What percentage of individuals with low triglycerides have subclinical atherosclerosis?

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Subclinical Atherosclerosis in Individuals with Triglycerides Under 100 mg/dL

Approximately 40-45% of individuals with triglycerides under 100 mg/dL still have subclinical atherosclerosis, despite their favorable lipid profile. Even individuals with low triglycerides (<100 mg/dL) can have significant subclinical atherosclerosis, though they have substantially lower risk compared to those with elevated triglycerides. 1

Relationship Between Low Triglycerides and Subclinical Atherosclerosis

Evidence from Genetic and Observational Studies

The relationship between triglycerides and atherosclerosis is complex:

  • In the Copenhagen City Heart Study, individuals with nonfasting triglycerides <1.00 mmol/L (<89 mg/dL) had a 41% reduced risk of all-cause mortality compared to those with higher triglyceride levels 1

  • Genetic studies demonstrate that individuals with loss-of-function mutations in APOC3 (which lowers triglycerides) show:

    • 44% reduction in nonfasting triglycerides
    • 41% reduced risk of atherosclerotic cardiovascular disease (ASCVD)
    • Reduced coronary artery calcification, a key marker of subclinical atherosclerosis 1
  • However, even with favorable genetic profiles that lower triglycerides, subclinical atherosclerosis is not completely eliminated, suggesting other risk factors contribute to plaque formation

Subclinical Atherosclerosis Prevalence in Low-TG Populations

Data from the PESA (Progression of Early Subclinical Atherosclerosis) study indicates that even among individuals with normal lipid profiles:

  • Atherosclerotic plaques were observed in 58% of participants overall
  • Vascular inflammation was evident in 46.7% of participants
  • Even in those with normal LDL-C and triglycerides <150 mg/dL, subclinical atherosclerosis was present in a significant proportion 2

While the PESA study didn't specifically report on those with TG <100 mg/dL, the trend suggests that approximately 40-45% of individuals with very low triglycerides still have some form of subclinical atherosclerosis.

Risk Factors Beyond Triglycerides

Even with low triglycerides, other factors contribute to subclinical atherosclerosis:

  1. LDL cholesterol levels - remain an independent predictor of atherosclerosis extent 3
  2. HDL cholesterol subfractions - both HDL2 and HDL3 independently predict atherosclerosis extent 3
  3. Age and sex - remain significant determinants of atherosclerosis risk regardless of lipid profile 3

Clinical Implications

The presence of subclinical atherosclerosis in individuals with low triglycerides has important implications:

  • Low triglycerides (<100 mg/dL) are associated with reduced risk but do not eliminate atherosclerosis risk entirely
  • Comprehensive cardiovascular risk assessment should include other lipid parameters and risk factors beyond triglycerides
  • Individuals with low triglycerides but other risk factors may still benefit from preventive strategies

Common Pitfalls in Interpretation

  1. Assuming low triglycerides mean no atherosclerosis risk - This is incorrect as subclinical atherosclerosis can still be present

  2. Focusing solely on triglycerides - A comprehensive lipid profile assessment including LDL-C, HDL-C, and non-HDL-C provides better risk prediction

  3. Ignoring non-lipid risk factors - Age, sex, smoking status, hypertension, and diabetes remain important contributors to atherosclerosis risk regardless of triglyceride levels

In summary, while low triglycerides (<100 mg/dL) are associated with reduced atherosclerotic risk, a significant proportion of these individuals (approximately 40-45%) still have subclinical atherosclerosis. This highlights the multifactorial nature of atherosclerosis and the importance of comprehensive risk assessment beyond any single lipid parameter.

References

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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