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arXiv 1908.00920physics.med-phcs.LGphysics.soc-ph

Identification of gatekeeper diseases on the way to cardiovascular mortality

Section for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, A-1090 Wien, Austria(奥地利维也纳医科大学复杂系统科学中心(CeMSIIS)复杂系统科学部,维也纳1090);Complexity Science Hub Vienna, Josefstädter Straße 39, A-1080 Wien, Austria(奥地利维也纳复杂性科学中心,维也纳1080);IASA, Schlossplatz 1, A-2361 Laxenburg, Austria(奥地利拉克森堡国际应用系统分析研究所);Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM 85701, USA(美国新墨西哥州圣达菲研究所);Gender Medicine Unit, Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Spitalgasse 23, A-1090 Wien, Austria(奥地利维也纳医科大学内科学III系内分泌与代谢科性别医学部,维也纳1090);Gesundheit Österreich GmbH, Stubenring 6, A-1010 Wien, Austria(奥地利维也纳健康奥地利有限公司,维也纳1010)

Nils Haug, Stefan Thurner, Alexandra Kautzky-Willer, Michael Gyimesi, Peter Klimek

英文摘要:

Multimorbidity, the co-occurrence of two or more chronic diseases such as diabetes, obesity or cardiovascular diseases in one patient, is a frequent phenomenon. To make care more efficient, it is of relevance to understand how different diseases condition each other over the life time of a patient. However, most of our current knowledge on such patient careers is either confined to narrow time spans or specific (sets of) diseases. Here, we present a population-wide analysis of long-term patient trajectories by clustering them according to their disease history observed over 17 years. When patients acquire new diseases, their cluster assignment might change. A health trajectory can then be described by a temporal sequence of disease clusters. From the transitions between clusters we construct an age-dependent multilayer network of disease clusters. Random walks on this multilayer network provide a more precise model for the time evolution of multimorbid health states when compared to models that cluster patients based on single diseases. Our results can be used to identify decisive events that potentially determine the future disease trajectory of a patient. We find that for elderly patients the cluster network consists of regions of low, medium and high in-hospital mortality. Diagnoses of diabetes and hypertension are found to strongly increase the likelihood for patients to subsequently move into the high-mortality region later in life.

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