New Study in Older Light — lower CVD may be due to lower triglycerides

The new study[1] that I mentioned in an article last week indicates that those with a genetic predisposition to having lower LDL cholesterol and systolic blood pressure have a lower lifetime risk of cardiovascular disease (CVD), but what the study doesn’t mention was that research published last year[2] found that people with the low LDL variant also having a genetic predisposition to lower levels of triglycerides. This begs the question as to whether it is really the lower LDL that lowers the lifetime risk of CVD, or the lower triglycerides or both.

*Note: special thanks to George Henderson (@puddleg) from Auckland, New Zealand for bringing this earlier study to my attention.

That is, it could very well be that perceived benefit of having a genetically lower LDL reported in this new study is actually due to the same people also having a genetic predisposition to having lower levels of triglycerides!

In a large-scale study published in 2018 [2], researchers analyzed data from several hundred thousand individuals. First they estimated associations from summary genetic data from more than 670, 000 people from 9 different European databases. Then they analyzed individual-level genetic data from >390 000 people and looked at the associations of naturally occurring genetic variation coding for lipoprotein lipase (LPL) inhibitors with cardiovascular and metabolic health outcomes. Researchers found that a subset of subjects with a genetic variant to lower LDL-cholesterol levels also had a genetic predisposition to lower triglyceride levels and the group that had both had the lowest odds of coronary artery disease [2]. This 2018 study [2] raises the issue as to whether the results of the current study [1] referred to in last week’s article really indicates that genetically lower LDL levels along with lower systolic blood pressure are responsible for lower rates of lower cardiovascular disease, or whether the lower rates of CVD are due to these same people also having genetically lower levels of triglycerides, (or perhaps a combination of both).

The Risk of Higher Triglycerides

A 2016 study published in the Journal of Circulation [3] examined the health risks associated with high levels of triglycerides in those with CVD. Researchers analyzed data from a large-scale study conducted in Israel (Bezafibrate Infarction Prevention (BIP) trial) which followed > 15,300 people with heart disease for a period of 22 years. At the start of the study, participants had their cholesterol and triglyceride levels measured, as well as other health markers. Based on fasting triglyceride levels, subjects were divided into 5 groups, ranging from low triglyceride levels to extremely high triglyceride levels.

Note: Triglycerides below 150 mg/dL (1.70 mmol/L) are considered normal, whereas triglycerides over 200 mg/dL (2.5 mmol/L) are considered high.

After more than two decades of follow-up, researchers found that compared to subjects with low triglycerides, those with the highest triglyceride levels (> 500 mg/dL / 5.6 mmol/L) had almost a 70% greater risk of death over the 22 year period. In fact, even with subjects with triglycerides of 100 to 149 mg/dL (1.13 – 1.68 mmol/L) the elevated risk of death was detected over subjects with lower triglycerides levels (<100 mg/dl / 1.12 mmol/L).

Evidence is emerging that plasma triglycerides represent a causal risk factor for CVD and that genetic variants in a least 6 genes that modulate plasma triglyceride levels have been linked to CVD [4-12].

Using a research method called multivariable Mendelian randomization, researchers are able to group study subjects based on their genetic markers, so they are naturally randomized.  Using this method, researchers are able to separate the effects on CVD associated with triglycerides from those associated with LDL [13]. It has been found that the effect of genetic variations involving triglyceride increases the risk of CVD independently of LDL concentration.

A 2016 review article [14] postulates that the risk factors surrounding increased plasma triglyceride concentration may involve the metabolism of lipoproteins that carry triglycerides in the blood, and that it could lie in a variant gene that encode for the enzyme lipoprotein lipase (which breaks down triglycerides), or for a gene that encodes for regulators of lipoprotein lipase [14].

Final Thoughts

It’s interesting to study whether those with a genetic predisposition to having lower LDL cholesterol have lower lifetime relative risk of cardiovascular events [1], but further study is needed to factor in the subset of subjects that also have a genetic predisposition to lower triglyceride levels, as well as a genetic variant to lower LDL.

More Info?

If you have been diagnosed as having “high cholesterol” and want to know how a low carbohydrate diet may help,  you can learn more about the services I provide under the Services tab or in the Shop. If you have questions, please feel free to send me a note using the Contact Me form above.
To your good health!

 

Joy

 

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References

  1. Ference BA, Bhatt DL, Catapano AL et al, Association of Genetic Variants Related to Combined Exposure to Lower Low-Density Lipoproteins and Lower Systolic Blood Pressure With Lifetime Risk of Cardiovascular Disease, JAMA. 2019 Sep 2. doi: 10.1001/jama.2019.14120. [Epub ahead of print]
  2. Lotta LA, Stewart ID, Sharp SJ, et al, Association of Genetically Enhanced Lipoprotein Lipase–Mediated Lipolysis and Low-Density Lipoprotein
    Cholesterol–Lowering Alleles With Risk of Coronary Disease
    and Type 2 Diabetes, JAMA Cardiology, 2018;3(10):957-966. doi:10.1001/jamacardio.2018.2866
  3. Klempfner R, Erez A, Ben-Zekry S et al, Elevated Triglyceride Level Is Independently Associated With Increased All-Cause Mortality in Patients With Established Coronary Heart Disease, Circulation: Cardiovascular Quality and Outcomes Vol 9(2), 2016, p 100-108, https://doi.org/10.1161/CIRCOUTCOMES.115.002104
  4. Voight BF, Peloso GM, Orho-Melander M, et al. Plasma HDL cholesterol and risk of myocardial infarction: a Mendelian randomisation study.
    Lancet. 2012;380:572–580. doi: 10.1016/S0140-6736(12)60312-2.
  5. Triglyceride Coronary Disease Genetics Consortium and Emerging
    Risk Factors Collaboration, Sarwar N, Sandhu MS, Ricketts SL, et al.
    Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies. Lancet. 2010;375:1634–1639.
  6.  Jørgensen AB, Frikke-Schmidt R, West AS, Grande P, Nordestgaard
    BG, Tybjærg-Hansen A. Genetically elevated non-fasting triglycerides
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  8. Pollin TI, Damcott CM, Shen H, Ott SH, Shelton J, Horenstein RB,
    Post W, McLenithan JC, Bielak LF, Peyser PA, Mitchell BD, Miller M,
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  9. TG and HDL Working Group of the Exome Sequencing Project, National
    Heart, Lung, and Blood Institute, Crosby J, Peloso GM, Auer PL, et al Loss-of-function mutations in APOC3, triglycerides, and coronary disease. N Engl J Med. 2014;371:22–31.
  10. Jørgensen AB, Frikke-Schmidt R, Nordestgaard BG, Tybjærg-Hansen A.
    Loss-of-function mutations in APOC3 and risk of ischemic vascular disease. N Engl J Med. 2014;371:32–41. doi: 10.1056/NEJMoa1308027.
  11. Folsom AR, Peacock JM, Demerath E, Boerwinkle E. Variation in
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