Donate Help Contact The AHA Sign In Home
American Heart Association
Stroke
Search: search_blue_button Advanced Search
Stroke. 2006;37:1668-1673
Published online before print June 1, 2006, doi: 10.1161/01.STR.0000227409.59195.d1
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
37/7/1668    most recent
01.STR.0000227409.59195.d1v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
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 Download to citation manager
Right arrow Request Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sundquist, K.
Right arrow Articles by Hemminki, K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sundquist, K.
Right arrow Articles by Hemminki, K.
Related Collections
Right arrow Acute Cerebral Hemorrhage
Right arrow Acute Cerebral Infarction
Right arrow Genetics of Stroke

(Stroke. 2006;37:1668.)
© 2006 American Heart Association, Inc.


Original Contributions

Familial Risk of Ischemic and Hemorrhagic Stroke

A Large-Scale Study of the Swedish Population

Kristina Sundquist, MD, PhD; Xinjun Li, MD, PhD Kari Hemminki, MD, PhD

From the Center for Family Medicine (K.S., X.L.), Karolinska Institute, Huddinge, Sweden; the Division of Molecular Genetic Epidemiology (K.H.), German Cancer Research Center (DKFZ), Heidelberg, Germany; and the Department of Biosciences at Novum (K.H.), Karolinska Institute, Huddinge, Sweden.

Correspondence to Dr Kristina Sundquist, Karolinska Institute, Center for Family and Community Medicine, Alfred Nobels allé 12, SE-141 83 Huddinge, Sweden. E-mail kristina.sundquist{at}klinvet.ki.se

Background and Purpose— Previous studies of familial risks have often combined ischemic and hemorrhagic stroke even though it seems unlikely that these 2 very different pathological conditions are under the same genetic influence. This study is the first to investigate the concordant (same subtype) and disconcordant (different subtype) association between ischemic and hemorrhagic stroke.

Methods— Data of first hospitalization for stroke were obtained from the Hospital Discharge Register during the study period 1987 to 2001. All individuals born in Sweden from 1932 onwards were included and linked to their siblings. Risks were calculated as standardized incidence ratios and compared with individuals without affected siblings. Results were standardized for age, gender, geographical region and socioeconomic status.

Results— Ischemic stroke (n=25 630) was associated only with ischemic stroke (n=7961), which was also the case for hemorrhagic stroke. The statistically significant standardized incidence ratios were 2.14 (95% CI, 1.21 to 3.74) and 1.82 (95% CI, 1.21 to 2.75), respectively. For discordant subtypes of stroke no significant associations were found.

Conclusions— The results suggest that ischemic and hemorrhagic stroke are not under the same genetic influence. However, further studies of the human genome are needed in order to identify the specific genes that play roles in the pathogenesis of common subtypes of stroke.


Key Words: cerebral ischemia • families • stroke • Sweden




This article has been cited by other articles:


Home page
J. Epidemiol. Community HealthHome page
K Hemminki, X Li, K Sundquist, and J Sundquist
Familial risks for chronic obstructive pulmonary disease among siblings based on hospitalisations in Sweden
J. Epidemiol. Community Health, May 1, 2008; 62(5): 398 - 401.
[Abstract] [Full Text] [PDF]