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  LDL cholesterol still a problem in old age? A Mendelian randomization study

Postmus, I., Deelen, J., Sedaghat, S., Trompet, S., de Craen, A. J., Heijmans, B. T., et al. (2015). LDL cholesterol still a problem in old age? A Mendelian randomization study. Int J Epidemiol, 44(2), 604-12. doi:10.1093/ije/dyv031.

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Postmus, I., Author
Deelen, J.1, Author           
Sedaghat, S., Author
Trompet, S., Author
de Craen, A. J., Author
Heijmans, B. T., Author
Franco, O. H., Author
Hofman, A., Author
Dehghan, A., Author
Slagboom, P. E., Author           
Westendorp, R. G., Author
Jukema, J. W., Author
Affiliations:
1Deelen – Genetics and Biomarkers of Human Ageing, Research Groups, Max Planck Institute for Biology of Ageing, Max Planck Society, ou_3394006              

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Free keywords: Adult Age Distribution Aged Aged, 80 and over Cardiovascular Diseases/*genetics/mortality Cholesterol, LDL/*genetics/metabolism Cross-Sectional Studies Female Genetic Predisposition to Disease/genetics Genotype Humans Hypercholesterolemia/*genetics/mortality Longevity/genetics Male Mendelian Randomization Analysis Middle Aged Netherlands/epidemiology Polymorphism, Single Nucleotide/*genetics LDL-cholesterol Mendelian randomization genetic risk score old age
 Abstract: BACKGROUND: Observational studies in older subjects have shown no or inverse associations between cholesterol levels and mortality. However, in old age plasma low-density lipoprotein cholesterol (LDL-C) may not reflect the lifetime level due to reverse causality, and hence the risk may be underestimated. In the current study, we used an LDL genetic risk score (GRS) to overcome this problem. METHODS: A weighted GRS was created using 51 single nucleotide polymorphisms associated with LDL-C levels. The LDL GRS was calculated in three Dutch cohorts: the Leiden Longevity Study (LLS) (n = 3270), the Leiden 85-plus study (n = 316) and the Rotterdam Study (n = 4035). We assessed the association between the LDL GRS and LDL-C levels, chronological age, familial longevity and mortality. RESULTS: Up to 90 years of age, in each age stratum individuals with high LDL GRS had higher LDL-C levels (P = 0.010 to P = 1.1 x 10(-16)). The frequency of LDL-increasing alleles decreased with increasing age [beta = -0.021 (SE = 0.01) per year, P = 0.018]. Moreover, individuals with a genetic predisposition for longevity had significantly lower LDL GRS compared with age-matched individuals of the general population [LLS nonagenarians vs > 90 years: beta = 0.73 (SE = 0.33), P = 0.029, LLS offspring vs partners: beta = 0.66 (SE = 0.23), P = 0.005]. In longitudinal analysis, high GRS was associated with increased all-cause mortality in individuals > 90 years, with a 13% increased risk in individuals with the highest LDL GRS (P-trend = 0.043). CONCLUSION: Results of the current study indicate that a genetic predisposition to high LDL-C levels contributes to mortality throughout life, including in the oldest old, and a beneficial LDL genetic risk profile is associated with familial longevity.

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 Dates: 2015-042015-04-10
 Publication Status: Issued
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 Identifiers: Other: 25855712
DOI: 10.1093/ije/dyv031
ISSN: 1464-3685 (Electronic)0300-5771 (Linking)
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Title: Int J Epidemiol
Source Genre: Journal
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Pages: - Volume / Issue: 44 (2) Sequence Number: - Start / End Page: 604 - 12 Identifier: -