Lack of aggregation of ischemic stroke subtypes within affected sibling pairs

P. G. Wiklund, W. M. Brown, Thomas G Brott, B. Stegmayr, Robert D Jr. Brown, S. Nilsson-Ardnor, J. A. Hardy, B. M. Kissela, A. Singleton, D. Holmberg, S. S. Rich, James F Meschia

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Abstract

OBJECTIVE: To establish whether subtypes of ischemic stroke aggregate within ischemic stroke-affected sibling pairs more than expected by chance alone. METHODS: This retrospective family study was based on a pooled analysis of two cohorts of male and female adult sibling pairs with symptomatic ischemic stroke. One hospital-based cohort of 404 individuals (first proband seen August 30, 1999) was recruited from the United States and Canada, and another population-based cohort of 198 individuals (first proband seen April 17, 1997) was recruited from Umeå, Sweden. Subtype diagnoses were based on Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria. RESULTS: Agreement for subtype diagnoses within families was poor (mean ± asymptotic SE κ = 0.17 ± 0.04). Occurrence of one ischemic stroke subtype in a proband was not associated with a greater likelihood of that subtype being the qualifying stroke subtype in the sibling. Comparable levels of agreement were seen when restricting the analysis to same-sex sibling pairs (κ = 0.22 ± 0.05) to sibling pairs in which the proband's stroke occurred before the age of 65 years (κ = 0.16 ± 0.05) or to pairs in which the proband's stroke occurred at or after the age of 65 years (κ = 0.19 ± 0.05). CONCLUSIONS: The subtype of ischemic stroke in a proband was a poor determinant of the subtype of ischemic stroke in the respective sibling. This suggests that many genetic risk factors for ischemic stroke may not be specific for one subtype.

Original languageEnglish (US)
Pages (from-to)427-431
Number of pages5
JournalNeurology
Volume68
Issue number6
DOIs
StatePublished - Feb 2007

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Siblings
Stroke
Sweden
Canada
Cohort Studies
Retrospective Studies

ASJC Scopus subject areas

  • Neuroscience(all)

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Lack of aggregation of ischemic stroke subtypes within affected sibling pairs. / Wiklund, P. G.; Brown, W. M.; Brott, Thomas G; Stegmayr, B.; Brown, Robert D Jr.; Nilsson-Ardnor, S.; Hardy, J. A.; Kissela, B. M.; Singleton, A.; Holmberg, D.; Rich, S. S.; Meschia, James F.

In: Neurology, Vol. 68, No. 6, 02.2007, p. 427-431.

Research output: Contribution to journalArticle

Wiklund, PG, Brown, WM, Brott, TG, Stegmayr, B, Brown, RDJ, Nilsson-Ardnor, S, Hardy, JA, Kissela, BM, Singleton, A, Holmberg, D, Rich, SS & Meschia, JF 2007, 'Lack of aggregation of ischemic stroke subtypes within affected sibling pairs', Neurology, vol. 68, no. 6, pp. 427-431. https://doi.org/10.1212/01.wnl.0000252955.17126.6a
Wiklund, P. G. ; Brown, W. M. ; Brott, Thomas G ; Stegmayr, B. ; Brown, Robert D Jr. ; Nilsson-Ardnor, S. ; Hardy, J. A. ; Kissela, B. M. ; Singleton, A. ; Holmberg, D. ; Rich, S. S. ; Meschia, James F. / Lack of aggregation of ischemic stroke subtypes within affected sibling pairs. In: Neurology. 2007 ; Vol. 68, No. 6. pp. 427-431.
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AU - Wiklund, P. G.

AU - Brown, W. M.

AU - Brott, Thomas G

AU - Stegmayr, B.

AU - Brown, Robert D Jr.

AU - Nilsson-Ardnor, S.

AU - Hardy, J. A.

AU - Kissela, B. M.

AU - Singleton, A.

AU - Holmberg, D.

AU - Rich, S. S.

AU - Meschia, James F

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N2 - OBJECTIVE: To establish whether subtypes of ischemic stroke aggregate within ischemic stroke-affected sibling pairs more than expected by chance alone. METHODS: This retrospective family study was based on a pooled analysis of two cohorts of male and female adult sibling pairs with symptomatic ischemic stroke. One hospital-based cohort of 404 individuals (first proband seen August 30, 1999) was recruited from the United States and Canada, and another population-based cohort of 198 individuals (first proband seen April 17, 1997) was recruited from Umeå, Sweden. Subtype diagnoses were based on Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria. RESULTS: Agreement for subtype diagnoses within families was poor (mean ± asymptotic SE κ = 0.17 ± 0.04). Occurrence of one ischemic stroke subtype in a proband was not associated with a greater likelihood of that subtype being the qualifying stroke subtype in the sibling. Comparable levels of agreement were seen when restricting the analysis to same-sex sibling pairs (κ = 0.22 ± 0.05) to sibling pairs in which the proband's stroke occurred before the age of 65 years (κ = 0.16 ± 0.05) or to pairs in which the proband's stroke occurred at or after the age of 65 years (κ = 0.19 ± 0.05). CONCLUSIONS: The subtype of ischemic stroke in a proband was a poor determinant of the subtype of ischemic stroke in the respective sibling. This suggests that many genetic risk factors for ischemic stroke may not be specific for one subtype.

AB - OBJECTIVE: To establish whether subtypes of ischemic stroke aggregate within ischemic stroke-affected sibling pairs more than expected by chance alone. METHODS: This retrospective family study was based on a pooled analysis of two cohorts of male and female adult sibling pairs with symptomatic ischemic stroke. One hospital-based cohort of 404 individuals (first proband seen August 30, 1999) was recruited from the United States and Canada, and another population-based cohort of 198 individuals (first proband seen April 17, 1997) was recruited from Umeå, Sweden. Subtype diagnoses were based on Trial of Org 10172 in Acute Stroke Treatment (TOAST) criteria. RESULTS: Agreement for subtype diagnoses within families was poor (mean ± asymptotic SE κ = 0.17 ± 0.04). Occurrence of one ischemic stroke subtype in a proband was not associated with a greater likelihood of that subtype being the qualifying stroke subtype in the sibling. Comparable levels of agreement were seen when restricting the analysis to same-sex sibling pairs (κ = 0.22 ± 0.05) to sibling pairs in which the proband's stroke occurred before the age of 65 years (κ = 0.16 ± 0.05) or to pairs in which the proband's stroke occurred at or after the age of 65 years (κ = 0.19 ± 0.05). CONCLUSIONS: The subtype of ischemic stroke in a proband was a poor determinant of the subtype of ischemic stroke in the respective sibling. This suggests that many genetic risk factors for ischemic stroke may not be specific for one subtype.

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