Intracranial blood flow velocities in patients with sickle cell disease and b-thalassemia intermediaTo the Editor: Thalassemia intermedia (TI) and sickle cell disease (SCD) represent two common forms of hereditary anemias that share many clinical manifestations and pathophysiologic mechanisms. Decreased nitric oxide production, endothelial dysfunction, and formation of reactive oxygen species play a role in increasing the thrombosis risk in both of these diseases [1,2]. Transcranial Doppler ultrasonography (TCD) detects patients with SCD who are at an increased risk of developing stroke. Despite the increased risk of cerebral thrombosis in TI, the role of TCD in identifying high-risk patients has not been properly evaluated. We aimed at comparing the mean maximal blood flow velocities (MBFV) in two populations of patients with SCD and TI, and we looked at the role of MBFV in predicting magnetic resonance imaging (MRI) abnormalities. We also evaluated the role of age and anemia in altering the intracranial blood flow.Between January 2011 and October 2011, a total of 60 patients with SCD and 20 patients with TI were enrolled in this study. After obtaining informed consent, the right and left, middle and anterior cerebral arteries (RMCA, LMCA, RACA, and LACA) were insonated using a temporal window approach. The MBFV of each artery was recorded separately. Demographic and recent (less than 3 months) laboratory information were collected for each patient. Sixteen out of the 20 patients with TI underwent brain MRI for another study. The MRI results were used as they were reported. All statistical analysis was done using SPSS version 19. Table I shows the baseline characteristics of the two groups of patients along with their respective MBFVs. There is no statistically significant difference between the distribution of sex and hemoglobin levels among the two groups; however, a statistically significant difference was detected regarding the age distribution. Fifty-four out of the 60 sickle cell patients have SS (90%) while 6/60 (10%) have Sb. Maximal blood flow velocity was significantly different among the two groups in the RACA (P 5 0.006), borderline significant in the LMCA (P 5 0.056), and not significant in the RMCA and LACA. Supporting Information Figs. 1 and 2 represent the linear trend lines correlating MBFV in the four arteries with age and hemoglobin in the TI and SCD group, respectively.Children with sickle cell have been found to have higher MBFV than the normal population in several studies [2]. Several mechanisms have been implicated including anemia, deficiency of nitric oxide synthesis, and endothelial dysfunction. The pathophysiology of SCD and TI includes disruption of the aforementioned mechanisms, thus one would expect the MBFV to be similar in these two diseases. In this study, the mean MBFV in 60 patients with SCD were higher than those of 20 patients with TI, despite similar hemoglobin levels. The difference was only statistically significant for the RACA and borderline significant for the LMCA. T...