Type 1 Diabetes (T1D) is an autoimmune disease where inflammation
in the Pancreas resulted in certain cells in the immune system attacking beta pancreatic
cells that secrete insulin. The damaged, failing beta cells could not produce
enough insulin, resulting in insulin deficiency.
An increasing body of research demonstrated that the
bacteria in our gut (microbiota) can influence our immune system and
inflammation status.
A small human study compared the microbial composition in
relation to blood glucose level of T1D versus healthy non-diabetic children. researchers
found that the ‘good bacteria’, Bacteroidetes, decreases significantly as blood
glucose level increases while The ‘bad
bacteria’, Clostridium, increases significantly as blood glucose level
increases in diabetic children. Healthy children have significantly more Bacteroidetes.
“At the genus level, we found a significant increase in the
number of Clostridium, Bacteroides and Veillonella and a significant decrease
in the number of Lactobacillus, Bifidobacterium, Blautia coccoides/Eubacterium
rectale group and Prevotella in the children with diabetes.” The authors added,
“Moreover, the quantity of bacteria essential to maintain gut integrity was
significantly lower in the children with diabetes than the healthy children.”
Since children with diabetes have a higher level of blood sugar compared to the
healthy group, the researchers suggested the increase of ‘bad bacteria’ may be related
to the glycemic level in the group with diabetes. The study showed Type 1 Diabetes
is associated with compositional changes in gut microbiota. [Maria Isabel
Queipo et al.]
Viruses are associated with T1D as well. In boys, human
parechovirus infection induces a subsequent appearance of diabetes-associated
autoantibodies.
Echovirus 4 and Coxsackie B virus are associated with T1D as
well. The latter may infect and destroy the insulin producing beta-cells in the
pancreas and also damage these cells via indirect autoimmune mechanisms. However,
Coxsackie B3 and B6 viruses were found to be associated with a reduced risk of
such autoimmunity (possibly due to immune cross-protection against Coxsackie B1
virus).
Not all bacteria and viruses within a particular species are
pathogenic. Some are commensal (benign). A Finnish study compared different
strains of Bifidobacteria And found that
children who developed islet autoimmunity and T1D later in life showed
significantly higher responses and have significantly higher autoantibodies against
a bacteria strain, Bifidobacteria adolescentis DSM 20083 proteins .
The researchers pointed out, biochemically detectable autoantibodies
can serve as reliable indicator for T1D development. [I Talja - 2014]
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