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Sökning: WFRF:(Mikkel Sirje) > (2022) > Characteristics of ...

Characteristics of white blood cell count in acute lymphoblastic leukemia : A COST LEGEND phenotype-genotype study

Helenius, Marianne (författare)
Tech Univ Denmark, Dept Hlth Technol, DK-2800 Copenhagen, Denmark.;Univ Hosp, Dept Pediat & Adolescent Med, Rigshosp, Copenhagen, Denmark
Vaitkeviciene, Goda (författare)
Vilnius Univ Hosp, Santaros Klin Ctr Pediat Oncol & Hematol, Vilnius, Lithuania.;Vilnius Univ, Vilnius, Lithuania
Abrahamsson, Jonas (författare)
Sahlgrens Univ Hosp, Inst Clin Sci, Dept Paediat, Gothenburg, Sweden
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Jonsson, Olafur Gisli (författare)
Landspitali Univ Hosp, Dept Pediat, Reykjavik, Iceland
Lund, Bendik (författare)
St Olavs Hosp, Dept Pediat, Trondheim, Norway
Harila-Saari, Arja H. (författare)
Uppsala universitet,Institutionen för kvinnors och barns hälsa
Vettenranta, Kim (författare)
Univ Helsinki, Helsinki, Finland.;Univ Helsinki, Childrens Hosp, Helsinki, Finland
Mikkel, Sirje (författare)
Univ Tartu, Dept Hematol & Oncol, Tartu, Estonia
Stanulla, Martin (författare)
Hannover Med Sch, Dept Pediat Hematol & Oncol, Hannover, Germany
Lopez-Lopez, Elixabet (författare)
Univ Basque Country UPV EHU, Fac Sci & Technol, Dept Genet Phys Anthropol & Anim Physiol, Leioa, Spain.;BioCruces Bizkaia Hlth Res Inst, Pediat Oncol Grp, Baracaldo, Spain
Waanders, Esme (författare)
Univ Med Ctr Utrecht, Dept Genet, Utrecht, Netherlands.;Princess Maxima Ctr Pediat Oncol, Utrecht, Netherlands
Madsen, Hans O. (författare)
Univ Hosp, Rigshosp, Dept Clin Immunol, Copenhagen, Denmark
Marquart, Hanne Vibeke (författare)
Univ Hosp, Rigshosp, Dept Clin Immunol, Copenhagen, Denmark
Modvig, Signe (författare)
Univ Hosp, Rigshosp, Dept Clin Immunol, Copenhagen, Denmark
Gupta, Ramneek (författare)
Tech Univ Denmark, Dept Hlth Technol, DK-2800 Copenhagen, Denmark.;Novo Nordisk Res Ctr Oxford, Oxford, England
Schmiegelow, Kjeld (författare)
Univ Hosp, Dept Pediat & Adolescent Med, Rigshosp, Copenhagen, Denmark.;Univ Copenhagen, Fac Med, Inst Clin Med, Copenhagen, Denmark
Nielsen, Rikke Linnemann (författare)
Tech Univ Denmark, Dept Hlth Technol, DK-2800 Copenhagen, Denmark.;Univ Hosp, Dept Pediat & Adolescent Med, Rigshosp, Copenhagen, Denmark.;Novo Nordisk Res Ctr Oxford, Oxford, England
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Tech Univ Denmark, Dept Hlth Technol, DK-2800 Copenhagen, Denmark;Univ Hosp, Dept Pediat & Adolescent Med, Rigshosp, Copenhagen, Denmark Vilnius Univ Hosp, Santaros Klin Ctr Pediat Oncol & Hematol, Vilnius, Lithuania.;Vilnius Univ, Vilnius, Lithuania (creator_code:org_t)
2022-03-22
2022
Engelska.
Ingår i: Pediatric Blood & Cancer. - : John Wiley & Sons. - 1545-5009 .- 1545-5017. ; 69:6
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background White blood cell count (WBC) as a measure of extramedullary leukemic cell survival is a well-known prognostic factor in acute lymphoblastic leukemia (ALL), but its biology, including impact of host genome variants, is poorly understood.Methods We included patients treated with the Nordic Society of Paediatric Haematology and Oncology (NOPHO) ALL-2008 protocol (N = 2347, 72% were genotyped by Illumina Omni2.5exome-8-Bead chip) aged 1-45 years, diagnosed with B-cell precursor (BCP-) or T-cell ALL (T-ALL) to investigate the variation in WBC. Spline functions of WBC were fitted correcting for association with age across ALL subgroups of immunophenotypes and karyotypes. The residuals between spline WBC and actual WBC were used to identify WBC-associated germline genetic variants in a genome-wide association study (GWAS) while adjusting for age and ALL subtype associations.Results We observed an overall inverse correlation between age and WBC, which was stronger for the selected patient subgroups of immunophenotype and karyotypes (rho(BCP-ALL )= -.17, rho(T-ALL )= -.19; p < 3 x 10(-4)). Spline functions fitted to age, immunophenotype, and karyotype explained WBC variation better than age alone (rho = .43, p << 2 x 10(-6)). However, when the spline-adjusted WBC residuals were used as phenotype, no GWAS significant associations were found. Based on available annotation, the top 50 genetic variants suggested effects on signal transduction, translation initiation, cell development, and proliferation.Conclusion These results indicate that host genome variants do not strongly influence WBC across ALL subsets, and future studies of why some patients are more prone to hyperleukocytosis should be performed within specific ALL subsets that apply more complex analyses to capture potential germline variant interactions and impact on WBC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Hematologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Hematology (hsv//eng)

Nyckelord

acute lymphoblastic leukemia (ALL)
genome-wide association studies (GWAS)
genotype
spline functions
white blood cell count (WBC)

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