Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.
Adult
Black or African American
/ genetics
Biopsy
/ methods
Bone Marrow Examination
/ methods
Duffy Blood-Group System
/ genetics
Female
Gene Expression Profiling
/ statistics & numerical data
Genetic Profile
Genome-Wide Association Study
Humans
Leukocyte Count
Male
Neutropenia
/ diagnosis
Polymorphism, Single Nucleotide
Receptors, Cell Surface
/ genetics
United States
/ epidemiology
Unnecessary Procedures
/ methods
Journal
JAMA internal medicine
ISSN: 2168-6114
Titre abrégé: JAMA Intern Med
Pays: United States
ID NLM: 101589534
Informations de publication
Date de publication:
01 08 2021
01 08 2021
Historique:
pubmed:
29
6
2021
medline:
18
1
2022
entrez:
28
6
2021
Statut:
ppublish
Résumé
Up to two-thirds of African American individuals carry the benign rs2814778-CC genotype that lowers total white blood cell (WBC) count. To examine whether the rs2814778-CC genotype is associated with an increased likelihood of receiving a bone marrow biopsy (BMB) for an isolated low WBC count. This retrospective genetic association study assessed African American patients younger than 90 years who underwent a BMB at Vanderbilt University Medical Center, Mount Sinai Health System, or Children's Hospital of Philadelphia from January 1, 1998, to December 31, 2020. The rs2814778-CC genotype. The proportion of individuals with the CC genotype who underwent BMB for an isolated low WBC count and had a normal biopsy result compared with the proportion of individuals with the CC genotype who underwent BMB for other indications and had a normal biopsy result. Among 399 individuals who underwent a BMB (mean [SD] age, 41.8 [22.5] years, 234 [59%] female), 277 (69%) had the CC genotype. A total of 35 patients (9%) had clinical histories of isolated low WBC counts, and 364 (91%) had other histories. Of those with a clinical history of isolated low WBC count, 34 of 35 (97%) had the CC genotype vs 243 of 364 (67%) of those without a low WBC count history. Among those with the CC genotype, 33 of 34 (97%) had normal results for biopsies performed for isolated low WBC counts compared with 134 of 243 individuals (55%) with biopsies performed for other histories (P < .001). In this genetic association study, among patients of African American race who had a BMB with a clinical history of isolated low WBC counts, the rs2814778-CC genotype was highly prevalent, and 97% of these BMBs identified no hematologic abnormality. Accounting for the rs2814778-CC genotype in clinical decision-making could avoid unnecessary BMB procedures.
Identifiants
pubmed: 34180972
pii: 2781474
doi: 10.1001/jamainternmed.2021.3108
pmc: PMC8239990
doi:
Substances chimiques
ACKR1 protein, human
0
Duffy Blood-Group System
0
Receptors, Cell Surface
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1100-1105Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM130791
Pays : United States
Organisme : NLM NIH HHS
ID : R01 LM010685
Pays : United States