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衰弱评分能否预测癌症的发生?来自两项大型基于人群的研究结果。

Can frailty scores predict the incidence of cancer? Results from two large population-based studies.

机构信息

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels Väg 12A, 171 77, Stockholm, Sweden.

Department of Clinical Sciences, Danderyd Hospital, Karolinska Institutet, Stockholm, Sweden.

出版信息

Geroscience. 2023 Jun;45(3):2051-2064. doi: 10.1007/s11357-023-00783-9. Epub 2023 Mar 30.

Abstract

While chronological age is the single biggest risk factor for cancer, it is less clear whether frailty, an age-related state of physiological decline, may also predict cancer incidence. We assessed the associations of frailty index (FI) and frailty phenotype (FP) scores with the incidence of any cancer and five common cancers (breast, prostate, lung, colorectal, melanoma) in 453,144 UK Biobank (UKB) and 36,888 Screening Across the Lifespan Twin study (SALT) participants, who aged 38-73 years and had no cancer diagnosis at baseline. During a median follow-up of 10.9 and 10.7 years, 53,049 (11.7%) and 4,362 (11.8%) incident cancers were documented in UKB and SALT, respectively. Using multivariable-adjusted Cox models, we found a higher risk of any cancer in frail vs. non-frail UKB participants, when defined by both FI (hazard ratio [HR] = 1.22; 95% confidence interval [CI] = 1.17-1.28) and FP (HR = 1.16; 95% CI = 1.11-1.21). The FI in SALT similarly predicted risk of any cancer (HR = 1.31; 95% CI = 1.15-1.49). Moreover, frailty was predictive of lung cancer in UKB, although this association was not observed in SALT. Adding frailty scores to models including age, sex, and traditional cancer risk factors resulted in little improvement in C-statistics for most cancers. In a within-twin-pair analysis in SALT, the association between FI and any cancer was attenuated within monozygotic but not dizygotic twins, indicating that it may partly be explained by genetic factors. Our findings suggest that frailty scores are associated with the incidence of any cancer and lung cancer, although their clinical utility for predicting cancers may be limited.

摘要

虽然年龄是癌症的最大单一风险因素,但衰弱(一种与年龄相关的生理衰退状态)是否也可以预测癌症的发生尚不清楚。我们评估了虚弱指数(FI)和虚弱表型(FP)评分与 453144 名英国生物库(UKB)和 36888 名筛查一生双胞胎研究(SALT)参与者中任何癌症和五种常见癌症(乳腺癌、前列腺癌、肺癌、结直肠癌、黑色素瘤)的发病率之间的关联,这些参与者年龄在 38-73 岁之间,在基线时没有癌症诊断。在中位随访 10.9 年和 10.7 年后,UKB 和 SALT 分别记录了 53049 例(11.7%)和 4362 例(11.8%)的新发癌症病例。使用多变量调整的 Cox 模型,我们发现与非虚弱的 UKB 参与者相比,虚弱参与者患任何癌症的风险更高,无论 FI(危险比[HR] = 1.22;95%置信区间[CI] = 1.17-1.28)还是 FP(HR = 1.16;95% CI = 1.11-1.21)定义。SALT 中的 FI 也同样预测了任何癌症的风险(HR = 1.31;95% CI = 1.15-1.49)。此外,虚弱与 UKB 中的肺癌有关,但在 SALT 中没有观察到这种关联。在包括年龄、性别和传统癌症风险因素在内的模型中加入虚弱评分,对大多数癌症的 C 统计数据的改善很小。在 SALT 中的双胞胎内分析中,FI 与任何癌症之间的关联在同卵双胞胎中减弱,但在异卵双胞胎中没有减弱,这表明它可能部分由遗传因素解释。我们的研究结果表明,虚弱评分与任何癌症和肺癌的发病率有关,但它们在预测癌症方面的临床应用可能有限。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4c/10400738/75d14ccaf2df/11357_2023_783_Fig1_HTML.jpg

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