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糖尿病肾病中的性别相关差异。

Sex and Gender Related Differences in Diabetic Kidney Disease.

机构信息

Division of Nephrology, Department of Medicine, University Health Network, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta.

Division of Nephrology, Department of Medicine, University Health Network, Toronto, Ontario, Canada; Department of Medicine, University of Toronto, Toronto, Ontario, Canada; Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta; Department of Cardiac Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta.

出版信息

Semin Nephrol. 2022 Mar;42(2):170-184. doi: 10.1016/j.semnephrol.2022.04.007.

DOI:10.1016/j.semnephrol.2022.04.007
PMID:35718364
Abstract

Diversity in sex and gender are important considerations in the pathogenesis, prognostication, research, and management of diabetic kidney disease (DKD). Sex and gender differences in the disease risk, disease-specific mechanisms, and outcomes in DKD may be attributed to biological differences between males and females at the cellular and tissue level, inconsistencies in the diagnostic and assessment tools used in chronic kidney disease and DKD, as well societal differences in the way men, women, and gender-diverse individuals self-manage and interact with health care systems. This review outlines key considerations related to the impact of sex on DKD, specifically elaborating on how they contribute to observed differences in disease epidemiology, pathogenesis, and treatment strategies. We also highlight the effect of gender on DKD progression and care.

摘要

性别和性别的多样性是糖尿病肾病(DKD)发病机制、预后、研究和管理中需要考虑的重要因素。DKD 疾病风险、疾病特异性机制和结局方面的性别差异可能归因于男性和女性在细胞和组织水平上的生物学差异、慢性肾脏病和 DKD 中使用的诊断和评估工具的不一致性,以及男性、女性和性别多样化个体在自我管理和与医疗保健系统互动方面的社会差异。这篇综述概述了与性别对 DKD 的影响相关的关键考虑因素,特别是详细阐述了它们如何导致疾病流行病学、发病机制和治疗策略方面观察到的差异。我们还强调了性别对 DKD 进展和护理的影响。

相似文献

1
Sex and Gender Related Differences in Diabetic Kidney Disease.糖尿病肾病中的性别相关差异。
Semin Nephrol. 2022 Mar;42(2):170-184. doi: 10.1016/j.semnephrol.2022.04.007.
2
Gender differences in the association between hyperuricemia and diabetic kidney disease in community elderly patients.社区老年患者高尿酸血症与糖尿病肾病关联中的性别差异
J Diabetes Complications. 2015 Nov-Dec;29(8):1042-9. doi: 10.1016/j.jdiacomp.2015.08.016. Epub 2015 Aug 22.
3
Multidisciplinary management of diabetic kidney disease: a systematic review and meta-analysis.糖尿病肾病的多学科管理:一项系统评价与荟萃分析
JBI Database System Rev Implement Rep. 2016 Jul;14(7):169-207. doi: 10.11124/JBISRIR-2016-003011.
4
Gender Differences in Diabetic Kidney Disease: Focus on Hormonal, Genetic and Clinical Factors.性别差异与糖尿病肾病:关注激素、遗传和临床因素。
Int J Mol Sci. 2021 May 28;22(11):5808. doi: 10.3390/ijms22115808.
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Clinical predictive factors in diabetic kidney disease progression.糖尿病肾病进展的临床预测因素。
J Diabetes Investig. 2017 Jan;8(1):6-18. doi: 10.1111/jdi.12533. Epub 2016 Jun 8.
6
Long noncoding RNA: an emerging player in diabetes and diabetic kidney disease.长链非编码 RNA:在糖尿病和糖尿病肾病中的新兴角色。
Clin Sci (Lond). 2019 Jun 20;133(12):1321-1339. doi: 10.1042/CS20190372. Print 2019 Jun 28.
7
Association of urinary acidification function with the progression of diabetic kidney disease in patients with type 2 diabetes.2 型糖尿病患者尿液酸化功能与糖尿病肾病进展的关系。
J Diabetes Complications. 2019 Nov;33(11):107419. doi: 10.1016/j.jdiacomp.2019.107419. Epub 2019 Aug 19.
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Hyperuricemia contributes to the faster progression of diabetic kidney disease in type 2 diabetes mellitus.高尿酸血症会促使2型糖尿病患者的糖尿病肾病进展加快。
J Diabetes Complications. 2016 Sep-Oct;30(7):1300-7. doi: 10.1016/j.jdiacomp.2016.06.002. Epub 2016 Jun 7.
9
Risk Factors and Comorbidities Associated with Diabetic Kidney Disease.与糖尿病肾病相关的风险因素和合并症。
J Prim Care Community Health. 2021 Jan-Dec;12:21501327211048556. doi: 10.1177/21501327211048556.
10
Insulin resistance, diabetic kidney disease, and all-cause mortality in individuals with type 2 diabetes: a prospective cohort study.2 型糖尿病患者的胰岛素抵抗、糖尿病肾病和全因死亡率:一项前瞻性队列研究。
BMC Med. 2021 Mar 15;19(1):66. doi: 10.1186/s12916-021-01936-3.

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