Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (11)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Bashir, S.
Right arrow Articles by Qizilbash, N
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Bashir, S.
Right arrow Articles by Qizilbash, N
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

International Journal of Epidemiology, Vol 26, 64-70, Copyright © 1997 by International Epidemiological Association


ARTICLES

Repeat measurement of case-control data: corrections for measurement error in a study of ischaemic stroke and haemostatic factors

SA Bashir, SW Duffy and N Qizilbash
MRC Biostatistics Unit, Institute of Public Health, University Forvie Site, Cambridge, UK.

BACKGROUND: Haemostatic factors are suspected to be involved in the aetiology of cerebrovascular events. METHODS: In a case-control study of 105 cases of transient ischaemic attack and minor ischaemic stroke, and 241 controls, data were available on levels of the haemostatic factors-von Willebrand factor (vWF), plasminogen activator inhibitor-1 (PAI), tissue plasminogen activator (TPA) and factor VII (FVII). These are subject to measurement error and within-person fluctuation of true levels, which may bias relative risk estimates. For all subjects, two determinations were performed on the same blood sample, which allowed estimation of pure measurement error. For estimation of within-person fluctuation, levels were measured from a repeat blood sample on 81 of the controls one year later. RESULTS: The pure measurement error accounted for a very small proportion of the total variation in all cases. Uncorrected for within-person fluctuation, the odds ratio estimates associated with exceeding the median of vWF, PAI, TPA and FVII respectively were 1.88, 0.87, 1.30 and 0.93. After correction for within-person fluctuation odds ratios were 3.56, 0.80, 1.41 and 0.91. Because the PAI determination was not robust to storage conditions, it was estimated that 75% of the variation in this factor was within- person rather than between-persons. Thus, estimates of relative risk relation to PAI cannot be regarded as reliable in this study. CONCLUSIONS: It is likely that elevated levels of vWF are associated with increased risk of ischaemic stroke, but interpretation must be tentative, due to relatively large within-person fluctuation of vWF levels.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
S. Su, S. Chen, J. Zhao, J. Huang, X. Wang, R. Chen, and D. Gu
Plasminogen Activator Inhibitor-1 Gene: Selection of Tagging Single Nucleotide Polymorphisms and Association With Coronary Heart Disease
Arterioscler Thromb Vasc Biol, April 1, 2006; 26(4): 948 - 954.
[Abstract] [Full Text] [PDF]


Home page
Eur Heart JHome page
G.D.O. Lowe, J. Danesh, S. Lewington, M. Walker, L. Lennon, A. Thomson, A. Rumley, and P.H. Whincup
Tissue plasminogen activator antigen and coronary heart disease: Prospective study and meta-analysis
Eur. Heart J., February 1, 2004; 25(3): 252 - 259.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
M. Roest, Y. T. van der Schouw, J. D. Banga, M. J. Tempelman, P. G. de Groot, J. J. Sixma, and D. E. Grobbee
Plasminogen Activator Inhibitor 4G Polymorphism Is Associated With Decreased Risk of Cerebrovascular Mortality in Older Women
Circulation, January 4, 2000; 101(1): 67 - 70.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.