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Lifetime risk for developing dyslipidemia: the Framingham Offspring Study
Mark R Cobain1, Michael J Pencina, Ralph B D'Agostino
1Department of Mathematics/Statistics and Biostatistics, Boston University, Boston, Mass, USA.
Insights
The lifetime risk of developing dyslipidemia is substantial, with most individuals developing high LDL or low HDL cholesterol over time. These risks significantly exceed previous prevalence estimates.
Area of Science:
- Cardiovascular Health
- Lipid Metabolism
- Preventive Medicine
Background:
- High serum low-density lipoprotein (LDL) cholesterol and low high-density lipoprotein (HDL) cholesterol are significant vascular risk factors.
- National surveys show high prevalence of borderline-high LDL (40%) and low HDL (13-34%) in the US.
- The lifetime risk of developing dyslipidemia remains largely unknown.
Purpose of the Study:
- To estimate the 10- to 30-year long-term risks of developing borderline-high LDL, high LDL, and low HDL cholesterol.
- To analyze these risks across different age groups and sexes.
- To assess risks considering baseline dyslipidemia prevalence.
Main Methods:
- Analysis of 4701 Framingham Offspring Study participants with at least two examinations between 1971 and 2000.
- Sex-specific risk estimations for age groups 30-54 years.
- Calculation of risks conditional on survival without dyslipidemia and accounting for baseline prevalence.
Main Results:
- Over 30 years, 60% developed borderline-high LDL, 40% developed high LDL, and 20-40% developed low HDL.
- Adjusted 30-year risks reached 80% for borderline-high LDL, 50% for high LDL, and 25-65% for low HDL.
- 20-50% had or developed both low HDL and high LDL; 30-year risks approximate lifetime risk for 50-year-olds.
Conclusions:
- Long-term risks for developing dyslipidemia are substantial in both men and women.
- These risks considerably surpass prevalence estimates derived from cross-sectional surveys.
- Individuals face a high likelihood of developing abnormal lipid profiles over their lifespan.
Background:
High serum low-density lipoprotein(LDL) cholesterol and low high-density lipoprotein (HDL) cholesterol are major vascular risk factors. National surveys indicate that 40% of individuals in the United States have borderline-high LDL cholesterol, and 13-34% have low HDL. The lifetime risk of developing dyslipidemia is unknown, however.
Methods:
We estimated the 10- to 30-year long-term risks of developing "borderline-high" LDL cholesterol (> or =130 mg/dL [3.4 mmol/L]), "high" LDL cholesterol (> or =160 mg/dL [4.1 mmol/L]) and "low" HDL cholesterol (<40 mg/dL [1.0 mmol/L]) in 4701 Framingham Offspring Study participants (53% women) who attended at least 2 examinations between 1971 and 2000. We performed sex-specific analyses (for age groups 30-34, 40-44, 50-54 years), and estimated risks conditional on surviving without the lipid abnormality up to the baseline age. We also estimated risks accounting for baseline prevalence of dyslipidemia (elevated LDL, low HDL).
Results:
Over a 30-year period, approximately 6 of 10 participants developed borderline-high LDL, 4 of 10 people developed high LDL, and 2 (women) to 4 (men) of 10 individuals developed low HDL levels; estimates were generally similar for different age groups. Adjustment for baseline prevalence of dyslipidemia increased these estimates: 30-year risks exceeded 80% for borderline-high LDL, 50% for high LDL, and 25% (women) to 65% (men) for low HDL; 20-50% had or developed a low HDL along with a high LDL level. The 30-year estimates approximate the lifetime risk in 50-year-olds.
Conclusions:
The long term risks of developing dyslipidemia are substantial in both sexes, and considerably exceed prevalence estimates from cross-sectional surveys.
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