癌症恶病质的 LDH 与 GLIM 标准之间的关系:系统回顾与元分析。

Joshua Thompson, Josh McGovern, Campbell Roxburgh, Joanne Edwards, Ross D Dolan, Donald C McMillan
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引用次数: 0

摘要

导言癌症恶病质是一种临床症状,其特点是伴随瘦身组织减少的可识别 "病态行为"。全球营养不良领导委员会(GLIM)提出了表型(无意的体重减轻、低体重指数和低肌肉质量)和病因(食物摄入减少、炎症或疾病负担)诊断标准。最近的研究表明,血清乳酸脱氢酶(LDH)可能是第三个病因学标准。但人们对其与 GLIM 的关系知之甚少。我们对它们的比较预后价值和关联性进行了系统回顾和荟萃分析:方法:对截至 2023 年 2 月的电子数据库(PubMed、Medline、Ovid、Cochrane)进行了检索,以确定对 LDH 和癌症 GLIM 标准的预后价值进行比较的研究。在数据可用的情况下,对 LDH 与 GLIM 各项指标之间的关系进行了分析。RevMan 5.4.1 用于对每种诊断标准进行荟萃分析,只要有 3 项或 3 项以上的研究报告了总生存期(OS)的危险比和 95% 的置信区间:结果:共审查了 119 项研究。晚期肺癌是研究最多的人群。纳入荟萃分析的研究包括:6 项关于 LDH 和体重减轻的研究(n=2,165)、17 项关于 LDH 和低体重指数的研究(n=7,540)、5 项关于 LDH 和低肌肉质量的研究(n=758)、0 项关于 LDH 和食物摄入量的研究以及 97 项关于 LDH 和炎症的研究(n=37,185)。血清 LDH 升高与低体重指数(OR 1.39,1.09 - 1.77;P=0.008)、NLR 升高(OR 2.04,1.57 - 2.65;P 结论:目前的文献表明,血清 LDH 升高与癌症中的炎症(GLIM 的病因学标准)有关,但还需要做更多的工作来确定 LDH 与 GLIM 表型成分之间的关系。此外,与 GLIM 标准相比,血清 LDH 升高似乎是癌症总生存期的一个比较预后指标。
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The relationship between LDH and GLIM criteria for cancer cachexia: Systematic Review and Meta-Analysis.

Introduction: Cancer cachexia is a clinical condition characterized by recognizable "sickness behaviors" accompanied by loss of lean body tissue. The Global Leadership on Malnutrition (GLIM) has proposed phenotypic (unintentional weight loss, low body mass index and low muscle mass) and aetiologic (reduced food intake and inflammation or disease burden) diagnostic criteria. Recent work has suggested serum lactate dehydrogenase (LDH) might represent a 3rd aetiologic criteria. Little is known of its relationship with GLIM. A systematic review and meta-analysis of their comparative prognostic value and association was performed.

Methods: A search of electronic databases (PubMed, Medline, Ovid, Cochrane) up to February 2023 was used to identify studies that compared the prognostic value of LDH and components of the GLIM criteria in cancer. An analysis of the relationship between LDH and the components of GLIM was undertaken where this data was available. RevMan 5.4.1 was used to perform a meta-analysis for each diagnostic criteria that had 3 or more studies which reported hazard ratios with a 95 per cent confidence interval for overall survival (OS).

Results: A total of 119 studies were reviewed. Advanced lung cancer was the most studied population. Included in the meta-analysis were 6 studies (n=2,165) on LDH and weight loss, 17 studies (n=7,540) on LDH and low BMI, 5 studies (n=758) on LDH and low muscle mass, 0 studies on LDH and food intake and 97 studies (n=37,185) on LDH and inflammation. There was a significant association between elevated serum LDH and each of low BMI (OR 1.39, 1.09 - 1.77; p=0.008), elevated NLR (OR 2.04, 1.57 - 2.65; p<0.00001) and elevated CRP (OR 2.58, 1.81 - 3.67; p<0.00001). There was no association between elevated serum LDH and low muscle mass. Only one study presented data on the association between LDH and unintentional weight loss. Elevated LDH showed a comparative OS (HR 1.86, 1.60 - 2.16; p<0.00001) to unintentional weight loss (HR 1.57, 1.23 - 1.99; p=0.0002) and had a similar OS (HR 2.01, 1.73 - 2.34; p<0.00001) to low BMI (HR 1.57, 1.29 -2.90; p<0.0001). LDH also showed an OS (HR 2.25, 1.76 - 2.87; p<0.00001) congruous with low muscle mass (HR 1.93, 1.14 - 3.27; p=0.01) and again, LDH conferred as poor an OS (HR 1.71, 1.60 - 1.82; p<0.00001) as elevated NLR (HR 1.57, 1.44 - 1.71; p<0.00001) or CRP (HR 1.53, 1.41 - 1.65; p<0.00001).

Conclusion: Current literature suggests elevated serum LDH is associated with inflammation in cancer (an aetiologic GLIM criterion), however more work is required to establish the relationship between LDH and the phenotypic components of GLIM. Additionally, elevated serum LDH appears to be a comparative prognosticator of overall survival in cancer when compared to the GLIM criteria.

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