Evidence map›Paper›PMID 30571611›Full record

SynthesisOmics : a journal of integrative biology2018

Genetic Determinants of Dyslipidemia in African-Based Populations: A Systematic Review.

Jean Jacques Noubiap, Edith Pascale M Mato, Magellan Guewo-Fokeng, Arnaud D Kaze, Houssam Boulenouar, Ambroise Wonkam

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Omics : a journal of integrative biology, 2018. 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 31% 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, 7 citations in OpenAlex.

  1. Article
  2. Global epidemiology of dyslipidaemias.Nature reviews. Cardiology · 2021
    Review
  3. 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

6 authors at 5 institutions in 4 countries.

Jean Jacques Noubiap1 Department of Medicine, University of Cape Town and Groote Schuur Hospital, Cape Town, South Africa.
Edith Pascale M Mato2 Molecular and Clinical Research Laboratory, Department of Pharmacology, University of Kwazulu-Natal, Durban, South Africa.
Magellan Guewo-Fokeng3 Department of Biochemistry, Faculty of Science, University of Yaoundé I, Yaoundé, Cameroon.
Arnaud D Kaze4 Department of Medicine, University of Maryland Medical Center Midtown Campus, Baltimore, Maryland.
Houssam Boulenouar5 Laboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de Technologie d'Oran Mohamed Boudiaf, Oran, Algeria.
Ambroise Wonkam8 Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
University of Cape Town · ZAUniversité de Yaoundé I · CMUniversity of Abou Bekr Belkaïd · DZUniversity of KwaZulu-Natal · ZAUniversity of Maryland, Baltimore · US

Funding

Sickle Africa Data Coordinating CenterU24HL135600 · NHLBI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA, WONKAM, AMBROISE · 2017 to 2025
$8.6M
Return of a Fragile X Syndrome genetic result: exploring the feedback of individual genetic findings and their relation to traditional knowledge in a village in Cameroon.U54HG009790 · NHGRI · UNIVERSITY OF CAPE TOWN · PI WONKAM, AMBROISE · 2017 to 2021
$2.5M
Exploring Perspectives on Genomics and Sickle Cell Public Health InterventionsU01HG007459 · NHGRI · UNIVERSITY OF CAPE TOWN · PI WONKAM, AMBROISE · 2013 to 2016
$622k
NHGRI NIH HHS U01 HG007459NHLBI NIH HHS U24 HL135600
6 · The paper itself

Abstract

Identification of genetic/genomic factors contributing to dyslipidemia is of great interest to prevention and reduction of the onset and burden of cardiovascular diseases in Africa. This systematic review summarizes available data on genetic variants associated with dyslipidemia in populations within Africa. A PubMed and EMBASE database search was conducted to identify all studies published until June 2018 on genetic susceptibility to dyslipidemia in African-based populations, excluding familial hypercholesterolemia. All studies on genetic predispositions of dyslipidemia and respecting the preestablished inclusion criteria were included in this systematic review. Because of high heterogeneity, the data were summarized narratively. Twenty-two studies investigated mostly the targeted genetic variants. A total of 51 polymorphisms in 28 susceptibility genes to dyslipidemia have been associated with a particular trait in the African populations, and through variable effects. Most polymorphisms investigated in Northern Africa seemed to have consistent effects on increasing the level of low-density lipoprotein cholesterol (LDL-C), total cholesterol, and triglycerides in patients with diabetes, myocardial infarction, coronary artery disease, and metabolic syndrome. By contrast, only Ser447Ter and C49620T variants were associated with increased LDL-C in sub-Saharan Africa. Despite few studies available in this context in the literature, certain genetic variants were consistently associated with dyslipidemia especially in Northern Africa as highlighted in this analysis. Further data, particularly from genome-wide association studies, would help establish an African-specific reference for genetic susceptibility markers of dyslipidemia.

Indexed as

Africa, NorthernAnimalsCardiovascular DiseasesDyslipidemiasGenome-Wide Association StudyHumansPolymorphism, GeneticAfricabiomarkerscardiovascular health and diseasedyslipidemiageneticsgenomicspolymorphism

Identifiers

PMID30571611
PMCPMC7001384
OpenAlexW2906637262

What OpenQuestion holds

Textmetadata
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.