However, this failed to produce patterns that made biological sense.
Most patients diagnosed with type 2 diabetes are treated with a "one-size-fits-all" protocol that is not tailored to each person custom infusion set physiology and may leave many cases inadequately managed.The previous research attempted to define more subtypes of type 2 diabetes based on indicators such as beta-cell function, insulin resistance, or body-mass index, but those traits can vary greatly through life and during the course of the disease. "We need a more granular approach that addresses the many different molecular processes leading to high blood sugar.A new study by scientists at Harvard University indicated that inherited genetic changes may underlie the variability observed among patients in the clinic, with several pathophysiological processes potentially leading to high blood sugar and its resulting consequences.Researchers then applied for a "soft-clustering" approach known as Bayesian non-negative matrix factorization, which allows each variant to fall into more than one cluster."The clusters from our study seem to recapitulate what we observe in clinical practice," said Florez.Turns out, the study of all genes at the DNA, mRNA, and proteome levels, as well as the cellular or tissue level or simply the Genomic study can help cure type 2 diabetes. They found nearly a third of patients scored highly for only one predominant cluster, suggesting that their diabetes may be driven predominantly by a single biological mechanism. However, this failed to produce patterns that made biological sense. Inherited genetic differences are present at birth, and so a more reliable method would be to create subtypes based on DNA variations that have been associated with diabetes risk in large-scale genetic studies. The other three clusters contain DNA variants related to insulin resistance, including one cluster mediated by obesity, one defined by disrupted metabolism of fats in the liver, and one driven by defects in the distribution of fat within the body, known as lipodystrophy.When they next analysed measurements of diabetes-related traits from high-scoring subjects, they saw patterns that strongly reflected the suspected biological mechanism and distinguished them from all other patients with type 2 diabetes - for example, patients who fell into the obesity-mediated cluster were indeed found to have increased body-mass # index and body fat percentage."It is known that type 2 diabetes can be broadly grouped into cases driven either by the inability of pancreatic beta cells to make enough insulin, known as insulin deficiency, or by the inability of liver, muscle or fat tissues to use insulin properly, known as insulin resistance. These variations can be grouped into clusters based on how they impact diabetes-related traits; for example, genetic changes linked to high triglyceride levels are likely to work through the same biological processes.Related StoriesFitness, physical activity can lower risk of type 2 diabetesEating walnuts may halve type 2 diabetes risk: StudyAir pollution increases risk of type 2 diabetes, says study.The work performed as the first step towards using genetics to identify subtypes of type 2 diabetes, which could help physicians prescribe interventions aimed at the cause of the disease, rather than just the symptoms.To further test whether each cluster had been assigned the correct biological mechanism, the researchers gathered data from four independent cohorts of patients with type 2 diabetes and first calculated the patients' individual genetic risk scores for each cluster."When treating type 2 diabetes, we have a dozen or so medications we can use, but after you start someone on the standard algorithm, it's primarily trial and error," said senior author Jose Florez."The findings appeared in the Journal of PLOS Medicine. Two of these clusters contain variants that suggest beta cells aren't working properly, but that differ in their impacts on levels of the insulin precursor, proinsulin. For example, people who scored high on the lipodystrophy-like cluster were likely to be thinner than average but have insulin-resistant diabetes, similar to a rare type of diabetes in which fat accumulates in the liver, which is a fundamentally different process from insulin resistance that results from obesity. "Now we need to determine whether these clusters translate to differences in disease progression, complications, and response to treatment.Genomic study may help cure diabetes.The results appeared to reflect some of the diversity observed by endocrinologists in the clinic.The new work revealed five clusters of genetic variants distinguished by distinct underlying cellular processes, within the existing major divisions of insulin-resistant and insulin-deficient disease.To confirm these observations, the team analysed data for biology and disease research.Early efforts to do so using a "hard-clustering" approach, in which each genetic variation was assigned to only one cluster."The soft-clustering method is better for studying complex diseases, in which.Representational Image.By analysing genomic data with a computational tool that incorporates genetic complexity, the researchers identified five distinct groups of DNA sites that appear to drive distinct forms of the illness in unique ways. They found that the genes contained in the clusters were more active in the tissue types one would expect.The results appeared to reflect some of the diversity observed by endocrinologists in the clinic
برچسب: ،