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. 2020 Jun 26;11(1):3223.
doi: 10.1038/s41467-020-16780-x.

Twelve-year clinical trajectories of multimorbidity in a population of older adults

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Twelve-year clinical trajectories of multimorbidity in a population of older adults

Davide L Vetrano et al. Nat Commun. .

Abstract

Multimorbidity-the co-occurrence of multiple diseases-is associated to poor prognosis, but the scarce knowledge of its development over time hampers the effectiveness of clinical interventions. Here we identify multimorbidity clusters, trace their evolution in older adults, and detect the clinical trajectories and mortality of single individuals as they move among clusters over 12 years. By means of a fuzzy c-means cluster algorithm, we group 2931 people ≥60 years in five clinically meaningful multimorbidity clusters (52%). The remaining 48% are part of an unspecific cluster (i.e. none of the diseases are overrepresented), which greatly fuels other clusters at follow-ups. Clusters contribute differentially to the longitudinal development of other clusters and to mortality. We report that multimorbidity clusters and their trajectories may help identifying homogeneous groups of people with similar needs and prognosis, and assisting clinicians and health care systems in the personalization of clinical interventions and preventive strategies.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1. Evolution of multimorbidity clusters and clinical trajectories of older adults with multimorbidity over 12 years.
The height of the boxes and the thickness of the stripes are proportional to the amount of people belonging to the cluster and moving from the cluster, respectively. MSK musculoskeletal. To note, for this analysis participants were assigned to the cluster they were more likely to belong in order to investigate the most likely trajectories.
Fig. 2
Fig. 2. Contribution of the baseline multimorbidity clusters to the 6-year follow-up clusters.
Numbers indicate the percentage (%) of people belonging to the 6-year follow-up clusters that moved from the baseline clusters. To note, for this analysis participants were assigned to the cluster they were more likely to belong.
Fig. 3
Fig. 3. Contribution of the 6-year follow-up multimorbidity clusters to the 12-year follow-up clusters.
Numbers indicate the percentage (%) of people belonging to the 12-year follow-up clusters that moved from the 6-year follow-up clusters. To note, for this analysis participants were assigned to the cluster they were more likely to belong.

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