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Association of Accelerated Phenotypic Aging, Genetic Risk, and Lifestyle with Progression of Type 2 Diabetes: A Prospective Study Using Multi-State Model

BMC medicine
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Lulu Pan, Yahang Liu, Chen Huang, Yifang Huang, Ruilang Lin, Kecheng Wei, Ye Yao, Guoyou Qin, Yongfu Yu

In a significant advancement in medical research, scientists from Fudan University have published a study that establishes a connection between accelerated biological aging and the progression of Type 2 Diabetes (T2D). This research transcends traditional markers of chronological age, examining how biological age, genetic predispositions, and lifestyle choices can impact diabetes outcomes.

Key Findings

  • Phenotypic Age Acceleration (PhenoAgeAccel): Individuals exhibiting higher PhenoAgeAccel are biologically older than their chronological age, which increases their risk of developing T2D and associated complications.

  • Genetic Risk and Lifestyle: Those with a high genetic risk and unhealthy lifestyle face significantly greater chances of T2D progression.

  • Mortality Rates: The study identified a strong link between accelerated aging and increased mortality among T2D patients.

"Being biologically older was associated with increased risks of transitions from baseline to T2D and even to diabetic complications," the study noted.

Why It Matters

Type 2 Diabetes presents a global health challenge, affecting approximately 500 million people worldwide. Understanding the complex factors contributing to its progression is essential for developing effective prevention and treatment strategies. Insights from this study into biological aging could transform how T2D is managed, paving the way for tailored interventions that account for an individual's biological age rather than solely their chronological age.

Research Details

This prospective cohort study utilized data from the UK Biobank, involving 376,083 adults who were initially free of T2D. Researchers employed PhenoAgeAccel, a novel metric based on nine clinical biomarkers, to assess biological aging. These biomarkers include albumin, creatinine, and glucose levels, among others.

The study utilized a multi-state model to monitor transitions from baseline to T2D, as well as from T2D to complications and mortality. With a median follow-up of 13.7 years, researchers observed 17,615 new T2D cases, with 4,524 developing further complications, and 28,373 deaths.

"PhenoAgeAccel was consistently associated with an increased risk of all transitions in T2D progression," the researchers emphasized.

Looking Ahead

The implications of this study are significant, suggesting that PhenoAgeAccel could be integrated with genetic risk assessments to identify individuals at higher risk for T2D earlier. This approach could lead to more personalized healthcare solutions, where interventions are customized not only to genetic risk but also to an individual's biological aging profile.

Additionally, the study highlights the importance of lifestyle choices in managing T2D risks. As the global burden of diabetes continues to rise, these findings could inform public health strategies that promote healthy living to mitigate both biological aging and genetic risks.

In conclusion, this groundbreaking study enhances our understanding of T2D progression and offers a potential roadmap for more effective, individualized care. As we delve deeper into the intersections of aging, genetics, and lifestyle, such research will be crucial in shaping the future of diabetes management.


By unraveling the complex relationship between biological age and diabetes, this research opens new avenues for medical science, encouraging further exploration and innovation in the pursuit of improved health outcomes worldwide.

Longevity