Trial reportDiabetologia2009

Apolipoproteins, cardiovascular risk and statin response in type 2 diabetes: the Collaborative Atorvastatin Diabetes Study (CARDS).

V Charlton-Menys, D J Betteridge, H Colhoun, J Fuller, M France, G A Hitman, S J Livingstone, H A W Neil, C B Newman, M Szarek and 2 more

Erratum issued Registry-linked trialOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Diabetologia, 2009. The graph read 1 number from its abstract, feeding 1 cell of the map, but it casts no vote: the report of the main result of NCT00327418 is not on the map. It also reports an association that does not count as treatment evidence, such as difference -32.0 (-51.2 to -5.40) for lipids. An erratum has been issued. It reports registered trial NCT00327418. Cited by 16 papers, 1 of them a synthesis that pooled it.

1number the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 7% 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.

Read, but not usablea number the graph found but could not read as for or against

Lipidsan association or prognostic statement, not a treatment comparison · head-to-head · dyslipidemia, hypertensionfeeds one cell of the map
decrease -32.0-51.2 to -5.40
The 27% decrease in the ApoB:ApoA-I ratio on atorvastatin predicted a 32% (95% CI 5.4-51.2%) risk reduction in CHD, close to the 36% decrease observed.

clause the extractor read what became the number

2 · Its place on the map

Where it lands on the map

Rows are treatments, columns are outcomes. The coloured squares are the cells this paper feeds, coloured by the vote it casts there. Click one to jump to what this paper adds to it.

supports the treatmentfavours the comparatorno clear differenceread, but no usable result
3 · What it changes

What it adds to each cell

For every cell the paper feeds: the belief in the claim with and without this paper, and this paper's estimate drawn against every other readable study in the cell. The ringed dot is this paper.

Statins×lipids

No readable resultOpen on the map →What to test next →

38 readable studies in this cell: 25 favour the treatment, 5 find no difference, 8 favour the comparator.

Belief with this paper
0.50contested · 21 families support, 7 contradict · against placebo
Without itNot a counted family in this claim, so removing it changes nothing.
← favours the treatmentfavours the comparator →
0 · no effect
NCT002899002,340 enrolled · 2006
Δ -13.2-16.8 to -9.60
reduced -66.0-73.0 to -58.0
NCT02546323543 enrolled · 2015
Δ -35.5-40.2 to -30.7
NCT01678820299 enrolled · 2012
Δ 0.50-4.80 to 5.80
NCT01218204287 enrolled · 2010
Δ 5.47-15.7 to 26.7
NCT0093525931 enrolled · 2009
Δ -51.7
reductions -33.6-38.8 to -28.4

This paper's own estimate is on a different scale from the rest of the cell, so it is not drawn here.

4 · 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.

NCT00327418 phase4completed

A Double Blind Placebo Controlled Study of Atorvastatin as Prevention of CHD in High Risk Patients With Non-Insulin Dependent Diabetes Mellitus (Collaborative Atorvastatin Study - CARDS)

Ran1997Enrolled2,800Registered outcomes7Posted comparisons0ConditionsAngina, Unstable, Cerebrovascular Accident, Coronary Artery Bypass Graft, Major Coronary EventArmsAtorvastatin
PMID 17065671other papers from this trial
Open the trial in the graph
5 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Statins for the primary prevention of cardiovascular disease.The Cochrane database of systematic reviews · 2013 · on this map
    Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. The effects of cranberry juice on serum glucose, apoB, apoA-I, Lp(a), and Paraoxonase-1 activity in type 2 diabetic male patients.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2012
    Article
  13. Review
  14. Review
  15. Article
  16. Article
6 · The record

Corrections and comments

  • Erratum issued
7 · Who and what money

Authors and funding

12 authors at 9 institutions in 2 countries.

V Charlton-MenysCardiovascular Research Group, School of Clinical & Laboratory Sciences, Core Technology Facility (3rd Floor), University of Manchester, 46 Grafton Street, Manchester M13 9NT, UK.
D J Betteridge
H Colhoun
J Fuller
M France
G A Hitman
S J Livingstone
H A W Neil
C B Newman
M Szarek
D A DeMicco
P N Durrington
Pfizer (United States) · USUniversity College London · GBUniversity of Manchester · GBManchester Royal Infirmary · GBNew York University · USNorth Middlesex Hospital · GBQueen Mary University of London · GBUniversity of Dundee · GBUniversity of Oxford · GB

Funding

Department of Health
8 · The paper itself

Abstract

The marked sentences are the ones the graph read a number from.

aims/hypothesisControversy surrounds whether the ratio of apolipoprotein B (ApoB) to apolipoprotein A-I (ApoA-I) is the best lipoprotein discriminator of CHD risk in non-diabetic populations, but the issue has never been investigated in type 2 diabetes.

methodsIn 2,627 participants without known vascular disease in the Collaborative Atorvastatin Diabetes Study, ApoB, ApoA-I, LDL-cholesterol (LDLC) and HDL-cholesterol (HDLC) were assayed at baseline.

resultsThere were 108 CHD and 59 stroke endpoints over 3.9 years. The ApoB:A-I ratio at baseline was the lipoprotein variable most closely predicting CHD risk both by comparison of the hazard ratio for a 1 SD change or tertiles of frequency distribution. The areas under the receiver-operator curve for the ApoB:ApoA-I and the LDLC to HDLC [corrected] ratios, although not significantly different from each other, were greater (p = 0.0005 and p = 0.0125 respectively) than that of non-HDLC:HDLC. The 27% decrease in the ApoB:ApoA-I ratio on atorvastatin predicted a 32% (95% CI 5.4-51.2%) risk reduction in CHD, close to the 36% decrease observed. Neither the ApoB:ApoA-I nor any other lipoprotein concentration or ratio predicted the stroke outcome. CONCLUSIONS/

interpretationOverall, the ApoB:ApoA-I ratio improved on the non-HDLC:HDLC ratio in predicting CHD, but, depending on the assessment chosen, its superiority over LDLC:HDLC may be marginal. The statin-induced decrease in stroke risk may not be lipoprotein mediated.

trial registrationClinicalTrials.gov NCT00327418.

fundingThe study was supported by unrestricted grants from Diabetes UK, the Department of Health and Pfizer to the University of Manchester and to University College, London.

Indexed as

AdultAgedApolipoprotein A-IApolipoproteinsAtorvastatinBiomarkersBlood PressureCardiovascular DiseasesDiabetes Mellitus, Type 2Diabetic AngiopathiesDouble-Blind MethodFemaleHeart RateHeptanoic AcidsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsApolipoprotein A-IApolipoproteinsAtorvastatinBiomarkersHeptanoic AcidsHydroxymethylglutaryl-CoA Reductase InhibitorsPyrrolesTriglycerides

Identifiers

PMID18972097
OpenAlexW2161679482

What OpenQuestion holds

Texttitle and abstract
Read underepoch 390

Registered trials

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.