100%

And that paper is only really discussing CAC

Not other risks like how Lp(a) contributes to calcification of the aortic valve, leading to aortic stenosis, or thrombosis formation risks.

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How would you diagnose the “calcification of the aortic valve”? Wouldn’t that show up in a CAC scan? So “discussing CAC” should cover that, no? What am I missing?

I ask, because I’ve had very high LDL all my life (and ApoB, as measured more recently), and also aky high Lp(a). I’ve only been on a low dose atorvastatin (10mg/day) for a little over five years. Yet, I had a CAC scan at age 65, and the score was zero. Of course I might have a lot of soft plaque. But the point being, is if we are talking about atherosclerosis impacted by Lp(a), how else would you discuss it other than in the context of CAC or angiogram.

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Good question: I looked into it a bit more and the answer is hopefully yes, but perhaps not it seems:

4o:

When radiologists interpret a CAC scan (or any cardiac CT), their primary task is to evaluate coronary calcification. However, they should also examine the aortic valve for calcifications. In the past, incidental valve calcium was often underreported - mild calcification might be overlooked or simply not mentioned in the official report . The focus used to be on coronary arteries, and unless the valve calcification was very pronounced, it might not make it into the summary.

Today, there is growing awareness that aortic valve calcification is clinically important. Consensus recommendations now urge radiologists to report any significant aortic valve calcification seen on routine chest CT scans (including CAC scans) . The British Society of Cardiovascular Imaging, for example, recommends that whenever the heart is visible on a CT (even one done for non-cardiac reasons), the reader should note calcifications in the coronary arteries and aortic valve . On a CAC scan report, a radiologist may add a line such as “Aortic valve calcification present” and often will qualitatively describe it (e.g. “mild,” “moderate,” or “severe”). There isn’t usually a numeric score given for the valve in routine practice, but if the calcification is heavy, some centers might quantify it or at least flag it.

(The general point that Lp(a) is risky for other reasons that normal arterial plack is still my main point)

Interesting. This is a quote from my December 2023 CAC scan at UCLA:

"FINDINGS:

Coronary artery calcification present in 0 vessels and the total CAC score is 0. The calcium score for each vessel is as follows:

Left main = 0

Left anterior descending = 0

Left circumflex = 0

Right coronary artery = 0

The ascending aorta measures 29 mm, which is normal. No aortic valve leaflet calcifications. No atherosclerotic calcifications of the partially visualized thoracic aorta."

I take the sentence: “No aortic valve leaflet calcifications.” to mean that they did in fact look for calcifications of the aortic valve.

If that is so, then it seems that Lp(a) impact on the aortic valve calcification can be assessed through a CAC scan.

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Something is very off about the communication about the KETO-CTA study, it’s the regular old bias probably, in this case bias that is expected to get people killed.

Didn’t report the primary outcome in the study:

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From Ethan Weiss (non-ideological keto dieter)

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https://x.com/ethanjweiss/status/1909686881425801227#m

It all just stinks ideology, having a conclusion and making the data fit it, I don’t mean this study but ALL data that exists on apoB and ASCVD progression. Missing the forest for the trees, not knowing, ignoring, or not understanding EXPECTED VALUE and reasoning under uncertainty.

But sure, plaque progression in metabolically healthy keto dieters is the same or WORSE than unhealthy cohorts (like Weiss pointed out), and much more disturbing at >100 CAC. What’s prevention of ASCVD? Where’s the reporting of the primary outcome as mentioned on ClinicalTrials.gov?

It’s pretty disturbing from an expected value perspective, but whatever.

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My question is, what would I do differently if I got a bad score?
The answer is nothing.
Being in the lower-the-lipids camp, I am already acting like I got a bad score.
I take atorvastatin and Brillo EZ. All of my lipids are in the low range except for HDL.

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CAC/CTCA can be helpful evidence to support insurance coverage, particularly of PCSK9-inhibitors, which can’t be sourced from India. Otherwise, agreed, if you’re already urgently lowering lipids and a positive scan won’t change your strategy, probably not much value.

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Can’t you monitor soft plaque progression with CTCA? Genuinely curious.

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Yes. Also could decide to intervene with stents or other surgery based on it.

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But I haven’t heard about anyone measuring efficacy of therapy or otherwise based on routine monitoring with CTCA. I’m thinking of e.g the case of someone who is still developing plaque at a low apoB and might e.g decide to lower it even further.

Like 99% have positive CAC eventually so might be important to be ahead on this.

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Arresting the primary cause of death.

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If you get +18mm3 over 1 year - no points!

I’m interested to know what you know about this.

I’ve considered getting the CLEERLY but I consulted with my soon to be ex cardiologist and my future cardiologist and they both told me that they don’t do preventative stents unless their patient is having symptoms. ?

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LMHR 7 times higher than a non-diabetic patient (2.5 mm3 vs. 18.8 mm3) and half the progression as in diabetic patients (18.8 mm3 vs. 31.2 mm3).

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You don’t have to get a stent to have the CTCA. My sister just got 2 of them done and they found some blockage, but said it wasn’t much so they let her go. People do them for the Cleerly all the time just because they want to know. I nearly did, but could not find out the rate of adverse events for a CTCA in a healthy person. I’m sure it depends on the skill of the team and of course I live in the sticks.

Also there are companies that do it without a doctors order. It’s about $500 here. Probably if the doc orders it for you then it’s covered, but the Cleerly isn’t and it’s more like $1200 here

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It would probably be whatever the rate of adverse events is for the contrast agent, which is typically iodine. Also the radiation dose. I doubt there’s anything specific to a CTCA regarding adverse events otherwise.

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I don’t know much about this, but a quick search shows

The primary endpoint of target vessel failure at 2 years (composite of death from cardiac causes, target vessel myocardial infarction [TV-MI], ischemia-driven target-vessel revascularization [ID-TLR], or hospitalization for unstable or progressive angina) for PCI + OMT vs. OMT alone, was: 0.4% vs. 3.4% (hazard ratio [HR] 0.11, 95% confidence interval [CI] 0.03-0.36, p = 0.0003).

Target vessel failure at 7 years: 6.5% vs. 9.4% (HR 0.54, 95% CI 0.33-0.87, p = 0.0097)

Key secondary outcomes for PCI + OMT vs. OMT:

  • All-cause mortality at 2 years: 0.5% vs. 1.3%, p > 0.05
  • All-cause mortality at 7 years: 5.2% vs. 7.4%, p > 0.05
  • All MI at 2 years: 1.1% vs. 1.7%, p > 0.05
  • All MI at 7 years: 2.4% vs. 3.5%, p > 0.05
  • ID-TLR at 2 years: 0.1% vs. 2.4%, p < 0.05
  • ID-TLR at 7 years: 4.9% vs. 8.0%, p < 0.05
  • All-cause mortality or TV-MI at 2 years: 0.6% vs. 1.9%, p < 0.05
  • All-cause mortality or TV-MI at 7 years: 6.2% vs. 8.6%, p > 0.05

These HRs and comparisons seem quite impressive.

The results of this trial suggest that PCI of focal non-FFR-positive plaques that are angiographically >50% and have evidence of vulnerability on intravascular imaging (preventive PCI) along with OMT is superior to OMT for clinical outcomes at 2 years among patients with predominantly SIHD

Symptoms was not one of the inclusion criteria.

Seems like the cardiologists you spoke to are out of date? Or perhaps they meant they refer out preventative work?

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I nearly did, but could not find out the rate of adverse events for a CTCA in a healthy person. I’m sure it depends on the skill of the team and of course I live in the sticks.

The tech on my CTCA messed up the first IV so I had two bruised veins instead of one. I guess that’s an adverse event.

Also need to take a heart rate lowering drug typically, like Metropolol, so add that in for adverse events.

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I was pretty excited by CT angiograms, until I dug deeper. While great accuracy is claimed, in fact when it comes to smaller blockages it can easily miss them. High cost and some associated risks with mediocre reliability of results - false negatives can happen (and false positives). So on balance, I passed.

Now maybe the CLEERLY protocol gives superior confidence, but I have not looked into it. I’m waiting for further progress in this space before I am tempted to dive in. YMMV.

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