Hyperhomocysteinemia and cardiovascular risk in postmenopausal women:: the role of folate supplementation

被引:8
作者
Villa, Paola
Suriano, Rosanna
Costantini, Barbara
Macri, Francesca
Ricciardi, Luigi
Campagna, Giuseppe
Lanzone, Antonio
机构
[1] Univ Cattolica Sacro Cuore, Dept Obstet & Gynecol, Rome, Italy
[2] OASI Inst Res, Unit Physiopathol Human Reprod, Troina, Italy
关键词
cardiovascular disease; endothelium; folate; homocysteine; postmenopausal;
D O I
10.1515/CCLM.2007.067
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
In the postmenopausal period, cardiovascular diseases are a frequent chronic condition leading to high risk of myocardial infarction and death. Recently hyperhomocysteinemia and even mildly elevated plasma concentrations of homocysteine have been recognized as independent risk factors for vascular damage predisposing to arteriosclerosis. Elevated plasma levels of homocysteine induce vascular endothelial damage and are frequently associated with low folate levels. In this review we evaluate literature data on some aspects related to menopause and homocysteine metabolism. In particular, we show the effect of folic acid supplementation on homocysteine concentrations and on homocysteine-related thiols, such as cysteine and cysteine-glycine, as well as the relationship with glucose, insulin, and lipidic metabolism in postmenopausal women. We also analyze the influence of folate supplementation on endothelial function, by brachial artery flow-mediated dilatation (endothelium-dependent) and nitro,glycerine-induced dilatation (endothelium-independent) before and after a methionine load. Folate administration in postmenopausal women is able to reduce high plasma homocysteine levels and to modify impaired endothelial function induced by hyperhomocysteinemia.
引用
收藏
页码:130 / 135
页数:6
相关论文
共 50 条
[1]   Plasma homocysteine concentrations in healthy volunteers are not related to differences in insulin-mediated glucose disposal [J].
Abbasi, F ;
Facchini, F ;
Humphreys, MH ;
Reaven, GR .
ATHEROSCLEROSIS, 1999, 146 (01) :175-178
[2]   Plasma homocysteine in women taking hormone replacement therapy: The Postmenopausal Estrogen/Progestin Interventions (PEPI) Trial [J].
Barnabei, VM ;
Phillips, TM ;
Hsia, J .
JOURNAL OF WOMENS HEALTH & GENDER-BASED MEDICINE, 1999, 8 (09) :1167-1172
[3]   The effect of estrogen replacement therapy on total plasma homocysteine in healthy postmenopausal women [J].
Berger, PB ;
Herrmann, RR ;
Dumesic, DA .
MAYO CLINIC PROCEEDINGS, 2000, 75 (01) :18-23
[4]   Long-term effects of oral and transdermal hormone replacement therapy on plasma homocysteine levels [J].
Chiantera, V ;
Sarti, CD ;
Fornaro, F ;
Farzati, A ;
De Franciscis, P ;
Sepe, E ;
Borrelli, AL ;
Colacurci, N .
MENOPAUSE-THE JOURNAL OF THE NORTH AMERICAN MENOPAUSE SOCIETY, 2003, 10 (04) :286-291
[5]   Low-dose folic acid supplementation reduces plasma levels of the cardiovascular risk factor homocysteine in postmenopausal women [J].
De Leo, V ;
la Marca, A ;
Morgante, G ;
Ciani, F ;
Zammarchi, E ;
Setacci, C .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2000, 183 (04) :945-947
[6]  
Dicker-Brown A, 1999, DIABETES, V48, pA135
[7]   Estrogen and homocysteine [J].
Dimitrova, KR ;
DeGroot, K ;
Myers, AK ;
Kim, YD .
CARDIOVASCULAR RESEARCH, 2002, 53 (03) :577-588
[8]   Folic acid improves endothelial function in coronary artery disease via mechanisms largely independent of homocysteine lowering [J].
Doshi, SN ;
McDowell, IFW ;
Moat, SJ ;
Payne, N ;
Durrant, HJ ;
Lewis, MJ ;
Goodfellow, J .
CIRCULATION, 2002, 105 (01) :22-26
[9]   Folate improves endothelial function in coronary artery disease - An effect mediated by reduction of intracellular superoxide? [J].
Doshi, SN ;
McDowell, IFW ;
Moat, SJ ;
Lang, D ;
Newcombe, RG ;
Kredan, MB ;
Lewis, MJ ;
Goodfellow, J .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (07) :1196-1202
[10]   Complex multivitamin supplementation improves homocysteine and resistance to LDL-C oxidation [J].
Earnest, CP ;
Wood, KA ;
Church, TS .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 2003, 22 (05) :400-407