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Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia

OBJECTIVE: Low levels of neutrophils can be an intrinsic condition, with no clinical consequences or immunity impairment. This condition is the benign constitutional neutropenia (BCN), defined as an absolute neutrophils count (ANC) [Formula: see text] 2000 cells/mm. Diagnosis of BCN is of exclusion...

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Autores principales: Barreto, Maria E.S.F., Lipay, Mariana E., Santos, Leandro D., Sirianni, Marilia F. Mascarenhas, Costa, Thiago H., Castilho, Lilian, Hamerschlak, Nelson, Kutner, José M., Bub, Carolina B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573039/
https://www.ncbi.nlm.nih.gov/pubmed/33184016
http://dx.doi.org/10.1016/j.htct.2020.08.015
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author Barreto, Maria E.S.F.
Lipay, Mariana E.
Santos, Leandro D.
Sirianni, Marilia F. Mascarenhas
Costa, Thiago H.
Castilho, Lilian
Hamerschlak, Nelson
Kutner, José M.
Bub, Carolina B.
author_facet Barreto, Maria E.S.F.
Lipay, Mariana E.
Santos, Leandro D.
Sirianni, Marilia F. Mascarenhas
Costa, Thiago H.
Castilho, Lilian
Hamerschlak, Nelson
Kutner, José M.
Bub, Carolina B.
author_sort Barreto, Maria E.S.F.
collection PubMed
description OBJECTIVE: Low levels of neutrophils can be an intrinsic condition, with no clinical consequences or immunity impairment. This condition is the benign constitutional neutropenia (BCN), defined as an absolute neutrophils count (ANC) [Formula: see text] 2000 cells/mm. Diagnosis of BCN is of exclusion where patients are submitted to blood tests and possibly to invasive diagnostic search until secondary causes of neutropenia are ruled out. The natural history of the disease suggests benign evolution and Brazilian study showed an overall frequency of 2.59%. The main mechanisms include reduced neutrophil production, increased marginalization, extravasation to the tissues and immune destruction. Genetic studies showed strong association between the single nucleotide variant rs2814778 located on chromosome 1q23.2 in the promoter region of the atypical chemokine receptor 1 (Duffy blood group system) gene (ACKR1, also termed DARC) and BCN. The aim of this study is to evaluate FY phenotypes and genotypes including the analysis of the rs2814778 SNP in Brazilian patients with BCN in order to determine an effective diagnostic tool, allowing reassurance of the patient and cost reduction in their care. METHODS: Case control study, with 94 individuals (18 patients and 76 controls). Phenotyping was performed by gel test and genotyping was performed by PCR-RFLP. RESULTS: White blood cell (WBC) and absolute neutrophils (AN) counts showed lower levels in patients compared to controls. In the patient group 83.3% were genotyped as FY*B/FY*B. The SNP rs2814778 (-67T > C) was identified in 77.8% of the patients genotyped as FY*B-67C/FY*B-67C. In the control group, 72.7% were homozygous for the wild type and 23.3% were heterozygous. CONCLUSION: This study reinforces that FY phenotyping and genotyping can be used to detect most people with BCN, avoiding excessive diagnostic investigation. Besides, this procedure may reduce health costs and be reproductible in clinical practice.
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spelling pubmed-85730392021-11-10 Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia Barreto, Maria E.S.F. Lipay, Mariana E. Santos, Leandro D. Sirianni, Marilia F. Mascarenhas Costa, Thiago H. Castilho, Lilian Hamerschlak, Nelson Kutner, José M. Bub, Carolina B. Hematol Transfus Cell Ther Original Article OBJECTIVE: Low levels of neutrophils can be an intrinsic condition, with no clinical consequences or immunity impairment. This condition is the benign constitutional neutropenia (BCN), defined as an absolute neutrophils count (ANC) [Formula: see text] 2000 cells/mm. Diagnosis of BCN is of exclusion where patients are submitted to blood tests and possibly to invasive diagnostic search until secondary causes of neutropenia are ruled out. The natural history of the disease suggests benign evolution and Brazilian study showed an overall frequency of 2.59%. The main mechanisms include reduced neutrophil production, increased marginalization, extravasation to the tissues and immune destruction. Genetic studies showed strong association between the single nucleotide variant rs2814778 located on chromosome 1q23.2 in the promoter region of the atypical chemokine receptor 1 (Duffy blood group system) gene (ACKR1, also termed DARC) and BCN. The aim of this study is to evaluate FY phenotypes and genotypes including the analysis of the rs2814778 SNP in Brazilian patients with BCN in order to determine an effective diagnostic tool, allowing reassurance of the patient and cost reduction in their care. METHODS: Case control study, with 94 individuals (18 patients and 76 controls). Phenotyping was performed by gel test and genotyping was performed by PCR-RFLP. RESULTS: White blood cell (WBC) and absolute neutrophils (AN) counts showed lower levels in patients compared to controls. In the patient group 83.3% were genotyped as FY*B/FY*B. The SNP rs2814778 (-67T > C) was identified in 77.8% of the patients genotyped as FY*B-67C/FY*B-67C. In the control group, 72.7% were homozygous for the wild type and 23.3% were heterozygous. CONCLUSION: This study reinforces that FY phenotyping and genotyping can be used to detect most people with BCN, avoiding excessive diagnostic investigation. Besides, this procedure may reduce health costs and be reproductible in clinical practice. Sociedade Brasileira de Hematologia e Hemoterapia 2021 2020-11-04 /pmc/articles/PMC8573039/ /pubmed/33184016 http://dx.doi.org/10.1016/j.htct.2020.08.015 Text en © 2020 Published by Elsevier Editora Ltda. on behalf of Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Barreto, Maria E.S.F.
Lipay, Mariana E.
Santos, Leandro D.
Sirianni, Marilia F. Mascarenhas
Costa, Thiago H.
Castilho, Lilian
Hamerschlak, Nelson
Kutner, José M.
Bub, Carolina B.
Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title_full Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title_fullStr Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title_full_unstemmed Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title_short Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropenia
title_sort duffy phenotyping and fy*b-67t/c genotyping as screening test for benign constitutional neutropenia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573039/
https://www.ncbi.nlm.nih.gov/pubmed/33184016
http://dx.doi.org/10.1016/j.htct.2020.08.015
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