Evidence map›Paper›PMID 27439317›Full record

ArticleBMC geriatrics2016

Cholesteryl ester transfer protein (CETP) I405V polymorphism and cardiovascular disease in eastern European Caucasians - a cross-sectional study.

Jasmin Bustami, Anna Sukiasyan, Juozas Kupcinskas, Jurgita Skieceviciene, Leonid Iakoubov, Malgorzata Szwed, Christoph Kleinle, Ralf R Schumann, Monika Puzianowska-Kuznicka, Lutz Hamann

Open access · goldAbstract read
In one paragraph

Article in BMC geriatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

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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 5 countries.

Jasmin BustamiInstitute of Microbiology and Hygiene, Charité University Medical Center Berlin, Rahel-Hirsch-Weg 3, 10117, Berlin, Germany.
Anna SukiasyanInstitute of Microbiology and Hygiene, Charité University Medical Center Berlin, Rahel-Hirsch-Weg 3, 10117, Berlin, Germany.
Juozas KupcinskasDepartment of Gastro-enterology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Jurgita SkiecevicieneInstitute for Digestive Research, Lithuanian University of Health Sciences, Kaunas, Lithuania.
Leonid IakoubovCellecta Inc, Mountain View, California, USA.
Malgorzata SzwedDepartment of Human Epigenetics, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland.
Christoph KleinleInstitute of Microbiology and Hygiene, Charité University Medical Center Berlin, Rahel-Hirsch-Weg 3, 10117, Berlin, Germany.
Ralf R SchumannInstitute of Microbiology and Hygiene, Charité University Medical Center Berlin, Rahel-Hirsch-Weg 3, 10117, Berlin, Germany.
Monika Puzianowska-KuznickaDepartment of Human Epigenetics, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland.
Lutz HamannInstitute of Microbiology and Hygiene, Charité University Medical Center Berlin, Rahel-Hirsch-Weg 3, 10117, Berlin, Germany. lutz.hamann@charite.de.
Charité - Universitätsmedizin Berlin · DELithuanian University of Health Sciences · LTCellecta (United States) · USMossakowski Medical Research Institute, Polish Academy of Sciences · PLPolish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe cholesteryl ester transfer protein (CETP) polymorphism I405V has been suggested to be involved in longevity and susceptibility to cardiovascular diseases. An enhanced reverse cholesterol transport due to enhanced HDL levels has been hypothesized to be the underlying mechanism. However, clinical trials with HDL-enhancing drugs failed to show beneficial effects. Consequently, it has been postulated that genetic variations enhancing HDL levels are cardioprotective only if they also decrease LDL levels.

methodsA cross-sectional study was conducted to genotype 1028 healthy blood donors and 1517 clinically well characterized elderly for CETP I405V.

resultsWe could not find any association of this polymorphism with age for both, males or females, in any of these cohorts (P = 0.71 and P = 0.57, respectively, for males and P = 0.55 and P = 0.88, respectively, for females). In addition, no association with cardiovascular diseases could be observed in the elderly cohort (males OR = 1.12 and females OR = 0.88). In the same cohort, the CETP V405V genotype was associated with significantly enhanced HDL levels (P = 0.03), mostly owing to the female sex (P = 0.46 for males, P = 0.02 for females), whereas LDL and triglyceride levels were unchanged (P = 0.62 and P = 0.18, respectively).

conclusionOur data support the recent hypothesis that variations enhancing HDL levels without affecting LDL levels are not associated with the risk for cardiovascular diseases.

Indexed as

Cardiovascular DiseasesAgedCholesterol Ester Transfer ProteinsCross-Sectional StudiesFemaleHumansLipoproteins, HDLMaleMiddle AgedPolymorphism, GeneticWhite PeopleCETP protein, humanCholesterol Ester Transfer ProteinsLipoproteins, HDLCardio vascular diseaseCholesteryl ester transfer proteinGenetic polymorphismHigh-density lipoproteinSingle nucleotide polymorphism

Identifiers

PMID27439317
PMCPMC4955243
OpenAlexW2480030066

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Registered trials

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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.