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足细胞在与早产相关的长期慢性肾脏病发病机制中的作用。

Podocyte involvement in the pathogenesis of preterm-related long-term chronic kidney disease.

机构信息

Department of Neonatology, Tianjin Central Hospital of Obstetrics and Gynecology, Tianjin, China.

Tianjin Key Laboratory of Human Development and Reproductive Regulation, Tianjin, China.

出版信息

Histol Histopathol. 2024 May;39(5):557-564. doi: 10.14670/HH-18-675. Epub 2023 Nov 15.

DOI:10.14670/HH-18-675
PMID:37994826
Abstract

With the continuous advancement of neonatal intensive care technology, the survival rate of preterm infants is gradually increasing. However, this improvement in survival is accompanied by long-term prognostic implications in various systems. In the field of renal diseases, current epidemiological data indicate that preterm birth is a significant risk factor for the development of long-term chronic kidney disease (CKD). This not only imposes an economic burden on patients families but also severely impacts their quality of life. Understanding the underlying mechanisms involved in this process could offer potential strategies for early prevention and management of CKD. Although the nephron number hypothesis is currently widely accepted as a mechanism, there has been limited exploration regarding podocytes - one of the most important structures within nephrons - in relation to long-term CKD associated with preterm birth. Therefore, this review aims to summarize current knowledge on how prematurity influences CKD development overall, while specifically focusing on our current understanding of podocytes in relation to prematurity.

摘要

随着新生儿重症监护技术的不断进步,早产儿的存活率逐渐提高。然而,这种生存率的提高伴随着各系统长期预后的影响。在肾脏疾病领域,目前的流行病学数据表明,早产是导致长期慢性肾脏病(CKD)的重要危险因素。这不仅给患者家庭带来了经济负担,也严重影响了他们的生活质量。了解这一过程中的潜在机制可能为 CKD 的早期预防和管理提供潜在策略。尽管目前广泛接受的是肾单位数量假说,但对于足细胞——肾单位中最重要的结构之一——与早产相关的长期 CKD 的关系,研究还很有限。因此,本综述旨在总结目前关于早产如何影响 CKD 发展的知识,同时特别关注我们对足细胞与早产相关的认识。

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本文引用的文献

1
Preterm birth leads to a decreased number of differentiated podocytes and accelerated podocyte differentiation.早产导致分化的足细胞数量减少,并加速足细胞分化。
Front Cell Dev Biol. 2023 Mar 2;11:1142929. doi: 10.3389/fcell.2023.1142929. eCollection 2023.
2
Prematurity and BPD: what general pediatricians should know.早产儿与支气管肺发育不良:一般儿科医生应该知道什么。
Eur J Pediatr. 2023 Apr;182(4):1505-1516. doi: 10.1007/s00431-022-04797-x. Epub 2023 Feb 10.
3
Omics and Artificial Intelligence in Kidney Diseases.肾脏疾病中的组学与人工智能
Adv Kidney Dis Health. 2023 Jan;30(1):47-52. doi: 10.1053/j.akdh.2022.11.005.
4
Long-term outcomes and life-impacts of necrotizing enterocolitis: A survey of survivors and parents.肠坏死性小肠结肠炎的长期预后和生活影响:对幸存者及其父母的调查。
Semin Perinatol. 2023 Feb;47(1):151696. doi: 10.1016/j.semperi.2022.151696. Epub 2022 Dec 31.
5
Low nephron endowment increases susceptibility to renal stress and chronic kidney disease.低肾小球数目的个体易患肾应激和慢性肾脏病。
JCI Insight. 2023 Feb 8;8(3):e161316. doi: 10.1172/jci.insight.161316.
6
Association between preterm births and socioeconomic development: analysis of national data.早产与社会经济发展的关联:全国数据分析。
BMC Public Health. 2022 Nov 3;22(1):2014. doi: 10.1186/s12889-022-14376-2.
7
The clinical burden of extremely preterm birth in a large medical records database in the United States: complications, medication use, and healthcare resource utilization.美国一个大型医疗记录数据库中极早产的临床负担:并发症、药物使用及医疗资源利用情况
J Matern Fetal Neonatal Med. 2022 Dec;35(26):10271-10278. doi: 10.1080/14767058.2022.2122035. Epub 2022 Sep 28.
8
Preterm Birth, Kidney Function and Cardiovascular Disease in Children and Adolescents.儿童和青少年的早产、肾功能与心血管疾病
Children (Basel). 2022 Jul 28;9(8):1130. doi: 10.3390/children9081130.
9
The developmental origins of health and chronic kidney disease: Current status and practices in Japan.健康与慢性肾脏病的发育起源:日本的现状与实践。
Pediatr Int. 2022 Jan;64(1):e15230. doi: 10.1111/ped.15230.
10
Urine podocyte mRNA loss in preterm infants and related perinatal risk factors.早产儿尿液足细胞 mRNA 丢失及其相关围生期危险因素。
Pediatr Nephrol. 2023 Mar;38(3):729-738. doi: 10.1007/s00467-022-05663-6. Epub 2022 Jun 27.