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Background And Objective: Bronchiectasis, which was previously regarded as a rare condition, has recently attracted increased attention with advancements in research and therapeutic strategies. However, heterogeneity remains a major challenge in the management of bronchiectasis. This review aims to elucidate the concepts of phenotypes and endotypes, facilitate a deeper understanding of bronchiectasis complexity, and pave the way for personalized treatment approaches.
Methods: The PubMed database was searched for relevant articles published in English between January 1990 and August 2024 using keywords "bronchiectasis", "phenotype", "endotype", "diagnosis", "disease management", "complexity", "eosino*", "neutrop*", and "precision medicine".
Key Content And Findings: We examined established clinical phenotypes, such as frequent exacerbator and chronic airway disease overlap, which significantly influence prognosis and therapeutic management. The significance of etiology-based phenotyping was also discussed while emphasizing how identifying specific underlying causes can guide targeted therapies. We further explored recent advancements in characterising bronchiectasis endotypes, particularly those marked by neutrophilic and eosinophilic inflammation. These endotypes provide valuable insights into underlying pathophysiological mechanisms and guide the selection of clinical management strategies. Recent cluster analysis research has identified distinct inflammatory endotypes in bronchiectasis, thereby improving the understanding of disease progression and identifying potential therapeutic targets. Integrating molecular endotyping with clinical phenotyping provides a more comprehensive perspective of the disease, underscoring the necessity of a dual approach to effectively address its inherent heterogeneity. Furthermore, we emphasize the significance of identifying treatable traits within these frameworks, which can enhance the precision of treatment strategies and improve patient outcomes. By exploring the interplay between clinical phenotypes, endotypes, and patient-specific characteristics, this review highlights the potential for advancing precision medicine for bronchiectasis.
Conclusions: Enhancing our understanding of bronchiectasis through these concepts is essential for developing tailored interventions that target the underlying biological mechanisms, thereby improving disease management and patients' quality of life.
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http://dx.doi.org/10.21037/jtd-2024-1945 | DOI Listing |
medRxiv
August 2025
Department of Sleep and Respiratory Medicine, Perth Children's Hospital, Perth, Western Australia, Australia.
Background: Early-life susceptibility to viral respiratory infections is associated with long-term respiratory morbidity in children. Currently, no reliable tools exist to predict susceptibility to these infections. Given its role in modulating pathogen virulence and airway inflammation, the endogenous microbiota represents a potential target for prevention.
View Article and Find Full Text PDFIntensive Care Med Exp
September 2025
Neurosciences Intensive Care Unit, John Radcliffe Hospital, Oxford, UK.
Delirium is a frequent and serious complication of critical illness, yet its pathophysiological mechanisms remain incompletely understood. Serum biomarkers offer a potential avenue for improved diagnosis, risk stratification, and mechanistic insight. This systematic review synthesises evidence from 28 studies evaluating 54 serum biomarkers in relation to delirium among critically ill adult patients.
View Article and Find Full Text PDFJ Clin Med
August 2025
Department of Respiratory Diseases, University of Bari, 70121 Bari, Italy.
Asthma has traditionally been viewed as a single disease, but recent research reveals its clinical and molecular complexity. This perspective highlights the need to shift from a traditional, uniform treatment paradigm to one that embraces the heterogeneity of asthma across individuals. Each patient presents a unique clinical story shaped by a complex interplay of genetic predispositions, developmental programming during critical early-life windows, the influence of sex and hormones, and lifelong environmental exposures.
View Article and Find Full Text PDFReprod Biomed Online
April 2025
State Research Institute Innovative Medicine Centre, Department of Regenerative Medicine, Vilnius, Lithuania; VilniusTech Faculty of Fundamental Sciences, Department of Chemistry and Bioengineering, Vilnius Gediminas Technical University, Vilnius, Lithuania. Electronic address: eiva.bernotiene@imcen
Research Question: Can the proteome of menstrual blood mesenchymal stromal cells (MenSC), their extracellular vesicles or extracellular-vesicle-depleted supernatant be employed for personalized identification of altered cellular processes in women with unexplained infertility (uIF), enabling their stratification into aetiopathogenetic endotypes?
Design: For MenSC isolation, menstrual blood was collected from 12 fertile healthy volunteers (control group) and eight patients with uIF. MenSC extracellular vesicles were isolated using iodixanol density gradient centrifugation, quantified by flow cytometry and characterized in accordance with the Minimal Information for Studies of Extracellular Vesicles (MISEV) guidelines by transmission electron microscopy, flow cytometry and western blot analysis. Proteomic analysis was undertaken using mass spectrometry and bioinformatic tools.
Int Forum Allergy Rhinol
August 2025
Department of Otolaryngology - Head and Neck Surgery, Emory University School of Medicine, Atlanta, Georgia, USA.
Background: Central compartment atopic disease (CCAD) is a nasal inflammatory condition associated with allergy and categorized as type 2 dominant chronic rhinosinusitis with nasal polyps (CRSwNP). Sinus opacification in this condition is secondary to obstruction from central tissue remodeling. Although the literature supports a unique phenotype of CCAD, controversy persists due to variations in published studies.
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