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常见良性基因型与非裔美国患者不必要的骨髓活检之间的关联。

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

机构信息

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

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

出版信息

JAMA Intern Med. 2021 Aug 1;181(8):1100-1105. doi: 10.1001/jamainternmed.2021.3108.

Abstract

IMPORTANCE

Up to two-thirds of African American individuals carry the benign rs2814778-CC genotype that lowers total white blood cell (WBC) count.

OBJECTIVE

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.

DESIGN, SETTING, AND PARTICIPANTS: 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.

EXPOSURE

The rs2814778-CC genotype.

MAIN OUTCOMES AND MEASURES

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.

RESULTS

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).

CONCLUSIONS AND RELEVANCE

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.

摘要

重要性

多达三分之二的非裔美国人携带降低总白细胞 (WBC) 计数的良性 rs2814778-CC 基因型。

目的

检查 rs2814778-CC 基因型是否与接受骨髓活检 (BMB) 以治疗孤立性低 WBC 计数的可能性增加相关。

设计、地点和参与者:这项回顾性遗传关联研究评估了 1998 年 1 月 1 日至 2020 年 12 月 31 日期间在范德比尔特大学医学中心、西奈山健康系统或费城儿童医院接受 BMB 的年龄在 90 岁以下的非裔美国患者。

暴露

rs2814778-CC 基因型。

主要结果和测量

与 CC 基因型患者因其他原因接受 BMB 且活检结果正常的比例相比,因孤立性低 WBC 计数接受 BMB 且活检结果正常的 CC 基因型患者的比例。

结果

在 399 名接受 BMB 的患者中(平均[SD]年龄为 41.8[22.5]岁,234[59%]为女性),277 名(69%)为 CC 基因型。共有 35 名患者(9%)有孤立性低 WBC 计数的临床病史,364 名(91%)有其他病史。在有孤立性低 WBC 计数病史的患者中,35 名中有 34 名(97%)为 CC 基因型,而在无低 WBC 计数病史的 364 名患者中,有 243 名(67%)为 CC 基因型。在 CC 基因型患者中,34 名(97%)因孤立性低 WBC 计数接受的 BMB 活检结果正常,而 243 名(55%)因其他原因接受 BMB 活检的患者中有 134 名(55%)活检结果正常(P<0.001)。

结论和相关性

在这项遗传关联研究中,在接受有孤立性低 WBC 计数临床病史的 BMB 的非裔美国患者中,rs2814778-CC 基因型非常普遍,其中 97%的 BMB 未发现血液异常。在临床决策中考虑 rs2814778-CC 基因型可以避免不必要的 BMB 程序。

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