Evidence map›Paper›PMID 19932775›Full record

SynthesisThe American journal of cardiology2009

Effects of combination lipid therapy on coronary stenosis progression and clinical cardiovascular events in coronary disease patients with metabolic syndrome: a combined analysis of the Familial Atherosclerosis Treatment Study (FATS), the HDL-Atherosclerosis Treatment Study (HATS), and the Armed Forces Regression Study (AFREGS).

Xue-Qiao Zhao, Richard A Krasuski, Jefferson Baer, Edwin J Whitney, Blazej Neradilek, Alan Chait, Santica Marcovina, John J Albers, B Greg Brown

Abstract readMeta-Analysis
In one paragraph

Synthesis in The American journal of cardiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
5.7field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. 2018 Guidelines for the management of dyslipidemia.The Korean journal of internal medicine · 2019
    Guideline
  2. Trial
  3. Article
  4. Atherosclerosis: Making a U Turn.Annual review of medicine · 2020
    Review
  5. 2018 Guidelines for the Management of Dyslipidemia in Korea.Journal of lipid and atherosclerosis · 2019
    Review
  6. Article
  7. Article
  8. Niacin: the evidence, clinical use, and future directions.Current atherosclerosis reports · 2012
    Review
  9. Metabolic syndrome in the Mediterranean region: Current status.Indian journal of endocrinology and metabolism · 2012
    Article
  10. Article
  11. Article
  12. Review
  13. High-density lipoprotein therapy: is there hope?Current treatment options in cardiovascular medicine · 2010
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Xue-Qiao ZhaoDepartment of Medicine, Division of Cardiology, University of Washington School of Medicine, Seattle, Washington, USA. xueqiao@u.washington.edu
Richard A Krasuski
Jefferson Baer
Edwin J Whitney
Blazej Neradilek
Alan Chait
Santica Marcovina
John J Albers
B Greg Brown
University of Washington · USCleveland Clinic · USEmory University · USSan Antonio Endovascular & Heart Institute · US

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
PILOT STUDY--CLINICAL NUTRITION RESEARCHP30DK035816 · NIDDK · UNIVERSITY OF WASHINGTON · PI Ellen A Schur · 1986 to 2026
$30.4M
Serum Amyloid and Inflammation in AtherogenesisP01HL030086 · NHLBI · UNIVERSITY OF WASHINGTON · PI HEINECKE, JAY W · 1985 to 2009
$14.7M
DOES ATHEROSCLEROSIS REGRESS WITH THERAPY FOR LOW HDLC?R01HL049546 · NHLBI · UNIVERSITY OF WASHINGTON · PI BROWN, BRUCE G · 1994 to 2000
$326k
FUNCTIONAL CHARACTERISTICS OF THE LEFT HEARTR01HL019451 · NHLBI · UNIVERSITY OF WASHINGTON · PI DODGE, HAROLD T · 1985 to 1990
–
NHLBI NIH HHS P01 HL030086NHLBI NIH HHS P01 HL30086NHLBI NIH HHS R01 HL049546NHLBI NIH HHS R01 HL19451NHLBI NIH HHS R01 HL49546NIDDK NIH HHS DK 17047NIDDK NIH HHS DK 35816NIDDK NIH HHS P30 DK017047NIDDK NIH HHS P30 DK035816
6 · The paper itself

Abstract

We examined the impact of metabolic syndrome (MS) on coronary stenosis progression and major cardiovascular (CV) events and investigated the mitigating effects of low-density lipoprotein (LDL) cholesterol lowering and LDL cholesterol lowering plus high-density lipoprotein (HDL) cholesterol increasing. This analysis combined individual patient data from 445 subjects who participated in 3 double-blinded, randomized, placebo-controlled trials (FATS, HATS, and AFREGS) comparing intensive lipid therapy to placebos on coronary stenosis progression by quantitative coronary angiography and on major CV events. The primary end points were change in mean proximal coronary diameter stenosis (Delta%S(prox)) over 3 years and the frequency of the predefined composite of coronary artery disease death, nonfatal myocardial infarction, stroke, and revascularization due to worsening ischemia. Patients with MS had 50% more rapid coronary stenosis progression and 64% increased CV event frequency compared to those without. More rapid coronary stenosis progression was significantly and independently associated with a 3.5-fold increased event risk (p <0.001). Combination lipid therapy significantly decreased stenosis progression by 83% (Delta%S(prox) 0.5 vs 2.9, p <0.001) in patients with MS and induced a small net regression in those without (Delta%S(prox) -0.3 vs 2.0, p <0.001). Combination therapy decreased the event rate by 54% (13% vs 28%, p = 0.03) in those with MS and by 82% (3% vs 17%, p = 0.002) without. On average, each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was significantly associated with a 0.3 Delta%S(prox) decrease. Each 10% decrease in LDL cholesterol or 10% increase in HDL cholesterol was associated with 11% (p = 0.02) or 22% (p <0.001) event risk decrease. In conclusion, patients with MS have significantly more rapid coronary stenosis progression and a higher frequency of CV events. Greater stenosis progression rate is associated with a higher event rate. LDL cholesterol-lowering and HDL cholesterol-increasing therapies independently and significantly decrease coronary stenosis progression and decrease CV events.

Indexed as

AdultAgedAnticholesteremic AgentsAtherosclerosisBiomarkersBody Mass IndexCholesterol, HDLCholesterol, LDLCoronary AngiographyCoronary StenosisDisease ProgressionDouble-Blind MethodFemaleFollow-Up StudiesHumansHydroxymethylglutaryl-CoA Reductase InhibitorsAnticholesteremic AgentsBiomarkersCholesterol, HDLCholesterol, LDLHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID19932775
PMCPMC2829987
OpenAlexW2026824875

What OpenQuestion holds

Texttitle and abstract
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.