Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

The discussion of the Linus Pauling vitamin C/lysine invention for chronic scurvy

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Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by ofonorow » Sun Mar 04, 2012 4:20 am

Dear Owen,
I was hoping you could you give me some advice on lowering my Lp(a), hs-CRP and Fribrogen? I am 50 years old with a history of CAD, MI when I was 30, Stroke in 2007, two stents placed in RCA in 2010, Hypertension and Hypothyroid. I have Factor V Leiden (heterozygous). I started somewhat following the PT in March 2011. My VAP Lab numbers did improve from Aug 2011 but my Lp(a), hs-CRP and Fribrogen all increased despite some lifestyle changes within the last 6-7 mo’s (lost 30 lbs, cut out trans fats, white flour, sugar, red meat, exercising more).

Here is my meds and supplements:

Losartin 100mg
Metoprolol 100mg
Plavix 75 mg
Ecotrin 81 mg
Levothyroxin 175 mg
Hydrochlorot 25 mg
Crestor 20 mg
Niaspan 1000 mg

Vit C 6-8 g
Lysine 3g
Proline 500mg
Multi-Twin Labs Daily One Cap
Vitamin D3 2000 IU
Magnesium 200 mg
Omega 3 Oil 2000 mg
CoQ10 (ubiquinol) 100 mg
Phytosterol Complex 1800mg
Petadolex 50 mg (been taking about a mo for migranes)

My Last VAP Lab numbers are as follows:
Cholest Total 144 mg/dl
LDL-C direct 81 mg/dl
HDL-C 40 mg/dl
Triglycer 109 mg/dl
Non-HDL-C 104 mg/dl
APO B 77 mg/dl
LDL-P 1406 nmol/L
sdLDL 20 mg/dl
% sdLDL 24 calculated
Apo A-1 140 mg/dl
HDL-P 29.5 umol/L
HDL2 12 mg/dl
Apo B:Apo A 0.55 ratio calculated
Lp(a) mass 94 mg/dl
Lp(a) Choles 11 mg/dl
Hs-CRP 4.3 mg/dl
Fibrinogen 489 mg/dl
Insulin 13
Vit D 51 ng/ml
Homocysteine 10 umol/L

Any help is greatly appreciated! Joe


Drugs worry me. Total cholesterol too low. Probably need more vitamin C just to help detoxify toxic drug load (don't eat grapefruits!) Where are Pauling's vitamins E? A? B-complex? Magnesium might be low.

Not use to Lp(a) being reported that way - but seems to imply large particles, which are usually less atherogenic.
Owen R. Fonorow
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American Scientist's Invention Could Prevent 350,000 Heart Bypass Operations a year

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Mon Mar 05, 2012 8:26 am

Owen,

I don't like the drugs either! Over the past 2 yrs since my stents I've felt lousy (brain fog, dizzy, forgetful). My goals is to get off as many as I can. Cardiologist doesn't seemed concerned about total Choles just wants to get my LDL's below 80. I don't eat
grapefruit. I get my Vit A (10,000 IU as beta carotene & retinyl palmitate), Vit E (100 IU as d-alpha tocopheryl acid succinate) and Vit B from my Multi-Vitamin. I also have other issues with Arthritus & psoriasis(past 10-15 yrs), diverticulitus(since 2009), IBS(since a kid), sinus troubles(most of adult life). Could this all be stemming from inflammation? What direction should I take?

Thanks,
Joe

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Thu Mar 08, 2012 2:56 pm

What does Pauling recommend in the way of Vitamins A, E & B's? Is my Multi vitamin sufficient for these? I am currently taking VC in pill form but I'm considering switching to powder form the next order (hard taking all those pills). Do you think the powder is more absorbable? Right now I'm taking 2g at a time. I'd like to increase this to 3g at a time. Any thoughts on using Nattokinase to reduce CRP and Fibrinogen?

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by ofonorow » Fri Mar 09, 2012 2:11 am

Pauling's recommendations are in his book HOW TO LIVE LONGER AND FEEL BETTER (around page 14). I have also copied them as the foundation of my recommendations,
http://www.practicingmedicinewithoutalicense.com/protocol/

Basics

Vitamin A - 25,000 iu daily
Vitamin E 400 to 800 iu daily
B-complex 1 or 2 daily
Vitamin C 6000 mg to 18000 mg daily
Good multi vitamin/mineral
Drink a lot of water, and reduce sugar intake


I think Pauling did make a mistake by not advocating vitamin D(3), partially because you can get a good supply from exposing the skin to sunlight. (This "mistake" may be why the vitamin D science has advanced without the same debunking other nutrients Pauling recommended have had to endure.)

As far as the Nattokinase enzyme - I personally tend to favor Pauling's orthomolecular approach - start with substances the body has evolved to know and use, such as all the essential vitamins, minerals and amino acids.
Owen R. Fonorow
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American Scientist's Invention Could Prevent 350,000 Heart Bypass Operations a year

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Fri Mar 09, 2012 3:38 am

Should VC be taken on empty stomach or with food?

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by Johnwen » Fri Mar 09, 2012 5:03 am

Not use to Lp(a) being reported that way - but seems to imply large particles, which are usually less atherogenic


Maybe this will help make it clearer.
LPa is high!
More Lysine...

http://www.mayomedicallaboratories.com/ ... tive/89005
To steal ideas from one person is plagiarism. To steal from many is
research!

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Fri Mar 09, 2012 9:31 am

Maybe this will help make it clearer.
LPa is high!
More Lysine...



Johnwen,

Currently taking 3g Lysine. Do I have to increase this slowly? How much do you think? Is that article mentioning a different test of the Lp(a)?

Thanks,
Joe

VanCanada

Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by VanCanada » Sat Mar 10, 2012 12:54 pm


VanCanada

Systemic enzymes are important orthomolecular substances

Post by VanCanada » Sat Mar 10, 2012 1:26 pm

Dr. William Wong, N.D. wrote:Systemic enzymes on the other hand are perfectly safe and free of dangerous side effects. They have no LD-50, or toxic dose. (6)

Reference (6): Enzymes: A Drug of the Future, Prof. Heinrich Wrba MD and Otto Pecher MD. Published 1993 Eco Med.

-quoted from: http://www.totalityofbeing.com/FramelessPages/Articles/WhatAreSystemicEnzymes.htm
Dr. William Wong, N.D. wrote:For at least the last 40 years most of us have been taking vitamin and mineral supplements and have been doing and feeling somewhat better. Almost daily now there is more and more information on the function of some nutrient and on its place in the overall scheme of health.

But I've got a question! If these nutrients fill their allotted functions then why don't they seem to work the same for everyone? In other words, they seem to help some folks and not to work at all in others! Is there some underlying thing that allows these nutrient substances to perform their actions? Are vitamins, minerals and herbs the do all end all of attaining wellness or, are they the bricks and cement that must be placed on a solid foundation before they can take up their tasks solidly?

Let's redefine some terms. In 1913, Dr. Funk discovered nutritional substances he called "Vital Amines" or Vitamins for short. Without getting into biochemistry it turns out that vitamins are not amines but coenzymes, substances that help enzymes to work. An enzyme is a huge protein that speeds up chemical reactions. Without enzymes, chemical reactions would happen so slowly that life would not be able to exist at all. The human body has some 3000+ enzymes and over 7000 enzymic reactions...

Most folks think of enzymes as being involved only in digestion. This is among the last things that enzymes do. Of all the enzymes in the body, the protein cleaving (or cutting-eating) ones are the most important. These have 4 primary actions, they:

1. Reduce inflammation
2. Balance the repair mechanism and prevent fibrosis, (the buildup of scar tissue)
3. Clean the blood
4. Modulate the immune system

Folks who do not experience the beneficial reactions expected from their coenzymes (vitamins) possibly don't have the enzymes that the coenzyme is supposed to help! The human body produces a finite amount of enzymes. From the age of 27 on, that enzyme production begins to wane. Dr. Max Wolf, an MD with 7 other Ph.D.'s after his name, researched enzymes and hormones at Columbia University from the 1930's through the 1960's. He found that round about 27 most folks stop making as many enzymes as they used to and that this event started the cycle of aging. In physiology we are taught that old age begins at 27! ...
(edit)
... When we only take vitamins, minerals and herbs, as important as they are, we are skirting around the outside of the essentials for health. If we just take supplements and not replace the enzymes we are wasting a good bit of money, expectation and time...

-quoted from http://www.totalityofbeing.com/FramelessPages/EssentialsPage.htm

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by Johnwen » Sun Mar 11, 2012 4:47 am

To steal ideas from one person is plagiarism. To steal from many is
research!

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Sun Mar 11, 2012 11:57 am


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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Sun Mar 11, 2012 12:14 pm

Regarding nattokinase, here are links to a podcast and to an online article.

(1) MP3 - WWCR Show #151 (Feb. 19, 2011) by Dr. William Wong, N.D. (For the nattokinase information, listen from the 7th minute and 50th second mark to the 10th minute and 52nd second mark. To hear a beautifully expressed rant from the good doctor, listen from the beginning.) MP3 file size = 13.6 MB

To paraphrase the most relevant bits of that podcast:
Nattokinase has no feedback mechanism like other enzymes do. The blood-thinning effect of nattokinase can go too far. Serrapeptase is a safer enzyme to use than nattokinase is.

Direct download link: http://www.naturalhealthpodcasts.com/Po ... 9_2011.mp3





Thank You Van! Nice Podcast! I will research systemic enzyme's and serrapeptase.

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Re: Age 50, history of CAD, MI, Stroke - Lp(a) increasing on PT

Post by JoMo145 » Fri Mar 23, 2012 4:14 am



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