Górski Paweł, Białas Adam J, Piotrowski Wojciech J
Department of Pneumology, Medical University of Lodz, 90-419 Lodz, Poland.
Department of Pulmonary Rehabilitation, Regional Medical Center for Lung Diseases and Rehabilitation, Blessed Rafal Chylinski Memorial Hospital for Lung Diseases, 91-520 Lodz, Poland.
Antioxidants (Basel). 2024 Dec 2;13(12):1480. doi: 10.3390/antiox13121480.
The aging process significantly impacts lung physiology and is a major risk factor for chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis (IPF), asthma, and non-IPF interstitial lung fibrosis. This narrative clinical review explores the molecular and biochemical hallmarks of aging, such as oxidative stress, telomere attrition, genomic instability, epigenetic modifications, proteostasis loss, and impaired macroautophagy, and their roles in lung senescence. Central to this process are senescent cells, which, through the senescence-associated secretory phenotype (SASP), contribute to chronic inflammation and tissue dysfunction. The review highlights parallels between lung aging and pathophysiological changes in respiratory diseases, emphasizing the role of cellular senescence in disease onset and progression. Despite promising research into modulating aging pathways with interventions like caloric restriction, mTOR inhibitors, and SIRT1 activators, clinical evidence for efficacy in reversing or preventing age-related lung diseases remains limited. Understanding the interplay between aging-related mechanisms and environmental factors, such as smoking and pollution, is critical for developing targeted therapies. This review underscores the need for future studies focusing on therapeutic strategies to mitigate aging's detrimental effects on lung health and improve outcomes for patients with chronic respiratory conditions.
衰老过程对肺生理有显著影响,是慢性呼吸道疾病的主要风险因素,包括慢性阻塞性肺疾病(COPD)、特发性肺纤维化(IPF)、哮喘和非IPF间质性肺纤维化。这篇叙述性临床综述探讨了衰老的分子和生化特征,如氧化应激、端粒损耗、基因组不稳定、表观遗传修饰、蛋白质稳态丧失和自噬受损,以及它们在肺衰老中的作用。这一过程的核心是衰老细胞,它们通过衰老相关分泌表型(SASP)促进慢性炎症和组织功能障碍。该综述强调了肺衰老与呼吸道疾病病理生理变化之间的相似之处,强调了细胞衰老在疾病发生和发展中的作用。尽管在通过热量限制、mTOR抑制剂和SIRT1激活剂等干预措施调节衰老途径方面有很有前景的研究,但逆转或预防与年龄相关的肺部疾病疗效的临床证据仍然有限。了解衰老相关机制与吸烟和污染等环境因素之间的相互作用,对于开发靶向治疗至关重要。这篇综述强调了未来研究的必要性,这些研究应聚焦于减轻衰老对肺部健康有害影响的治疗策略,并改善慢性呼吸道疾病患者的预后。