Data-driven identification of ageing-related diseases from electronic health records

被引:22
作者
Kuan, Valerie [1 ,2 ,3 ]
Fraser, Helen C. [4 ]
Hingorani, Melanie [5 ]
Denaxas, Spiros [1 ,2 ,3 ,6 ]
Gonzalez-Izquierdo, Arturo [1 ,2 ]
Direk, Kenan [1 ,2 ]
Nitsch, Dorothea [7 ]
Mathur, Rohini [7 ]
Parisinos, Constantinos A. [1 ]
Lumbers, R. Thomas [1 ,2 ,3 ,8 ]
Sofat, Reecha [1 ,2 ,3 ]
Wong, Ian C. K. [9 ,10 ]
Casas, Juan P. [11 ,12 ]
Thornton, Janet M. [13 ]
Hemingway, Harry [1 ,2 ,3 ,14 ]
Partridge, Linda [4 ,15 ]
Hingorani, Aroon D. [2 ,3 ,16 ]
机构
[1] UCL, Inst Hlth Informat, London, England
[2] UCL, Hlth Data Res UK London, London, England
[3] UCL, British Heart Fdn Res Accelerator, London, England
[4] UCL, Inst Hlth Ageing, Dept Genet Evolut & Environm, London, England
[5] Moorfields Eye Hosp, London, England
[6] Alan Turing Inst, London, England
[7] London Sch Hyg & Trop Med, Dept Noncommunicable Dis Epidemiol, London, England
[8] St Bartholomews Hosp, Barts Heart Ctr, London, England
[9] UCL, Sch Pharm, London WC1N 1AX, England
[10] Univ Hong Kong, Ctr Safe Medicat Practice & Res, Dept Pharmacol & Pharm, Pok Fu Lam, Hong Kong, Peoples R China
[11] Harvard Med Sch, Dept Med, Brigham & Womens Hosp, Boston, MA 02115 USA
[12] VA Boston Healthcare Syst, Massachusetts Vet Epidemiol Res & Informat Ctr MA, Boston, MA USA
[13] European Bioinformat Inst EMBL EBI, European Mol Biol Lab, Wellcome Genome Campus, Hinxton CB10 1SD, Cambs, England
[14] UCL, Natl Inst Hlth Res, Univ Coll London Hosp, Biomed Res Ctr, London W1T 7DN, England
[15] Max Planck Inst Biol Ageing, Cologne, Germany
[16] UCL, Inst Cardiovasc Sci, London, England
基金
英国医学研究理事会; 英国惠康基金; 英国工程与自然科学研究理事会; 英国经济与社会研究理事会;
关键词
VALIDATION; VALIDITY; DIAGNOSES;
D O I
10.1038/s41598-021-82459-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Reducing the burden of late-life morbidity requires an understanding of the mechanisms of ageing-related diseases (ARDs), defined as diseases that accumulate with increasing age. This has been hampered by the lack of formal criteria to identify ARDs. Here, we present a framework to identify ARDs using two complementary methods consisting of unsupervised machine learning and actuarial techniques, which we applied to electronic health records (EHRs) from 3,009,048 individuals in England using primary care data from the Clinical Practice Research Datalink (CPRD) linked to the Hospital Episode Statistics admitted patient care dataset between 1 April 2010 and 31 March 2015 (mean age 49.7 years (s.d. 18.6), 51% female, 70% white ethnicity). We grouped 278 high-burden diseases into nine main clusters according to their patterns of disease onset, using a hierarchical agglomerative clustering algorithm. Four of these clusters, encompassing 207 diseases spanning diverse organ systems and clinical specialties, had rates of disease onset that clearly increased with chronological age. However, the ages of onset for these four clusters were strikingly different, with median age of onset 82 years (IQR 82-83) for Cluster 1, 77 years (IQR 75-77) for Cluster 2, 69 years (IQR 66-71) for Cluster 3 and 57 years (IQR 54-59) for Cluster 4. Fitting to ageing-related actuarial models confirmed that the vast majority of these 207 diseases had a high probability of being ageing-related. Cardiovascular diseases and cancers were highly represented, while benign neoplastic, skin and psychiatric conditions were largely absent from the four ageing-related clusters. Our framework identifies and clusters ARDs and can form the basis for fundamental and translational research into ageing pathways.
引用
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页数:17
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