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本文引用的文献

1
Clinical Spectrum Associated with Wolfram Syndrome Type 1 and Type 2: A Review on Genotype-Phenotype Correlations.Wolfram 综合征 1 型和 2 型的临床特征:基因型-表型相关性综述。
Int J Environ Res Public Health. 2021 Apr 30;18(9):4796. doi: 10.3390/ijerph18094796.
2
Current Landscape of Treatments for Wolfram Syndrome.沃尔姆综合征治疗现状。
Trends Pharmacol Sci. 2019 Oct;40(10):711-714. doi: 10.1016/j.tips.2019.07.011. Epub 2019 Aug 13.
3
Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations.意大利人群中的沃勒姆综合征 1:基因型-表型相关性。
Pediatr Res. 2020 Feb;87(3):456-462. doi: 10.1038/s41390-019-0487-4. Epub 2019 Jul 2.
4
Activation of GLP-1 receptor signalling alleviates cellular stresses and improves beta cell function in a mouse model of Wolfram syndrome.GLP-1 受体信号激活可减轻沃勒氏综合征小鼠模型中的细胞应激并改善β细胞功能。
Diabetologia. 2018 Oct;61(10):2189-2201. doi: 10.1007/s00125-018-4679-y. Epub 2018 Jul 28.
5
Preventive treatment with liraglutide protects against development of glucose intolerance in a rat model of Wolfram syndrome.利拉鲁肽预防性治疗可预防沃尔弗拉姆综合征大鼠模型葡萄糖不耐受的发展。
Sci Rep. 2018 Jul 5;8(1):10183. doi: 10.1038/s41598-018-28314-z.
6
Longitudinal hearing loss in Wolfram syndrome.Wolfram 综合征的纵向听力损失。
Orphanet J Rare Dis. 2018 Jun 27;13(1):102. doi: 10.1186/s13023-018-0852-0.
7
Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease.Wolfram 综合征 1 的遗传和临床方面,一种严重的神经退行性疾病。
Pediatr Res. 2018 May;83(5):921-929. doi: 10.1038/pr.2018.17. Epub 2018 Feb 28.
8
Clinical utility gene card for: Wolfram syndrome.Wolfram综合征的临床应用基因卡片
Eur J Hum Genet. 2016 Nov;24(11). doi: 10.1038/ejhg.2016.49. Epub 2016 May 25.
9
Wolfram Syndrome: Diagnosis, Management, and Treatment.沃夫勒姆综合征:诊断、管理与治疗
Curr Diab Rep. 2016 Jan;16(1):6. doi: 10.1007/s11892-015-0702-6.
10
Selective cognitive and psychiatric manifestations in Wolfram Syndrome.沃夫勒姆综合征的选择性认知和精神症状
Orphanet J Rare Dis. 2015 May 30;10:66. doi: 10.1186/s13023-015-0282-1.

沃尔夫拉明综合征 1 患者队列的临床特征。

Clinical Peculiarities in a Cohort of Patients with Wolfram Syndrome 1.

机构信息

Department of Human Pathology in Adult and Developmental Age "Gaetano Barresi", University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy.

Unit of Pediatric Nephrology and Dialysis, Department of Human Pathology in Adult and Developmental Age "Gaetano Barresi", University of Messina, 98125 Messina, Italy.

出版信息

Int J Environ Res Public Health. 2022 Jan 4;19(1):520. doi: 10.3390/ijerph19010520.

DOI:10.3390/ijerph19010520
PMID:35010780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8744633/
Abstract

Wolfram syndrome 1 is a rare, autosomal recessive, neurodegenerative, progressive disorder. Insulin-dependent, non-autoimmune diabetes mellitus and bilateral progressive optic atrophy are both sensitive and specific criteria for clinical diagnosis. The leading cause of death is central respiratory failure resulting from brainstem atrophy. We describe the clinical features of fourteen patients from seven different families followed in our Diabetes Center. The mean age at Wolfram syndrome 1 diagnosis was 12.4 years. Diabetes mellitus was the first clinical manifestation, in all patients. Sensorineural hearing impairment and central diabetes insipidus were present in 85.7% of patients. Other endocrine findings included hypogonadotropic hypogonadism (7.1%), hypergonadotropic hypogonadism (7.1%), and Hashimoto's thyroiditis (21.4%). Neuropsychiatric disorders were detected in 35.7% of patients, and urogenital tract abnormalities were present in 21.4%. Finally, heart diseases were found in 14.2% of patients. Eight patients (57.1%) died at the mean age of 27.3 years. The most common cause of death was respiratory failure which occurred in six patients. The remaining two died due to end-stage renal failure and myocardial infarction. Our data are superimposable with those reported in the literature in terms of mean age of onset, the clinical course of the disease, and causes of death. The frequency of deafness and diabetes insipidus was higher in our patients. The incidence of urogenital diseases was lower although it led to the death of one patient. Long-term follow-up studies including large patient cohorts are necessary to establish potential genotype-phenotype correlation in order to personalize the most suitable clinical approach for each patient.

摘要

沃尔弗拉姆综合征 1 是一种罕见的常染色体隐性、神经退行性、进行性疾病。胰岛素依赖型、非自身免疫性糖尿病和双侧进行性视神经萎缩均为临床诊断的敏感和特异性标准。导致死亡的主要原因是由于脑干萎缩导致的中枢性呼吸衰竭。我们描述了在我们的糖尿病中心随访的七个不同家庭的 14 名患者的临床特征。沃尔弗拉姆综合征 1 的平均诊断年龄为 12.4 岁。糖尿病是所有患者的首发临床表现。85.7%的患者存在感音神经性听力损失和中枢性尿崩症。其他内分泌发现包括促性腺激素低下性性腺功能减退症(7.1%)、促性腺激素过多性性腺功能减退症(7.1%)和桥本甲状腺炎(21.4%)。35.7%的患者检测到神经精神障碍,21.4%的患者存在泌尿生殖道异常。最后,14.2%的患者存在心脏病。8 名患者(57.1%)在平均 27.3 岁时死亡。最常见的死亡原因是呼吸衰竭,有 6 名患者发生。其余两名患者死于终末期肾衰竭和心肌梗死。我们的数据在发病年龄、疾病的临床过程和死亡原因方面与文献报道的相似。我们的患者中耳聋和尿崩症的发生率更高。泌尿生殖系统疾病的发生率较低,但导致一名患者死亡。需要进行长期的随访研究,包括大型患者队列,以确定潜在的基因型-表型相关性,从而为每位患者制定最合适的个性化临床治疗方案。