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. 2014 Feb 21;165(5):699–706. doi: 10.1111/bjh.12791

Table 3. Associations between demographic, laboratory variables and genetic variants with CBFv as a continuous measurementa.

Predictors β‐Coefficient (95% CI) P‐value Observations (n)
Age (years)b −2·28 (−3·21 to −1·35) <0·0001 525
Sex (male vs female)b 3·512 (−3·56–10·58) 0·329 525
Haemoglobin (g/l)b −4·60 (−7·91 to−1·29) 0·007 525
Fetal haemoglobin (%)b −0·197 (−1·11–0·72) 0·672 525
Haptoglobin HP11c
HP12 0·28 (−9·61–10·17) 0·956 410
HP22 −2·994 (−15·32–9·33) 0·633
α‐Thalassaemia normalc
1 Deletion −6·32 (−13·78–1·14) 0·097 549
2 Deletions −16·14 (−26·271 to −6·0135) 0·002
G6PD Phenotype normalc
Mild (A‐B) −8·80 (−19·44–1·84) 0·105 564
Affected (A‐Z or A‐A‐) −1·81 (−11·83–8·21) 0·723
a

Only velocity values >0 cm/s included for multiple linear regression.

b

Results for multivariable regression including the marked variables.

c

Adjusted for age and survey year CBFv, cerebral blood flow velocity; 95% CI, 95% confidence interval.