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Abnormal cytokine profiles in patients with idiopathic dilated cardiomyopathy and their asymptomatic relatives
- Source :
- Heart. 75:287-290
- Publication Year :
- 1996
- Publisher :
- BMJ, 1996.
-
Abstract
- Objectives-Immunological abnormalities in idiopathic dilated cardiomyopathy (DCM) include an increase in soluble interleukin(IL)-2 receptor, disease specific cardiac autoantibodies, an HLADR4 association, and familial aggregation of disease; however, cytokine profiles have not been defined. Serum concentrations of IL-2, IL-4, IL-10, and IL-12 were measured in patients with DCM (WHO criteria), relatives with asymptomatic left ventricular enlargement (LVE), patients with ischaemic heart failure (IHD), and healthy controls. Design-Serum from 20 individuals from each of the four groups was assayed for cytokine concentrations by a commercial enzyme linked immunosorbent assay. Results-IL-2 concentrations were abnormally increased in DCM patients and relatives with LVE. Concentrations of IL-10 were increased in DCM patients. Concentrations ofIL-4 and IL-12 were not increased in any of the groups. Conclusion-These abnormalities may reflect defective/inappropriate T cell function in patients with DCM and in their relatives with LVE. (Heart 1996;75:287-290)
- Subjects :
- Adult
Cardiomyopathy, Dilated
Male
medicine.medical_specialty
Adolescent
Heart disease
medicine.medical_treatment
Cardiomegaly
Enzyme-Linked Immunosorbent Assay
Disease
Gastroenterology
Asymptomatic
Pathogenesis
Internal medicine
Idiopathic dilated cardiomyopathy
medicine
Humans
cardiovascular diseases
Heart Failure
business.industry
Autoantibody
Interleukin
Family aggregation
Dilated cardiomyopathy
General Medicine
Middle Aged
medicine.disease
Interleukin-12
Interleukin-10
Cytokine
Heart failure
cardiovascular system
Cardiology
Cytokines
Interleukin-2
Female
Interleukin-4
medicine.symptom
Cardiology and Cardiovascular Medicine
business
Research Article
Subjects
Details
- ISSN :
- 13556037
- Volume :
- 75
- Database :
- OpenAIRE
- Journal :
- Heart
- Accession number :
- edsair.doi.dedup.....151a5424f915488f487c00deb60ddc6c