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Shaun Sabico

Associate Professor

Associate Professor and Deputy Director

Sciences
Chair for Biomarkers of Chronic Diseases, Biochemistry Department, College of Science, KSU

Structured lifestyle modification and biological aging: effects on PhenoAge, sclerostin, and GDF-15 in arab adults with prediabetes

Background:

Lifestyle modification programs (LMP) such as diabetes prevention programs may influence phenotypic aging trajectories, but evidence in Middle Eastern populations remains limited. This study examined the effects of a structured LMP on phenotypic age (PhenoAge) as the primary endpoint and circulating sclerostin (SOST) and growth differentiation factor-15 (GDF-15) as secondary endpoints in a cohort of Arab adults with prediabetes.

Participants and Methods:

In this randomized clinical trial (RCT), a total of 181 adults (130 males, 51 females; mean age 50.8 ± 10.9 years, body mass index, BMI 30.0 ± 4.8 kg/m2) were enrolled. Participants were allocated to either a structured LMP or Control Group (CG) and followed for 6 months. The LMP group was requested to reduce weight by 5%, moderate exercise (150 min/week), reduce fat intake (30%) and increase fiber intake (15g/1 kcal). CG was given brochure. PhenoAge was calculated and assessed alongside anthropometrics, blood biomarkers (HbA1c, fasting glucose, albumin, creatinine, GDF15, SOST), and dietary parameters at baseline and after 6 months.

Results:

Compared with the CG, participants in the lifestyle modification program (LMP) showed a significant reduction in PhenoAge (−4.9 vs. +1.3 years; between-group p < 0.001). Significant between-group improvements were also observed in weight (−5.7 kg), BMI (−2.0 kg/m2), waist circumference (−6.3 cm), and HbA1c (−0.4%; all p < 0.001). Neither GDF-15 nor SOST demonstrated a significant intervention-specific effect.

Conclusion:

A structured lifestyle intervention significantly improved PhenoAge, accompanied by improvements in metabolic parameters in Arab adults with prediabetes. Changes in GDF-15 and SOST appeared time-dependent rather than intervention-specific. These findings support lifestyle modification as a potential strategy to slow a composite clinical measure of biological aging. ClinicalTrial Registration (NCT06440681).

Publisher Name
Frontiers in Aging
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