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Hyperhomocysteinemia in patients with symptomatic chronic heart failure: prevalence and prognostic importance--pilot
Marek Naruszewicz1, Ewa A Jankowska, Robert Zymlinski
1Department of Clinical Biochemistry and Laboratory Diagnostics, Pomeranian Medical University, al. Powstańców Wlkp. 72, 70-111 Szczecin, Poland. mnarusze@sci.pam.szczecin.pl
Insights
Hyperhomocysteinemia (HHcy) is prevalent in chronic heart failure (CHF) patients, linked to disease severity and poor prognosis. Addressing HHcy may improve outcomes in CHF.
Area of Science:
- Cardiology
- Metabolic Medicine
- Clinical Research
Background:
- Chronic heart failure (CHF) patients may be susceptible to adverse effects of hyperhomocysteinemia (HHcy).
- Prevalence, clinical determinants, and prognostic implications of HHcy in CHF require further investigation.
Purpose of the Study:
- To assess the prevalence of HHcy (plasma homocysteine [Hcy] ≥ 14 µmol/L) in an unselected CHF cohort.
- To identify clinical and metabolic determinants of HHcy in CHF.
- To evaluate the prognostic impact of HHcy on mortality in CHF patients.
Main Methods:
- Study included 108 consecutive CHF patients (mean age 66±11 years).
- Plasma Hcy levels were measured, with HHcy defined as ≥ 14 µmol/L.
- Multivariable regression models were used to identify predictors of HHcy and its association with mortality.
Main Results:
- 35% of CHF patients (38 out of 108) had HHcy (mean Hcy 12.5±5.5 µmol/L).
- Advanced NYHA class, elevated NT-proBNP, reduced peak oxygen consumption, lower glomerular filtration rate, and hyperuricemia predicted HHcy.
- HHcy was independently associated with increased 3-year mortality (HR=3.26), with survival rates of 37% vs. 73% for normal Hcy levels (P<0.0001).
Conclusions:
- HHcy is common in CHF patients.
- HHcy is associated with disease severity and generalized metabolic imbalance, including hyperuricemia.
- HHcy independently predicts a poor long-term prognosis in CHF.
Background:
Patients with chronic heart failure (CHF) may be particularly susceptible to unfavorable effects of hyperhomocysteinemia (HHcy). The aim of this study was to assess the prevalence of HHcy (plasma homocysteine [Hcy]>or=14 micromol/L) in an unselected cohort of CHF patients, its clinical determinants, and prognostic implications.
Methods And Results:
In 108 consecutive CHF patients (81 men, age: 66+/-11 years) with mean plasma Hcy level 12.5+/-5.5 micromol/L (range 2.3-28.3 micromol/L), 38 (35%) patients demonstrated HHcy. Among clinical and metabolic parameters, in multivariable regression models, advanced NYHA class (P<0.0001), plasma NT-proBNP (P<0.001), peak oxygen consumption (P<0.05), reduced glomerular filtration rate (P<0.0001) and elevated serum uric acid (P<0.05) predicted high plasma Hcy level. HHcy was related to increased mortality (HR=3.26, 95% CI: 1.78-5.98, P=0.0001), also when adjusted for conventional prognosticators in multivariable models (all P<0.01). In patients with HHcy, a 3-year survival was 37% (95% CI: 22-52%) as compared to 73% (95% CI: 63-83%) in those with normal Hcy levels (P<0.0001).
Conclusions:
HHcy is common in CHF, is related to the disease severity, depicts generalized metabolic imbalance (evidenced by hyperuricaemia), and independently predicts poor long-term prognosis.
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