Department of Children's Diseases and Pediatric Surgery, I.Horbachevsky Ternopil National Medical University, Ternopil, Ukraine.
Clinic of Pediatric Immunology and Rheumatology, Western Ukrainian Specialized Children's Medical Centre, Lviv, Ukraine.
Front Immunol. 2024 Jun 28;15:1428724. doi: 10.3389/fimmu.2024.1428724. eCollection 2024.
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.
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.
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.
Improvements in diagnosis, including prenatal screening, newborn screening, monitoring, and expanding treatment options, will lead to better outcomes for NBS patients.
尼曼匹克氏症候群(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 在斯拉夫人群中最为普遍,包括乌克兰。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、免疫参数和治疗情况。
我们进行了一项回顾性研究,纳入了 1999 年至 2023 年间在乌克兰不同地区诊断出的 84 名 NBS 患者。我们利用乌克兰 NBS 登记处的数据和通过开发的问卷从治疗医生那里获得的信息进行了分析。
84 名 NBS 患者中,55 名(65.5%)存活,25 名(29.8%)死亡,4 名失访。患者的中位年龄为 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%),尽管近年来,来自中部和东南部地区的诊断病例有所增加,这扩大了我们对 NBS 患病率的认识。每年诊断出的患者数量平均为 3.4 例,近年来从 2.7 例增加到 4.8 例。1999 年至 2007 年,NBS 的中位诊断年龄为 4.0 岁(范围 0.1-16 岁),而在过去 6 年中降至 2.7 岁。大多数儿童在十岁之前都有发育迟缓的情况。所有儿童都经历过感染,41.3%的儿童有反复感染。严重感染是 12%患者死亡的原因。NBS 的第二大常见临床表现是恶性肿瘤(37.5%),其中淋巴瘤的患病率最高(63.3%)。恶性肿瘤是 NBS 患者死亡的最常见原因(72%的病例)。89.6%的患者观察到 CD4+和 CD19+水平下降,其次是 CD3+(81.8%)和 CD8+(62.5%)下降。NK 细胞水平升高至 62.5%。72.9%的患者 IgG 浓度下降,56.3%的患者 IgA 浓度下降。58.7%的患者接受了免疫球蛋白替代治疗。定期进行免疫球蛋白替代治疗有助于减少严重呼吸道感染的频率和严重程度。
改善诊断方法,包括产前筛查、新生儿筛查、监测和扩大治疗选择,将为 NBS 患者带来更好的预后。