Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American Patients.


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
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

1100-1105

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM130791
Pays : United States
Organisme : NLM NIH HHS
ID : R01 LM010685
Pays : United States

Auteurs

Sara L Van Driest (SL)

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Noura S Abul-Husn (NS)

Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Joseph T Glessner (JT)

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.
The Center for Applied Genomics, the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

Lisa Bastarache (L)

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.

Sharon Nirenberg (S)

Department of Scientific Computing, Icahn School of Medicine at Mount Sinai, New York, New York.

Jonathan S Schildcrout (JS)

Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee.

Meghana S Eswarappa (MS)

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Gillian M Belbin (GM)

Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York.

Christian M Shaffer (CM)

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Frank Mentch (F)

The Center for Applied Genomics, the Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.

John Connolly (J)

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.

Mingjian Shi (M)

Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.

C Michael Stein (CM)

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee.

Dan M Roden (DM)

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee.

Hakon Hakonarson (H)

Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia.

Nancy J Cox (NJ)

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.

Scott C Borinstein (SC)

Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee.

Jonathan D Mosley (JD)

Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee.

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Classifications MeSH