Evidence map›Paper›PMID 41743830›Full record

ArticleTransplantation direct2026

Lower Limit of Normal of Pulmonary Function to Define Baseline Lung Allograft Dysfunction.

Michael Gerckens, Susanne Simon, Carlo Mümmler, Paola Arnold, Jürgen Barton, Ali Önder Yildirim, Jürgen Behr, Nikolaus Kneidinger, Jens Gottlieb

Abstract read
In one paragraph

Article in Transplantation direct, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

9 authors.

Michael GerckensDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.ORCID https://orcid.org/0000-0002-2251-4382
Susanne SimonDepartment of Respiratory Medicine and Infectious Diseases, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0009-0000-8532-9427
Carlo MümmlerDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.ORCID https://orcid.org/0000-0002-2501-3356
Paola ArnoldDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.
Jürgen BartonDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.
Ali Önder YildirimInstitute of Lung Health and Immunity (LHI), Helmholtz Munich, Comprehensive Pneumology Center (CPC-M)/Member of the German Center for Lung Research (DZL), Munich, Germany.ORCID https://orcid.org/0000-0003-1969-480X
Jürgen BehrDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.ORCID https://orcid.org/0000-0002-9151-4829
Nikolaus KneidingerDepartment of Medicine V, University Hospital, LMU Munich, Comprehensive Pneumology Center (CPC-M), German Center for Lung Research (DZL), Munich, Germany.ORCID https://orcid.org/0000-0001-7583-0453
Jens GottliebDepartment of Respiratory Medicine and Infectious Diseases, Hannover Medical School, Hannover, Germany.ORCID https://orcid.org/0000-0002-9540-9022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Subnormal lung function after lung transplantation (LTx) has increasingly been recognized as an independent risk factor for mortality. Historically, baseline lung allograft dysfunction (BLAD) has been defined using the fixed "< 80% predicted" threshold from population-wide reference equations, which disregards age- and sex-related variability in spirometric values and can lead to systematic overdiagnosis, particularly in older and female recipients. While the lower limit of normal (LLN), derived from Global Lung Initiative reference equations, has been accepted as technical standard in spirometry, it has not yet been applied to define BLAD. Methods: A retrospective multicenter study included LTx recipients transplanted between 2014 and 2018. Lung function trajectories and allograft survival were followed-up until August 2024. The association of BLAD defined by forced expiratory volume in 1 s (FEV1) or forced vital capacity (FVC) < LNN as time-dependent variable with graft loss was studied using time-dependent Cox proportional hazard models. Results: We analyzed 726 patients after LTx including 102 unilateral LTx recipients, of whom 470 (65%) of the cohort achieved normal baseline lung function defined as FEV1 and FVC ≥ LLN. Two hundred thirty-six patients experienced graft loss (n = 2 redo LTx) and 179 developed chronic lung allograft dysfunction. After adjusting for age, disease, transplant type, and chronic lung allograft dysfunction, baseline FEV1 or FVC < LLN was associated with graft loss (hazard ratio, 1.822; 95% confidence interval, 1.372-2.418; Conclusions: BLAD defined by concurrent baseline FEV1 or FVC below the LLN was strongly associated with increased risk of graft loss. These findings extend prior studies that used the fixed 80% threshold by demonstrating that an LLN-based, age- and sex-adjusted definition of BLAD identifies lung transplant recipients at risk, thereby avoiding fixed cutoff associated age- and sex-bias.

Identifiers

PMID41743830
PMCPMC12931945

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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.