Evidence map›Paper›PMID 42128815›Full record

ArticleESC heart failure2026

FEV1 is a major prognostic factor in diverse heart failure populations: findings from the Global Heart Failure registry.

MyLinh Duong, Shofiqul Islam, Philip Joseph, Darryl Leong, Alex Grinvalds, Tara McCready, Kelley R Branch, Andrzej Budaj, Albertino Damasceno, Juan Manuel Dominguez and 15 more

Abstract readMulticenter Study
In one paragraph

Article in ESC heart failure, 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

25 authors.

MyLinh DuongDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.ORCID 0000-0002-9197-2547
Shofiqul IslamDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.ORCID 0000-0001-8196-8598
Philip JosephDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Darryl LeongDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Alex GrinvaldsDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Tara McCreadyDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.
Kelley R BranchCardiology, University of Washington, Seattle, Washington State, USA.
Andrzej BudajCentre of Postgraduate Medical Education, Department of Cardiology, Grochowski Hospital, Warsaw, Poland.ORCID 0000-0002-6395-2098
Albertino DamascenoFaculty of Medicine, Eduardo Mondlane University, Maputo, Mozambique.ORCID 0000-0003-0925-494X
Juan Manuel DominguezEstudios Clínicos Latino America Collaborative Group, Rosario, Argentina.
Anastase DzudieDepartment of Global Health and Population, Lown Scholars Program, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
Camilla HageDepartment of Medicine, Cardiology Unit, Karolinska Institutet, Stockholm, Sweden.
Charles MondoKiruddu National Referral Hospital, King Ceasor University, Kampala, Uganda.
Julius Chacha MwitaInternal Medicine, University of Botswana, Gaborone, Botswana.ORCID 0000-0002-5947-3684
Francesco OrsoANMCO Research Center, Heart Care Foundation, Florence, Italy.ORCID 0000-0003-0809-1771
Alexander ParkhomenkoEmergency Cardiology Department, National Scientific Centre, Strazhesko Institute of Cardiology, Kiev, Ukraine.
Jeffrey ProbstfieldCardiology, University of Washington, Seattle, Washington State, USA.ORCID 0000-0002-4899-9971
Jean RouleauMontreal Heart Institute, Université de Montréal, Montreal, Quebec, Canada.
Sanjib Kumar SharmaB P Koirala Institute of Health Sciences, Dharan, Nepal.ORCID 0000-0002-8392-8028
Jose Silva-CardosoFaculty of Medicine, University of Porto, Porto, Portugal.
Stefan StörkDepartment of Clinical Research & Epidemiology, Comprehensive Heart Failure Center, University Hospital Würzburg, Würzburg, Germany.
Thomas WittlingerDepartment of Cardiology, Asklepios Hospital Goslar, Goslar, Germany.
Gerald YongaDepartment of Clinical Medicine and Therapeutics, University of Nairobi, Nairobi, Nairobi City County, Kenya.
Jun ZhuNational Center for Cardiovascular Diseases, Fuwai Hospital, Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC), Beijing, China.ORCID 0000-0002-4309-5789
Salim YusufDepartment of Medicine, Population Health Research Institute, McMaster University and Hamilton Health Sciences, Hamilton, Ontario, Canada.ORCID 0000-0003-4776-5601

Funding

Bayer AG
6 · The paper itself

Abstract

aimsPulmonary abnormalities are commonly reported in heart failure (HF) and may have prognostic implications. Current evidence is limited to high-income countries. We examined the relationship between forced expiratory volume in 1 second (FEV1), HF burden, and long-term clinical outcomes in a diverse multi-national HF cohort. METHODS AND

resultsIn a sub-study within the multinational Global Congestive Heart Failure registry, which collected clinical data including spirometry from HF participants in 28 high-, middle-, and low-income countries, and followed for a median 3.8 (IQR 2.1, 5.0) years. Baseline FEV1 was transformed into z-scores standardized for age, sex, and height. The association between baseline FEV1 with all-cause mortality, cardiovascular (CV) deaths, and all-cause hospitalizations was examined.

findingsThe analysis included 3359 HF participants (mean age 61.9 [SD 14.1] years, 66.4% males). Participants with lower FEV1 z-scores, even within the normal range (z-score>-2), showed increasing burden of HF, cardiac structural and functional impairment, and lower health-related quality of life. FEV1 z-score ≤ -2 was independently associated with higher risks of all-cause (HR 2.20 [95%CI 1.61-3.01]), CV mortality (HR 2.45 [1.64-3.66]), and hospitalizations (HR 1.40 [1.12-1.74]). The effect sizes were comparable to those of other major prognostic factors. The association was consistent across populations from diverse socio-economic development, HF aetiology, HF types, and airflow obstruction.

conclusionIn a diverse, multi-national HF cohort, reductions in FEV1 were independently associated with higher HF burden and poor health outcomes. The effect of lower FEV1 was generalizable across the HF spectrum and comparable to other major established HF prognostic factors.

Indexed as

Heart FailureQuality of LifeRegistriesAgedFemaleFollow-Up StudiesForced Expiratory VolumeGlobal HealthHumansMaleMiddle AgedPrognosisSpirometrySurvival RateFEV1Global populationHeart failureLung functionOutcomes

Identifiers

PMID42128815
PMCPMC13195515

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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.