Ectopic and visceral fat deposition in aging, obesity, and idiopathic pulmonary fibrosis: an interconnected role

被引:15
作者
Cheng, Xiaoyun [1 ,2 ]
Jiang, Shuhan [1 ,2 ]
Pan, Boyu [3 ]
Xie, Wei [4 ]
Meng, Jie [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp 3, Dept Pulm & Crit Care Med, Tongzipo Rd 138, Changsha 410000, Peoples R China
[2] Hunan Key Lab Organ Fibrosis, Tongzipo Rd 138, Changsha 410000, Peoples R China
[3] Third Hosp Changsha, Dept Orthoped, Laodong West Rd 176, Changsha 410000, Peoples R China
[4] Cent South Univ, Xiangya Hosp, Dept Cardiol, Furong Middle Rd 36, Changsha 410000, Peoples R China
基金
中国国家自然科学基金;
关键词
Idiopathic pulmonary fibrosis; Aging; Ectopic fat deposition; Inflammation; Visceral adipose tissue; RENIN-ANGIOTENSIN SYSTEM; ADIPOSE-TISSUE; LUNG FIBROSIS; T-CELLS; DISEASE; INJURY; ABNORMALITIES; INFLAMMATION; ADIPONECTIN; RECRUITMENT;
D O I
10.1186/s12944-023-01964-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Idiopathic pulmonary fibrosis (IPF) is considered an age-related disease. Age-related changes, along with other factors such as obesity, hormonal imbalances, and various metabolic disorders, lead to ectopic fat deposition (EFD). This accumulation of fat outside of its normal storage sites is associated with detrimental effects such as lipotoxicity, oxidative stress, inflammation, and insulin resistance. This narrative review provides an overview of the connection between ectopic and visceral fat deposition in aging, obesity, and IPF. It also elucidates the mechanism by which ectopic fat deposition in the airways and lungs, pericardium, skeletal muscles, and pancreas contributes to lung injury and fibrosis in patients with IPF, directly or indirectly. Moreover, the review discusses the impact of EFD on the severity of the disease, quality of life, presence of comorbidities, and overall prognosis in IPF patients. The review provides detailed information on recent research regarding representative lipid-lowering drugs, hypoglycemic drugs, and lipid-targeting drugs in animal experiments and clinical studies. This may offer new therapeutic directions for patients with IPF.
引用
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页数:19
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