(Sep. 19, 2012) — Could a capsule of insulin
crystals a day stop the development of type 1 diabetes? There are
indications that this could be the case. In the international TrialNet
study, which follows relatives of individuals with type 1 diabetes,
researchers are investigating whether oral insulin could prevent or
delay the disease.
Type 1 diabetes is the autoimmune form of diabetes, in which the
patients' insulin-producing beta cells are destroyed by their own immune
system. "We know that if a person has two autoantibodies and one of
them is against insulin, there is a 50 per cent risk that they will
develop type 1 diabetes within five years. It doesn't matter how old you
are," says Åke Lernmark, Professor of Experimental Diabetes Research at
Lund University in Sweden.
"There are indications that oral insulin may prevent or delay the
clinical onset of type 1 diabetes among individuals with autoantibodies
against insulin, who are thus in the risk zone," says Åke Lernmark, who
will be initiating and coordinating the Swedish TrialNet study.
Åke Lernmark refers to a study presented earlier in the year by
American and Canadian researchers. In the study, which ran from 1994 to
2003, participants with relatives who had type 1 diabetes and at least
two autoantibodies, one of which against insulin, took either oral
insulin or placebo capsules containing an inactive substance. At first,
the results were a disappointment. Just as many people in the treatment
group became ill as in the placebo group.
"However, the subsequent analyses showed something different. Among
those who had high levels of insulin autoantibodies at the start of the
study, the oral insulin had an effect and the development of type 1
diabetes was delayed. The delaying effect lasted for as long as the
participants took the insulin," says Åke Lernmark, adding that those who
are now being recruited for the Swedish TrialNet study with oral
insulin also have high levels of autoantibodies against insulin.
No one knows how oral insulin might stop type 1 diabetes. However,
Åke Lernmark believes a possible explanation could be that the immune
system becomes accustomed to the low daily doses of insulin in the
gastrointestinal tract. The insulin is not perceived as a foreign
substance to be rejected by the immune system.
This line of reasoning is the same as for desensitisation for
allergies, in which the dose of the substance that provokes the allergy
is gradually increased.
The oral insulin study will run for several years and is open to all
those who meet the requirements and are aged between 3 and 45.
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