205-215
[8]   Loss of Incretin Effect Is a Specific, Important, and Early Characteristic of Type 2 Diabetes [J].
Holst, Jens J. ;
Knop, Filip K. ;
Vilsboll, Tina ;
Krarup, Thure ;
Madsbad, Sten .
DIABETES CARE, 2011, 34 :S251-S257
[9]   Dipeptidyl peptidase-4 inhibitor use is not associated with elevated risk of severe joint pain in patients with type 2 diabetes: a population-based cohort study [J].
Hou, Wen-Hsuan ;
Chang, Kai-Cheng ;
Li, Chung-Yi ;
Ou, Huang-Tz .
PAIN, 2016, 157 (09) :1954-1959
[10]   DPP-4 Inhibitor-Induced Rheumatoid Arthritis Among Diabetics: A Nested Case-Control Study [J].
Kathe, Niranjan ;
Shah, Anuj ;
Said, Qayyim ;
Painter, Jacob T. .
DIABETES THERAPY, 2018, 9 (01) :141-151