There's a good paper (METEOR study) in the current JAMA.
http://jama.ama-assn.org/cgi/content/full/297.12.1344
And there's a very perceptive editorial, also.
http://jama.ama-assn.org/cgi/content/full/297.12.1376v1
Abstract:
Context Atherosclerosis is often advanced before symptoms appear and it is
not clear whether treatment is beneficial in middle-aged individuals with a
low Framingham risk score (FRS) and mild to moderate subclinical
atherosclerosis.
Objective To assess whether statin therapy could slow progression and/or
cause regression of carotid intima-media thickness (CIMT) over 2 years.
Design, Setting, and Participants Randomized, double-blind,
placebo-controlled study (Measuring Effects on Intima-Media Thickness: an
Evaluation of Rosuvastatin [METEOR]) of 984 individuals, with either age
(mean, 57 years) as the only coronary heart disease risk factor or a 10-year
FRS of less than 10%, modest CIMT thickening (1.2-<3.5 mm), and elevated LDL
cholesterol (mean, 154 mg/dL); conducted at 61 primary care centers in the
United States and Europe between August 2002 and May 2006.
Intervention Participants received either a 40-mg dose of rosuvastatin or
placebo.
Main Outcome Measures Rate of change in maximum CIMT (assessed with B-mode
ultrasound) for 12 carotid sites; changes in maximum CIMT of the common
carotid artery, carotid bulb, and internal carotid artery sites and in mean
CIMT of the common carotid artery sites. CIMT regression was assessed in the
rosuvastatin group only.
Results Among participants in the rosuvastatin group, the mean (SD)
baseline LDL cholesterol level of 155 (24.1) mg/dL declined to 78 (27.5)
mg/dL, a mean reduction of 49% (P<.001 vs placebo group). The change in
maximum CIMT for the 12 carotid sites was 0.0014 (95% CI, 0.0041 to
0.0014) mm/y for the rosuvastatin group vs 0.0131 (95% CI, 0.0087-0.0174)
mm/y for the placebo group (P<.001). The change in maximum CIMT for the
rosuvastatin group was 0.0038 (95% CI, 0.0064 to 0.0013) mm/y for the
common carotid artery sites (P<.001), 0.0040 (95% CI, 0.0090 to 0.0010)
mm/y for the carotid bulb sites (P<.001), and 0.0039 (95% CI, 0.0009 to
0.0088) mm/y for the internal carotid artery sites (P = .02). The change in
mean CIMT for the rosuvastatin group for the common carotid artery sites was
0.0004 (95% CI, 0.0011 to 0.0019) mm/y (P<.001). All P values are vs
placebo group. Overall, rosuvastatin was well tolerated with infrequent
serious adverse cardiovascular events (6 participants [0.86%] had 8 events
[1.1%] over 2 years).
Conclusions In middle-aged adults with an FRS of less than 10% and evidence
of subclinical atherosclerosis, rosuvastatin resulted in statistically
significant reductions in the rate of progression of maximum CIMT over 2
years vs placebo. Rosuvastatin did not induce disease regression. Larger,
longer-term trials are needed to determine the clinical implications of
these findings.
--
Jim Chinnis Warrenton, Virginia, USA
William Wagner - 26 Mar 2007 21:44 GMT
> There's a good paper (METEOR study) in the current JAMA.
> http://jama.ama-assn.org/cgi/content/full/297.12.1344
[quoted text clipped - 53 lines]
> --
> Jim Chinnis Warrenton, Virginia, USA
...................
>>>And there's a very perceptive editorial, also.
>>> http://jama.ama-assn.org/cgi/content/full/297.12.1376v1
"And finally, where to go from here? Should low-risk individuals undergo
routine arterial imaging followed by statin therapy when evidence of
asymptomatic disease is discovered? On the basis of current evidence,
including the METEOR trial, the answer is clearly no. However, like a
shooting star in the night, the METEOR findings reflect a warning of
problems lurking "out there" in the vast person-time space of the
low-risk population.
Epidemiological data have provided overwhelming evidence that low-risk
populations are the source of most clinical disease.
The METEOR investigators have now provided biological evidence for a
plausible but unproved strategy."
Bill who is looking for the VA Stent vs Drug info to be released. I
heard Tuesday but TV said today due to leaks. Seems investing public
gets info before us users.

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Andrew B. Chung, MD/PhD - 27 Mar 2007 12:00 GMT
> > There's a good paper (METEOR study) in the current JAMA.
> > http://jama.ama-assn.org/cgi/content/full/297.12.1344
[quoted text clipped - 76 lines]
> heard Tuesday but TV said today due to leaks. Seems investing public
> gets info before us users.
Prayerfully in Jesus' ever-lasting love,
Andrew <><
--
Andrew B. Chung, MD/PhD
http://EmoryCardiology.com
May HIS immortal brethren pray for our dying mortal friends and
neighbors:
http://HeartMDPhD.com/Convicts
Especially dear Bob(this one) Pastorio:
http://bobs-amanuensis.livejournal.com/4211.html
http://pics.livejournal.com/bobs_amanuensis/pic/0000z24f/g1
Many in the "low-risk populations" have undiagnosed metabolic syndrome
(MetS).
Folks with MetS are actually high risk and are the real source of most
clinical disease.
May GOD bless you.
Andrew B. Chung, MD/PhD - 27 Mar 2007 14:11 GMT
> There's a good paper (METEOR study) in the current JAMA.
> http://jama.ama-assn.org/cgi/content/full/297.12.1344
[quoted text clipped - 51 lines]
> longer-term trials are needed to determine the clinical implications of
> these findings.
IME, disease regression does not occur until the visceral adipose
tissue (VAT), which is the proximate cause of metabolic syndrome
(MetS) via pro-inflammatory cytokines, is lost.
Prayerfully in Jesus' ever-lasting love,
Andrew <><
--
Andrew B. Chung, MD/PhD
http://EmoryCardiology.com
May HIS immortal brethren pray for our dying mortal friends and
neighbors:
http://HeartMDPhD.com/Convicts
Especially dear Bob(this one) Pastorio:
http://bobs-amanuensis.livejournal.com/4211.html
http://pics.livejournal.com/bobs_amanuensis/pic/0000z24f/g1
eml - 27 Mar 2007 23:23 GMT
On Mar 27, 9:11 am, "Andrew B. Chung, MD/PhD"
<ach...@emorycardiology.com> wrote:
> > There's a good paper (METEOR study) in the current JAMA.
> >http://jama.ama-assn.org/cgi/content/full/297.12.1344
[quoted text clipped - 68 lines]
>
> - Show quoted text -
sounds like such a novel idea--losing weight to reduce VAT vs taking a
pill for one's lifetime...a pill that has so many "pleiotropic
effects" it is studied for its anti-immune and anti cancer effects....
Andrew B. Chung, MD/PhD - 28 Mar 2007 10:02 GMT
> Andrew, in the Holy Spirit, boldly wrote:
> > > There's a good paper (METEOR study) in the current JAMA.
[quoted text clipped - 60 lines]
> pill for one's lifetime...a pill that has so many "pleiotropic
> effects" it is studied for its anti-immune and anti cancer effects....
The 2PD-OMER Approach has been around for nearly 10 years now:
http://HeartMDPhD.com/HolySpirit/overweight.asp
This Approach now even comes with a million dollar guarantee:
http://TruthRUS.org/Guarantee
May GOD bless you.
Prayerfully in Jesus' ever-lasting love,
Andrew <><
--
Andrew B. Chung, MD/PhD
http://EmoryCardiology.com
May HIS immortal brethren pray for our dying mortal friends and
neighbors:
http://HeartMDPhD.com/Convicts
Especially dear Bob(this one) Pastorio:
http://bobs-amanuensis.livejournal.com/4211.html
http://pics.livejournal.com/bobs_amanuensis/pic/0000z24f/g1
As for knowing who are the very elect, these you will know by the
unconditional love they have for everyone including their enemies
(Matthew 5:44-45, 1 Corinthians 13:3, James 2:14-17).
http://HeartMDPhD.com/Love