A first study on diabetes and the underlying genetic cause confirms the role of certain genes that predispose one to type 1 diabetes.
Highlights:
- The world health organization (WHO) has projected that diabetes is to become the 7th largest reason for deaths by 2030; this indicates the rapid progression of the disease into today’s world.
- Type 1 diabetes (T1D) is an auto immune disease where the insulin producing cells in the body are destroyed by the body’s own cells.
- While the exact cause of the T1D is not understood today, a new study has identified genes that predispose an individual to T1D.
What is Type 1 Diabetes?
T1D is an autoimmune disease where the body’s own cells attack the cells in the pancreas called the islets, which are responsible for producing a chemical called insulin. Insulin allows the body cells to take up sugar, thereby reducing the sugar levels in the bloodstream. In T1D, a sufficient number of insulin producing cells are destroyed which results in very low or no insulin production by the pancreas. This ultimately results in high sugar levels.Symptoms
- Increased urine output
- Extreme thirst
- Fatigue and weight loss
- Constant hunger
Late Onset Type 1 Diabetes
T1D was previously called juvenile or childhood - onset diabetes. This was due to the fact that T1D usually affected children and young adults. In recent years, T1D was also diagnosed in adults above the age of 30; in this case, it is called late onset type 1 diabetes. Theresa May, Prime Minister of UK, was diagnosed with late onset T1D at the age of 56. More often than not people with late onset T1D are misdiagnosed for type 2 diabetes which is more common in adults.Predisposition to late onset T1D is in your genes
In the fist study of its kind, researchers suggest that there are certain genetic alterations in different genes that predispose an individual to develop late onset T1D. This could explain why some people develop T1D at childhood and others well into adulthood.Genes associated with regulation of the immune system in humans are known to be linked to risk of developing T1D. These genes are the DR3 and DR4 alleles of the group of genes called the HLA complex, which regulated the human immune system.
Researchers at the University of Exeter, UK, investigated whether the high risk of T1D that is seen in children with DR3 and DR4 genotypes persists into adulthood.
Every gene has two alleles, one is inherited from each parent.
Example: Allele from mother/Allele from father
The strongest risk factor for late onset T1D is when these two allelic variants (DR3 and DR4) are inherited in pairs.
For example: Homozygous type(2 same alleles): DR3/DR3 or DR4/DR4
Heterozygous type (different alleles): DR3/DR4
The research team analyzed the development of T1D in 120,000 individuals from birth till the age of 60 in individuals who had the highest risk HLA group.The study finding was surprising. It was observed that although the high risk individuals formed only 6.4% of the UK population, the very same individuals contributed to 61% of all cases of type 1 diabetes.
Other key findings
- 71% cases of late onset T1D associated with DR4/DR4 genotype
- 26% cases of late onset T1D was associated with DR3/DR3 genotype
- 40% cases of late onset T1D associated with DR3/DR4
- The average age of diagnosis was highest for DR4/DR4 genotype at age 38, followed by DR3/DR4 at 28 and DR3/DR3 at 17 years of age.
References:
- Type 1 diabetes - (1. http://www.mayoclinic.org/diseases-conditions/type-1-diabetes/home/ovc-20340976)
Source-Medindia