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肾脏和尿路先天性异常与成年期尿路癌风险

Congenital Anomalies of the Kidney and Urinary Tract and Adulthood risk of Urinary Tract Cancer.

作者信息

Calderon-Margalit Ronit, Efron Gil, Pleniceanu Oren, Tzur Dorit, Stern-Zimmer Michal, Afek Arnon, Erlich Tomer, Derazne Estela, Kark Jeremy D, Keinan-Boker Lital, Twig Gilad, Vivante Asaf

机构信息

Hadassah-Hebrew University Braun School of Public Health, Jerusalem, Israel.

Department of Military Medicine, Hebrew University of Jerusalem, Jerusalem and the Israel Defense Forces Medical Corps, Ramat Gan, Israel.

出版信息

Kidney Int Rep. 2021 Jan 10;6(4):946-952. doi: 10.1016/j.ekir.2021.01.003. eCollection 2021 Apr.

DOI:10.1016/j.ekir.2021.01.003
PMID:33912744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8071628/
Abstract

INTRODUCTION

Congenital anomalies of the kidney and urinary tract (CAKUT) are the most common kidney diseases in childhood. Alterations in genes governing nephrogenesis may cause CAKUT, and in some cases may contribute to development of urinary tract (UT) tumors later in life. We aimed to assess the association between CAKUT and UT cancer in adulthood.

METHODS

We conducted a population-based historical cohort study encompassing 1,510,042 recruits to the Israeli army between 1967 and 1997. CAKUT exposure was determined by army medical coding of CAKUT in childhood. Incidence of UT cancer (kidney, ureter, or bladder) was available through record linkage with the Israeli Cancer Registry. Recruits were followed from the prerecruitment assessment until cancer diagnosis, death, or study termination, in 2012. Cox proportional hazards models were constructed to estimate the hazard ratios (HRs) for UT cancer in participants with vs. without CAKUT.

RESULTS

During a mean follow-up of 30.4 years, 2959 participants (2573 men and 386 women) developed UT cancer. Men with CAKUT exhibited an increased risk of UT cancer compared with men without CAKUT, yielding an adjusted HR of 1.98 (95% confidence interval [CI] 1.03-3.82). Among women CAKUT was associated with a HR of 5.88 (95% CI 2.19-15.76). Notably, upon stratification according to age of cancer diagnosis, the association between CAKUT and UT cancer was statistically significant only before 45 years of age in women and only after 45 years of age in men.

CONCLUSION

CAKUT is associated with a significantly increased risk of UT cancer, although the incidence and absolute risk remained quite low.

摘要

引言

先天性肾和尿路畸形(CAKUT)是儿童时期最常见的肾脏疾病。调控肾发生的基因改变可能导致CAKUT,在某些情况下可能会促使日后发生尿路(UT)肿瘤。我们旨在评估CAKUT与成年期UT癌症之间的关联。

方法

我们进行了一项基于人群的历史性队列研究,纳入了1967年至1997年间应征加入以色列军队的1,510,042名新兵。儿童时期的CAKUT暴露情况通过军队医疗记录中CAKUT的编码来确定。UT癌症(肾脏、输尿管或膀胱)的发病率可通过与以色列癌症登记处的记录链接获得。从入伍前评估开始对新兵进行随访,直至2012年癌症诊断、死亡或研究终止。构建Cox比例风险模型以估计有CAKUT与无CAKUT参与者发生UT癌症的风险比(HR)。

结果

在平均30.4年的随访期间,2959名参与者(2573名男性和386名女性)发生了UT癌症。与无CAKUT的男性相比,有CAKUT的男性发生UT癌症的风险增加,校正后的HR为1.98(95%置信区间[CI] 1.03 - 3.82)。在女性中,CAKUT与HR为5.88(95% CI 2.19 - 15.76)相关。值得注意的是,根据癌症诊断年龄分层后,CAKUT与UT癌症之间的关联仅在女性45岁之前以及男性45岁之后具有统计学意义。

结论

CAKUT与UT癌症风险显著增加相关,尽管发病率和绝对风险仍然相当低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed2f/8071628/8e71e754d44b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed2f/8071628/23ec3dfc61a6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed2f/8071628/8e71e754d44b/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed2f/8071628/23ec3dfc61a6/fx1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed2f/8071628/8e71e754d44b/gr1.jpg

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本文引用的文献

1
The Therapeutic Landscape of Renal Cell Carcinoma: From the Dark Age to the Golden Age.肾细胞癌的治疗前景:从黑暗时代到黄金时代。
Semin Nephrol. 2020 Jan;40(1):28-41. doi: 10.1016/j.semnephrol.2019.12.004.
2
Adolescent obesity and midlife cancer risk: a population-based cohort study of 2·3 million adolescents in Israel.青少年肥胖与中年癌症风险:基于人群的以色列 230 万青少年队列研究。
Lancet Diabetes Endocrinol. 2020 Mar;8(3):216-225. doi: 10.1016/S2213-8587(20)30019-X. Epub 2020 Feb 3.
3
History of Childhood Kidney Disease and Risk of Adult End-Stage Renal Disease.
双集合系统肾脏中上尿路尿路上皮癌的管理
J Pers Med. 2024 Jan 30;14(2):158. doi: 10.3390/jpm14020158.
4
The risks of birth defects and childhood cancer with conception by assisted reproductive technology.辅助生殖技术受孕与出生缺陷和儿童癌症风险。
Hum Reprod. 2022 Oct 31;37(11):2672-2689. doi: 10.1093/humrep/deac196.
5
The genetic basis of congenital anomalies of the kidney and urinary tract.先天性肾和泌尿道畸形的遗传学基础。
Pediatr Nephrol. 2022 Oct;37(10):2231-2243. doi: 10.1007/s00467-021-05420-1. Epub 2022 Feb 4.
儿童期肾脏疾病史与成人终末期肾脏疾病风险。
N Engl J Med. 2018 Feb 1;378(5):428-438. doi: 10.1056/NEJMoa1700993.
4
Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract.单基因先天性肾脏和泌尿道畸形发病机制的新见解。
J Am Soc Nephrol. 2018 Jan;29(1):36-50. doi: 10.1681/ASN.2017050561. Epub 2017 Oct 27.
5
Renal lineage cells as a source for renal regeneration.肾系细胞作为肾脏再生的来源。
Pediatr Res. 2018 Jan;83(1-2):267-274. doi: 10.1038/pr.2017.255. Epub 2017 Nov 15.
6
Immunohistochemical and molecular characterizations in urothelial carcinoma of bladder in patients less than 45 years.45岁以下膀胱尿路上皮癌患者的免疫组织化学和分子特征
J Cancer. 2017 Feb 5;8(3):323-331. doi: 10.7150/jca.17482. eCollection 2017.
7
Association between Congenital Lung Malformations and Lung Tumors in Children and Adults: A Systematic Review.先天性肺畸形与儿童和成人肺部肿瘤的相关性:系统综述。
J Thorac Oncol. 2016 Nov;11(11):1837-1845. doi: 10.1016/j.jtho.2016.06.023. Epub 2016 Jul 15.
8
Epidemiology of bladder cancer.膀胱癌流行病学
Hematol Oncol Clin North Am. 2015 Apr;29(2):177-89, vii. doi: 10.1016/j.hoc.2014.10.001.
9
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.人类肾脏和尿路先天性异常(CAKUT)的单基因病因。
Pediatr Nephrol. 2014 Apr;29(4):695-704. doi: 10.1007/s00467-013-2684-4. Epub 2014 Jan 8.
10
Defining early-onset kidney cancer: implications for germline and somatic mutation testing and clinical management.定义早发性肾癌:对种系和体细胞突变检测及临床管理的影响。
J Clin Oncol. 2014 Feb 10;32(5):431-7. doi: 10.1200/JCO.2013.50.8192. Epub 2013 Dec 30.