Laufer Menachem, Perelman Maxim, Sarfaty Michal, Itelman Edward, Segal Gad
Department of Urology, Chaim Sheba Medical Center, Ramat Gan, Israel.
Department of Internal Medicine T, Chaim Sheba Medical Center, Ramat Gan, Israel.
Eur Urol Open Sci. 2023 Aug 22;55:38-44. doi: 10.1016/j.euros.2023.07.007. eCollection 2023 Sep.
Sarcopenia is characterized by loss of muscle mass and function and is associated with frailty, a syndrome with higher likelihood of falls, fractures, physical disability, and mortality. Both frailty and sarcopenia are known markers of shorter survival in various cancer patient populations. Low alanine aminotransferase (ALT), reflecting loss of muscle mass (sarcopenia), may be associated with greater frailty and shorter survival in multiple cancers.
To assess the potential association between low ALT and shorter survival among prostate cancer (PCa) patients and survivors.
This was a retrospective analysis of a historical cohort of PCa patients and survivors. Patients were defined as those still actively receiving PCa treatment, while those no longer receiving such treatment were classified as PCa survivors.
ALT data were obtained from results for basic biochemical blood testing carried out for patients on their first hospital admission. Patients were divided into two groups: those with ALT ≥17 IU/l and those with ALT <17 IU/l. Univariate and multivariable analyses were conducted for between-group survival comparisons.
We identified 9489 PCa records. The final study cohort with ALT data available included 4064 patients with ALT <40 IU/l. Of this cohort, 536 patients were actively receiving medical anticancer therapy for PCa. The mean age for the entire cohort was 74.6 yr (standard deviation 9.6) and the median ALT level was 19.28 IU/l; 1676 patients (41%) had low ALT (<17 IU/l). On univariate analysis, low ALT was associated with a 78% increase in mortality risk (95% confidence interval [CI] 1.62-1.97; < 0.001). A sensitivity analysis of the 536 patients actively receiving medical anticancer treatment revealed that low ALT was associated with a 48% increase in mortality risk (95% CI 1.19-1.85; = 0.001). In a multivariable model controlled for age, kidney disease, history of cerebrovascular event/transient ischemic attack, and baseline prostate-specific antigen, low ALT was still associated with a 35% increase in mortality risk (95% CI 1.12-1.63; = 0.001). Limitations include the single-center, retrospective design.
Low ALT, which is indicative of sarcopenia and frailty, is associated with shorter survival among PCa patients and survivors and could potentially be used for treatment personalization.
We compared survival for prostate cancer patients and survivors according to their blood level of the protein alanine aminotransferase (ALT). Low ALT levels in the general population are associated with loss of muscle mass. We found that in our group of prostate cancer patients and survivors, the risk of death from any cause was higher for those with low ALT levels.
肌肉减少症的特征是肌肉质量和功能丧失,与衰弱相关,衰弱是一种跌倒、骨折、身体残疾和死亡风险更高的综合征。衰弱和肌肉减少症都是各种癌症患者群体生存时间缩短的已知标志物。低丙氨酸转氨酶(ALT)反映肌肉质量丧失(肌肉减少症),可能与多种癌症患者更严重的衰弱和更短的生存期有关。
评估前列腺癌(PCa)患者及幸存者中低ALT与较短生存期之间的潜在关联。
设计、设置和参与者:这是一项对PCa患者及幸存者历史队列的回顾性分析。患者被定义为仍在积极接受PCa治疗的人,而不再接受此类治疗的人则被归类为PCa幸存者。
ALT数据来自患者首次入院时进行的基本生化血液检测结果。患者分为两组:ALT≥17 IU/l的患者和ALT<17 IU/l的患者。进行单因素和多因素分析以比较两组之间的生存期。
我们识别出9489条PCa记录。最终纳入的有可用ALT数据的研究队列包括4064例ALT<40 IU/l的患者。在该队列中,536例患者正在积极接受PCa的抗癌治疗。整个队列的平均年龄为74.6岁(标准差9.6),ALT中位数水平为19.28 IU/l;1676例患者(41%)ALT较低(<17 IU/l)。单因素分析显示,低ALT与死亡风险增加78%相关(95%置信区间[CI]1.62 - 1.97;P<0.0)。对536例正在积极接受抗癌治疗的患者进行的敏感性分析显示,低ALT与死亡风险增加48%相关(95%CI 1.19 - 1.85;P = 0.001)。在控制了年龄、肾脏疾病、脑血管事件/短暂性脑缺血发作史和基线前列腺特异性抗原的多因素模型中,低ALT仍与死亡风险增加35%相关(95%CI 1.12 - 1.63;P = 0.001)。局限性包括单中心、回顾性设计。
低ALT表明存在肌肉减少症和衰弱,与PCa患者及幸存者的生存期较短相关,并且可能可用于个性化治疗。
我们根据前列腺癌患者及幸存者血液中丙氨酸转氨酶(ALT)蛋白水平比较了他们的生存期。一般人群中低ALT水平与肌肉质量丧失有关。我们发现,在我们的前列腺癌患者及幸存者群体中,ALT水平低的患者因任何原因死亡的风险更高。