Evidence map›Paper›PMID 38454004›Full record

ArticleNPJ digital medicine2024

Unraveling cradle-to-grave disease trajectories from multilayer comorbidity networks.

Elma Dervić, Johannes Sorger, Liuhuaying Yang, Michael Leutner, Alexander Kautzky, Stefan Thurner, Alexandra Kautzky-Willer, Peter Klimek

Open access · goldAbstract read
In one paragraph

Article in NPJ digital medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
8.1field-weighted citation impact, top 2% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

Elma DervićComplexity Science Hub Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0001-7168-3310
Johannes SorgerComplexity Science Hub Vienna, Vienna, Austria.
Liuhuaying YangComplexity Science Hub Vienna, Vienna, Austria.
Michael LeutnerMedical University of Vienna, Department of Internal Medicine III, Clinical Division of Endocrinology and Metabolism, Vienna, Austria.
Alexander KautzkyMedical University of Vienna, Department of Psychiatry and Psychotherapy, Vienna, Austria.
Stefan ThurnerComplexity Science Hub Vienna, Vienna, Austria.
Alexandra Kautzky-WillerMedical University of Vienna, Department of Internal Medicine III, Clinical Division of Endocrinology and Metabolism, Vienna, Austria.ORCID http://orcid.org/0000-0002-3520-4105
Peter KlimekComplexity Science Hub Vienna, Vienna, Austria. peter.klimek@meduniwien.ac.at.ORCID http://orcid.org/0000-0003-1187-6713
Medical University of Vienna · ATComplexity Science Hub · ATAustrian Research Institute for Artificial Intelligence · ATAustrian Standards · ATSanta Fe Institute · US

Funding

Vienna Science and Technology Fund (Wiener Wissenschafts-, Forschungs- und Technologiefonds) MA16- 045
6 · The paper itself

Abstract

We aim to comprehensively identify typical life-spanning trajectories and critical events that impact patients' hospital utilization and mortality. We use a unique dataset containing 44 million records of almost all inpatient stays from 2003 to 2014 in Austria to investigate disease trajectories. We develop a new, multilayer disease network approach to quantitatively analyze how cooccurrences of two or more diagnoses form and evolve over the life course of patients. Nodes represent diagnoses in age groups of ten years; each age group makes up a layer of the comorbidity multilayer network. Inter-layer links encode a significant correlation between diagnoses (p < 0.001, relative risk > 1.5), while intra-layers links encode correlations between diagnoses across different age groups. We use an unsupervised clustering algorithm for detecting typical disease trajectories as overlapping clusters in the multilayer comorbidity network. We identify critical events in a patient's career as points where initially overlapping trajectories start to diverge towards different states. We identified 1260 distinct disease trajectories (618 for females, 642 for males) that on average contain 9 (IQR 2-6) different diagnoses that cover over up to 70 years (mean 23 years). We found 70 pairs of diverging trajectories that share some diagnoses at younger ages but develop into markedly different groups of diagnoses at older ages. The disease trajectory framework can help us to identify critical events as specific combinations of risk factors that put patients at high risk for different diagnoses decades later. Our findings enable a data-driven integration of personalized life-course perspectives into clinical decision-making.

Identifiers

PMID38454004
PMCPMC10920888
OpenAlexW4392560640

What OpenQuestion holds

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LicenceCC BY
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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.