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肾功能 eGFR 范围内的癌症结局的性别差异。

Sex differences in cancer outcomes across the range of eGFR.

机构信息

NHS Greater Glasgow and Clyde, G12 0XH, UK.

School of Medicine, Dentistry and Nursing, University of Glasgow, Glasgow G12 8QQ, UK.

出版信息

Nephrol Dial Transplant. 2024 Oct 30;39(11):1799-1808. doi: 10.1093/ndt/gfae059.

Abstract

BACKGROUND

People with chronic kidney disease (CKD) have increased incidence and mortality of most cancer types. We hypothesized that the odds of presenting with advanced cancer may vary according to differences in estimated glomerular filtration rate (eGFR), that this could contribute to increased all-cause mortality and that sex differences may exist.

METHODS

Data were from Secure Anonymised Information Linkage Databank, including people with de novo cancer diagnosis (2011-17) and two kidney function tests within 2 years prior to diagnosis to determine baseline eGFR (mL/min/1.73 m2). Logistic regression models determined the odds of presenting with advanced cancer by baseline eGFR. Cox proportional hazards models tested associations between baseline eGFRCr and all-cause mortality.

RESULTS

eGFR <30 was associated with higher odds of presenting with advanced cancer of prostate, breast and female genital organs, but not other cancer sites. Compared with eGFR >75-90, eGFR <30 was associated with greater hazards of all-cause mortality in both sexes, but the association was stronger in females [female: hazard ratio (HR) 1.71, 95% confidence interval (CI) 1.56-1.88; male versus female comparison: HR 0.88, 95% CI 0.78-0.99].

CONCLUSIONS

Lower or higher eGFR was not associated with substantially higher odds of presenting with advanced cancer across most cancer sites, but was associated with reduced survival. A stronger association with all-cause mortality in females compared with males with eGFR <30 is concerning and warrants further scrutiny.

摘要

背景

患有慢性肾病(CKD)的人群发生大多数癌症类型的发病率和死亡率均增加。我们假设,出现晚期癌症的可能性可能因估计肾小球滤过率(eGFR)的差异而有所不同,这可能导致全因死亡率增加,并且可能存在性别差异。

方法

数据来自安全匿名信息链接数据库,包括新诊断患有癌症的患者(2011-17 年)以及在诊断前 2 年内进行的两次肾功能检查,以确定基线 eGFR(mL/min/1.73 m2)。逻辑回归模型确定了基线 eGFR 下出现晚期癌症的几率。Cox 比例风险模型检验了基线 eGFR/Cr 与全因死亡率之间的关联。

结果

eGFR <30 与前列腺癌、乳腺癌和女性生殖器官癌的晚期癌症发病几率较高相关,但与其他癌症部位无关。与 eGFR >75-90 相比,eGFR <30 与两性全因死亡率的风险增加相关,但在女性中关联更强[女性:危险比(HR)1.71,95%置信区间(CI)1.56-1.88;男性与女性比较:HR 0.88,95%CI 0.78-0.99]。

结论

较低或较高的 eGFR 与大多数癌症部位的晚期癌症发病几率的显著增加无关,但与生存率降低有关。eGFR <30 的女性与男性相比,与全因死亡率的关联更强,令人担忧,需要进一步审查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0455/11648947/013eb780db6a/gfae059fig1g.jpg

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