Bristol Medical School, Translational Health Sciences, University of Bristol, Learning and Research Building, Level 2, Southmead Hospital, Bristol, UK.
Bristol Medical School, Population Health Sciences, University of Bristol, Bristol, UK.
Sci Rep. 2021 Jan 11;11(1):320. doi: 10.1038/s41598-020-79345-4.
Obesity is associated with an increased risk of advanced, recurrent and fatal prostate cancer. Adipokines may mediate this relationship. We conducted a systematic review and meta-analysis of associations of leptin and adiponectin with overall and aggressive prostate cancer. Bibliographic databases were systematically searched up to 1st April 2017. Log Odds Ratios (ORs) per 2.5 unit increase in adiponectin or leptin levels were derived and pooled. All analyses were stratified by study type (cross-sectional/prospective). 746 papers were retrieved, 34 eligible studies identified, 31 of these could be included in the meta-analysis. Leptin was not consistently associated with overall prostate cancer (pooled OR 1.00, 95%CI 0.98-1.02, per 2.5 ng/ml increase, prospective study OR 0.97, 95%CI 0.95-0.99, cross-sectional study OR 1.19, 95%CI 1.13-1.26) and there was weak evidence of a positive association with aggressive disease (OR 1.03, 95%CI 1.00-1.06). There was also weak evidence of a small inverse association of adiponectin with overall prostate cancer (OR 0.96, 95%CI 0.93-0.99, per 2.5 µg/ml increase), but less evidence of an association with aggressive disease (OR 0.98, 95%CI 0.94-1.01). The magnitude of any effects are small, therefore levels of circulating adiponectin or leptin alone are unlikely to be useful biomarkers of risk or prognosis.
肥胖与晚期、复发性和致命性前列腺癌的风险增加有关。脂肪因子可能介导这种关系。我们对瘦素和脂联素与总体和侵袭性前列腺癌的相关性进行了系统评价和荟萃分析。系统地检索了截至 2017 年 4 月 1 日的文献数据库。根据脂联素或瘦素水平每增加 2.5 个单位,得出并汇总了对数优势比(OR)。所有分析均按研究类型(横断面/前瞻性)分层。共检索到 746 篇论文,确定了 34 项符合条件的研究,其中 31 项可纳入荟萃分析。瘦素与总体前列腺癌无一致性相关性(汇总 OR 1.00,95%CI 0.98-1.02,每增加 2.5ng/ml,前瞻性研究 OR 0.97,95%CI 0.95-0.99,横断面研究 OR 1.19,95%CI 1.13-1.26),且与侵袭性疾病呈弱正相关(OR 1.03,95%CI 1.00-1.06)。脂联素与总体前列腺癌也呈弱负相关(OR 0.96,95%CI 0.93-0.99,每增加 2.5μg/ml),但与侵袭性疾病的相关性证据较少(OR 0.98,95%CI 0.94-1.01)。任何效应的幅度都很小,因此循环脂联素或瘦素的水平本身不太可能成为风险或预后的有用生物标志物。