Literature DB >> 29723869

Genetic Analysis of TREM2 Variants in Tunisian Patients with Alzheimer's Disease.

Zied Landoulsi1, Mouna Ben Djebara1,2, Imen Kacem1,2, Youssef Sidhom1,2, Rym Kefi3, Sonia Abdelhak3, Amina Gargouri-Berrechid1,2, Riadh Gouider1,2.   

Abstract

OBJECTIVE: Rare variants in the TREM2 gene have been reported to significantly increase the risk of Alzheimer's disease in Caucasian populations. Hitherto, this association was not studied in North African populations. In this work, we aimed to study the association between TREM2 exon 2 variants and the risk of late-onset Alzheimer's disease (LOAD) in a Tunisian population. SUBJECTS AND METHODS: We sequenced exon 2 of TREM2 in a Tunisian cohort of 172 LOAD patients and 158 control subjects. We used the Fisher exact test to compare the distribution of allelic frequencies between the two groups.
RESULTS: We identified 4 previously reported nonsynonymous variants (p.Asp39Glu, p.Arg62His, p.Thr96Lys, and p.Val126Gly) and 1 novel synonymous variant (p.Gln109Gln), none of which was significantly associated with the risk of Alzheimer's disease. Moreover, the rare TREM2 variant (p.Arg47His), which was considered to be a risk factor for Alzheimer's disease in European descent populations, was not detected in our cohort.
CONCLUSION: These findings do not support a major role for TREM2 in the pathogenesis of LOAD in the Tunisian population.
© 2018 The Author(s) Published by S. Karger AG, Basel.

Entities:  

Keywords:  Alzheimer’s disease; Case-control study; North-African population; TREM2 gene; Variants

Mesh:

Substances:

Year:  2018        PMID: 29723869      PMCID: PMC6167692          DOI: 10.1159/000489779

Source DB:  PubMed          Journal:  Med Princ Pract        ISSN: 1011-7571            Impact factor:   1.927


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