Evidence map›Paper›PMID 14583798›Full record

ArticleThe pharmacogenomics journal2003

Haplotypes of the cholesteryl ester transfer protein gene predict lipid-modifying response to statin therapy.

B R Winkelmann, M M Hoffmann, M Nauck, A M Kumar, K Nandabalan, R S Judson, B O Boehm, A R Tall, G Ruaño, W März

Abstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Association ofInternational journal of molecular sciences · 2023
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Polymorphisms in maternal and fetal genes encoding for proteins involved in extracellular matrix metabolism alter the risk for small-for-gestational-age.The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians · 2011
    Article
  9. Article
  10. Article
  11. Article
  12. Pharmacogenetics of cardiovascular drug therapy.Clinical cases in mineral and bone metabolism : the official journal of the Italian Society of Osteoporosis, Mineral Metabolism, and Skeletal Diseases · 2009
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

10 authors at 5 institutions in 2 countries.

B R WinkelmannCooperation Unit of Pharmacogenomics/Applied Genomics, Ruprecht Karls-University, Heidelberg, Germany. bernhard_winkelmann@med.uni-heidelberg.de
M M Hoffmann
M Nauck
A M Kumar
K Nandabalan
R S Judson
B O Boehm
A R Tall
G Ruaño
W März
Biohaven Pharmaceuticals (United States) · USUniversity of Freiburg · DEColumbia University · USHeidelberg University · DEUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholesteryl ester transfer protein (CETP) plays a central role in high-density lipoprotein (HDL) metabolism. Single nucleotide polymorphisms (SNPs) and haplotypes in the CETP gene were determined in 98 patients with untreated dyslipidemias and analyzed for associations with plasma CETP and plasma lipids before and during statin treatment. Individual CETP SNPs and haplotypes were both significantly associated with CETP enzyme mass and activity. However, only certain CETP haplotypes, but not individual SNPs, significantly predicted the magnitude of change in HDL cholesterol (HDL-C) and triglycerides. After adjusting for covariates and multiple testing, the TTCAAA haplotype showed a gene-dose effect in predicting the HDL-C increase (P=0.03), while the TTCAAAGGG and AAAGGG haplotypes predicted a decrease in triglycerides (P=0.04 both). This is the first study to demonstrate that SNP haplotypes derived from allelic SNP combinations in the CETP gene were more informative than single SNPs in predicting the response to lipid-modifying therapy with statins.

Indexed as

GlycoproteinsAgedCardiovascular DiseasesCarrier ProteinsCholesterol Ester Transfer ProteinsCohort StudiesFemaleGenetic VariationHaplotypesHumansHydroxymethylglutaryl-CoA Reductase InhibitorsLipidsMaleMiddle AgedPredictive Value of TestsCarrier ProteinsCETP protein, humanCholesterol Ester Transfer ProteinsGlycoproteinsHydroxymethylglutaryl-CoA Reductase InhibitorsLipids

Identifiers

PMID14583798
OpenAlexW2034267806

What OpenQuestion holds

Texttitle and abstract
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.