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子宫肌瘤和瘢痕疙瘩纤维化的起源:纤维增殖性疾病的小型综述。

Uterine leiomyomata and keloids fibrosis origins: a mini-review of fibroproliferative diseases.

机构信息

Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee, United States.

Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, United States.

出版信息

Am J Physiol Cell Physiol. 2023 Oct 1;325(4):C817-C822. doi: 10.1152/ajpcell.00181.2023. Epub 2023 Aug 29.

Abstract

Diseases such as uterine leiomyomata (fibroids and benign tumors of the uterus) and keloids (raised scars) may share common etiology. Fibroids and keloids can co-occur in individuals, and both are highly heritable, suggesting they may share common genetic risk factors. Fibroproliferative diseases are common and characterized by scarring and overgrowth of connective tissue, impacting multiple organ systems. These conditions both have racial disparities in prevalence, with the highest prevalence observed among individuals of African ancestry. Several fibroproliferative diseases are more severe and common in populations of sub-Saharan Africa. This mini-review aims to provide a broad overview of the current knowledge of the evolutionary origins and causes of fibroproliferative diseases. We also discuss current hypotheses proposing that the increased prevalence of these diseases in African-derived populations is due to the selection for profibrotic alleles that are protective against helminth infections and provide examples from knowledge of uterine fibroid and keloid research.

摘要

疾病,如子宫肌瘤(子宫纤维瘤和良性肿瘤)和瘢痕疙瘩(隆起的疤痕)可能具有共同的病因。纤维瘤和瘢痕疙瘩可能在个体中共存,且两者具有高度遗传性,表明它们可能具有共同的遗传风险因素。纤维增生性疾病很常见,其特征是结缔组织的疤痕和过度生长,影响多个器官系统。这些疾病在患病率上存在种族差异,在非洲裔个体中观察到的患病率最高。一些纤维增生性疾病在撒哈拉以南非洲人群中更为严重和常见。本篇迷你综述旨在提供对纤维增生性疾病的进化起源和病因的广泛概述。我们还讨论了目前的假说,即这些疾病在非洲裔人群中的高患病率是由于对纤维化等位基因的选择,这些等位基因对寄生虫感染具有保护作用,并从子宫纤维瘤和瘢痕疙瘩研究中举例说明。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7de1/10635651/1e370d29d6dd/c-00181-2023r01.jpg

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