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. Author manuscript; available in PMC: 2012 Oct 1.
Published in final edited form as: Expert Rev Hematol. 2011 Dec;4(6):597–606. doi: 10.1586/ehm.11.61

Table 3.

Genetic risk factors for stroke in children with sickle cell disease.

Study (year) Gene Odds ratio (95% CI) p-value Participants Comments Ref.
Flanagan et al. (2011) ANXA2 2.7 (1.3–5.8) 0.007 130 with stroke All ischemic [71]
TGFBR3 2.5 (1.3–5.0) 0.005 103 without stroke
TEK 2.2 (1.1–4.2) 0.016
ADCY9 0.47 (0.3–0.8) 0.003
HbA2 α-thalassemia 3.7 kb deletion 0.45 (0.2–0.8) 0.009

Adams et al. (1994) HbA2 α-thalassemia deletion 0.42 (0.2–0.9) 0.02 44 with stroke 256 without stroke Unspecified stroke type [72]

Sebastiani et al. (2005) HbA2 α-thalassemia deletion Bayesian network NA 92 with stroke Hemorrhagic and ischemic [18]
BMP6 1306 without stroke
SELP
MET

Hoppe et al. (2004) ADRB2 0.53 0.033 36 with ischemic stroke CSSCD infant cohort [73]
HLA-A 7.7 0.013 159 with normal MRI
IL4R 2.5 0.006
VCAM1 (−1594)C 1.1 0.72

Taylor et al. (2002) VCAM1 G1238C 0.35 (0.2–0.8) 0.02 51 with and without stroke Unspecified stroke type [74]

Sebastiani et al. (2005) HbA2 α-thalassemia deletion Bayesian network NA 92 with stroke Hemorrhagic and ischemic [18]
BMP6 1306 without stroke
SELP
MET

Tang et al. (2001) AGT repeat 4 (1.3–13) 0.02 21 with stroke Unspecified [75]
Allele 3 or 4 42 without stroke stroke type

Romana et al. (2004) Allele 3 or 4 0.2 (0.03–1) 0.06 8 children with stroke Unspecified [76]
Allele 1 3.9 (1.01–15) 0.047 148 without stroke stroke type

CSSCD: Cooperative Study of Sickle Cell Disease; NA: Not applicable.