Evidence map›Paper›PMID 42116176›Full record

ReviewDiabetology & metabolic syndrome2026

Obesity and respiratory diseases: mechanisms, phenotypes, and clinical implications.

Amin R Soliman, Amany Abouzeid, Hebatallah Hesham Ahmed

Abstract readReview
In one paragraph

Review in Diabetology & metabolic syndrome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Amin R SolimanDepartment of internal medicine and Nephrology, Faculty of Medicine, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0002-5589-1037
Amany AbouzeidDepartment of chest diseases, Faculty of Medicine, Cairo University, Cairo, Egypt.ORCID http://orcid.org/0000-0002-4805-1902
Hebatallah Hesham AhmedDepartment of chest diseases, Faculty of Medicine, Cairo University, Cairo, Egypt. hebatallah40987@kasralainy.edu.eg.ORCID http://orcid.org/0009-0003-7233-3429

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObesity has emerged as a global pandemic with profound implications for respiratory health. The complex interplay between excessive adiposity and pulmonary function encompasses mechanical, metabolic, and inflammatory pathways that significantly impact morbidity and mortality.

objectivesThis comprehensive review synthesizes current evidence on obesity-related respiratory disorders, examining pathophysiological mechanisms, clinical phenotypes, epidemiological trends, and therapeutic considerations across the spectrum of respiratory diseases. This review provides a novel integrative framework unifying mechanical, inflammatory, and metabolic mechanisms across all major obesity-related respiratory conditions, with emphasis on clinically actionable phenotyping and emerging pharmacological therapies.

methodsWe conducted a narrative review of peer-reviewed literature (PubMed/MEDLINE, Embase, and Cochrane Database, January 2000 - December 2024, using pre-specified MeSH terms; study selection and quality assessment followed SANRA guidelines focusing on the relationship between obesity and respiratory disorders including asthma, obstructive sleep apnea (OSA), obesity hypoventilation syndrome (OHS), chronic obstructive pulmonary disease (COPD), respiratory infections, and lung cancer.

resultsObesity profoundly affects respiratory mechanics through a right-shift of the static volume-pressure relationship of the chest wall, reducing FRC and ERV without a true restrictive pattern, altered respiratory muscle function, and systemic inflammation. Asthma prevalence increases with body mass index, demonstrating distinct phenotypes including atopic, insulin-resistant, dyslipidemic, and non-Th2 neutrophilic subtypes. OSA affects 22% of men and 17% of women, with obesity being the principal modifiable risk factor. OHS occurs in 8-20% of obese patients with sleep-disordered breathing, characterized by daytime hypercapnia (arising from impaired neuromuscular ventilatory drive and progressive nocturnal hypoventilation) and increased cardiovascular mortality. Paradoxically, obesity appears protective in advanced COPD by reducing FRC, thereby increasing inspiratory capacity and limiting dynamic pulmonary hyperinflation, and ARDS-the so-called obesity paradox-while conferring increased risk in COVID-19 pneumonitis. In lung cancer, obesity demonstrates complex relationships with risk and prognosis that vary by sex, smoking status, and disease stage.

conclusionsObesity-related respiratory disorders represent a multifaceted clinical challenge requiring integrated multidisciplinary approaches. Understanding distinct phenotypes and pathophysiological mechanisms is essential for personalized therapeutic strategies addressing both weight management and respiratory-specific interventions. Emerging pharmacological therapies including GLP-1 receptor agonists and dual GIP/GLP-1 agonists show particular promise in improving OSA severity and airway inflammation.

Indexed as

AdipokinesAsthma phenotypesCOVID-19GLP-1 receptor agonistsMetabolic syndromeObesityObesity hypoventilation syndromeObesity paradoxObstructive sleep apneaRespiratory diseases

Identifiers

PMID42116176
PMCPMC13169587

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.