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| Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00005482 |
Purpose
To test the hypotheses that the risk of myocardial infarction and/or stroke is associated with elevated plasma levels of homocysteine, and low plasma levels of folate, vitamins B12 and B6.
| Condition |
|---|
|
Cardiovascular Diseases Cerebrovascular Accident Coronary Disease Myocardial Infarction Heart Diseases Hyperhomocysteinemia |
| Study Type: | Observational |
| Study Design: | Natural History |
| Study Start Date: | September 1995 |
| Estimated Study Completion Date: | March 1999 |
BACKGROUND:
Elevated plasma homocyst(e)ine is a risk factor for vascular disease in middle-aged men. Supplementation with folate, and to some extent vitamins B12 and B6, can reduce plasma homocyst(e)ine levels. There is also evidence from in vitro studies that the adverse atherogenic or thrombotic effects of Lp(a) may be greatly enhanced by homocyst(e)ine. The high prevalence of low levels of folate and vitamins B12 and B6 among the elderly in the United States has led to the hypothesis that a substantial portion of cardiovascular morbidity and mortality among older persons could be prevented by increasing intake of these nutrients to reduce plasma levels of homocysteine. Little is known, however, regarding the relationship of homocysteine, folate, B vitamins, and Lp(a) to cardiovascular disease among the elderly, among whom CVD represents the leading cause of morbidity and mortality.
DESIGN NARRATIVE:
In this ancillary study to the prospective Cardiovascular Health Study (CHS), a case-cohort design was used to test hypotheses that the risk of myocardial infarction and/or stoke was associated with elevated plasma levels of homocysteine, and low plasma levels of folate, vitamins B12 and B6.
Further, a determination was made whether elevated plasma levels of homocysteine and Lp(a) interacted to increase substantially the risk of myocardial infarction and/or stroke above that due to either factor alone. The sub-cohort was used to study the relationship between the factors under study and progression of sub-clinical atherosclerosis. For each case and sub-cohort member, an aliquot of fasting plasma drawn at baseline was analyzed for homocysteine, folate B12, and B6 concentrations. [Values of plasma Lp(a) were determined at baseline.] Results of these assays were combined with other CHS data to address the hypothesis that the risk of myocardial infarction and/or stroke was associated with elevated plasma levels of homocysteine, and low plasma levels of folate, vitamins B12 and B6.
Eligibility| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
No eligibility criteria
Contacts and Locations
More Information
| Study ID Numbers: | 4969 |
| Study First Received: | May 25, 2000 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00005482 History of Changes |
| Health Authority: | United States: Federal Government |
|
Cerebral Infarction Myocardial Ischemia Arteriosclerosis Brain Diseases Cerebrovascular Disorders Metabolism, Inborn Errors Necrosis Vitamins Brain Ischemia Myocardial Infarction Metabolic Disorder Arterial Occlusive Diseases Heart Diseases |
Metabolic Diseases Hyperhomocysteinemia Amino Acid Metabolism, Inborn Errors Stroke Vascular Diseases Central Nervous System Diseases Ischemia Coronary Disease Genetic Diseases, Inborn Inborn Amino Acid Metabolism Disorder Brain Infarction Infarction Coronary Artery Disease |
|
Cerebral Infarction Myocardial Ischemia Arteriosclerosis Brain Diseases Cerebrovascular Disorders Metabolism, Inborn Errors Necrosis Pathologic Processes Brain Ischemia Cardiovascular Diseases Myocardial Infarction Arterial Occlusive Diseases Metabolic Diseases |
Heart Diseases Hyperhomocysteinemia Amino Acid Metabolism, Inborn Errors Stroke Nervous System Diseases Vascular Diseases Central Nervous System Diseases Ischemia Coronary Disease Genetic Diseases, Inborn Brain Infarction Infarction Coronary Artery Disease |