Lower neutrophil count without clinical consequence among children of African ancestry living with HIV in Canada

Isabelle Bernard, D. Ransy, Jason Brophy, Fatima Kakkar, Ari Bitnun, Laura Sauvé, L. Samson, Stanley Read, Hugo Soudeyns, Michael T Hawkes
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Abstract

To investigate the association between African ancestry and neutrophil counts among children living with HIV (CLWH). We also examined whether medications, clinical conditions, hospitalization, or HIV virologic control were associated with low neutrophil counts or African ancestry. We conducted a secondary analysis of the Early Pediatric Initiation Canada Child Cure Cohort (EPIC4) Study, a multicenter prospective cohort study of CLWH across eight Canadian pediatric HIV care centers. We classified CLWH according to African ancestry, defined as “African,” “Caribbean” or “Black” maternal race. Longitudinal laboratory data (white blood cells (WBCs), neutrophils, lymphocytes, viral load, CD4 count) and clinical data (hospitalizations, AIDS-defining conditions, treatments) were abstracted from medical records. Among 217 CLWH (median age 14, 55% female), 145 were of African ancestry and 72 were of non-African ancestry. African ancestry was associated with lower neutrophil counts, WBC counts, and neutrophil-lymphocyte ratios. Neutrophil count<1.5×109/L was detected in 60% of CLWH of African ancestry, compared to 31% of CLWH of non-African ancestry (p<0.0001), representing a 2.0-fold higher relative frequency (95% CI 1.4-2.9). Neutrophil count was on average 0.74×109/L (95%CI 0.45-1.0) lower in CLWH of African ancestry (p<0.0001). Neither neutrophil count<1.5×109/L nor African ancestry was associated with medications, hospitalizations, AIDS-defining conditions, or markers of virologic control (viral load, sustained viral suppression, lifetime nadir CD4). In CLWH, African ancestry is associated with lower neutrophil counts, without clinical consequences. A flexible evaluation of neutrophil counts in CLWH of African ancestry may avoid unnecessary interventions.
在加拿大感染艾滋病毒的非洲裔儿童中,中性粒细胞计数较低却没有临床后果
研究非洲血统与艾滋病病毒感染儿童(CLWH)中性粒细胞计数之间的关系。我们还研究了药物、临床状况、住院治疗或艾滋病病毒学控制是否与中性粒细胞计数低或非洲血统有关。 我们对加拿大儿童早期起始治疗队列(EPIC4)研究进行了二次分析,该研究是一项针对加拿大八家儿科艾滋病护理中心的CLWH的多中心前瞻性队列研究。 我们根据非洲血统对 CLWH 进行了分类,定义为 "非洲"、"加勒比海 "或 "黑人 "母亲种族。我们从医疗记录中抽取了纵向实验室数据(白细胞、中性粒细胞、淋巴细胞、病毒载量、CD4计数)和临床数据(住院、艾滋病定义病症、治疗)。 在 217 名 CLWH(中位年龄为 14 岁,55% 为女性)中,145 人为非洲血统,72 人为非非洲血统。非洲血统与中性粒细胞计数、白细胞计数和中性粒细胞-淋巴细胞比率较低有关。在 60% 的非洲血统 CLWH 中检测到中性粒细胞计数<1.5×109/L,而在 31% 的非非洲血统 CLWH 中检测到中性粒细胞计数<1.5×109/L(p<0.0001),相对频率高出 2.0 倍(95% CI 1.4-2.9)。非洲血统的 CLWH 中性粒细胞计数平均低 0.74×109/L(95%CI 0.45-1.0)(p<0.0001)。中性粒细胞计数<1.5×109/L或非洲血统均与用药、住院、艾滋病定义病症或病毒控制指标(病毒载量、持续病毒抑制、终生最低CD4)无关。 在慢性淋巴细胞白血病患者中,非洲血统与较低的中性粒细胞计数有关,但不会产生临床后果。对有非洲血统的 CLWH 患者的中性粒细胞计数进行灵活评估可避免不必要的干预。
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