Cluster analysis of angiotensin biomarkers to identify antihypertensive drug treatment in population studies.


Journal

BMC medical research methodology
ISSN: 1471-2288
Titre abrégé: BMC Med Res Methodol
Pays: England
ID NLM: 100968545

Informations de publication

Date de publication:
27 05 2023
Historique:
received: 20 01 2023
accepted: 23 04 2023
medline: 29 5 2023
pubmed: 28 5 2023
entrez: 27 5 2023
Statut: epublish

Résumé

The recent progress in molecular biology generates an increasing interest in investigating molecular biomarkers as markers of response to treatments. The present work is motivated by a study, where the objective was to explore the potential of the molecular biomarkers of renin-angiotensin-aldosterone system (RAAS) to identify the undertaken antihypertensive treatments in the general population. Population-based studies offer an opportunity to assess the effectiveness of treatments in real-world scenarios. However, lack of quality documentation, especially when electronic health record linkage is unavailable, leads to inaccurate reporting and classification bias. We present a machine learning clustering technique to determine the potential of measured RAAS biomarkers for the identification of undertaken treatments in the general population. The biomarkers were simultaneously determined through a novel mass-spectrometry analysis in 800 participants of the Cooperative Health Research In South Tyrol (CHRIS) study with documented antihypertensive treatments. We assessed the agreement, sensitivity and specificity of the resulting clusters against known treatment types. Through the lasso penalized regression, we identified clinical characteristics associated with the biomarkers, accounting for the effects of cluster and treatment classifications. We identified three well-separated clusters: cluster 1 (n = 444) preferentially including individuals not receiving RAAS-targeting drugs; cluster 2 (n = 235) identifying angiotensin type 1 receptor blockers (ARB) users (weighted kappa κ Unsupervised clustering of angiotensin-based biomarkers is a viable technique to identify individuals on specific antihypertensive treatments, pointing to a potential application of the biomarkers as useful clinical diagnostic tools even outside of a controlled clinical setting.

Sections du résumé

BACKGROUND
The recent progress in molecular biology generates an increasing interest in investigating molecular biomarkers as markers of response to treatments. The present work is motivated by a study, where the objective was to explore the potential of the molecular biomarkers of renin-angiotensin-aldosterone system (RAAS) to identify the undertaken antihypertensive treatments in the general population. Population-based studies offer an opportunity to assess the effectiveness of treatments in real-world scenarios. However, lack of quality documentation, especially when electronic health record linkage is unavailable, leads to inaccurate reporting and classification bias.
METHOD
We present a machine learning clustering technique to determine the potential of measured RAAS biomarkers for the identification of undertaken treatments in the general population. The biomarkers were simultaneously determined through a novel mass-spectrometry analysis in 800 participants of the Cooperative Health Research In South Tyrol (CHRIS) study with documented antihypertensive treatments. We assessed the agreement, sensitivity and specificity of the resulting clusters against known treatment types. Through the lasso penalized regression, we identified clinical characteristics associated with the biomarkers, accounting for the effects of cluster and treatment classifications.
RESULTS
We identified three well-separated clusters: cluster 1 (n = 444) preferentially including individuals not receiving RAAS-targeting drugs; cluster 2 (n = 235) identifying angiotensin type 1 receptor blockers (ARB) users (weighted kappa κ
CONCLUSIONS
Unsupervised clustering of angiotensin-based biomarkers is a viable technique to identify individuals on specific antihypertensive treatments, pointing to a potential application of the biomarkers as useful clinical diagnostic tools even outside of a controlled clinical setting.

Identifiants

pubmed: 37245005
doi: 10.1186/s12874-023-01930-8
pii: 10.1186/s12874-023-01930-8
pmc: PMC10224304
doi:

Substances chimiques

Antihypertensive Agents 0
Angiotensins 0
Angiotensin-Converting Enzyme Inhibitors 0
Angiotensin Receptor Antagonists 0
Biomarkers 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

131

Informations de copyright

© 2023. The Author(s).

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Auteurs

Maeregu Woldeyes Arisido (MW)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy. maeregu.arisido@fht.org.
Health Data Science Center, Human Technopole, Viale Rita Levi Montalcini, 1, 20157, Milan, Italy. maeregu.arisido@fht.org.

Luisa Foco (L)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy.

Robin Shoemaker (R)

Department of Dietetics and Human Nutrition, University of Kentucky, Lexington, USA.

Roberto Melotti (R)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy.

Christian Delles (C)

School of Cardiovascular and Metabolic Health , University of Glasgow, Glasgow, UK.

Martin Gögele (M)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy.

Stefano Barolo (S)

Hospital of Schlanders/Silandro, Schlanders/Silandro, Italy.

Stephanie Baron (S)

National Institute of Health and Medical Research (Inserm), Paris, France.

Michel Azizi (M)

National Institute of Health and Medical Research (Inserm), Paris, France.
Hypertension Department and DMU CARTE, AP-HP, Hôpital Européen Georges-Pompidou, Paris, France.
Université Paris Cité, Paris, France.

Anna F Dominiczak (AF)

School of Cardiovascular and Metabolic Health , University of Glasgow, Glasgow, UK.

Maria-Christina Zennaro (MC)

National Institute of Health and Medical Research (Inserm), Paris, France.

Peter P Pramstaller (P)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy.

Marko Poglitsch (M)

Attoquant Diagnostics, Vienna, Austria.

Cristian Pattaro (C)

Institute for Biomedicine (affiliated to the University of Lübeck), Eurac Research, Via Volta 21, 39100, Bolzano, Italy. cristian.pattaro@eurac.edu.

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