Determinants of plasma homocysteine in relation to hematological and biochemical variables in patients with acute myocardial infarction

被引:7
作者
Marouf, Rajaa
Zubaid, Mohammad
Mojiminiyi, Olusegun A.
Qurtom, Mohammad
Abdella, Nabila A.
Al Wazzan, Hanan
Al Humood, Salah
机构
[1] Kuwait Univ, Fac Med, Dept Pathol, Safat 13110, Kuwait
[2] Kuwait Univ, Fac Med, Dept Med, Safat 13110, Kuwait
[3] Minist Hlth, Kuwait, Kuwait
关键词
homocysteine; myocardial infarction; coronary disease; risk factors;
D O I
10.1097/01.smj.0000231245.44439.47
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Elevated plasma total homocysteine (tHcy) is a risk factor for coronary artery disease (CAD), but the mechanism is not known. This study evaluates the determinants and associations of tHcy in patients presenting with acute myocardial infarction (AMI). Methods: Plasma concentration of tHcy, protein C, protein S, and antitbrombin were measured in 210 (177 males and 33 females) patients with first AMI and 167 (87 males and 80 females) controls. Serum vitamin 13,21 folate, creatinine, lipid profile, fasting glucose, full blood count and red cell folate were determined. Creatinine clearance was calculated using the modification of diet in renal disease formula. Univariate and multivariate analyses were used to determine the associations of tHcy. Results: Mean tHcy was higher in male than female patients. On logistic regression analysis, the most important determinants of tHcy in the patients were age, creatinine, creatinine clearance, vitamin B 12 and red cell folate. When study patients were compared with the controls, tHcy, fasting glucose and serum creatinine were significantly higher, while creatinine clearance and HDL cholesterol were significantly lower in the study patients. Logistic regression analysis showed significant association of tHcy with AMI, odds ratio = 1.39, in the presence of other confounding factors. Conclusions: Our results show that tHcy is a significant risk factor for CAD in our patient population. The determinants in the patients are age, glomerular filtration rate and the status of vitamins B-12 and folate. The above determinants should be kept in mind when using tHcy as a risk factor for CAD.
引用
收藏
页码:811 / 816
页数:6
相关论文
共 33 条
[1]   Associations of plasma homocysteine concentration in subjects with type 2 diabetes mellitus [J].
Abdella, NA ;
Mojiminiyi, OA ;
Akanji, AO ;
Moussa, MA .
ACTA DIABETOLOGICA, 2002, 39 (04) :183-190
[2]   MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C [J].
BERTINA, RM ;
KOELEMAN, BPC ;
KOSTER, T ;
ROSENDAAL, FR ;
DIRVEN, RJ ;
DERONDE, H ;
VANDERVELDEN, PA ;
REITSMA, PH .
NATURE, 1994, 369 (6475) :64-67
[3]   Antiphospholipid syndrome and thrombosis [J].
Bick, RL ;
Baker, WF .
SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1999, 25 (03) :333-350
[4]  
Booth GL, 2000, CAN MED ASSOC J, V163, P21
[5]   The investigation and management of inherited thrombophilia [J].
Cumming, AM ;
Shiach, CR .
CLINICAL AND LABORATORY HAEMATOLOGY, 1999, 21 (02) :77-92
[6]   FAMILIAL THROMBOPHILIA DUE TO A PREVIOUSLY UNRECOGNIZED MECHANISM CHARACTERIZED BY POOR ANTICOAGULANT RESPONSE TO ACTIVATED PROTEIN-C - PREDICTION OF A COFACTOR TO ACTIVATED PROTEIN-C [J].
DAHLBACK, B ;
CARLSSON, M ;
SVENSSON, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (03) :1004-1008
[7]   Acute methionine load-induced hyperhomocysteinemia enhances platelet aggregation thromboxane biosynthesis, and macrophage-derived tissue factor activity in rats [J].
Durand, P ;
LussierCacan, S ;
Blache, D .
FASEB JOURNAL, 1997, 11 (13) :1157-1168
[8]   British Cardiac Society Working Group on the definition of myocardial infarction [J].
Fox, KAA ;
Birkhead, J ;
Wilcox, R ;
Knight, C ;
Barth, J .
HEART, 2004, 90 (06) :603-609
[9]  
FRIEDEWALD WT, 1972, CLIN CHEM, V18, P499
[10]   Lupus anticoagulants are stronger risk factors for thrombosis than anticardiolipin antibodies in the antiphospholipid syndrome: a systematic review of the literature [J].
Galli, M ;
Luciani, D ;
Bertolini, G ;
Barbui, T .
BLOOD, 2003, 101 (05) :1827-1832