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Phenotypic Disease Network-Based Multimorbidity Analysis in Idiopathic Cardiomyopathy Patients with Hospital
Lei Wang1, Ye Jin2, Jingya Zhou3,4
1State Key Laboratory of Complex Severe and Rare Diseases, Department of Cardiology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100730, China.
Insights
Aging significantly increases the comorbidity burden in Idiopathic Cardiomyopathy (ICM) patients, affecting multiple systems. Network analysis reveals key disease clusters and age-specific patterns, aiding integrated care for this rare disease.
Area of Science:
- Cardiology and Internal Medicine
- Complex Systems Science
- Public Health and Epidemiology
Background:
- Idiopathic Cardiomyopathy (ICM) is a rare condition associated with significant multimorbidity across physiological systems.
- Understanding chronic disease co-occurrence in ICM is limited, especially in developing regions, due to small patient cohorts.
- Investigating age-related differences in ICM multimorbidity patterns is crucial for comprehensive patient care.
Purpose of the Study:
- To develop a multidimensional model for Idiopathic Cardiomyopathy (ICM) multimorbidity.
- To analyze age-specific differences in disease co-occurrence patterns within ICM patients.
- To identify key comorbidities associated with heart failure in ICM.
Main Methods:
- Retrospective analysis of 1036 Idiopathic Cardiomyopathy (ICM) inpatients and matched controls from 2012-2021.
- Focus on chronic illnesses with >1% prevalence using ICD-10 codes.
- Construction of age-specific multimorbidity networks and application of Associated Rule Mining (ARM) for heart failure comorbidities.
Main Results:
- Idiopathic Cardiomyopathy (ICM) patients exhibited a 78% higher comorbidity burden compared to controls, with intensified interactions in those over 50.
- Central disease clusters involved metabolic, musculoskeletal, genitourinary, respiratory, and digestive systems.
- Age-specific findings highlighted impaired coagulation in younger adults and malignant neoplasms/circulatory issues in older adults; heart failure comorbidities included diabetes and metabolic disorders.
Conclusions:
- Aging is a primary driver of the increased comorbidity load in Idiopathic Cardiomyopathy (ICM).
- ICM comorbidities are concentrated in circulatory, metabolic, musculoskeletal, genitourinary, respiratory, and digestive systems.
- A network-based approach enhances understanding of ICM multimorbidity and optimizes integrated care strategies.
Background:
Idiopathic cardiomyopathy (ICM) is a rare disease affecting numerous physiological and biomolecular systems with multimorbidity. However, due to the small sample size of uncommon diseases, the whole spectrum of chronic disease co-occurrence, especially in developing nations, has not yet been investigated. To grasp the multimorbidity pattern, we aimed to present a multidimensional model for ICM and differences among age groups.
Methods:
Hospital discharge records were collected from a rare disease centre of ICM inpatients (n = 1036) over 10 years (2012 to 2021) for this retrospective analysis. One-to-one matched controls were also included. First, by looking at the first three digits of the ICD-10 code, we concentrated on chronic illnesses with a prevalence of more than 1%. The ICM and control inpatients had a total of 71 and 69 chronic illnesses, respectively. Second, to evaluate the multimorbidity pattern in both groups, we built age-specific cosine-index-based multimorbidity networks. Third, the associated rule mining (ARM) assessed the comorbidities with heart failure for ICM, specifically.
Results:
The comorbidity burden of ICM was 78% larger than that of the controls. All ages were affected by the burden, although those over 50 years old had more intense interactions. Moreover, in terms of disease connectivity, central, hub, and authority diseases were concentrated in the metabolic, musculoskeletal and connective tissue, genitourinary, eye and adnexa, respiratory, and digestive systems. According to the age-specific connection, the impaired coagulation function was required for raising attention (e.g., autoimmune-attacked digestive and musculoskeletal system disorders) in young adult groups (ICM patients aged 20-49 years). For the middle-aged (50-60 years) and older (≥70 years) groups, malignant neoplasm and circulatory issues were the main confrontable problems. Finally, according to the result of ARM, the comorbidities and comorbidity patterns of heart failure include diabetes mellitus and metabolic disorder, sleeping disorder, renal failure, liver, and circulatory diseases.
Conclusions:
The main cause of the comorbid load is aging. The ICM comorbidities were concentrated in the circulatory, metabolic, musculoskeletal and connective tissue, genitourinary, eye and adnexa, respiratory, and digestive systems. The network-based approach optimizes the integrated care of patients with ICM and advances our understanding of multimorbidity associated with the disease.
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