Dipeptidyl peptidase-4 inhibitors and risk of arthralgia: A systematic review and meta-analysis

被引:22
作者
Men, P. [1 ]
He, N. [1 ,2 ]
Song, C. [3 ]
Zhai, S. [1 ]
机构
[1] Peking Univ, Dept Pharm, Hosp 3, 49 Huayuan North Rd, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Pharmaceut Sci, Dept Pharm Adm & Clin Pharm, Beijing, Peoples R China
[3] Peking Univ, Hosp 3, Dept Orthopaed, Beijing, Peoples R China
关键词
Arthralgia; Dipeptidyl peptidase-4 inhibitors; Meta-analysis; Systematic review; RHEUMATOID-ARTHRITIS; SAFETY; SITAGLIPTIN; EFFICACY; TOLERABILITY; MONOTHERAPY;
D O I
10.1016/j.diabet.2017.05.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. - The US Food and Drug Administration has warned that treatment with dipeptidyl peptidase (DPP)-4 inhibitors may promote serious arthralgia. However, the clinical evidence for this is relatively lacking. Objective. - For this reason, a systematic review and meta-analysis of randomized controlled trials (RCTs) were carried out to determine the relationship between DPP -4 inhibitors and risk of arthralgia, and also to investigate any potential risk factors. Methods. - An extensive electronic search for RCTs comparing DPP -4 inhibitors with any comparators was performed up to July 2016. Outcomes of interest were overall and serious arthralgia. Summary risk ratios (RRs) with 95% confidence intervals (CIs) were calculated. Results. - A total of 67 RCTs (involving 79,110 patients) was ultimately included. Pooled results showed that DPP -4 inhibitors were associated with a slightly but significantly increased risk of overall arthralgia (RR: 1.13, 95% CI: 1.04-1.22; P = 0.003) and a non-significant increased risk of serious arthralgia (RR: 1.44, 95% CI: 0.83-2.51; P = 0.20). Also, subgroup analyses showed that add-on/combination therapy and longer diabetes duration (> 5 years) were possible factors associated with the increased risk of overall arthralgia. Conclusion. - These findings suggest that DPP -4 inhibitors can increase the risk of arthralgia. Thus, the benefits of glycaemic control must be weighed against the risk of arthralgia when prescribing DPP -4 inhibitors. Further studies are now needed to identify and confirm these risk factors. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:493 / 500
页数:8
相关论文
共 29 条
[1]  
[Anonymous], 2016, IDF Diabetes Atlas, V7th
[2]  
[Anonymous], 2015, FDA DRUG SAF COMM FD
[3]   Effect of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2 diabetes [J].
Aschner, Pablo ;
Kipnes, Mark S. ;
Lunceford, Jared K. ;
Sanchez, Matilde ;
Mickel, Carolyn ;
Williams-Herman, Debora E. .
DIABETES CARE, 2006, 29 (12) :2632-2637
[4]   Influence of HLA DRB1 alleles in the susceptibility of rheumatoid arthritis and the regulation of antibodies against citrullinated proteins and rheumatoid factor [J].
Balsa, Alejandro ;
Cabezon, Arancha ;
Orozco, Gisela ;
Cobo, Tatiana ;
Miranda-Carus, Eugenia ;
Angel Lopez-Nevot, Miguel ;
Luis Vicario, Jose ;
Martin-Mola, Emilio ;
Martin, Javier ;
Pascual-Salcedo, Dora .
ARTHRITIS RESEARCH & THERAPY, 2010, 12 (02)
[5]  
Bekiari E, 2015, ENDOCRINE, V52, P1
[6]   A highly efficacious lymphocyte chemoattractant, stromal cell-derived factor 1 (SDF-1) [J].
Bleul, CC ;
Fuhlbrigge, RC ;
Casasnovas, JM ;
Aiuti, A ;
Springer, TA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (03) :1101-1109
[7]   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
[8]   Dipeptidyl peptidase-4 inhibition and the treatment of type 2 diabetes - Preclinical biology and mechanisms of action [J].
Drucker, Daniel J. .
DIABETES CARE, 2007, 30 (06) :1335-1343
[9]   A review of newer treatment approaches for type-2 diabetes: Focusing safety and efficacy of incretin based therapy [J].
George, Regin Elsa ;
Joseph, Siby .
SAUDI PHARMACEUTICAL JOURNAL, 2014, 22 (05) :403-410
[10]   Quantifying heterogeneity in a meta-analysis [J].
Higgins, JPT ;
Thompson, SG .
STATISTICS IN MEDICINE, 2002, 21 (11) :1539-1558