Evidence map›Paper›PMID 28458923›Full record

ArticleCholesterol2017

Cholesterol Levels in Genetically Determined Familial Hypercholesterolaemia in Russian Karelia.

V A Korneva, T Yu Kuznetsova, T Yu Bogoslovskaya, D S Polyakov, V B Vasilyev, A V Orlov, M Yu Mandelshtam

Open access · hybridAbstract read
In one paragraph

Article in Cholesterol, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. TheGenes · 2021
    Observational
  3. 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

7 authors at 4 institutions in 1 country.

V A KornevaDepartment of Faculty Therapy, Phthisiology, Infectious Diseases and Epidemiology, Institute of Medicine, Petrozavodsk State University, 33 Lenin Str., Petrozavodsk, Republic of Karelia 185910, Russia.
T Yu KuznetsovaDepartment of Faculty Therapy, Phthisiology, Infectious Diseases and Epidemiology, Institute of Medicine, Petrozavodsk State University, 33 Lenin Str., Petrozavodsk, Republic of Karelia 185910, Russia.ORCID 0000-0002-6654-1382
T Yu BogoslovskayaDepartment of Molecular Genetics, Institute of Experimental Medicine, 12 Pavlov Street, St. Petersburg 197376, Russia.ORCID 0000-0002-9480-1073
D S PolyakovDepartment of Molecular Genetics, Institute of Experimental Medicine, 12 Pavlov Street, St. Petersburg 197376, Russia.
V B VasilyevDepartment of Molecular Genetics, Institute of Experimental Medicine, 12 Pavlov Street, St. Petersburg 197376, Russia.
A V OrlovDepartment of Analysis of Competitive Systems, National Research Nuclear University "MEPhI", Kashirskoye Shosse 31, Moscow 115409, Russia.
M Yu MandelshtamDepartment of Molecular Genetics, Institute of Experimental Medicine, 12 Pavlov Street, St. Petersburg 197376, Russia.
Institute of Experimental Medicine · RUPetrozavodsk State University · RUSt Petersburg University · RUNational Research Nuclear University MEPhI · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Familial hypercholesterolaemia (FH) is a rare disease that tends to be diagnosed lately. In Russia, the genetic and phenotypic characteristics of the disease are not well defined. We investigated 102 patients with definite FH. In 52 of these patients (50.9%) genetic analysis was performed, revealing pathogenic mutations of the low density lipoprotein (LDL) receptor gene in 22 patients. We report here five mutations of the LDL receptor gene found in the Karelian FH sample for the first time. The detection rate of mutations in definite FH patients was 42.3%. Two groups of patients with a definite diagnosis of FH according to the Dutch Lipid Clinic Network criteria were compared: the first group had putatively functionally important LDL receptor gene mutations, while in the second group LDL receptor gene mutations were excluded by single-strand conformation polymorphism analysis. Total and LDL cholesterol levels were higher in the group with LDL receptor mutations compared to the mutation-free population. The frequency of mutations in patients with LDL cholesterol > 6.5 mmol/L was more than 3 times higher than that in patients with LDL < 6.5 mmol/L. Total and LDL cholesterol levels and the frequency of coronary heart disease and myocardial infarction were higher in the group with definite FH compared to groups with probable and possible FH. Cholesterol figures in FH patients of different age and sex from the Karelian population were comparable.

Identifiers

PMID28458923
PMCPMC5387824
OpenAlexW2600314747

What OpenQuestion holds

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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.