Suppr超能文献

巴特综合征中性粒细胞减少症:特征、风险和管理。

Neutropenia in Barth syndrome: characteristics, risks, and management.

机构信息

NHS Specialised Services Barth Syndrome Service, Royal Hospital for Children.

School of Cellular and Molecular Medicine, University of Bristol, Bristol, UK.

出版信息

Curr Opin Hematol. 2019 Jan;26(1):6-15. doi: 10.1097/MOH.0000000000000472.

Abstract

PURPOSE OF REVIEW

Barth syndrome (BTHS) is an X-linked disease characterized by defective remodeling of phospholipid side chains in mitochondrial membranes. Major features include neutropenia, dilated cardiomyopathy, motor delay and proximal myopathy, feeding problems, and constitutional growth delay. We conducted this review of neutropenia in BTHS to aid in the diagnosis of this disease, and to improve understanding of both the consequences of neutropenia and the benefits of treatment with granulocyte colony-stimulating factor (G-CSF).

RECENT FINDINGS

In 88 patients with BTHS, neutropenia, that is, at least one count below 1.5 × 10/l, was detected in 74 (84%) and 44% had severe chronic neutropenia, with multiple counts below 0.5 × 10/l. The pattern of neutropenia varied between intermittent and unpredictable, chronic and severe, or cyclical with mathematically regular oscillations. Monocytosis, that is, monocytes more than 1.0 × 10/l, was observed at least once in 64 of 85 (75%) patients. G-CSF was administered to 39 of 88 patients (44%). Weekly average G-CSF doses ranged from 0.12 to 10.92 μg/kg/day (mean 1.16 μg/kg/day, median 1.16 μg/kg/day). Antibiotic prophylaxis was additionally employed in 21 of 26 neutropenic patients. Pretreatment bone marrow evaluations predominantly showed reduced myeloid maturation which normalized on G-CSF therapy in seven of 13 examined. Consistent clinical improvement, with reduced signs and symptoms of infections, was observed in response to prophylactic G-CSF ± prophylactic antibiotics. However, despite G-CSF and antibiotics, one adult patient died with multiple infections related to indwelling medical devices and gastrostomy site infection after 15.5 years on G-CSF and a pediatric patient required gastrostomy removal for recurrent abdominal wall cellulitis.

SUMMARY

BTHS should be considered in any men with neutropenia accompanied by any of the characteristic features of this syndrome. Prophylaxis with G-CSF ± antibiotics prevents serious bacterial infections in the more severe neutropenic patients although infections remain a threat even in patients who are very compliant with therapy, especially in those with indwelling devices.

摘要

目的综述

巴特综合征(BTHS)是一种 X 连锁疾病,其特征是线粒体膜中磷脂侧链的重塑缺陷。主要特征包括中性粒细胞减少症、扩张型心肌病、运动发育迟缓及近端肌病、喂养问题和生长发育迟缓。我们对 BTHS 中的中性粒细胞减少症进行了综述,以帮助诊断这种疾病,并更好地了解中性粒细胞减少症的后果和粒细胞集落刺激因子(G-CSF)治疗的益处。

最近的发现

在 88 例 BTHS 患者中,74 例(84%)检测到中性粒细胞减少症,即至少一次计数低于 1.5×10/l,44%存在严重慢性中性粒细胞减少症,多次计数低于 0.5×10/l。中性粒细胞减少症的模式在间歇性和不可预测性、慢性和严重性、或周期性且具有数学规律的波动之间变化。85 例患者中至少有 64 例(75%)观察到单核细胞增多症,即单核细胞超过 1.0×10/l。88 例患者中有 39 例(44%)接受了 G-CSF 治疗。每周平均 G-CSF 剂量范围为 0.12 至 10.92μg/kg/天(平均 1.16μg/kg/天,中位数 1.16μg/kg/天)。26 例中性粒细胞减少症患者中有 21 例还接受了抗生素预防治疗。21 例患者中有 13 例进行了预处理骨髓评估,主要表现为骨髓粒细胞成熟减少,其中 7 例在 G-CSF 治疗后恢复正常。预防性 G-CSF±预防性抗生素治疗后,观察到一致的临床改善,感染症状和体征减少。然而,尽管使用了 G-CSF 和抗生素,一名成年患者在接受 G-CSF 治疗 15.5 年后,因留置医疗设备和胃造口部位感染导致多重感染死亡,一名儿科患者因反复腹壁蜂窝织炎而需要胃造口管移除。

总结

任何伴有中性粒细胞减少症和巴特综合征特征的男性都应考虑巴特综合征。G-CSF±抗生素预防可预防严重的细菌感染,但即使在非常依从治疗的患者中,感染仍然是一个威胁,尤其是在有留置设备的患者中。

相似文献

2
Barth syndrome.巴特综合征。
Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23.

引用本文的文献

5
Tafazzin regulates neutrophil maturation and inflammatory response.tafazzin调节中性粒细胞成熟和炎症反应。
EMBO Rep. 2025 Mar;26(6):1590-1619. doi: 10.1038/s44319-025-00393-w. Epub 2025 Feb 17.
6
The metabolic basis of inherited neutropenias.遗传性中性粒细胞减少症的代谢基础。
Br J Haematol. 2024 Jan;204(1):45-55. doi: 10.1111/bjh.19192. Epub 2023 Dec 4.

本文引用的文献

3
New targets for monitoring and therapy in Barth syndrome.巴特综合征监测与治疗的新靶点
Genet Med. 2016 Oct;18(10):1001-10. doi: 10.1038/gim.2015.204. Epub 2016 Feb 4.
7
Clinical laboratory studies in Barth Syndrome.巴思综合征的临床实验室研究。
Mol Genet Metab. 2014 Jun;112(2):143-7. doi: 10.1016/j.ymgme.2014.03.007. Epub 2014 Mar 30.
9
Barth syndrome.巴特综合征。
Orphanet J Rare Dis. 2013 Feb 12;8:23. doi: 10.1186/1750-1172-8-23.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验