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端粒长度作为骨质疏松症的预测生物标志物(综述)

Telomere length as a predictive biomarker in osteoporosis (Review).

作者信息

Kakridonis Fotios, Pneumatikos Spyros G, Vakonaki Elena, Berdiaki Aikaterini, Tzatzarakis Manolis N, Fragkiadaki Persefoni, Spandidos Demetrios A, Baliou Stella, Ioannou Petros, Hatzidaki Eleftheria, Nikitovic Dragana, Tsatsakis Aristidis, Vasiliadis Elias

机构信息

5th Department of Orthopaedics, KAT Attica General Hospital, 14561 Athens, Greece.

3rd Department of Orthopaedics, KAT Attica General Hospital, 14561 Athens, Greece.

出版信息

Biomed Rep. 2023 Oct 3;19(5):87. doi: 10.3892/br.2023.1669. eCollection 2023 Nov.

Abstract

Telomeres are the ends of chromosomes that protect them from DNA damage. There is evidence to suggest that telomere shortening appears with advanced age. Since aging is a significant risk factor for developing age-related complications, it is plausible that telomere shortening may be involved in the development of osteoporosis. The present review summarizes the potential of telomere shortening as a biomarker for detecting the onset of osteoporosis. For the purposes of the present review, the following scientific databases were searched for relevant articles: PubMed/NCBI, Cochrane Library of Systematic Reviews, Scopus, Embase and Google Scholar. The present review includes randomized and non-randomized controlled studies and case series involving humans, irrespective of the time of their publication. In six out of the 11 included studies providing data on humans, there was at least a weak association between telomere length and osteoporosis, with the remaining studies exhibiting no such association. As a result, telomere shortening may be used as a biomarker or as part of a panel of biomarkers for tracking the onset and progression of osteoporosis.

摘要

端粒是染色体的末端,可保护其免受DNA损伤。有证据表明,端粒缩短会随着年龄的增长而出现。由于衰老 是发生与年龄相关并发症的一个重要风险因素,因此端粒缩短可能与骨质疏松症的发生有关这一说法是合理的。本综述总结了端粒缩短作为检测骨质疏松症发病生物标志物的潜力。为了本综述的目的,在以下科学数据库中搜索了相关文章:PubMed/NCBI、Cochrane系统评价图书馆、Scopus、Embase和谷歌学术。本综述包括涉及人类的随机和非随机对照研究以及病例系列,无论其发表时间如何。在纳入的11项提供人类数据的研究中,有6项研究表明端粒长度与骨质疏松症之间至少存在微弱关联,其余研究则未显示出这种关联。因此,端粒缩短可作为一种生物标志物或作为一组生物标志物的一部分,用于追踪骨质疏松症的发病和进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b412/10594068/a07764c40768/br-19-05-01669-g00.jpg

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