Evidence map›Paper›PMID 32151252›Full record

ArticleBMC medicine2020

High-risk multimorbidity patterns on the road to cardiovascular mortality.

Nina Haug, Carola Deischinger, Michael Gyimesi, Alexandra Kautzky-Willer, Stefan Thurner, Peter Klimek

Abstract read
In one paragraph

Article in BMC medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

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

  1. Pooled it
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  17. Heart Failure and Multimorbidity in Asia.Current heart failure reports · 2023
    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

6 authors.

Nina HaugSection for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Carola DeischingerGender Medicine Unit, Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Michael GyimesiGesundheit Österreich GmbH, Stubenring 6, Vienna, A-1010, Austria.
Alexandra Kautzky-WillerGender Medicine Unit, Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Stefan ThurnerSection for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria.
Peter KlimekSection for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, Vienna, A-1090, Austria. peter.klimek@meduniwien.ac.at.

Funding

European Commission H2020 SmartResilience No. 700621\"{O}sterreichische Forschungsf\"{o}rderungsgesellschaft (AT) 857136Wiener Wissenschafts-, Forschungs- und Technologiefonds MA16-045
6 · The paper itself

Abstract

backgroundMultimorbidity, the co-occurrence of two or more diseases in one patient, is a frequent phenomenon. Understanding how different diseases condition each other over the lifetime of a patient could significantly contribute to personalised prevention efforts. However, most of our current knowledge on the long-term development of the health of patients (their disease trajectories) is either confined to narrow time spans or specific (sets of) diseases. Here, we aim to identify decisive events that potentially determine the future disease progression of patients.

methodsHealth states of patients are described by algorithmically identified multimorbidity patterns (groups of included or excluded diseases) in a population-wide analysis of 9,000,000 patient histories of hospital diagnoses observed over 17 years. Over time, patients might acquire new diagnoses that change their health state; they describe a disease trajectory. We measure the age- and sex-specific risks for patients that they will acquire certain sets of diseases in the future depending on their current health state.

resultsIn the present analysis, the population is described by a set of 132 different multimorbidity patterns. For elderly patients, we find 3 groups of multimorbidity patterns associated with low (yearly in-hospital mortality of 0.2-0.3%), medium (0.3-1%) and high in-hospital mortality (2-11%). We identify combinations of diseases that significantly increase the risk to reach the high-mortality health states in later life. For instance, in men (women) aged 50-59 diagnosed with diabetes and hypertension, the risk for moving into the high-mortality region within 1 year is increased by the factor of 1.96 ± 0.11 (2.60 ± 0.18) compared with all patients of the same age and sex, respectively, and by the factor of 2.09 ± 0.12 (3.04 ± 0.18) if additionally diagnosed with metabolic disorders.

conclusionsOur approach can be used both to forecast future disease burdens, as well as to identify the critical events in the careers of patients which strongly determine their disease progression, therefore constituting targets for efficient prevention measures. We show that the risk for cardiovascular diseases increases significantly more in females than in males when diagnosed with diabetes, hypertension and metabolic disorders.

Indexed as

AgedCardiovascular DiseasesFemaleHumansMaleMiddle AgedMultimorbiditySurvival RateCardiovascular diseaseComorbiditiesDisease trajectoriesMachine learningMetabolic syndrome

Identifiers

PMID32151252
PMCPMC7063814

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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.