Association between circulating leptin concentration and G-2548A gene polymorphism in patients with breast cancer: a meta-analysis

The aim of this meta-analysis was to summarize the evidence on the serum/plasma leptin concentrations in breast cancer (BC) patients, as well as the associations between leptin gene polymorphisms and susceptibility to BC. Potentially relevant studies about serum/plasma leptin levels and leptin gene...

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Veröffentlicht in:Archives of medical science 2019-03, Vol.15 (2), p.275-283
Hauptverfasser: Hao, Ji-Qing, Zhang, Qian-Kun, Zhou, Yi-Xin, Chen, Li-Hao, Wu, Peng-Fei
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Sprache:eng
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Zusammenfassung:The aim of this meta-analysis was to summarize the evidence on the serum/plasma leptin concentrations in breast cancer (BC) patients, as well as the associations between leptin gene polymorphisms and susceptibility to BC. Potentially relevant studies about serum/plasma leptin levels and leptin gene polymorphism were selected using the electronic databases PubMed, EMBASE and The Cochrane Library (from January 1 1995 to Jun 30 2017, no language restrictions). The potential sources of heterogeneity were assessed by the statistic and quantified using ; publication bias was qualitatively assessed by funnel plot and quantitatively assessed by Egger's linear regression test. A total of 1141 articles were retrieved after database searches, and 27 studies with 9516 subjects (4542 BC patients/4974 controls) were finally included. The results indicated that BC patients had significantly higher leptin levels compared with healthy controls (SMD = 1.65, 95% CI: 1.21-2.09, < 0.001), but there was no association between leptin polymorphism and BC (OR = 1.05, 95% CI: 0.80-1.39, 0.722). Subgroup analyses demonstrated increased leptin levels in BC patients of different region, race, body mass index and waist circumference. Our results revealed a significantly higher leptin level in BC patients than in healthy controls, but no association between leptin polymorphism and BC susceptibility was found.
ISSN:1734-1922
1896-9151
DOI:10.5114/aoms.2018.75638