Sex-based differences in cardiac ischaemic injury and protection: therapeutic implications

被引:73
作者
Ostadal, B. [1 ]
Ostadal, P. [2 ]
机构
[1] Acad Sci Czech Republ, Inst Physiol, CR-14220 Prague 4, Czech Republic
[2] Na Homolce Hosp, Dept Cardiol, Cardiovasc Ctr, Prague, Czech Republic
关键词
acute coronary syndrome; cardioprotection; oestrogen; heart; ischaemia; reperfusion injury; sex differences; therapeutic implications; ACUTE CORONARY SYNDROMES; ACUTE MYOCARDIAL-INFARCTION; ESTROGEN-RECEPTOR-ALPHA; POSTMENOPAUSAL HORMONE-THERAPY; GENDER-DIFFERENCES; REPERFUSION INJURY; ISCHEMIA/REPERFUSION INJURY; CARDIOVASCULAR-DISEASE; PRENATAL HYPOXIA; RAT HEARTS;
D O I
10.1111/bph.12270
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ischaemic heart disease (IHD) is the most frequent cause of mortality among men and women. Many epidemiological studies have demonstrated that premenopausal women have a reduced risk for IHD compared with their male counterparts. The incidence of IHD in women increases after menopause, suggesting that IHD is related to declining oestrogen levels. Experimental observations have confirmed the results of epidemiological studies investigating sex-specific differences in cardiac tolerance to ischaemia. Female sex appears also to favourably influence cardiac remodelling after ischaemia/reperfusion injury. Furthermore, sex-related differences in ischaemic tolerance of the adult myocardium can be influenced by interventions during the early phases of ontogenetic development. Detailed mechanisms of these sex-related differences remain unknown; however, they involve the genomic and non-genomic effects of sex steroid hormones, particularly the oestrogens, which have been the most extensively studied. Although the protective effects of oestrogen have many potential therapeutic implications, clinical trials have shown that oestrogen replacement in postmenopausal women may actually increase the incidence of IHD. The results of these trials have illustrated the complexity underlying the mechanisms involved in sex-related differences in cardiac tolerance to ischaemia. Sex-related differences in cardiac sensitivity to ischaemia/reperfusion injury may also influence therapeutic strategies in women with acute coronary syndrome. Women undergo coronary intervention less frequently and a lower proportion of women receive evidence-based therapy compared with men. Although our understanding of this important topic has increased in recent years, there is an urgent need for intensive experimental and clinical research to develop female-specific therapeutic strategies. Only then we will be able to offer patients better evidence-based treatment, a better quality of life and lower mortality.
引用
收藏
页码:541 / 554
页数:14
相关论文
共 148 条
[1]   Gender differences among patients with acute coronary syndromes undergoing percutaneous coronary intervention in the American College of Cardiology-National Cardiovascular Data Registry (ACC-NCDR) [J].
Akhter, Nausheen ;
Milford-Beland, Sarah ;
Roe, Matthew T. ;
Piana, Robert N. ;
Kao, John ;
Shroff, Adhir .
AMERICAN HEART JOURNAL, 2009, 157 (01) :141-148
[2]   THE CONCISE GUIDE TO PHARMACOLOGY 2013/14: OVERVIEW [J].
Alexander, Stephen P. H. ;
Benson, Helen E. ;
Faccenda, Elena ;
Pawson, Adam J. ;
Sharman, Joanna L. ;
McGrath, John C. ;
Catterall, William A. ;
Spedding, Michael ;
Peters, John A. ;
Harmar, Anthony J. .
BRITISH JOURNAL OF PHARMACOLOGY, 2013, 170 (08) :1449-1458
[3]   Gender differences in management and outcome in non-ST-elevation acute coronary syndrome [J].
Alfredsson, Joakim ;
Stenestrand, Ulf ;
Wallentin, Lars ;
Swahn, Eva .
HEART, 2007, 93 (11) :1357-1362
[4]   Genetic and pharmacologic strategies to determine the function of estrogen receptor α and estrogen receptor β in the cardiovascular system [J].
Arias-Loza, Paula Anahi ;
Jazbutyte, Virginija ;
Pelzer, Theo .
GENDER MEDICINE, 2008, 5 :S34-S45
[5]   Gender differences in cardioprotection against Ischemia/Reperfusion injury in adult rat hearts: Focus on Akt and protein kinase C signaling [J].
Bae, SC ;
Zhang, LB .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 315 (03) :1125-1135
[6]   In utero programming of cardiovascular disease [J].
Barker, DJP .
THERIOGENOLOGY, 2000, 53 (02) :555-574
[7]   GROWTH INUTERO, BLOOD-PRESSURE IN CHILDHOOD AND ADULT LIFE, AND MORTALITY FROM CARDIOVASCULAR-DISEASE [J].
BARKER, DJP ;
OSMOND, C ;
GOLDING, J ;
KUH, D ;
WADSWORTH, MEJ .
BRITISH MEDICAL JOURNAL, 1989, 298 (6673) :564-567
[8]   Changing incidence and survival for heart failure in a well-defined older population, 1970-1974 and 1990 1994 [J].
Barker, WH ;
Mullooly, JP ;
Getchell, W .
CIRCULATION, 2006, 113 (06) :799-805
[9]  
Bassuk SS, 2010, PRINCIPLES OF GENDER-SPECIFIC MEDICINE, 2ND EDITION, P162, DOI 10.1016/B978-0-12-374271-1.00015-0
[10]  
Bazett HC, 1920, HEART-J STUD CIRC, V7, P353