Progesterone treatment for experimental stroke: an individual animal meta-analysis

被引:43
作者
Wong, Raymond [1 ]
Renton, Cheryl [1 ]
Gibson, Claire L. [2 ]
Murphy, Stephanie J. [3 ]
Kendall, David A. [4 ]
Bath, Philip M. W. [1 ]
机构
[1] Univ Nottingham, Div Stroke, Nottingham NG5 1PB, England
[2] Univ Leicester, Sch Psychol, Leicester, Leics, England
[3] Oregon Hlth & Sci Univ, Dept Anesthesiol & Perioperat Med, Portland, OR 97201 USA
[4] Univ Nottingham, Sch Biomed Sci, Nottingham NG5 1PB, England
基金
英国医学研究理事会;
关键词
individual animal data; meta-analysis; neuroprotection; progesterone; steroid hormones; systematic review; CEREBRAL-ARTERY OCCLUSION; ACUTE ISCHEMIC-STROKE; INFARCT VOLUME; NXY-059; INJURY; BIAS; ALLOPREGNANOLONE; ESTROGEN; MODELS; SAFETY;
D O I
10.1038/jcbfm.2013.120
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Preclinical studies suggest progesterone is neuroprotective after cerebral ischemia. The gold standard for assessing intervention effects across studies within and between subgroups is to use meta-analysis based on individual animal data (IAD). Preclinical studies of progesterone in experimental stroke were identified from searches of electronic databases and reference lists. Corresponding authors of papers of interest were contacted to obtain IAD and, if unavailable, summary data were obtained from the publication. Data are given as standardized mean differences (SMDs, continuous data) or odds ratios (binary data), with 95% confidence intervals (95% CIs). In an unadjusted analysis of IAD and summary data, progesterone reduced standardized lesion volume (SMD 0.766, 95% CI 1.173 to 0.358, P<0.001). Publication bias was apparent on visual inspection of a Begg's funnel plot on lesion volume and statistically using Egger's test (P = 0.001). Using individual animal data alone, progesterone was associated with an increase in death in adjusted analysis (odds ratio 2.64, 95% CI 1.17 to 5.97, P = 0.020). Although progesterone significantly reduced lesion volume, it also appeared to increase the incidence of death after experimental stroke, particularly in young ovariectomized female animals. Experimental studies must report the effect of interactions on death and on modifiers, such as age and sex.
引用
收藏
页码:1362 / 1372
页数:11
相关论文
共 52 条
[1]  
Adamson Joy, 2004, J Stroke Cerebrovasc Dis, V13, P171, DOI 10.1016/j.jstrokecerebrovasdis.2004.06.003
[2]   Neuroprotective effects of female gonadal steroids in reproductively senescent female rats [J].
Alkayed, NJ ;
Murphy, SJ ;
Traystman, RJ ;
Hurn, PD .
STROKE, 2000, 31 (01) :161-167
[3]   The influence of stroke risk factors and comorbidities on assessment of stroke therapies in humans and animals [J].
Ankolekar, Sandeep ;
Rewell, Sarah ;
Howells, David W. ;
Bath, Philip M. W. .
INTERNATIONAL JOURNAL OF STROKE, 2012, 7 (05) :386-397
[4]   An alternative method for the quantitation of neuronal damage after experimental middle cerebral artery occlusion in rats: Analysis of behavioral deficit [J].
Aronowski, J ;
Samways, E ;
Strong, R ;
Rhoades, HM ;
Grotta, JC .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (04) :705-713
[5]   Potential Animal Models of Lacunar Stroke A Systematic Review [J].
Bailey, Emma L. ;
McCulloch, James ;
Sudlow, Cathie ;
Wardlaw, Joanna M. .
STROKE, 2009, 40 (06) :E451-E458
[6]   Effects of NXY-059 in experimental stroke: an individual animal meta-analysis [J].
Bath, P. M. W. ;
Gray, L. J. ;
Bath, A. J. G. ;
Buchan, A. ;
Miyata, T. ;
Green, A. R. .
BRITISH JOURNAL OF PHARMACOLOGY, 2009, 157 (07) :1157-1171
[7]  
Bath PMW, 2000, STROKE, V31, P2257
[8]   Neuroprotective effects of progesterone after transient middle cerebral artery occlusion in rat [J].
Chen, JL ;
Chopp, M ;
Li, Y .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 171 (01) :24-30
[9]   17 β-estradiol prevents focal cerebral ischemic damages via activation of Akt and CREB in association with reduced PTEN phosphorylation in rats [J].
Choi, YC ;
Lee, JH ;
Hong, KW ;
Lee, KS .
FUNDAMENTAL & CLINICAL PHARMACOLOGY, 2004, 18 (05) :547-557
[10]   Sustained levels of progesterone prior to the onset of cerebral ischemia are not beneficial to female mice [J].
Coomber, Ben ;
Gibson, Claire L. .
BRAIN RESEARCH, 2010, 1361 :124-132