Female-specific aspects in the pharmacotherapy of chronic cardiovascular diseases

被引:199
作者
Jochmann, N [1 ]
Stangl, K [1 ]
Garbe, E [1 ]
Baumann, G [1 ]
Stangl, V [1 ]
机构
[1] Univ Med Berlin, Inst Klin Pharmakol, Med Klin Schwerpunkt Kardiol, D-10117 Berlin, Germany
关键词
gender; women; cardiovascular; therapy; pharmacokinetics; drugs;
D O I
10.1093/eurheartj/ehi397
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Differences in pharmacokinetics, pharmacodynamics, and physiology contribute to the phenomenon that women and men frequently respond differently to cardiovascular drugs. Hormonal influences, in addition, can play an important role: for example, the menstrual cycle, menopause, and pregnancy as a result of fluctuations in concentrations of sexual steroids, and of changes in total body water-can be associated with gender-specific differences in the plasma levels of cardiovascular drugs. Clinical relevance accordingly results, especially for substances with a narrow therapeutic margin. This review treats the most important pharmacodynamic gender-retevant differences in this context, and surveys available evidence on the benefits of therapy of chronic cardiovascular diseases in women. On the whole, the study situation for women is appreciably less favourabte than for men: owing to the fact that women are under-represented in most studies, and that few gender-specific analyses have been conducted.
引用
收藏
页码:1585 / 1595
页数:11
相关论文
共 129 条
[1]   Assessment of sex differences in pharmacokinetics and pharmacodynamics of amlodipine in a bioequivalence study [J].
Abad-Santos, F ;
Novalbos, J ;
Gálvez-Múgica, MA ;
Gallego-Sandín, S ;
Almeida, S ;
Vallée, F ;
García, AG .
PHARMACOLOGICAL RESEARCH, 2005, 51 (05) :445-452
[2]  
[Anonymous], 1989, NEW ENGL J MED, V321, P406
[3]  
[Anonymous], 1988, LANCET, V2, P349
[4]  
[Anonymous], 2005, PHYS DESK REFERENCE, V59th
[5]  
Baigent C, 2002, BMJ-BRIT MED J, V324, P71, DOI 10.1136/bmj.324.7329.71
[6]  
Bazett HC, 1920, HEART-J STUD CIRC, V7, P353
[7]   Torsades do Pointes associated with nonantiarrhythmic drugs and observations on gender and QTc [J].
Bednar, MM ;
Harrigan, EP ;
Ruskin, JN .
AMERICAN JOURNAL OF CARDIOLOGY, 2002, 89 (11) :1316-+
[8]   Greater quinidine-induced QTc interval prolongation in women [J].
Benton, RE ;
Sale, M ;
Flockhart, DA ;
Woosley, RL .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 67 (04) :413-418
[9]  
Berra K, 2000, J Cardiovasc Nurs, V14, P59
[10]   Double-blind study of the safety of clopidogrel with and without a loading dose in combination with aspirin compared with ticlopidine in combination with aspirin after coronary stenting - The Clopidogrel Aspirin Stent International Cooperative Study (CLASSICS) [J].
Bertrand, ME ;
Rupprecht, HJ ;
Urban, P ;
Gershlick, AH .
CIRCULATION, 2000, 102 (06) :624-629