Proteomic biomarkers and pathway analysis for progression to heart failure in three epidemiological representative cohorts
(2024) In European Journal of Heart Failure- Abstract
AIMS: Biomarkers associated with asymptomatic ventricular dysfunction might improve risk stratification and identify pathways leading to heart failure (HF). We explored the association between proteomic biomarkers and left ventricular hypertrophy (LVH), diastolic dysfunction (DD) and incident HF in three population-based cohorts.
METHODS AND RESULTS: A chip was used to measure 92 protein biomarkers in blood samples from >1500 Malmö Preventive Project (MPP) participants, of whom 514 had LVH (34%), 462 had DD (32.4%) and, over a median follow-up of 13 (11-14) years, 130 developed HF (7.7%). Findings were confirmed in the STANISLAS (n > 1500, 238 participants with LVH, 76 with DD) and HOMAGE case-control (562 cases of incident... (More)
AIMS: Biomarkers associated with asymptomatic ventricular dysfunction might improve risk stratification and identify pathways leading to heart failure (HF). We explored the association between proteomic biomarkers and left ventricular hypertrophy (LVH), diastolic dysfunction (DD) and incident HF in three population-based cohorts.
METHODS AND RESULTS: A chip was used to measure 92 protein biomarkers in blood samples from >1500 Malmö Preventive Project (MPP) participants, of whom 514 had LVH (34%), 462 had DD (32.4%) and, over a median follow-up of 13 (11-14) years, 130 developed HF (7.7%). Findings were confirmed in the STANISLAS (n > 1500, 238 participants with LVH, 76 with DD) and HOMAGE case-control (562 cases of incident HF, 871 controls) cohorts. In multivariable logistic or Cox regression analyses adjusted for age, sex and cardiovascular risk factors, N-terminal pro-B-type natriuretic peptide (NT-proBNP) was associated with LVH, DD and incident HF in all cohorts: MPP (LVH odds ratio [OR] [95% confidence interval] 1.48 [1.28-1.71]; DD OR 1.71 [1.53-1.92]; HF HR 1.98 [1.66-2.36]); STANISLAS (LVH OR 1.20 [1.02-1.41]; DD OR 1.46 [1.12-1.90]); HOMAGE (HF HR 1.85 [1.62-2.12]). Galectin-4, growth differentiation factor 15 and suppression of tumorigenicity-2 were associated with incident HF in MPP and HOMAGE. A pathway enrichment analysis suggested that inflammation and viral infection were related to incident HF.
CONCLUSION: In conclusion, our study reinforces the role of NT-proBNP as a key biomarker for asymptomatic cardiac dysfunction and incident HF, consistent with its established use in clinical practice. This underscores the value of NT-proBNP for identifying patients at high risk for HF, and provides insights into pathways leading to HF and potential therapeutic targets.
(Less)
- author
- organization
-
- Cardiovascular Research - Hypertension (research group)
- MultiPark: Multidisciplinary research focused on Parkinson's disease
- EXODIAB: Excellence of Diabetes Research in Sweden
- EpiHealth: Epidemiology for Health
- Family Medicine and Community Medicine (research group)
- Internal Medicine - Epidemiology (research group)
- WCMM-Wallenberg Centre for Molecular Medicine
- publishing date
- 2024-10-28
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- European Journal of Heart Failure
- publisher
- Elsevier
- external identifiers
-
- scopus:85207916356
- pmid:39466935
- ISSN
- 1879-0844
- DOI
- 10.1002/ejhf.3502
- language
- English
- LU publication?
- yes
- additional info
- © 2024 The Author(s). European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
- id
- 0690a040-c0ea-4f7f-91c8-db48480800c2
- date added to LUP
- 2024-11-04 09:27:55
- date last changed
- 2025-07-09 23:51:20
@article{0690a040-c0ea-4f7f-91c8-db48480800c2, abstract = {{<p>AIMS: Biomarkers associated with asymptomatic ventricular dysfunction might improve risk stratification and identify pathways leading to heart failure (HF). We explored the association between proteomic biomarkers and left ventricular hypertrophy (LVH), diastolic dysfunction (DD) and incident HF in three population-based cohorts.</p><p>METHODS AND RESULTS: A chip was used to measure 92 protein biomarkers in blood samples from >1500 Malmö Preventive Project (MPP) participants, of whom 514 had LVH (34%), 462 had DD (32.4%) and, over a median follow-up of 13 (11-14) years, 130 developed HF (7.7%). Findings were confirmed in the STANISLAS (n > 1500, 238 participants with LVH, 76 with DD) and HOMAGE case-control (562 cases of incident HF, 871 controls) cohorts. In multivariable logistic or Cox regression analyses adjusted for age, sex and cardiovascular risk factors, N-terminal pro-B-type natriuretic peptide (NT-proBNP) was associated with LVH, DD and incident HF in all cohorts: MPP (LVH odds ratio [OR] [95% confidence interval] 1.48 [1.28-1.71]; DD OR 1.71 [1.53-1.92]; HF HR 1.98 [1.66-2.36]); STANISLAS (LVH OR 1.20 [1.02-1.41]; DD OR 1.46 [1.12-1.90]); HOMAGE (HF HR 1.85 [1.62-2.12]). Galectin-4, growth differentiation factor 15 and suppression of tumorigenicity-2 were associated with incident HF in MPP and HOMAGE. A pathway enrichment analysis suggested that inflammation and viral infection were related to incident HF.</p><p>CONCLUSION: In conclusion, our study reinforces the role of NT-proBNP as a key biomarker for asymptomatic cardiac dysfunction and incident HF, consistent with its established use in clinical practice. This underscores the value of NT-proBNP for identifying patients at high risk for HF, and provides insights into pathways leading to HF and potential therapeutic targets.</p>}}, author = {{Dieden, Anna and Girerd, Nicolas and Ottosson, Filip and Molvin, John and Pareek, Manan and Melander, Olle and Bachus, Erasmus and Råstam, Lennart and Lindblad, Ulf and Daka, Bledar and Leósdóttir, Margrét and Nilsson, Peter M and Olsen, Michael H and Clark, Andrew L and Cleland, John G F and Delles, Christian and González, Arantxa and Lamiral, Zohra and Duarte, Kevin and Rossignol, Patrick and Zannad, Faiez and Gudmundsson, Petri and Jujić, Amra and Magnusson, Martin}}, issn = {{1879-0844}}, language = {{eng}}, month = {{10}}, publisher = {{Elsevier}}, series = {{European Journal of Heart Failure}}, title = {{Proteomic biomarkers and pathway analysis for progression to heart failure in three epidemiological representative cohorts}}, url = {{http://dx.doi.org/10.1002/ejhf.3502}}, doi = {{10.1002/ejhf.3502}}, year = {{2024}}, }