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Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):80-86. doi: 10.1080/21678421.2017.1361444. Epub 2017 Aug 10.

Lack of association between the P413L variant of chromogranin B and ALS risk or age at onset: a meta-analysis.

Yang X1,2, Li S3, Xing D4, Li P4, Li C4, Qi L4, Xu Y2, Ren H1.

Author information

1
a Department of Geriatric Neurology , First Affiliated Hospital of Kunming Medical University , Kunming , Yunan Province , P.R. China.
2
b Department of Neurology , West China Hospital, Sichuan University , Chengdu , Sichuan Province , P.R. China.
3
c Department of Anesthesia , Kunming Xishan District People's Hospital , Kunming , Yunnan Province , P.R. China , and.
4
d Department of Neurology , The Third People's Hospital of Yunnan Province , Kunming , Yunnan Province , P.R. China.

Abstract

BACKGROUND:

Amyotrophic lateral sclerosis (ALS), the most common motor neuron disease, is thought to result from interaction of genetic and environmental risk factors. Whether the potentially functional exonic P413L variant in the chromogranin B gene influences ALS risk and age at onset is controversial.

METHOD:

We meta-analysed or other studies assessing the association between the P413L variant and ALS risk or age at ALS onset indexed in Web of Science, PubMed, Embase, Chinese National Knowledge Infrastructure, Wanfang, and SinoMed databases.

RESULTS:

Five case-control studies were analysed, involving 2639 patients with sporadic ALS, 201 with familial ALS and 3381 controls. No association was detected between risk of either ALS type and the CT + TT genotype or T-allele of the P413L variant. Age at ALS onset was similar between carriers and non-carriers of the T-allele.

CONCLUSION:

The available evidence suggests that the P413L variant of chromogranin B is not associated with ALS risk or age at ALS onset. These results should be validated in large, well-designed studies.

KEYWORDS:

Amyotrophic lateral sclerosis; chromogranin B; genetics; meta-analysis

PMID:
28795874
DOI:
10.1080/21678421.2017.1361444
[Indexed for MEDLINE]

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