Evidence map›Paper›PMID 41094466›Full record

Observational studyBMC pulmonary medicine2025

Exploring the association between ceramide, phosphatidylcholine, and COPD prevalence and incidence: a FINRISK population-based cohort study.

Mohammadreza Shoghli, Juha Sinisalo, A Inkeri Lokki, Mitja Lääperi, Marja-Liisa Lokki, Mika Hilvo, Antti Jylhä, Jaakko Tuomilehto, Reijo Laaksonen

Abstract readObservational Study
In one paragraph

Observational study in BMC pulmonary medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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.

Mohammadreza ShoghliDepartment of Population Health, University of Helsinki, Helsinki, 00014, Finland.
Juha SinisaloHeart and Lung Center, Helsinki University Hospital, University of Helsinki, Helsinki, 00014, Finland.
A Inkeri LokkiDepartment of Bacteriology and Immunology, University of Helsinki, Helsinki, 00014, Finland.
Mitja LääperiZora Biosciences Oy, Espoo, Espoo, 02620, Finland.
Marja-Liisa LokkiDepartment of Pathology, University of Helsinki, Helsinki, 00290, Finland.
Mika HilvoVTT Technical Research Centre of Finland, Espoo, 02044, Finland.
Antti JylhäZora Biosciences Oy, Espoo, Espoo, 02620, Finland.
Jaakko TuomilehtoPopulation Health Unit, Finnish Institute for Health and Welfare, Helsinki, 00271, Finland. jaakko.tuomilehto@helsinki.fi.
Reijo LaaksonenZora Biosciences Oy, Espoo, Espoo, 02620, Finland. reijo.laaksonen@tuni.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCeramides (Cers) and phosphatidylcholines (PCs) are potential lipid biomarkers in obstructive pulmonary disease (COPD). Even though they are linked to inflammation and lipid dysregulation, little is known about how these factors affect the prevalence and incidence of COPD in population-based cohorts. This study investigates these associations, addressing knowledge gaps regarding the interplay of Cers, PCs, and COPD risk, focusing on sex-specific differences and smoking.

methodsThis observational study analysed data from the population-based FINRISK 2002 cohort, with 7,722 participants for prevalence and 7,662 for incidence analyses. Logistic regression models were used to assess associations between lipid biomarkers and prevalent COPD, while Cox regression models were applied for incident COPD. CERT1 and CERT2 (Cardiovascular Event Risk Test 1 and 2) are lipid-based scores derived from ceramide (Cer) ratios that estimate cardiovascular risk; in this study, they were used to examine their association with COPD. Kaplan-Meier curves were used to evaluate the impact of CERT scores on COPD risk, stratified by smoking status.

resultsElevated CERT1 and CERT2 scores were associated with both prevalent and incident COPD. For CERT1, the association with prevalent COPD was significant (univariable OR = 1.81, 95% CI: 1.41-2.33, p = < 0.001), as was the association with incident COPD (univariable HR = 1.33, 95% CI: 1.16-1.53, p = < 0.001). CERT2 was also significantly associated with prevalent COPD (adjusted OR = 1.57, 95% CI: 1.15-2.16, p = 0.005) and with incident COPD (univariable HR = 1.53, 95% CI: 1.32-1.77, p = < 0.001). PC species (14:0/22:6) was significantly associated with a lower risk of incident COPD (adjusted HR = 0.85, 95% CI: 0.73-0.98, p = 0.023). The Cer(d18:1/18:0)/PC (14:0/22:6) ratio was associated with both prevalent COPD (adjusted OR = 1.37, 95% CI: 1.01-1.86, p = 0.041) and incident COPD (HR = 1.24, 95% CI: 1.07-1.44, p = 0.004). Smokers had an elevated risk of COPD with increasing CERT scores.

conclusionThese findings support the role of lipid biomarkers, particularly Cers and CERT scores, in improving COPD risk prediction and management, with potential implications for targeted interventions in smokers.

Indexed as

CeramidesPhosphatidylcholinesPulmonary Disease, Chronic ObstructiveAdultAgedBiomarkersCohort StudiesFemaleFinlandHumansIncidenceKaplan-Meier EstimateLogistic ModelsMaleMiddle AgedPrevalenceBiomarkersCeramidesPhosphatidylcholinesCeramidesCERT scoresCOPDFINRISK cohortIncidenceLipid biomarkersPhosphatidylcholinePrevalenceSmoking

Identifiers

PMID41094466
PMCPMC12522678

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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.