98%
921
2 minutes
20
Background: Pulmonary fibrosis (PF) is a serious respiratory complication observed in coronavirus disease 2019 (COVID-19) patients, and people with diabetes mellitus (DM) are at an increased risk of developing severe COVID-19. However, whether DM is a risk factor for post-COVID-19 pulmonary fibrosis (PCPF) remains unknown.
Methods: We conducted a meta-analysis of observational studies to evaluate the association between DM and the development of PCPF. We searched PubMed, EMBASE, and the Cochrane Library for relevant studies published before February 1, 2023, without language or publication type restrictions. We calculated odds ratio (OR) with 95% confidence interval (CI) to compare the prevalence of DM among COVID-19 patients with PCPF with that among non-PCPF controls.
Results: This meta-analysis included a total of 5,088 COVID-19 patients. We found a significant association between DM and the development of PCPF (OR = 2.18, 95% CI: 1.15-4.13, P < 0.001), with high heterogeneity among the studies (I = 82.2%). Subgroup analysis showed that the association between DM and PCPF was consistent across different geographic regions, study designs, sample sizes, mean ages, DM types, assessment times after COVID-19 onset, and NOS quality ratings.
Conclusions: This meta-analysis offers evidence supporting a correlation between DM and the development of PCPF among COVID-19 patients. Despite the considerable heterogeneity in this studies, this research retains significant implications for the clinical management of COVID-19 patients. DM is a potential risk factor for PCPF. It is imperative for clinicians to remain vigilant regarding the development of PCPF in COVID-19 patients who complicated with DM.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12341327 | PMC |
http://dx.doi.org/10.1186/s12890-025-03880-x | DOI Listing |
Open Access Rheumatol
August 2025
Department of Rheumatology and Immunology, the First Affiliated Hospital, Jinan University, Guangzhou, 510632, People's Republic of China.
Objective: To evaluate the efficacy of baricitinib in combination therapy for managing refractory, rapidly progressive systemic sclerosis (SSc) with severe cardiac conduction defects and interstitial lung disease (ILD).
Methods: A 48-year-old male patient with SSc complicated by significant cardiac enlargement, third-degree atrioventricular block, heart failure, progressive ILD, and partial intestinal obstruction was included in the study. Prior treatments with mycophenolate mofetil (MMF), tacrolimus, and cyclophosphamide (CTX) had shown limited efficacy.
Front Pediatr
August 2025
Division of Pediatric Pulmonology, Department of Pediatrics, Oregon Health & Science University, Portland, OR, United States.
Background: Modulator therapy restores CFTR function and has led to health benefits for persons with cystic fibrosis (CF) (PwCF), including lower rates of pulmonary exacerbations. It is unknown if modulators affect lung function trajectories after inpatient treatment of pulmonary exacerbations (PEx).
Methods: We conducted a retrospective review of hospital encounters for PEx for subjects 6-25 years old with mild to moderate lung disease admitted to a large tertiary care center from 2014 to 2021 to capture hospitalizations of PwCF before and after starting modulators.
Front Pharmacol
August 2025
Department of Pharmacy, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Shanghai, China.
Dipeptidyl peptidase 1 (DPP1) inhibitors constitute a major advance in respiratory disease therapeutics. Through selective blockade of neutrophil serine protease (NSP) activation, these agents establish novel treatment paradigms for inflammatory respiratory conditions characterized by neutrophil-driven pathology. This comprehensive review examines the development status, clinical efficacy, and safety profile of DPP1 inhibitors in neutrophil-driven diseases, particularly non-cystic fibrosis bronchiectasis (NCFBE) and chronic obstructive pulmonary disease (COPD).
View Article and Find Full Text PDFFront Med (Lausanne)
August 2025
Department of Respiratory Medicine, Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Traditional studies of pulmonary fibrosis (PF) have focused on alveolar epithelial cells injury and abnormal myofibroblast aggregation, but recent studies have revealed that imbalances in pulmonary capillary homeostasis also play pivotal roles in this disease. The pulmonary microvasculature, composed of aerocyte capillary (aCap) and general capillary (gCap) endothelial cells, forms the core structure of the alveolar-capillary membrane. It performs key roles in gas exchange and nutrient/metabolite transport, while modulating the trafficking of inflammatory factors and immune cells and regulating alveolar damage repair.
View Article and Find Full Text PDFImmune Netw
August 2025
Center for Metabolic and Degenerative Diseases, The Brown Foundation Institute of Molecular Medicine for Prevention of Human Diseases, UTHealth-McGovern Medical School, Houston, TX 77030, USA.
Complement anaphylatoxins C3a and C5a are potent immunomodulators whose impact extends well beyond their traditional roles in innate immunity. Acting through G protein-coupled receptors C3aR, C5aR1, and C5aR2, these peptides take part in coordinating immune cell recruitment, vascular tone, and tissue remodeling. Yet their functions are deeply context-dependent: while they play essential roles in microbial clearance and immune coordination, their overactivation contributes to immunopathology in a wide range of diseases.
View Article and Find Full Text PDF