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本文引用的文献

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Absolute neutrophil count by Duffy status among healthy Black and African American adults.根据达菲血型状态划分的健康黑人和非裔美国人成年人的中性粒细胞绝对计数。
Blood Adv. 2023 Feb 14;7(3):317-320. doi: 10.1182/bloodadvances.2022007679.
2
When non-Whiteness becomes a condition.当非白色成为一种条件。
Blood. 2021 Jan 7;137(1):13-15. doi: 10.1182/blood.2020008600.
3
Ethnic benign neutropenia: A phenomenon finds an explanation.遗传性良性中性粒细胞减少症:现象有了合理解释。
Pediatr Blood Cancer. 2018 Dec;65(12):e27361. doi: 10.1002/pbc.27361. Epub 2018 Aug 16.
4
Complete Blood Count Reference Intervals and Patterns of Changes Across Pediatric, Adult, and Geriatric Ages in Korea.韩国儿科、成人和老年人群的全血细胞计数参考区间和变化模式。
Ann Lab Med. 2018 Nov;38(6):503-511. doi: 10.3343/alm.2018.38.6.503.
5
Verification of reference intervals in routine clinical laboratories: practical challenges and recommendations.参考区间在常规临床实验室中的验证:实际挑战与建议。
Clin Chem Lab Med. 2018 Dec 19;57(1):30-37. doi: 10.1515/cclm-2018-0059.
6
Characteristics of systemic lupus erythematosus in a sample of the Egyptian population: a retrospective cohort of 1109 patients from a single center.埃及人群样本中系统性红斑狼疮的特征:来自单一中心的1109例患者的回顾性队列研究
Lupus. 2018 May;27(6):1030-1038. doi: 10.1177/0961203317751856. Epub 2018 Feb 10.
7
Duffy blood group system: New genotyping method and distribution in a Brazilian extra-Amazonian population.达菲血型系统:一种新的基因分型方法及其在巴西亚马孙河以外人群中的分布。
Mol Cell Probes. 2017 Oct;35:20-26. doi: 10.1016/j.mcp.2017.06.001. Epub 2017 Jun 3.
8
Benign Ethnic Neutropenia and Clozapine Use: A Systematic Review of the Evidence and Treatment Recommendations.良性种族性中性粒细胞减少症与氯氮平的使用:证据及治疗建议的系统评价
J Clin Psychiatry. 2016 Jul;77(7):e909-16. doi: 10.4088/JCP.15r10085.
9
Role of Plasmodium vivax Duffy-binding protein 1 in invasion of Duffy-null Africans.间日疟原虫达菲结合蛋白1在达菲阴性非洲人入侵中的作用。
Proc Natl Acad Sci U S A. 2016 May 31;113(22):6271-6. doi: 10.1073/pnas.1606113113. Epub 2016 May 17.
10
Identification and Clinical Characterization of Children With Benign Ethnic Neutropenia.良性家族性中性粒细胞减少症患儿的识别与临床特征
J Pediatr Hematol Oncol. 2016 Apr;38(3):e140-3. doi: 10.1097/MPH.0000000000000528.

因无症状性中性粒细胞减少而就诊患者的临床结局:以血液学中的种族差异为重点

Clinical outcomes of patients referred for asymptomatic neutropenia: A focus on racial disparities in hematology.

机构信息

Division of Internal Medicine, Oregon Health & Science University, Portland, Oregon, USA.

Department of Biomedical Engineering, Oregon Health & Science University, School of Medicine, Portland, Oregon, USA.

出版信息

Eur J Haematol. 2023 Jul;111(1):41-46. doi: 10.1111/ejh.13963. Epub 2023 Mar 28.

DOI:10.1111/ejh.13963
PMID:36951011
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10272056/
Abstract

BACKGROUND

Asymptomatic neutropenia is a common hematology referral, though standardized reference ranges and published clinical outcomes are lacking.

METHODS

In our retrospective analysis, we evaluated demographics, laboratory, and clinical outcomes of adult patients referred to an academic hematology practice for evaluation of neutropenia from 2010 to 2018. Primary and secondary outcomes included incidence of hematologic disorders and rates of Duffy-null positivity by race, respectively. In a separate analysis, we reviewed absolute neutrophil count (ANC) reference ranges from publicly available Association of American Medical Colleges Medical School Member laboratory directories to assess institutional variations.

RESULTS

In total, 163 patients were included, with disproportionate number of Black patients referred compared to local demographics. Twenty-three percent of patients (n = 38) were found to have a clinically relevant hematologic outcome (mean ANC of 0.59 × 10 /L), and only six were identified with ANC ≥1.0 × 10 /L. Incidence of hematologic outcomes was lowest among Black patients (p = .05), and nearly all Blacks who underwent Duffy-null phenotype testing were positive (93%), compared to 50% of Whites (p = .04). In separate review of laboratory directories, we confirmed wide variation in ANC lower limit of normal (0.91-2.40 × 10 /L).

CONCLUSION

Hematologic disorders were rare in patients with mild neutropenia and among Blacks, highlighting the need to standardize hematological ranges representative of non-White communities.

摘要

背景

无症状性中性粒细胞减少症是一种常见的血液学转诊病症,但缺乏标准化的参考范围和已发表的临床结果。

方法

在我们的回顾性分析中,我们评估了 2010 年至 2018 年期间因中性粒细胞减少症到学术血液科就诊的成年患者的人口统计学、实验室和临床结果。主要和次要结局分别为血液系统疾病的发生率和按种族划分的 Duffy 阴性率。在另一项分析中,我们查阅了美国医师协会医学学校成员实验室目录中公开提供的协会的绝对中性粒细胞计数(ANC)参考范围,以评估机构间的差异。

结果

共有 163 名患者入组,其中黑人患者的转诊比例不成比例,与当地人口统计学数据相比。23%的患者(n=38)发现有临床相关的血液学结果(平均 ANC 为 0.59×10/L),只有 6 名患者 ANC≥1.0×10/L。血液学结果的发生率在黑人中最低(p=0.05),几乎所有接受 Duffy 阴性表型检测的黑人都是阳性(93%),而白人的阳性率为 50%(p=0.04)。在对实验室目录的单独审查中,我们证实 ANC 正常下限存在广泛差异(0.91-2.40×10/L)。

结论

在轻度中性粒细胞减少症患者和黑人中,血液系统疾病很少见,这突出表明需要标准化代表非白人社区的血液学范围。