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英格兰1b型糖原贮积病的自然病史:一项多中心调查。

The natural history of glycogen storage disease type Ib in England: A multisite survey.

作者信息

Halligan Rebecca, White Fiona J, Schwahn Bernd, Stepien Karolina M, Kamarus Jaman Nazreen, McSweeney Mel, Kitchen Steve, Gribben Joanna, Dawson Charlotte, Lewis Katherine, Cregeen David, Mundy Helen, Santra Saikat

机构信息

Inherited Metabolic Disorders Birmingham Children's Hospital Birmingham UK.

Inherited Metabolic Diseases Evelina London Children's Hospital London UK.

出版信息

JIMD Rep. 2021 Jan 24;59(1):52-59. doi: 10.1002/jmd2.12200. eCollection 2021 May.

Abstract

Glycogen storage disease type Ib (GSDIb) is characterized by hepatomegaly and fasting hypoglycaemia as well as neutropaenia and recurrent infections. We conducted a retrospective observational study on a cohort of patients with GSDIb across England. A total of 35 patients, with a median age of 9.1 years (range 1-39 years), were included in the study. We examined the genotype and phenotype of all patients and reported 14 novel alleles. The phenotype of GSDIb in England involves a short fasting tolerance that extends into adulthood and a high prevalence of gastrointestinal symptoms. Growth is difficult to manage and neutropaenia and recurrent infections persist throughout life. Liver transplantation was performed in nine patients, which normalized fasting tolerance but did not correct neutropaenia. This is the first natural history study on the cohort of GSDIb patients in England.

摘要

I型糖原贮积病(GSDIb)的特征为肝肿大、空腹低血糖、中性粒细胞减少和反复感染。我们对英国一组GSDIb患者进行了一项回顾性观察研究。共有35例患者纳入研究,中位年龄为9.1岁(范围1 - 39岁)。我们检查了所有患者的基因型和表型,并报告了14个新的等位基因。英国GSDIb的表型包括成年期仍存在的短时间空腹耐受力以及胃肠道症状的高发生率。生长难以控制,中性粒细胞减少和反复感染终生持续。9例患者接受了肝移植,这使空腹耐受力恢复正常,但未纠正中性粒细胞减少。这是英国关于GSDIb患者队列的第一项自然史研究。

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