Why the study?
Is plasma homocyst(e)ine level an independent risk factor and inherited abnormality associated with early familial coronary heart disease?
Population
85 participants including 37 with early familial coronary heart disease and 48 age- and sex-matched controls…
Comparison
Elevated plasma homocyst(e)ine (H(e)) levels vs Age- and sex-matched control subjects
Design
Case-control
Authors
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Supports homocysteine as potential inherited marker in early familial CHD; observational data leave causal role and therapeutic implications open.
Is plasma homocyst(e)ine level an independent risk factor and inherited abnormality associated with early familial coronary heart disease?
Hyperhomocyst(e)inemia is an independent predictor and inherited abnormality that may explain some occurrences of early familial coronary heart disease.
Williams et al. (1990) studied this question.
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