{"title":"多囊卵巢综合征与非酒精性脂肪肝风险的相关性:一项荟萃分析。","authors":"Kui Yao, Heng Zheng, Hongling Peng","doi":"10.5603/ep.93291","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>There have been many studies assessing whether abnormal metabolic and hormone levels among women with polycystic ovary syndrome (PCOS) are associated with a greater risk of non-alcoholic fatty liver disease (NAFLD). However, previous studies repported no consistent outcomes. To provide a comprehensive evaluation regarding the role of PCOS in the risk of NAFLD, we updated the published literature and conducted this systemic review and meta-analysis.</p><p><strong>Material and methods: </strong>Electronic databases (Web of Science and PubMed) were searched for literature up to October 2022. We used STATA 12.0 software to compute odds ratios (ORs) and 95% confidence intervals (CIs), to evaluate the association between PCOS and risk of NAFLD.</p><p><strong>Results: </strong>The study indicated that PCOS was significantly related to an elevated risk of NAFLD (OR = 2.93, 95% CI 2.38 to 3.62, I2 = 83.7%, p < 0.001). Meta-regression analysis showed that age and body mass index (BMI) were not responsible for heterogeneity across the studies (age: p = 0.096; BMI: p = 0.418). Sensitivity analysis indicated no alteration in the direction of effect when any study was eliminated. Begg's test, Egger's test, Begg's test, and funnel plot indicated a significant risk of publication bias (Egger's test: p = 0.028; Begg's test: p < 0.001).</p><p><strong>Conclusion: </strong>This meta-analysis reported that PCOS was associated with an elevated risk of NAFLD. Early proper detection of NAFLD for PCOS women is essential. All patients with PCOS should undergo appropriate diagnostics for early detection of fatty liver and fibrosis.</p>","PeriodicalId":93990,"journal":{"name":"Endokrynologia Polska","volume":" ","pages":"520-527"},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association between polycystic ovary syndrome and risk of non-alcoholic fatty liver disease: a meta-analysis.\",\"authors\":\"Kui Yao, Heng Zheng, Hongling Peng\",\"doi\":\"10.5603/ep.93291\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>There have been many studies assessing whether abnormal metabolic and hormone levels among women with polycystic ovary syndrome (PCOS) are associated with a greater risk of non-alcoholic fatty liver disease (NAFLD). However, previous studies repported no consistent outcomes. To provide a comprehensive evaluation regarding the role of PCOS in the risk of NAFLD, we updated the published literature and conducted this systemic review and meta-analysis.</p><p><strong>Material and methods: </strong>Electronic databases (Web of Science and PubMed) were searched for literature up to October 2022. We used STATA 12.0 software to compute odds ratios (ORs) and 95% confidence intervals (CIs), to evaluate the association between PCOS and risk of NAFLD.</p><p><strong>Results: </strong>The study indicated that PCOS was significantly related to an elevated risk of NAFLD (OR = 2.93, 95% CI 2.38 to 3.62, I2 = 83.7%, p < 0.001). Meta-regression analysis showed that age and body mass index (BMI) were not responsible for heterogeneity across the studies (age: p = 0.096; BMI: p = 0.418). Sensitivity analysis indicated no alteration in the direction of effect when any study was eliminated. Begg's test, Egger's test, Begg's test, and funnel plot indicated a significant risk of publication bias (Egger's test: p = 0.028; Begg's test: p < 0.001).</p><p><strong>Conclusion: </strong>This meta-analysis reported that PCOS was associated with an elevated risk of NAFLD. Early proper detection of NAFLD for PCOS women is essential. 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引用次数: 0
摘要
引言:已有许多研究评估多囊卵巢综合征(PCOS)女性代谢和激素水平异常是否与非酒精性脂肪肝(NAFLD)的更大风险相关。然而,先前的研究没有报告一致的结果。为了对多囊卵巢综合征在NAFLD风险中的作用进行全面评估,我们更新了已发表的文献,并进行了系统综述和荟萃分析。材料和方法:检索电子数据库(Web of Science和PubMed)中截至2022年10月的文献。我们使用STATA 12.0软件计算比值比(OR)和95%置信区间(CI),评估PCOS与NAFLD风险之间的相关性。结果:研究表明,PCOS与非酒精性肝病风险升高显著相关(OR=2.93,95%CI 2.38至3.62,I2=83.7%,p<0.001)。荟萃回归分析显示,年龄和体重指数(BMI)不是研究异质性的原因(年龄:p=0.096;BMI:p=0.418)。敏感性分析表明在消除任何研究时,作用方向没有改变。Begg检验、Egger检验、Begg检验和漏斗图显示有显著的发表偏倚风险(Egger检验:p=0.028;Begg检验:p<0.001)。结论:该荟萃分析报告PCOS与NAFLD风险升高有关。PCOS妇女早期正确检测NAFLD是至关重要的。所有多囊卵巢综合征患者都应接受适当的诊断,以早期发现脂肪肝和纤维化。
Association between polycystic ovary syndrome and risk of non-alcoholic fatty liver disease: a meta-analysis.
Introduction: There have been many studies assessing whether abnormal metabolic and hormone levels among women with polycystic ovary syndrome (PCOS) are associated with a greater risk of non-alcoholic fatty liver disease (NAFLD). However, previous studies repported no consistent outcomes. To provide a comprehensive evaluation regarding the role of PCOS in the risk of NAFLD, we updated the published literature and conducted this systemic review and meta-analysis.
Material and methods: Electronic databases (Web of Science and PubMed) were searched for literature up to October 2022. We used STATA 12.0 software to compute odds ratios (ORs) and 95% confidence intervals (CIs), to evaluate the association between PCOS and risk of NAFLD.
Results: The study indicated that PCOS was significantly related to an elevated risk of NAFLD (OR = 2.93, 95% CI 2.38 to 3.62, I2 = 83.7%, p < 0.001). Meta-regression analysis showed that age and body mass index (BMI) were not responsible for heterogeneity across the studies (age: p = 0.096; BMI: p = 0.418). Sensitivity analysis indicated no alteration in the direction of effect when any study was eliminated. Begg's test, Egger's test, Begg's test, and funnel plot indicated a significant risk of publication bias (Egger's test: p = 0.028; Begg's test: p < 0.001).
Conclusion: This meta-analysis reported that PCOS was associated with an elevated risk of NAFLD. Early proper detection of NAFLD for PCOS women is essential. All patients with PCOS should undergo appropriate diagnostics for early detection of fatty liver and fibrosis.