Evidence map›Paper›PMID 36209412›Full record

ArticleBriefings in bioinformatics2022

Data-driven patient stratification of UK Biobank cohort suggests five endotypes of multimorbidity.

Bodhayan Prasad, Anthony J Bjourson, Priyank Shukla

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
–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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

3 authors.

Bodhayan PrasadPersonalised Medicine Centre, School of Medicine, Ulster University, UK. He holds a MSc in Computational and Integrative Sciences from Jawaharlal Nehru University, India.ORCID 0000-0002-7383-2460
Anthony J BjoursonPersonalised Medicine Centre, School of Medicine, Ulster University, UK. He holds a PhD in Genomics and Molecular Biology from Queen's University, Northern Ireland.ORCID 0000-0002-1105-7147
Priyank ShuklaPersonalised Medicine Centre, School of Medicine, Ulster University, UK. He holds a PhD in Computer Science with area of research in Bioinformatics from University of Bologna, Italy.ORCID 0000-0002-4985-9305

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Science Foundation Ireland
6 · The paper itself

Abstract

Multimorbidity generally refers to concurrent occurrence of multiple chronic conditions. These patients are inherently at high risk and often lead a poor quality of life due to delayed treatments. With the emergence of personalized medicine and stratified healthcare, there is a need to stratify patients right at the primary care setting. Here we developed multimorbidity analysis pipeline (MulMorPip), which can stratify patients into multimorbid subgroups or endotypes based on their lifetime disease diagnosis and characterize them based on demographic features and underlying disease-disease interaction networks. By implementing MulMorPip on UK Biobank cohort, we report five distinct molecular subclasses or endotypes of multimorbidity. For each patient, we calculated the existence of broad disease classes defined by Charlson's comorbidity classification using the International Classification of Diseases-10 encoding. We then applied multiple correspondence analysis in 77 524 patients from UK Biobank, who had multimorbidity of more than one disease, which resulted in five multimorbid clusters. We further validated these clusters using machine learning and were able to classify 20% model-blind test set patients with an accuracy of 97% and an average Jaccard similarity of 84%. This was followed by demographic characterization and development of interlinking disease network for each cluster to understand disease-disease interactions. Our identified five endotypes of multimorbidity draw attention to dementia, stroke and paralysis as important drivers of multimorbidity stratification. Inclusion of such patient stratification at the primary care setting can help general practitioners to better observe patients' multiple chronic conditions, their risk stratification and personalization of treatment strategies.

Indexed as

MultimorbidityMultiple Chronic ConditionsBiological Specimen BanksHumansQuality of LifeUnited Kingdomcharlson comorbidity index (CCI)clusteringcomorbiditydisease interaction networkendotypesmachine learningmultimorbiditymultiple correspondence analysis (MCA)patient stratificationUK Biobank

Identifiers

PMID36209412
PMCPMC9677496

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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.