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CRP genetic variants are associated with mortality and depressive symptoms in chronic heart failure patients
S Kittel-Schneider1, M Kaspar2, D Berliner3
1Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital of Frankfurt, Frankfurt, Germany; Comprehensive Heart Failure Center, University Hospital of Würzburg, Würzburg, Germany.
Insights
Certain genetic variations in the C-reactive protein (CRP) gene are linked to higher mortality risk and increased depressive symptoms in heart failure (HF) patients. These findings suggest inflammation may connect HF prognosis and depression.
Area of Science:
- Cardiology
- Genetics
- Psychiatry
Background:
- Heart failure (HF) is a complex condition influenced by genetic and other factors.
- Inflammatory mechanisms and depressive symptoms are increasingly recognized in HF pathogenesis and outcomes.
- Depression is prevalent in HF patients and acts as a risk factor for cardiovascular disease.
Purpose of the Study:
- To investigate the association between genetic variants of CRP and IL-6 and mortality in HF patients.
- To explore the relationship between CRP and IL-6 genetic variants, CRP/IL-6 blood levels, and depressive symptoms.
Main Methods:
- Analyzed blood levels of C-reactive protein (CRP) and Interleukin-6 (IL-6) in 936 heart failure patients.
- Examined single nucleotide polymorphisms (SNPs) in the CRP and IL6 genes for their impact on mortality.
- Assessed depressive symptoms using the PHQ-9 scale.
Main Results:
- Recessive genotypes of two CRP gene SNPs (rs1800947 and rs11265263) were associated with significantly higher mortality risk.
- These CRP variants correlated with elevated CRP blood levels and increased depressive symptoms.
- No significant association was found between IL-6 gene variants and mortality.
Conclusions:
- Less common CRP genetic variants may be linked to increased mortality, depressive symptoms, and CRP levels in HF patients.
- The inflammatory system might serve as a link between poor HF prognosis and depressive symptoms.
- Further research into CRP genetics could elucidate pathways connecting inflammation, HF outcomes, and depression.
Objective:
Heart failure (HF) is a complex medical condition with a multitude of genetic and other factors being involved in the pathogenesis. Emerging evidence points to an involvement of inflammatory mechanisms at least in subgroups of patients. The same is true for depression and depressive symptoms, which have a high prevalence in HF patients and are risk factors for the development and outcomes of cardiovascular disease.
Methods:
In 936 patients of the Interdisciplinary Network Heart Failure (INH) program, CRP and IL-6 protein blood levels were measured and genetic variants (single nucleotide polymorphisms) of the CRP and IL6 gene analyzed regarding their influence on mortality.
Results:
Less common recessive genotypes of two single nucleotide polymorphisms in the CRP gene (rs1800947 and rs11265263) were associated with significantly higher mortality risk (p < 0.006), higher CRP levels (p = 0.029, p = 0.006) and increased depressive symptoms in the PHQ-9 (p = 0.005, p = 0.003). Variants in the IL-6 gene were not associated with mortality.
Conclusion:
Our results hint towards an association of less common CRP genetic variants with increased mortality risk, depressive symptoms and peripheral CRP levels in this population of HF patients thereby suggesting a possible role of the inflammatory system as link between poor prognosis in HF and depressive symptoms.
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