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捐献,而非疾病!关于捐献后肾病发生的多重打击假说。

Donation, Not Disease! A Multiple-Hit Hypothesis on Development of Post-Donation Kidney Disease.

作者信息

Cheng Xingxing S, Glassock Richard J, Lentine Krista L, Chertow Glenn M, Tan Jane C

机构信息

Division of Nephrology, Department of Medicine, Stanford University, 750 Welch Road, Suite 200, Mail code 5785, Palo Alto, CA 94304 USA.

Department of Medicine, David Geffen School of Medicine at UCLA, Los Angeles, CA USA.

出版信息

Curr Transplant Rep. 2017;4(4):320-326. doi: 10.1007/s40472-017-0171-8. Epub 2017 Nov 4.

DOI:10.1007/s40472-017-0171-8
PMID:29201600
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5691123/
Abstract

PURPOSE OF REVIEW

The risks following living kidney donation has been the subject of rigorous investigation in the past several decades. How to utilize the burgeoning new knowledge base to better the risk assessment, education, and health maintenance of donors is unclear. We review the physiologic and epidemiologic evidences on the post-donation state and submit a multiple-hit hypothesis to reconcile the finite elevation in risk of kidney disease after donation with the benign course of most kidney donors.

RECENT FINDINGS

The risk of end-stage kidney disease is higher in kidney donors compared to similarly healthy non-kidney donors. Nonetheless, post-donation kidney disease is uncommon and arises mostly in the setting of other "hits"-either a "first hit" present at birth or a "second hit" acquired later in life.

SUMMARY

The transplant community's focus should be directed toward (1) personalized risk assessment to inform consent before donation and (2) preventing and treating development of "second hits" following kidney donation.

摘要

综述目的

在过去几十年中,活体肾捐赠后的风险一直是严格研究的主题。如何利用迅速增长的新知识基础来改善捐赠者的风险评估、教育和健康维护尚不清楚。我们回顾了关于捐赠后状态的生理学和流行病学证据,并提出一种多重打击假说,以调和捐赠后肾病风险的有限升高与大多数肾捐赠者的良性病程之间的矛盾。

最新发现

与健康状况相似的非肾捐赠者相比,肾捐赠者患终末期肾病的风险更高。尽管如此,捐赠后肾病并不常见,且大多发生在存在其他“打击”的情况下——要么是出生时就存在的“首次打击”,要么是生命后期获得的“第二次打击”。

总结

移植界的重点应转向:(1)进行个性化风险评估,以便在捐赠前告知相关情况并取得同意;(2)预防和治疗肾捐赠后“第二次打击”的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/5691123/ffe3465b8292/40472_2017_171_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/5691123/6b81f6d89fc2/40472_2017_171_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/5691123/ffe3465b8292/40472_2017_171_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/5691123/6b81f6d89fc2/40472_2017_171_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/5691123/ffe3465b8292/40472_2017_171_Fig2_HTML.jpg

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本文引用的文献

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KDIGO Clinical Practice Guideline on the Evaluation and Care of Living Kidney Donors.KDIGO 活体肾捐献者评估与管理临床实践指南
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Quantifying Postdonation Risk of ESRD in Living Kidney Donors.量化活体肾供者捐献后发生终末期肾病的风险。
J Am Soc Nephrol. 2017 Sep;28(9):2749-2755. doi: 10.1681/ASN.2016101084. Epub 2017 Apr 27.
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A developmental approach to the prevention of hypertension and kidney disease: a report from the Low Birth Weight and Nephron Number Working Group.
国际活体肾供体候选者的评估与护理:应对常见考量因素和挑战的策略
Clin Transplant. 2020 Mar;34(3):e13792. doi: 10.1111/ctr.13792. Epub 2020 Feb 29.
4
Postdonation eGFR and New-Onset Antihypertensive Medication Use After Living Kidney Donation.活体肾捐献后的捐赠后估算肾小球滤过率及新发抗高血压药物使用情况。
Transplant Direct. 2019 Jul 25;5(8):e474. doi: 10.1097/TXD.0000000000000913. eCollection 2019 Aug.
预防高血压和肾脏疾病的发育学方法:低出生体重与肾单位数量工作组的报告
Lancet. 2017 Jul 22;390(10092):424-428. doi: 10.1016/S0140-6736(17)30576-7. Epub 2017 Mar 9.
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Obesity increases the risk of end-stage renal disease among living kidney donors.肥胖会增加活体肾供者发生终末期肾病的风险。
Kidney Int. 2017 Mar;91(3):699-703. doi: 10.1016/j.kint.2016.10.014. Epub 2016 Dec 29.
5
Integrating APOL1 Gene Variants Into Renal Transplantation: Considerations Arising From the American Society of Transplantation Expert Conference.将载脂蛋白L1(APOL1)基因变异纳入肾移植:美国移植学会专家会议引发的思考
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Understanding and Communicating Medical Risks for Living Kidney Donors: A Matter of Perspective.理解并传达活体肾供体的医疗风险:视角问题
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