代谢功能障碍相关性脂肪肝和骨质疏松症:脂肪的机制和作用。

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM Osteoporosis International Pub Date : 2024-12-01 Epub Date: 2024-08-13 DOI:10.1007/s00198-024-07217-y
Jie Tao, Hong Li, Honggang Wang, Juan Tan, Xiaozhong Yang
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引用次数: 0

摘要

非酒精性脂肪肝(NAFLD)最近已被国际共识更名为代谢功能障碍相关性脂肪肝(MAFLD)。非酒精性脂肪肝和骨质疏松症都是高发的代谢性疾病。最近的证据表明,非酒精性脂肪肝增加了低骨质密度和骨质疏松症的风险,这很可能是由肥胖引起的。非酒精性脂肪肝与肥胖和其他代谢性疾病密切相关。虽然以前认为肥胖可以防止骨质流失,但现在却增加了骨质疏松性骨折的风险。本综述总结了目前肥胖、非酒精性脂肪肝和骨质疏松症之间的临床相关性,并重点介绍了最近对这三种疾病相互关联的潜在机制的见解。本研究回顾了有关肥胖、非酒精性脂肪肝和骨质疏松症之间关系的科学文献,以及揭示三者之间潜在病理生理机制的科学文献。新的证据表明,肥胖在非酒精性脂肪肝和骨质疏松症之间的关系中起着关键的中介作用。不断积累的实验室证据支持肥胖、非酒精性脂肪肝和骨质疏松症之间存在似是而非的病理生理学联系,包括炎症途径、胰岛素抵抗、肠道微生物群失调、骨髓脂肪过多以及胰岛素样生长因子-1 信号的改变。肥胖与非酒精性脂肪肝和骨质疏松症有重要关联,三者之间的潜在病理生理机制可能为这一复杂的患者群体提供新的治疗靶点。
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Metabolic dysfunction-associated fatty liver disease and osteoporosis: the mechanisms and roles of adiposity.

Nonalcoholic fatty liver disease (NAFLD) has recently been renamed metabolic dysfunction-associated fatty liver disease (MAFLD) by international consensus. Both MAFLD and osteoporosis are highly prevalent metabolic diseases. Recent evidence indicates that NAFLD increases the risk of low bone mineral density and osteoporosis, likely mediated by obesity. NAFLD has a close association with obesity and other metabolic disorders. Although obesity was previously thought to protect against bone loss, it now heightens osteoporotic fracture risk. This overview summarizes current clinical correlations between obesity, NAFLD, and osteoporosis, with a focus on recent insights into potential mechanisms interconnecting these three conditions. This study reviewed the scientific literature on the relationship between obesity, nonalcoholic fatty liver disease, and osteoporosis as well as the scientific literature that reveals the underlying pathophysiologic mechanisms between the three. Emerging evidence suggests obesity plays a key role in mediating the relationship between NAFLD and osteoporosis. Accumulating laboratory evidence supports plausible pathophysiological links between obesity, NAFLD, and osteoporosis, including inflammatory pathways, insulin resistance, gut microbiota dysbiosis, bone marrow adiposity, and alterations in insulin-like growth factor-1 signaling. Adiposity has important associations with NAFLD and osteoporosis, the underlying pathophysiologic mechanisms between the three may provide new therapeutic targets for this complex patient population.

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来源期刊
Osteoporosis International
Osteoporosis International 医学-内分泌学与代谢
CiteScore
8.10
自引率
10.00%
发文量
224
审稿时长
3 months
期刊介绍: An international multi-disciplinary journal which is a joint initiative between the International Osteoporosis Foundation and the National Osteoporosis Foundation of the USA, Osteoporosis International provides a forum for the communication and exchange of current ideas concerning the diagnosis, prevention, treatment and management of osteoporosis and other metabolic bone diseases. It publishes: original papers - reporting progress and results in all areas of osteoporosis and its related fields; review articles - reflecting the present state of knowledge in special areas of summarizing limited themes in which discussion has led to clearly defined conclusions; educational articles - giving information on the progress of a topic of particular interest; case reports - of uncommon or interesting presentations of the condition. While focusing on clinical research, the Journal will also accept submissions on more basic aspects of research, where they are considered by the editors to be relevant to the human disease spectrum.
期刊最新文献
Correction: Exposure to air pollution might decrease bone mineral density and increase the prevalence of osteoporosis: A mendelian randomization study. Type 2 diabetes incidence in patients initiating denosumab or alendronate treatment: a primary care cohort study. Real-world efficacy of a teriparatide biosimilar (RGB-10) compared with reference teriparatide on bone mineral density, trabecular bone score, and bone parameters assessed using quantitative ultrasound, 3D-SHAPER® and high-resolution peripheral computer tomography in postmenopausal women with osteoporosis and very high fracture risk. One versus 2 years of alendronate following denosumab: the CARD extension. Association of proton-density fat fraction with osteoporosis: a systematic review and meta-analysis.
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