Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II

S Ouadghiri1, K El Alaoui Toussi, C Brick

  • 1Unité d'immunologie, service de transfusion sanguine et d'hémovigilance, CHU Ibn-Sina, Rabat, Morocco; UPR d'immunologie, faculté de médecine et de pharmacie de Rabat, université Mohamed V, Souissi, Rabat, Morocco.

Pathologie-Biologie
|July 16, 2013
PubMed
Abstract

Insights

The HLA-DRB1*15 allele is linked to increased multiple sclerosis (MS) risk in the Moroccan population. This genetic marker may play a role in MS susceptibility for this group.

Area of Science:

  • Immunogenetics
  • Neurology
  • Human Genetics

Background:

  • Multiple sclerosis (MS) is an autoimmune CNS disease primarily affecting young adults.
  • The human leukocyte antigen (HLA) class II genes, particularly HLA-DRB1*15, are associated with MS susceptibility across diverse ethnicities.
  • Genetic factors influencing MS risk in specific populations require further investigation.

Purpose of the Study:

  • To determine the frequency of HLA-DRB1* and -DQB1* alleles in the Moroccan population.
  • To assess the association of these HLA alleles with susceptibility to multiple sclerosis in Morocco.

Main Methods:

  • Case-control study comparing 57 Moroccan MS patients with 172 healthy controls.
  • HLA class II (DRB1* and DQB1*) typing using PCR-SSP and/or Luminex (PCR-SSO).
  • Statistical analysis of allelic and haplotypic frequencies, odds ratios (OR), and confidence intervals (CI).

Main Results:

  • A significant elevation in the frequency of the HLA-DRB1*15 allele was observed in MS patients (17.6%) compared to controls (8.4%).
  • The HLA-DRB1*15-DQB1*06 haplotype was also significantly more frequent in Moroccan MS patients (8.8% vs 4.08%).
  • No significant association was found for HLA-DQB1* alleles or the DR15 allele with sex or age at onset.

Conclusions:

  • The HLA-DRB1*15 allele is implicated in the predisposition to multiple sclerosis in the Moroccan population.
  • This study provides the first genetic marker analysis for MS susceptibility in Moroccans.
  • Further validation with larger sample sizes is recommended to confirm these findings.

Related Concept Videos

Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu01:29

Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu

Genetic variations significantly influence drug response through pharmacokinetics, receptor interactions, and biologic milieu modifications. Pharmacokinetic alterations impact drug metabolism and clearance, affecting efficacy and toxicity. Variants in drug-metabolizing enzymes, such as CYP2C9 and CYP2C19, alter drug activation and elimination. For example, CYP2C9 loss-of-function variants require lower warfarin doses to prevent excessive bleeding, while CYP2C19 variants reduce clopidogrel...
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
Genetic Lingo01:11

Genetic Lingo

Overview
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
Principles of Pharmacogenetics: Types of Genetic Variants01:27

Principles of Pharmacogenetics: Types of Genetic Variants

The human genome is over 99.9% identical between individuals, yet genetic differences exist at millions of bases. The human genome contains approximately 3 million variant positions per individual, many of which are heterozygous, contributing to genetic diversity and individual traits. Genetic variations include single-nucleotide polymorphisms (SNPs), insertions, deletions, and copy number variations (CNVs).SNPs, the most common variation, involve single-base changes in DNA. These can be...