Evidence map›Paper›PMID 27488495›Full record

ArticleBMC pulmonary medicine2016

Adiposity influences airway wall thickness and the asthma phenotype of HIV-associated obstructive lung disease: a cross-sectional study.

Julia H Barton, Alex Ireland, Meghan Fitzpatrick, Cathy Kessinger, Danielle Camp, Renee Weinman, Deborah McMahon, Joseph K Leader, Fernando Holguin, Sally E Wenzel and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. HIV-associated lung disease.Nature reviews. Disease primers · 2023
    Review
  5. Review
  6. Article
  7. Adiponectin and Asthma: Knowns, Unknowns and Controversies.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

12 authors at 1 institution in 1 country.

Julia H BartonDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Alex IrelandDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Meghan FitzpatrickDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Cathy KessingerDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Danielle CampDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Renee WeinmanDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Deborah McMahonDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Joseph K LeaderDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Fernando HolguinDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Sally E WenzelDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Alison MorrisDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA.
Matthew R GingoDepartment of Medicine, University of Pittsburgh, Pittsburgh, USA. gingomr@upmc.edu.
University of Pittsburgh · US

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
Pneumocystis in Pathogenesis of HIV-associated EmphysemaR01HL083461 · NHLBI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MORRIS, ALISON · 2005 to 2009
$2.2M
HIV infection and AsthmaK23HL108697 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GINGO, MATTHEW R. · 2011 to 2015
$662k
Mentoring and Patient-Oriented Research in HIV Obstructive Lung DiseaseK24HL123342 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MORRIS, ALISON · 2014 to 2018
$571k
IMMUNE COMPETENCE OF HUMAN PLEURAL MESOTHELIAL CELLSF32HL008346 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI CAMP, MARK A · 1991 to 1991
–
NCRR NIH HHS UL1 RR024153NHLBI NIH HHS HL083461SNHLBI NIH HHS K23 HL108697NHLBI NIH HHS K24 HL123342NHLBI NIH HHS R01 HL083461PHS HHS K24 1233342
6 · The paper itself

Abstract

backgroundAirflow obstruction, which encompasses several phenotypes, is common among HIV-infected individuals. Obesity and adipose-related inflammation are associated with both COPD (fixed airflow obstruction) and asthma (reversible airflow obstruction) in HIV-uninfected persons, but the relationship to airway inflammation and airflow obstruction in HIV-infected persons is unknown. The objective of this study was to determine if adiposity and adipose-associated inflammation are associated with airway obstruction phenotypes in HIV-infected persons.

methodsWe performed a cross-sectional analysis of 121 HIV-infected individuals assessed with pulmonary function testing, chest CT scans for measures of airway wall thickness (wall area percent [WA%]) and adipose tissue volumes (mediastinal and subcutaneous), as well as HIV- and adipose-related inflammatory markers. Participants were defined as COPD phenotype (post-bronchodilator FEV1/FVC < lower limit of normal) or asthma phenotype (doctor-diagnosed asthma or bronchodilator response). Pearson correlation coefficients were calculated between adipose measurements, WA%, and pulmonary function. Multivariable logistic and linear regression models were used to determine associations of airflow obstruction and airway remodeling (WA%) with adipose measurements and participant characteristics.

resultsTwenty-three (19 %) participants were classified as the COPD phenotype and 33 (27 %) were classified as the asthma phenotype. Body mass index (BMI) was similar between those with and without COPD, but higher in those with asthma compared to those without (mean [SD] 30.7 kg/m(2) [8.1] vs. 26.5 kg/m(2) [5.3], p = 0.008). WA% correlated with greater BMI (r = 0.55, p < 0.001) and volume of adipose tissue (subcutaneous, r = 0.40; p < 0.001; mediastinal, r = 0.25; p = 0.005). Multivariable regression found the COPD phenotype associated with greater age and pack-years smoking; the asthma phenotype with younger age, female gender, smoking history, and lower adiponectin levels; and greater WA% with greater BMI, younger age, higher soluble CD163, and higher CD4 counts.

conclusionsAdiposity and adipose-related inflammation are associated with an asthma phenotype, but not a COPD phenotype, of obstructive lung disease in HIV-infected persons. Airway wall thickness is associated with adiposity and inflammation. Adipose-related inflammation may play a role in HIV-associated asthma.

Indexed as

Airway RemodelingAdultAsthmaBody Mass IndexCross-Sectional StudiesFemaleForced Expiratory VolumeHIV InfectionsHumansLinear ModelsLogistic ModelsLungMaleMiddle AgedMultivariate AnalysisObesityAdiponectinAsthmaCOPDHIVLipodystrophyObesityObstructive lung disease

Identifiers

PMID27488495
PMCPMC4973076
OpenAlexW2498169211

What OpenQuestion holds

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Registered trials

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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.