The research was led by Prof. Leif Groop, of the Lund University Diabetes Centre in Sweden and the Institute for Molecular Medicine Finland in Helsinki.
In the United States alone, around 30.3 million people are living with diabetes.
Excluding gestational diabetes â€” diabetes that develops during pregnancy â€” there are two main types: type 1 and type 2.
In type 1 diabetes, the beta cells of the pancreas â€” which produce insulin, the hormone that regulates blood sugar levels â€” are mistakingly attacked and destroyed by the immune system.
Type 2 diabetes is the most common form, accounting for around 90â€“95 percent of all cases. This occurs when the bodyâ€™s cells stop responding to insulin, or the beta cells are unable to produce sufficient amounts of the hormone.
In both forms of the condition, blood sugar levels can become too high â€” a condition known as hyperglycemia. Unless controlled, this can lead to a number of complications, including kidney disease, cardiovascular disease, and nerve damage.
The heterogeneity of diabetes
A diabetes diagnosis is normally made using the fasting plasma glucose (FPG) test or the A1C test. The FPG test assesses a personâ€™s blood glucose level at a single time point, while the A1C test measures average blood glucose levels over the previous 3 months.
When it comes to determining which type of diabetes a person has, healthcare professionals might look for diabetes-related autoantibodies in the blood. These are proteins produced by the immune system that can attack the bodyâ€™s own cells.
The presence of such autoantibodies is an indicator of type 1 diabetes. If a person does not have these autoantibodies, they are considered to have type 2 diabetes.
â€œDiabetes is a group of chronic metabolic disorders,â€ says Dr. Rob Sladek, of the McGill University and GÃ©nome QuÃ©bec Innovation Centre in Canada, in an editorial linked to the study, â€œthat share the common feature of hyperglycemia, meaning that, in principle, diabetes can be diagnosed via measurement of a single blood component.â€
â€œHowever, elevations in blood glucose can be caused by a number of genetic and acquired factors that reduce the circulating concentrations of insulin or decrease its effectiveness, leading to heterogeneity in the clinical presentation and progression of the disease.â€
Prof. Groop and his team say that a â€œrefined classificationâ€ of diabetes based on its heterogeneity could help healthcare professionals better predict which individuals are most likely to develop complications and allow a more personalized approach to treatment.
In their study, the researchers propose that diabetes should no longer be categorized as two types. Instead, they say that the condition should be classified into five distinct types.
The five â€˜clustersâ€™ of diabetes
The researchers came to their proposal by analyzing the data of four study cohorts. These included a total of 14,775 adults from Sweden and Finland, all of whom had been newly diagnosed with diabetes.
As part of the analysis, the scientists looked at six measures in each subject that each represent different features of diabetes.
These measures were: body mass index (BMI); age at diabetes diagnosis; hemoglobin A1C (HbA1C), a measure of long-term blood sugar control; beta cell functioning; insulin resistance; and the presence of diabetes-related autoantibodies.
As well as conducting genetic analyses of the participants, the researchers also compared their disease progression, complications, and treatment.
The study revealed five distinct forms of diabetes, three of which were severe and two that were mild. The team categorized these as follows:
- Cluster 1: severe autoimmune diabetes (currently known as type 1 diabetes), characterized by insulin deficiency and the presence of autoantibodies. This was identified in 6â€“15 percent of subjects. Cluster 2: severe insulin- deficient diabetes, characterized by younger age, insulin deficiency, and poor metabolic control, but no autoantibodies. This was identified in 9â€“20 percent of subjects.
- Cluster 3: severe insulin-resistant diabetes, characterized by severe insulin resistance and a significantly higher risk of kidney disease. This was identified in 11â€“17 percent of subjects. Cluster 4: mild obesity- related diabetes, most common in obese individuals. This affected 18â€“23 percent of subjects.
- Cluster 5: mild age-related diabetes, most common in elderly individuals. This was the most common form, affecting 39â€“47 percent of subjects.
The researchers note that each of these five types â€œwere also genetically distinct,â€ meaning that there were no genetic mutations that were shared across all five clusters.
A â€˜step toward precision medicineâ€™
When the researchers assessed the treatment received by adults in each of the five clusters, they noticed that some were being treated inappropriately.
As an example, the team points out that just 42 percent of patients in cluster 1 and 29 percent of patients in cluster 2 received insulin therapy from the point of disease onset.
They say that this indicates that the current classifications of diabetes fail to target the underlying features of the disease.
As such, Prof. Groop and colleagues propose that diabetes should be categorized into five distinct types.
While further research is required to refine these five clusters â€” by using biomarkers and genetic risk scores, for example â€” the team believes that this study is a great stride toward tailored treatments for diabetes.
â€œExisting treatment guidelines,â€ concludes Prof. Groop, â€œare limited by the fact they respond to poor metabolic control when it has developed, but do not have the means to predict which patients will need intensified treatment.
â€œThis study moves us towards a more clinically useful diagnosis, and represents an important step towards precision medicine in diabetes.â€
Prof. Leif Groop
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