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奈梅亨断裂综合征:乌克兰 25 年诊断和治疗经验

英文原题:Nijmegen breakage syndrome: 25-year experience of diagnosis and treatment in Ukraine.

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Nijmegen breakage syndrome: 25-year experience of diagnosis and treatment in Ukraine.

PubMed 2024/06/28(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

研究概要

诊断方面的改进,包括产前筛查、新生儿筛查、监测以及不断扩大的治疗选择,将为NBS患者带来更好的结局。

研究思路结论见上方概要

奈梅亨断裂综合征(NBS)是一种常染色体隐性遗传病,以小头畸形、免疫缺陷和DNA修复受损为特征。NBS在包括乌克兰在内的斯拉夫人群中最为流行。我们的研究旨在全面评估乌克兰NBS患者的患病率、诊断、临床数据、免疫学参数和治疗情况。

我们进行了一项回顾性综述,纳入1999-2023年确诊的来自乌克兰不同地区的84例NBS患者。分析使用了乌克兰NBS登记处的数据以及通过制定的问卷从治疗医师处获得的信息。

在84例NBS患者中,55例(65.5%)存活,25例(29.8%)死亡,4例失访。患者中位年龄为11岁,范围为1至34岁。大多数患者来自乌克兰西部地区(57.8%),但近年来来自中部和东南部地区的诊断有所增加,扩展了我们对NBS患病率的认识。每年诊断患者数平均为3.4例,近年来从2.7例增加至4.8例。1999-2007年NBS诊断中位年龄为4.0岁(范围0.1-16),过去6年降至2.7岁。大多数儿童在十岁之前出现体格发育迟缓。所有儿童均经历过感染,其中41.3%有反复感染。严重感染是12%患者的死亡原因。NBS第二常见的临床表现是恶性肿瘤(37.5%),以淋巴瘤为主(63.3%)。恶性肿瘤一直是NBS患者最常见的死亡原因(占72%)。89.6%的患者观察到CD4+和CD19+水平降低,其次是CD3+(81.8%)和CD8+(62.5%)减少。NK细胞水平升高占62.5%。IgG浓度降低占72.9%,IgA降低占56.3%。58.7%的患者接受了免疫球蛋白替代治疗。定期免疫球蛋白替代治疗有助于减少严重呼吸道感染的发生频率和严重程度。

展开英文摘要原文

INTRODUCTION: Nijmegen breakage syndrome (NBS) is an autosomal recessive disorder, characterized by microcephaly, immunodeficiency, and impaired DNA repair. NBS is most prevalent among Slavic populations, including Ukraine. Our study aimed to comprehensively assess the prevalence, diagnosis, clinical data, immunological parameters, and treatment of NBS patients in Ukraine. METHODS: We conducted a retrospective review that included 84 NBS patients from different regions of Ukraine who were diagnosed in 1999-2023. Data from the Ukrainian Registry of NBS and information from treating physicians, obtained using a developed questionnaire, were utilized for analysis. RESULTS: Among 84 NBS patients, 55 (65.5%) were alive, 25 (29.8%) deceased, and 4 were lost to follow-up. The median age of patients was 11 years, ranging from 1 to 34 years. Most patients originate from western regions of Ukraine (57.8%), although in recent years, there has been an increase in diagnoses from central and southeastern regions, expanding our knowledge of NBS prevalence. The number of diagnosed patients per year averaged 3.4 and increased from 2.7 to 4.8 in recent years. The median age of NBS diagnosis was 4.0 years (range 0.1-16) in 1999-2007 and decreased to 2.7 in the past 6 years. Delayed physical development was observed in the majority of children up to the age of ten years. All children experienced infections, and 41.3% of them had recurrent infections. Severe infections were the cause of death in 12%. The second most common clinical manifestation of NBS was malignancies (37.5%), with the prevalence of lymphomas (63.3%). Malignancies have been the most common cause of death in NBS patients (72% of cases). Decreased levels of CD4+ and CD19+ were observed in 89.6%, followed by a reduction of CD3+ (81.8%) and CD8+ (62.5%). The level of NK cells was elevated at 62.5%. IgG concentration was decreased in 72.9%, and IgA - in 56.3%. Immunoglobulin replacement therapy was administered to 58.7% of patients. Regular immunoglobulin replacement therapy has helped reduce the frequency and severity of severe respiratory tract infections. CONCLUSION: Improvements in diagnosis, including prenatal screening, newborn screening, monitoring, and expanding treatment options, will lead to better outcomes for NBS patients.

论文信息

作者
Boyarchuk O、Kostyuchenko L、Akopyan H、Bondarenko A、Volokha A、Hilfanova A、Savchak I、Nazarenko L
第一作者单位
Department of Children's Diseases and Pediatric Surgery, I.Horbachevsky Ternopil National Medical University, Ternopil, Ukraine.Ukraine
通讯作者单位
Department of the Research and Biotechnology, Scientific Medical Genetic Center LeoGENE, Lviv, Ukraine.Ukraine
期刊
Frontiers in immunology2024
原文标识
PubMed 39007137 · DOI 10.3389/fimmu.2024.1428724