A major scientific breakthrough has raised fresh hope for improved treatment and prevention of Type 2 diabetes, a condition affecting millions worldwide.
According to new research published in Nature Communications, scientists have identified a gene that plays a central role in the development of Type 2 diabetes. Experts say the discovery could pave the way for more effective and targeted therapies in the future.
The study highlights the role of the SMOC1 gene in the pancreas, where blood glucose regulation occurs. Researchers found that abnormal activity of this gene alters insulin-producing cells, disrupting the body’s ability to regulate glucose levels.
In people with Type 2 diabetes, insulin-producing beta cells gradually lose their normal function. Instead of producing insulin, they begin acting like alpha cells, which release glucagon. This shift leads to higher blood sugar levels and worsens disease symptoms.
The hormone adrenomedullin disrupts insulin signaling in blood vessel cells, contributing to systemic insulin resistance in obesity-associated type 2 diabetes, according to a Science study from earlier this year in mice.
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In healthy individuals, beta cells and alpha cells work together to maintain blood glucose homeostasis. Beta cells release insulin to lower glucose levels, while alpha cells release glucagon when blood sugar drops. In Type 2 diabetes, this balance is disrupted, leading to insulin deficiency and hyperglucagonemia.
Researchers argue that understanding this change in cellular identity is critical. By targeting the SMOC1 gene, future treatments may be able to restore normal beta-cell function rather than only managing symptoms.
Experts believe this discovery marks an important step toward addressing the root causes of Type 2 diabetes. While further research is needed, the findings offer renewed optimism for developing therapies that could significantly improve patients’ quality of life.