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神经元蜡样脂褐质沉积症中基因型、表型和组织学之间的相关性:一项个体患者数据荟萃分析

Correlation Among Genotype, Phenotype, and Histology in Neuronal Ceroid Lipofuscinoses: An Individual Patient Data Meta-Analysis.

作者信息

Aungaroon Gewalin, Hallinan Barbara, Jain Puneet, Horn Paul S, Spaeth Christine, Arya Ravindra

机构信息

Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

Division of Neurology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.

出版信息

Pediatr Neurol. 2016 Jul;60:42-48.e4. doi: 10.1016/j.pediatrneurol.2016.03.018. Epub 2016 Apr 8.

Abstract

BACKGROUND

Neuronal ceroid lipofuscinoses (NCL) are heterogeneous neurodegenerative disorders. A better understanding of genotype-phenotype-histology correlation is expected to improve patient care and enhance understanding for phenotypic variability. This meta-analysis studies the correlation of NCL genotypes with clinical phenotypes, ages of onset, and pathologic findings.

METHODS

A structured MEDLINE search was performed using search strings incorporating relevant Medical Subject Headings (MeSH) terms. Studies of NCL patients with genetic, clinical, and histologic data were included. Individual patient data were extracted. Chi-square statistic was used to test the genotype differences in clinical phenotypes and histology. The distribution of age(s) of onset as a function of genotype was explored. Pairwise comparisons were performed with robust analysis of variance.

RESULTS

Sixty-eight studies including a total of 440 individuals with NCL were analyzed. Genetic testing was performed on 395 patients, and a pathologic mutation was identified in 372 of 395 of them. A significant clustering of genotypes into juvenile-onset (only CLN3) and infantile-onset (all others) phenotypes was observed (P < 0.0001). However, the CLN6 genotype showed a bimodal onset and included 14 of 17 subjects with the adult-onset phenotype. The estimated age of onset was respectively lower for subjects with CLN1 mutation (3.01 years, 95% confidence interval [CI] = 2.54 to 3.49) and higher for those with CLN6 mutation (16.33 years, 95% CI = 15.68 to 16.98), compared with other genotypes (P < 0.05 for pairwise comparisons). There was a significant (P < 0.0001) clustering of genotype observed according to the sampled tissue types and electron microscopic findings.

CONCLUSIONS

NCL genotypes significantly differ in terms of ages of onset and clinical phenotypes. There is a distinct segregation of genotypes and electron microscopic findings and high-yield tissue types for pathologic study. This information can possibly facilitate testing and diagnosis in resource-limited settings.

摘要

背景

神经元蜡样脂褐质沉积症(NCL)是一组异质性神经退行性疾病。更好地理解基因型 - 表型 - 组织学之间的相关性有望改善患者护理,并增进对表型变异性的理解。本荟萃分析研究了NCL基因型与临床表型、发病年龄和病理结果之间的相关性。

方法

使用包含相关医学主题词(MeSH)的检索词对MEDLINE进行结构化检索。纳入了具有遗传、临床和组织学数据的NCL患者研究。提取个体患者数据。采用卡方统计检验临床表型和组织学方面的基因型差异。探讨了发病年龄作为基因型函数的分布情况。采用稳健方差分析进行两两比较。

结果

分析了68项研究,共纳入440例NCL患者。对395例患者进行了基因检测,其中395例中有372例鉴定出病理性突变。观察到基因型明显聚集成青少年发病型(仅CLN3)和婴儿发病型(其他所有类型)表型(P < 0.0001)。然而,CLN6基因型表现为双峰发病型,17例成人发病型表型患者中有14例属于该基因型。与其他基因型相比,CLN1突变患者的估计发病年龄较低(3.01岁,95%置信区间[CI] = 2.54至3.49),而CLN6突变患者的估计发病年龄较高(16.33岁,95%CI = 15.68至16.98)(两两比较P < 0.05)。根据采样组织类型和电子显微镜检查结果观察到基因型有显著聚类(P < 0.0001)。

结论

NCL基因型在发病年龄和临床表型方面存在显著差异。基因型与电子显微镜检查结果以及用于病理研究的高产出组织类型之间存在明显的分离。这些信息可能有助于在资源有限的环境中进行检测和诊断。

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