Efficacy and safety of hydroxychloroquine for managing glycemia in type-2 diabetes: A systematic review and meta-analysis

被引:5
|
作者
Dutta, D. [1 ]
Jindal, R. [2 ,3 ]
Mehta, D. [4 ]
Kumar, M. [5 ]
Sharma, M. [6 ]
机构
[1] CEDAR Superspecial Clin, Dept Endocrinol, New Delhi, India
[2] Vardhman Mahavir Med Coll, Dept Endocrinol, New Delhi, India
[3] Safdarjang Hosp, New Delhi, India
[4] CEDAR Superspecial Clin, Dept Gastroenterol, New Delhi, India
[5] CEDAR Superspecial Clin, Dept Endocrinol, Zirakpur, India
[6] CEDAR Superspecial Clin, Dept Rheumatol, New Delhi, India
关键词
Hydroxychloroquine; inflammation; meta-analysis; retinopathy; type-2; diabetes; DOUBLE-BLIND; MELLITUS; TENELIGLIPTIN; CHLOROQUINE; COMBINATION; METFORMIN; QUALITY; THERAPY;
D O I
10.4103/jpgm.JPGM_301_21
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: No Cochrane meta-analysis with grading of evidence is available on use of hydroxychloroquine (HCQ) in type-2 diabetes (T2DM). This meta-analysis evaluated the efficacy and safety of HCQ in T2DM.Methods: Electronic databases were searched using a Boolean search strategy: ((hydroxychloroquine) OR (chloroquine*)) AND ((diabetes) OR ("diabetes mellitus") OR (glycemia) OR (glucose) OR (insulin)) for studies evaluating hydroxychloroquine for glycemic control in T2DM. The primary outcome was a change in glycated haemoglobin (HbA1c). The secondary outcomes were changes in other glycemic/lipid parameters and adverse effects.Results: Data from 11 randomized controlled trials (RCTs) (3 having placebo as controls [passive controls] and 8 having anti-diabetes medications as controls [active controls]) involving 2,723 patients having a median follow-up of 24 weeks were analyzed. About 54.54% of the RCTs were of poor quality as evaluated by the Jadad scale. The performance bias and detection bias were at high risk in 63.64% of the RCTs. The HbA1c reduction with HCQ was marginally better compared to the active (mean differences [MD]-0.17% [95%, CI:-0.30--0.04;P=0.009;I-2=89%; very low certainty of evidence, VLCE]), and passive (MD-1.35% [95%CI:-2.10--0.59;P=0.005;I-2=74%]) controls. A reduction in fasting glucose (MD-16.63mg/dL[95%, CI:-25.99 --7.28mg/dL;P<0.001;I-2=97%;VLCE]) and post-prandial glucose [MD-8.41mg/dL (95%CI:-14.71 --2.12mg/ dL;P=0.009;I-2=87%;VLCE]), appeared better with HCQ compared to active controls. The total adverse events (risk ratio [RR]0.93 [95% CI:0.68-1.28]; P=0.65;I-2=66%) were not different with HCQ compared to the controls.Conclusion: The routine use of HCQ in T2DM cannot be recommended based on the current evidence.
引用
收藏
页码:85 / 92
页数:8
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