Use of FGF21 analogs for the treatment of metabolic disorders: a systematic review and meta-analysis

被引:7
|
作者
Carbonetti, Maria Paula [1 ]
Almeida-Oliveira, Fernanda [2 ]
Majerowicz, David [1 ,3 ]
机构
[1] Univ Fed Rio de Janeiro, Fac Farm, Rio De Janeiro, RJ, Brazil
[2] Univ Fed Rio de Janeiro, Inst Bioquim Med Leopoldo de Meis, Rio De Janeiro, RJ, Brazil
[3] Univ Estado Rio de Janeiro, Programa Posgrad Biociencias, Rio De Janeiro, RJ, Brazil
来源
关键词
FGF21; blood glucose; metabolic syndrome; glycated hemoglobin A; fasting; blood pressure; obesity; lipids; BROWN ADIPOSE-TISSUE; NONALCOHOLIC STEATOHEPATITIS; INSULIN GLARGINE; PEGYLATED FGF21; BODY-WEIGHT; FIBROBLAST; GLUCOSE; FGF-21; MICE; PHARMACOKINETICS;
D O I
10.20945/2359-4292-2022-0493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
FGF21 is a hormone produced primarily by the liver with several metabolic functions, such as induction of heat production, control of glucose homeostasis, and regulation of blood lipid levels. Due to these actions, several laboratories have developed FGF21 analogs to treat patients with metabolic disorders such as obesity and diabetes. Here, we performed a systematic review and metaanalysis of randomized controlled trials that used FGF21 analogs and analyzed metabolic outcomes. Our search yielded 236 articles, and we included eight randomized clinical trials in the meta-analysis. The use of FGF21 analogs exhibited no effect on fasting blood glucose, glycated hemoglobin, HOMA index, blood free fatty acids or systolic blood pressure. However, the treatment significantly reduced fasting insulinemia, body weight and total cholesterolemia. None of the included studies were at high risk of bias. The quality of the evidence ranged from moderate to very low, especially due to imprecision and indirection issues. These results indicate that FGF21 analogs can potentially treat metabolic syndrome. However, more clinical trials are needed to increase the quality of evidence and confirm the effects seen thus far.
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页数:14
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