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Lower serum CETP levels found in the oldest members of Greek long-lived families (Open Cardiovasc Med J 2018)

Original title: Biomarkers and Gene Polymorphisms in Members of Long- and Short-lived Families: A Longevity Study

Open Cardiovasc Med J · · 6

Kolovou V, Diakoumakou O, Papazafiropoulou AK, Katsiki N, Fragopoulou E, Vasiliadis I, Degiannis D, Duntas L, Antonopoulou S, Kolovou G

Researchers studied 149 Greek individuals from long-lived families (three generations spanning long-lived members aged 90 or older, their offspring, and grandchildren) and short-lived families (two generations where both parents died before age 75), measuring serum CETP and other biomarkers alongside CETP, ADIPOQ, IGFBP3, and ACE gene polymorphisms. Serum CETP was significantly lower in the oldest long-lived members than in their offspring or grandchildren (P = 0.03 for both comparisons), while adiponectin was higher. Across the youngest generations of both family types, individuals with the CETP TaqIB B2B2 genotype had significantly lower serum CETP than B1B1 carriers (P = 0.007), a difference that held after adjusting for age and sex in the oldest and youngest groups (P = 0.004 and 0.007). The authors suggest CETP genotype and serum levels merit further attention as biomarkers relevant to human lifespan.

Read the paper (DOI)PubMed

Original abstract

Background: The influence of biomarkers in human lifespan has been investigated but with no clear results yet.

Materials And Methods: Lipids, Uric Acid (UA), Adiponectin (ADIPOQ), Insulin-like Growth Factor (IGF-1), cholesteryl ester transfer protein (CETP) and angiotensin-converting enzyme (ACE) proteins, as well as CETP, ADIPOQ, insulin-like growth factor binding protein-3 (IGFBP3) and ACE-gene polymorphisms were evaluated in 149 Greek individuals. The Long-Lived Families (LON) (n=84) comprised of 3 generations: long-lived aged ≥90 years (P), offspring (FL1) and their grandchildren (FL2), while the Short-Lived Families (EAD) (n=65) where both parents died <75 years, comprised of 2 generations: middle-aged (FD1) and children (FD2).

Results: Serum CETP and IGF-1 levels were lower, whereas AdipoQ concentrations were higher in P compared with FL1 and FL2 members (CETP: p = 0.03 for both comparisons; IGF-1 p < 0.001 for both comparisons and ADIPOQ: p = 0.001 and p = 0.004, respectively). Furthermore, serum triglycerides, UA and glucose concentrations were higher in FD1 compared with FD2 subjects (p=0.001, 0.02 and ≤0.001, respectively). In FD2 and FL2, CETP levels were lower in individuals with B2B2 compared with B1B1 genotype (p=0.007). Additionally, ACE concentrations were higher in individuals with DD compared with II genotype in both Families (p=0.001). After adjustment for age and gender, CETP levels were lower in P and FL2 individuals with B2B2 compared with the B1B1 genotype (p=0.004 and 0.007, respectively).

Conclusion: Increase serum TGs, UA and GL concentrations were higher in the middle-aged individuals compared with their children in families independently of their lifespan. The serum adiponectin concentration was the highest in the oldest old individuals implying beneficial influence on lifespan. Independently of family's lifespan history, the youngest individuals with CETPB2B2 genotype, compared with individuals with CETPB1B1 genotypes, had lower serum CETP concentrations. The knowledge of the unfavourable gene(s)influencing human lifespan may be helpful in encouraging individuals to follow healthier lifestyle habits and better control their high-risk biomarkers.

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Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.