Organ iron accumulation in chronically transfused children with sickle cell anaemia: baseline results from the TWiTCH trial. (2nd November 2015)

• Record Type: Journal Article
• Authors: Wood, John C.; Cohen, Alan R.; Pressel, Sara L.; Aygun, Banu; Imran, Hamayun; Luchtman‐Jones, Lori; Thompson, Alexis A.; Fuh, Beng; Schultz, William H.; Davis, Barry R.; Ware, Russell E.
• Is Part Of: British journal of haematology. Volume 172:Number 1(2016)
• Page Start: 122
• Page End: 130
• Publication Date: 2015-11-02
• Subjects: iron overload -- sickle cell anaemia -- sickle cell radiology -- MRI -- transfusions; Hematology -- Periodicals; Blood -- Diseases -- Periodicals; 616.15
• DOI: 10.1111/bjh.13791
• Languages: English
• ISSNs: 0007-1048

Abstract

Summary: Transcranial Doppler (TCD) With Transfusions Changing to Hydroxyurea (TWiTCH) trial is a randomized, open‐label comparison of hydroxycarbamide (also termed hydroxyurea) versus continued chronic transfusion therapy for primary stroke prevention in patients with sickle cell anaemia (SCA) and abnormal TCD. Severity and location of iron overload is an important secondary outcome measure. We report the baseline findings of abdominal organ iron burden in 121 participants. At enrollment, patients were young (9·8 ± 2·9 years), predominantly female (60:40), and previously treated with transfusions (4·1 ± 2·4 years) and iron chelation (3·1 ± 2·1 years). Liver iron concentration (LIC; 9·0 ± 6·6 mg/g dry weight) and serum ferritin were moderately elevated (2696 ± 1678 μg/l), but transferrin was incompletely saturated (47·2 ± 23·6%). Spleen R2* was 509 ± 399 Hz (splenic iron ~13·9 mg/g) and correlated with LIC ( r 2 = 0·14, P = 0·0008). Pancreas R2* was increased in 38·3% of patients but not to levels associated with endocrine toxicity. Kidney R2* was increased in 80·7% of patients; renal iron correlated with markers of intravascular haemolysis and was elevated in patients with increased urine albumin‐creatinine ratios. Extra‐hepatic iron deposition is common among children with SCA who receive chronic transfusions, and could potentiate oxidative stress caused by reperfusion injury and decellularized haemoglobin.