Fetal hemoglobin level is a heritable complex trait that strongly correlates swith the clinical severity of sickle cell disease. Only few genetic loci have been identified as robustly associated with fetal hemoglobin in patients with sickle cell disease, primarily adults. The sole approved pharmacologic therapy for this disease is hydroxyurea, with effects largely attributable to induction of fetal hemoglobin.
In a multi-site observational analysis of children with sickle cell disease, candidate single nucleotide polymorphisms associated with baseline fetal hemoglobin levels in adult sickle cell disease were examined in children at baseline and induced by hydroxyurea therapy. For baseline levels, single marker analysis demonstrated significant association with BCL11A and the beta and epsilon globin loci (HBB and HBE, respectively), with an additive attributable variance from these loci of 23%. Among a subset of children on hydroxyurea, baseline fetal hemoglobin levels explained 33% of the variance in induced levels. The variant in HBE accounted for an additional 13% of the variance in induced levels, while variants in the HBB and BCL11A loci did not contribute beyond baseline levels.
These findings clarify the overlap between baseline and hydroxyurea-induced fetal hemoglobin levels in pediatric disease. Studies assessing influences of specific sequence variants in these and other genetic loci in larger populations and in unusual hydroxyurea responders are needed to further understand the maintenance and therapeutic induction of fetal hemoglobin in pediatric sickle cell disease.
Citation: Green NS, Ender KL, Pashankar F, Driscoll C, Giardina PJ, et al. (2013) Candidate Sequence Variants and Fetal Hemoglobin in Children with Sickle Cell Disease Treated with Hydroxyurea. PLoS ONE 8(2): e55709. doi:10.1371/journal.pone.0055709
Editor: Dimas Tadeu Covas, University of Sao Paulo - USP, Brazil
Received: June 28, 2012; Accepted: December 29, 2012; Published: February 7, 2013
Copyright: © 2013 Green et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by a grant from the National Institutes of Health (NIH) to Columbia University from the Best Pharmaceutical for Children’s Act (3UL1RR024156-04S4 to NSG), the St. Giles Foundation (to Gary M. Brittenham) and a gift from Henry Taub (to NSG). Additional support was provided by NIH Clinical Translational Science Awards (CTSAs) at Columbia University (5UL1RR024156), Albert Einstein College of Medicine (5UL1RR025750), Weill-Cornell School of Medicine (5UL1RR024996), University of Rochester (5UL1RR024160), Yale (5UL1RR024139) and Oakland Children’s-UCSF (5UL1RR024131). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
In sickle cell disease, higher fetal hemoglobin (HbF) levels diminish de-oxygenated sickle globin polymerization in vitro  and reduce the incidence of disease morbidities in vivo , . HbF is a heritable complex trait , . Only three genetic loci have been validated as strongly associated with higher HbF in sickle cell disease: the 5′ beta globin locus (HBB) , , , , , although not the sickle mutation; the BCL11A repressor of HbF , , , , , ; and the HS1L-MYB intergenic region , , , . Other candidate regions have not been confirmed , , .
Hydroxyurea is the only approved pharmacologic therapy for sickle cell disease. Its clinical and laboratory effect is understood to result largely from enhanced HbF expression , , , although induction occurs to a highly variable extent , , , , . Children generally have higher baseline HbF levels than adults ,  and a stable  and overall more robust HbF response to hydroxyurea , , . Hydroxyurea-induced HbF is also a heritable trait  that generally correlates with baseline levels , , . To date, only limited reports have examined relationships between hydroxyurea-induced HbF and specific genetic polymorphisms in adults with sickle cell disease ,  and did not explore the recently identified major loci of interest. Genetic determinants for this clinically relevant marker of drug response have not been confirmed in children , . Such insight would be useful for elucidating mechanisms of hydroxyurea induction and for predicting individual response.
Our multi-site observational study examined associations between baseline and hydroxyurea-induced HbF in children with sickle cell disease and candidate single nucleotide polymorphisms (SNP) in several genes associated with adult sickle cell HbF levels. Our results indicate: 1) A 33% contribution of baseline to induced levels; 2) Confirmation of single marker associations between the HBB and epsilon globin (HBE) and BCL11A loci and baseline HbF in children; 2) Association between HBE and hydroxyurea-induced HbF; 3) Additive effects of these SNPs on baseline and induced HbF in children.
Studies were performed under the policies of and with specific approval from the Institutional Review Board (IRB) at Columbia University and the corresponding body at each of the other participating institutions: Yale University IRB, Albert Einstein College of Medicine IRB, Weill Cornell University Medical School IRB, University of Rochester Research Subjects Review Board, Children's Mercy Hospitals and Clinics IRB, Children’s Hospital & Research Center Oakland IRB. Written informed consent from parents of participating children and informed assent from children were obtained according to each institution’s IRB policies.
Observational analysis of children attending sickle cell clinic was performed at five sites (see author affiliations), including prospective observation during 2010. The Oakland site provided archived data and samples. Clinical inclusion and exclusion criteria conformed to those previously described , . Inclusion criteria are: HbSS or HbS-B0 thalassemia, ages 5–21 years. Exclusions criteria are: pregnancy, current or recent painful crisis, fever or other acute illness within three weeks prior to evaluation, transfusion within the prior 100 days or active transfusion therapy, abnormal elevated serum creatinine or liver transaminases. We excluded siblings to ensure genetic independence. Laboratory data at steady state represented the most recent values obtained during routine care or an average of three values from well visits over the preceding 6–12 months, if available. Percent HbF (%HbF) was determined by routine HPLC and was used as a quantitative trait at steady state for baseline and for drug-induced levels.
Duration of hydroxyurea treatment was for at least six months and was initiated for comparable clinical indications across sites (nearly all for repetitive painful crises and/or acute chest episodes). Stable hydroxyurea dosing was three months at or near maximal dose by ANC criteria, excluding data from subjects on less than 20 mg/kg/day, even if for dose-limiting toxicity. Across the six sites, drug dose averages ranged from 23.8–29 mg/kg/day and did not statistically differ between sites (F = 1.554, p = 0.210). Adherence to hydroxyurea was defined as parent report of at least 80% of prescribed doses. Laboratory data at steady state represented recent values during routine care or averaged three values from well visits over the preceding 6–12 months, if available. Percentage of HbF (HbF%) was used as a quantitative trait. Baseline HbF had not been recorded prior to treatment for nine of the 47 subjects on hydroxyurea, thus is not available. Hydroxyurea-associated increased mean red cell volume and decreased white blood cell count were used to confirm data quality. For children on hydroxyurea therapy, where available, clinical response to hydroxyurea was assessed by retrospective chart review of the number of sickle-related hospitalizations over the two-year periods preceding and while on hydroxyurea treatment.
Description of Procedures
Twenty SNPs previously reported as associated with HbF% in sickle cell disease , , , , , , ,  were genotyped (Table 1): nine in the BCL11A locus; two in HBS1L-MYB intergenic region on chromosome 6q23; three in the globin locus on chromosome 11: two 5′ sites in HBB (including the previously identified XmnI site  and one in HBE ; one in OR51 that is upstream of HBB ; one in the glucagon-like peptide-2 receptor, GLP2R, found by genome-wide analysis ; two SNPs from the hydroxyurea-induced SAR1A locus ; one SNP each in ARG1 and ARG2  (SNP sequences available by request).
Table 1. 19 SNPs associations with baseline, maximum and delta HbF%.doi:10.1371/journal.pone.0055709.t001
SNP marker genotyping of minor allele frequencies ranging from 0.07 to 0.45 was performed using Sequenom MassArray iPLEX platform with matrix-assisted laser desorption/ionization time of flight mass spectrometry (Sequenom, San Diego, CA). PCR assays and mass extension reactions were designed using mass array assay design software (Sequenom). PCR assays used Applied Biosystems Geneamp PCR thermocyclers (Foster City, CA) and analyzed by mass array compact mass spectrometer (Bruker Daltonik, Billerica, MA) and Spectro TYPER software (Sequenom). (SNP sequences, PCR and analytic conditions are available upon request.) Genotyping was performed in duplicate with separate assays, with genotype frequency distribution at each SNP tested for deviations from Hardy-Weinberg equilibrium. Accurate genotyping of SAR1A SNP rs4282891 required sequencing. The sickle genotype, rs334, was assayed to confirm the diagnosis for each sample.
Relationships between each of the three quantitative HbF values were assessed by Pearson correlation analysis. Genetic associations were assessed for candidate SNPs with %HbF at baseline, on hydroxyurea treatment (“maximum HbF”), and the hydroxyurea-induced increment over baseline (“delta HbF”) (Table 1). For each HbF value, quantitative associations with a dose effect model of the minor allele were tested using a linear regression analysis, adjusted for sex and age. Baseline HbF levels were log10 transformed to fit a normal distribution; maximum and delta HbF were normally distributed. Significance is reported for nominal p-values of 0.05 or less, and with Bonferroni adjustment of p-values for multiple testing (adjusted p-value of 3×10−3 for the 19 SNPs tested – see below). Given the fixed sample size, power was estimated based on the smallest detectable differences in the average levels of baseline and hydroxyurea-induced fetal hemoglobin HbF. Power was computed using QUANTO software (http://hydra.usc.edu/gxe/) assuming an additive allele effects model, an alpha threshold of 0.05, a range of different values for effect sizes (β) and SNP allele frequency (Figure S2) .
Limited number of subjects of each genotype precluded analysis of potential dose effect of homozygotes. Trend analysis was performed by analysis of variance tested for individual and additive effects for each allele. Percentage of variance attributable to SNPs in BCL11A, HBB and HBE was estimated using linear regression analysis comparing models consisting of age, sex, individual SNPs and multiple SNPs with a reduced model consisting of sex and age (SPSS Inc., Chicago, IL). To evaluate whether BCL11A haplotypes was in closer linkage disequilibrium with causal variants than single SNPs, haplotype association analysis was performed with PLINK software  using a haplotype block of four BCL11A SNPs in strong linkage disequilibrium (r2>0.70) .
117 children from the six sites met study criteria (Data from each site are shown in Table S1). The mean age and standard deviation was 12.5 (SD = 4.9), with 52% male. Six subjects (5.1%) had HbS-B0 thalassemia (Table S1A). A subset of children (N = 47) was on hydroxyurea, 38 of whom had recorded baseline and maximum HbF values. Hydroxyurea dosing ranged from 20–30.7 mg/kg/day, averaging 25.3 (SD = 3.0) mg/kg/day. During the two years prior to hydroxyurea therapy, children (N = 22 with available data) had 0–13 hospital admissions (mean = 3.7, SD = 2.8); only one child had no hospitalizations. During a two year period while on hydroxyurea therapy, these same children had 0–6 hospitalizations (mean = 1.4,SD = 1.5). While on hydroxyurea, nearly all had fewer hospitalizations over a two year period (p = 0.001), and 32% had none.
Mean HbF% values were: baseline HbF 8.0 (SD = 4.9, N = 108), maximum HbF 18.2 (SD = 7.1, N = 47), and delta HbF 11.6 (SD = 6.3, N = 38). Among those subjects with complete data for baseline and hydroxyurea-induced HbF (N = 38), distributions of baseline and induced HbF were comparable to those previously reported for children on hydroxyurea (Figure 1, Figure S1)  thereby validating our observational data. No significant effect of gender was detected for any of the three quantitative traits; age appeared to have some influence on baseline HbF. Mean baseline HbF at each site ranged from 6.8 (SD = 5.0) to 9.8 (SD = 5.6), with no significant difference in mean values (F = 0.808, p = 0.523), excluding the average value of 12.9% from Rochester (N = 8). At the three sites with at least four subjects on hydroxyurea (Columbia, Yale and Oakland), no differences were found in induced maximum or delta HbF (F = 0.668, p = 0.418 and F = 0.404, p = 0.530, respectively).
Figure 1. Baseline and hydroxyurea-induced maximum HbF for each subject (comparable to References 18, 19, 26).doi:10.1371/journal.pone.0055709.g001
Pearson correlation for the 38 children with complete baseline and hydroxyurea-induced HbF demonstrated high levels of relatedness for: baseline and induced maximum HbF levels (r2 = 0.59, p<0.001), similar to previously reported ; maximum and delta HbF (r2 = 0.86, p<0.001); but not between baseline and delta HbF (r2 = 0.08, p = 0.632). Those in the lowest quartile for baseline levels were highly likely to remain in the lowest quartile (Q1) for induced HbF (r2 = 0.565, p<0.001) (Figure 1). Only two children (5.3%) were induced from the lowest to highest quartiles (Q3+Q4), and did not appear to differ by age, sex, sickle type, hydroxyurea dose, genotype, or other discernible variable, although the small number precluded statistical analysis. By linear regression analysis adjusted for age and sex, overall percentage of variance in hydroxyurea-induced HbF attributable to baseline levels was 33%.
Call rates uniformly exceeded 97% for each SNP. One SAR1A gene SNP, rs428289,  was monomorphic in subjects treated with hydroxyurea, precluding analysis of variants. Genotyping of the other 19 SNPs revealed minor allele frequencies that were comparable across the six sites (Table S1B) and to allele frequencies among sickle cell populations in the U.S and elsewhere , confirming validity of our pooling strategy. Log10 transformation of baseline HbF had no effect on SNP associations; non-transformed results are shown for comparison with induced values (Table 1).
Given the fixed sample size and SNP allele frequencies, the study had 90% power to detect differences in average levels of baseline HbF% between 2.0 and 2.5 (Figure S2A). Single marker SNP analysis revealed several significant associations to baseline HbF (Table 1). One of two SNPs tested within the HBB locus, rs7482144 , and the HBE SNP  were significantly associated with baseline HbF after Bonferroni correction. Six BCL11A SNPs were significantly associated with baseline HbF, of which five withstood correction for multiple comparisons, including the intronic variant, rs4671393 , . To test for closer linkage disequilibrium with causal variants within the BCL11A haplotype block than single SNPs , analysis revealed several common haplotypes (frequency = 0.05), with statistical association and effect size comparable to those seen with single marker analysis (data not shown). Power was insufficient to detect effects sizes of <3, such as for markers in the HBS1L-MYB intergenic region (Table 1).
Trend analysis using the SNP allele associated with higher baseline HbF values (“favorable allele”) in one or both of the BCL11A (rs4671393) and HBE (rs7130110) loci demonstrated a statistically significant additive effect of each SNP and a two-fold difference for both (ptrend<0.004) (Table 2). The HBB marker (rs7482144) had effects identical to those of HBE (not shown). By linear regression analysis of individual markers accounting for age and sex, the percentage of baseline HbF variance attributable each to the BCL11A or HBE SNP was 13%, and 10% for HBB (Table S2A). In the multiple marker model, the BCL11A SNP combined with either globin marker had an additive effect to 21–23%. Contributions from HBE and HBB appeared to be redundant. These two markers are in strong linkage disequilibrium within the globin locus (r2 = 0.86, p<0.001), with different prevalence of the minor allele: 18% for HBE and 12% for HBB.
Table 2. Incremental effect of allelotypes in BCL11A and HBE on Baseline and Maximum HbF%.doi:10.1371/journal.pone.0055709.t002
The study had ≥80% power to detect SNPs with effect sizes larger than 2.5 with allele frequencies of 0.25 or higher; estimated power decreased with lower SNP allele frequencies (Figure S2B). Among all single markers tested, only the HBE SNP  was significantly associated with maximum HbF after correction for multiple testing, and remained nominally associated even after adjusting for baseline HbF (p = 0.001) (Table 1). This same SNP was also unique in being associated with the hydroxyurea-induced increment, delta HbF (p = 0.004). Nominal associations were also found between maximum HbF and four of the same six BCL11A SNPs associated with baseline HbF (Table 1). However, no association of BCL11A single marker with maximum HbF withstood adjustment for baseline HbF (Table 1). Haplotype analysis of BCL11A indicated nominal association with hydroxyurea-induced HbF, remaining at borderline significant even after adjustment for baseline HbF (data not shown).
By trend analysis, subjects with a favorable allele in at least one of the BCL11A or HBE loci had higher average values, 20.8 (SD = 7.5, N = 23), compared to 15.5 (SD = 5.6, N = 24) for those without either allele (ptrend = 0.009) (Table 2). As with single SNP analysis, statistical significance of this trend analysis did not withstand adjustment for baseline fetal hemoglobin (p = 0.0.086). As seen for baseline HbF, the HBB marker (rs7482144) had effects identical to those of HBE (ptrend = 0.018, not shown). By linear regression analysis of the three markers, alone or in combination, only the HBE SNP independently and significantly added to the phenotypic variance contributed by the baseline levels. In combination, baseline level (33%) and the HBE (13%, p<0.001) contributed an estimated 46% of the variance (Table S2B).
The GLP2R allele, not associated with baseline HbF, was nominally associated with maximum HbF; the SAR1A SNP, rs2310991,  was not.
Children with sickle cell disease generally have higher baseline HbF levels than adults and more pronounced HbF response to hydroxyurea , , , , , , , , , , , . Findings from this multi-site, observational analysis corroborate in children the correlation between baseline and hydroxyurea-induced HbF levels , , and demonstrate that one third of the variance in induced HbF is attributable to baseline levels. In contrast to the induced HbF, the treatment-associated increment appears to be a less relevant marker, as baseline and delta levels did not correlate and those with high baseline more likely have highly inducible HbF%.
For baseline HbF, we confirm in children the associations between single candidate markers in the BCL11A and HBB or HBE loci . Comparable marker contributions to baseline HbF were reported for BCL11A and HBB in adult sickle cell disease , . In our analysis, statistical effects on HbF from BCL11A and either globin marker were additive, and were associated with two-fold higher levels for patients with favorable alleles in both loci. An apparent redundant influence exists between HBB and HBE markers, suggesting a statistical effect stemming from tight linkage and/or overlapping biologic effects.
For hydroxyurea-induced HbF, the HBE marker was the most robustly associated with drug-induced HbF levels, an effect that was independent of and additive to baseline levels. Despite a sample size limiting statistical power for individual SNPs, trend analysis with BCL11A and HBE or HBB markers suggests substantially higher induced levels associated with one or both favorable alleles. In combination with baseline levels, the HBE accounted for almost half of the variance of induced levels. Taken together, these data support a model of overlapping genetic regulation of HbF in pediatric SCD for both steady states .
Roles of other SNP markers are less clear. Nominal association with GLP2R for hydroxyurea-induced HbF, but not baseline, will need confirmation and biologic rationale. No associations were detected with SNPs in other candidate loci such as HBS1L-MYB, presumably from insufficient power and its lesser impact on baseline HbF in sickle cell disease . Another hematologic parameter, alpha-thalassemia status, is not independently associated with hydroxyurea-induced HbF in children . Effects of the drug’s pharmaco-kinetics on HbF response are unclear .
Limitations: Study limitations include sample size and observational assessment, where therapeutic approaches to hydroxyurea and drug adherence may vary among sites despite inclusion criteria. Nonetheless, hydroxyurea dose and distribution of drug-induced HbF were comparable to those from prospective pediatric hydroxyurea studies . Moreover, a threshold hydroxyurea dose of 20 mg/kg/day was employed to reduce HbF variability from low drug dosing.
Clinically, HbF level is arguably the strongest predictor of disease severity , . Baseline HbF in children remains the best forecaster of hydroxyurea-induced HbF but accounts for only a portion of drug response . Despite a modest sample size, clinically relevant differences in HbF ,  in our study population appeared to be associated with specific alleles in three genetic loci. These findings suggest that induced levels in pediatric disease share some of the major regulatory loci associated with baseline levels. Our HBE marker data also suggest that induced levels may reflect effects that are additive to those of baseline. In summary, our findings suggest that baseline and hydroxyurea-induced HbF likely are influenced by these genetic loci, while distinct genetic, pharmacologic, and clinical determinants also exist , . Genetic studies examining larger pediatric populations on hydroxyurea and unusual responders are needed to assess the specific sequence variants in these and other genetic loci responsible for HbF response.
Histograms for Baseline, Maximum and Delta HbF%.
Power analyses based on minor allele frequencies. S2A. Baseline HbF. S2B. Maximum HbF
Clinical and Genetic Data by Study Site. S1A. Clinical data by study site. S1B. Minor allele frequencies by study site.
HbF linear regression analysis to compare full model consisting of age, sex, individual and multiple SNPs. S2A. Baseline HbF%. S2B. Maximum HbF%
We acknowledge the contributions of Maureen Licursi, MS, CPNP; Mara Burney, RN, MPH; Columbia’s Human Genetics Resources Core; and the participating families and coordinators at each site.
Conceived and designed the experiments: NSG KLE SB. Performed the experiments: NSG KLE FP CD PJG CAM LNC DM JC SK KAN CH SB. Analyzed the data: NSG KLE LC SK SB. Contributed reagents/materials/analysis tools: NSG KLE FP CD PJG CAM LNC DM JC SK KAN CH SB. Wrote the paper: NSG KLE CAM LNC SB.
- 1. Bunn HF (1987) Subunit assembly of hemoglobin: an important determinant of hematologic phenotype. Blood 69: 1–6.
- 2. Powars DR, Weiss JN, Chan LS, Schroeder WA (1984) Is there a threshold level of fetal hemoglobin that ameliorates morbidity in sickle cell anemia? Blood 63: 921–926.
- 3. Platt OS (2008) Hydroxyurea for the treatment of sickle cell anemia. N Engl J Med 358: 1362–1369. doi: 10.1056/nejmct0708272
- 4. Steinberg MH, Voskaridou E, Kutlar A, Loukopoulos D, Koshy M, et al. (2003) Concordant fetal hemoglobin response to hydroxyurea in siblings with sickle cell disease. Am J Hematol 72: 121–126. doi: 10.1002/ajh.10264
- 5. Thein SL, Menzel S, Lathrop M, Garner C (2009) Control of fetal hemoglobin: new insights emerging from genomics and clinical implications. Hum Mol Genet 18: R216–223. doi: 10.1093/hmg/ddp401
- 6. Galarneau G, Palmer CD, Sankaran VG, Orkin SH, Hirschhorn JN, et al. (2010) Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation. Nat Genet 42: 1049–1051. doi: 10.1038/ng.707
- 7. Lettre G, Sankaran VG, Bezerra MA, Araujo AS, Uda M, et al. (2008) DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proc Natl Acad Sci U S A 105: 11869–11874. doi: 10.1073/pnas.0804799105
- 8. Makani J, Menzel S, Nkya S, Cox SE, Drasar E, et al. (2011) Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia. Blood 117: 1390–1392. doi: 10.1182/blood-2010-08-302703
- 9. Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, et al. (2008) Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations. Am J Hematol 83: 189–195. doi: 10.1002/ajh.21048
- 10. Bhatnagar P, Purvis S, Barron-Casella E, Debaun MR, Casella JF, et al. (2011) Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. J Hum Genet 56: 316–323. doi: 10.1038/jhg.2011.12
- 11. Sedgewick AE, Timofeev N, Sebastiani P, So JC, Ma ES, et al. (2008) BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies. Blood Cells Mol Dis 41: 255–258. doi: 10.1016/j.bcmd.2008.06.007
- 12. Bae HT, Baldwin CT, Sebastiani P, Telen MJ, Ashley-Koch A, et al. (2012) Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans. Blood 120: 1961–1962. doi: 10.1182/blood-2012-06-432849
- 13. Ma Q, Wyszynski DF, Farrell JJ, Kutlar A, Farrer LA, et al. (2007) Fetal hemoglobin in sickle cell anemia: genetic determinants of response to hydroxyurea. Pharmacogenomics J 7: 386–394. doi: 10.1038/sj.tpj.6500433
- 14. Solovieff N, Milton JN, Hartley SW, Sherva R, Sebastiani P, et al. (2010) Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster. Blood 115: 1815–1822. doi: 10.1182/blood-2009-08-239517
- 15. Meier ER, Byrnes C, Weissman M, Noel P, Luban NL, et al. (2011) Expression patterns of fetal hemoglobin in sickle cell erythrocytes are both patient- and treatment-specific during childhood. Pediatr Blood Cancer 56: 103–109. doi: 10.1002/pbc.22643
- 16. Steinberg MH, Lu ZH, Barton FB, Terrin ML, Charache S, et al. (1997) Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea. Blood 89: 1078–1088.
- 17. Green NS, Barral S (2011) Genetic modifiers of HbF and response to hydroxyurea in sickle cell disease. Pediatr Blood Cancer 56: 177–181. doi: 10.1002/pbc.22754
- 18. Ware RE, Eggleston B, Redding-Lallinger R, Wang WC, Smith-Whitley K, et al. (2002) Predictors of fetal hemoglobin response in children with sickle cell anemia receiving hydroxyurea therapy. Blood 99: 10–14. doi: 10.1182/blood.v99.1.10
- 19. Ware RE, Despotovic JM, Mortier NA, Flanagan JM, He J, et al. (2011) Pharmacokinetics, pharmacodynamics, and pharmacogenetics of hydroxyurea treatment for children with sickle cell anemia. Blood 118: 4985–4991. doi: 10.1182/blood-2011-07-364190
- 20. Charache S (1997) Mechanism of action of hydroxyurea in the management of sickle cell anemia in adults. Semin Hematol 34: 15–21.
- 21. Kumkhaek C, Taylor JGt, Zhu J, Hoppe C, Kato GJ, et al. (2008) Fetal haemoglobin response to hydroxycarbamide treatment and sar1a promoter polymorphisms in sickle cell anaemia. Br J Haematol 141: 254–259. doi: 10.1111/j.1365-2141.2008.07045.x
- 22. Zimmerman SA, Schultz WH, Davis JS, Pickens CV, Mortier NA, et al. (2004) Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood 103: 2039–2045. doi: 10.1182/blood-2003-07-2475
- 23. Green NS, Fabry ME, Kaptue-Noche L, Nagel RL (1993) Senegal haplotype is associated with higher HbF than Benin and Cameroon haplotypes in African children with sickle cell anemia. Am J Hematol 44: 145–146. doi: 10.1002/ajh.2830440214
- 24. Gauderman WJ, Morrison JM (2006) QUANTO 1.1: A computer program for power and sample size calculations for genetic-epidemiology studies.
- 25. Purcell S, Neale B, Todd-Brown K, Thomas L, Ferreira MA, et al. (2007) PLINK: a tool set for whole-genome association and population-based linkage analyses. Am J Hum Genet 81: 559–575. doi: 10.1086/519795
- 26. Ender KL, Lee MT, Sheth S, Licursi M, Crotty J, et al. (2011) Fetal hemoglobin levels in African American and Hispanic children with sickle cell disease at baseline and in response to hydroxyurea. J Pediatr Hematol Oncol 33: 496–499. doi: 10.1097/mph.0b013e31822dcc21