Evidence map›Paper›PMID 27168072›Full record

ArticlePloS one2016

APOE Genotype in the Ethnic Majority and Minority Groups of Laos and the Implications for Non-Communicable Diseases.

Kaoru Midorikawa, Douangdao Soukaloun, Kongsap Akkhavong, Bouavanh Southivong, Oudayvone Rattanavong, Vikham Sengkhygnavong, Amphay Pyaluanglath, Saymongkhonh Sayasithsena, Satoshi Nakamura, Yutaka Midorikawa and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 5 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

11 authors at 6 institutions in 2 countries.

Kaoru MidorikawaDepartment of Environmental and Molecular Medicine, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
Douangdao SoukalounMahosot Hospital, Ministry of Health, Vientiane, Lao PDR.
Kongsap AkkhavongNational Institute of Public Health, Ministry of Health, Vientiane, Lao PDR.
Bouavanh SouthivongDepartment of Health Care, Ministry of Health, Vientiane, Lao PDR.
Oudayvone RattanavongMahosot Hospital, Ministry of Health, Vientiane, Lao PDR.
Vikham SengkhygnavongMahosot Hospital, Ministry of Health, Vientiane, Lao PDR.
Amphay PyaluanglathMahosot Hospital, Ministry of Health, Vientiane, Lao PDR.
Saymongkhonh SayasithsenaMahosot Hospital, Ministry of Health, Vientiane, Lao PDR.
Satoshi NakamuraLaboratory of Epidemiology and Public Health, Graduate School of Nursing Science and Faculty of Nursing, Hiroshima Bunka Gakuen University, Kure, Hiroshima, Japan.
Yutaka MidorikawaDepartment of Medical Nutrition, Faculty of Health, Suzuka University of Medical Science, Suzuka, Mie, Japan.
Mariko MurataDepartment of Environmental and Molecular Medicine, Mie University Graduate School of Medicine, Tsu, Mie, Japan.
Mahosot Hospital · LAMie University · JPHiroshima Bunka Gakuen University · JPMinistry of Health · LANational Institute of Public Health · LASuzuka University of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIncreasing age is associated with elevated risk of non-communicable diseases, including dementia and Alzheimer's disease (AD). The apolipoprotein E (APOE) ε4 allele is a risk factor not only for AD, but also for cognitive decline, depressive symptoms, stroke, hypertension, coronary heart disease, cardiovascular disease, and diabetes. The Lao People's Democratic Republic (Laos) is undergoing development; consequently, life expectancy has risen. To evaluate the future risk of non-communicable diseases, we investigated APOE genotypes and anthropometric characteristics in the Laotian population. METHODOLOGY/PRINCIPAL

findingsSubjects were 455 members of the Lao Loum majority and 354 members of ethnic minorities. APOE genotypes, anthropometric characteristics, blood pressure, and blood glucose were recorded. To compare individual changes, health examination data collected 5 years apart were obtained from a subset of Lao Loum subjects. APOE ε4 allele frequencies were higher among minorities (31.3%) than among Lao Loum (12.6%). In Lao Loum, but not in minorities, mean waist circumference and blood pressure increased significantly across age groups. Comparisons of health conditions between the beginning and end of the 5-year period revealed significant increases in obesity and blood glucose levels in Lao Loum. APOE ε4 carriers exhibited significant increases in resting heart rate in both ethnic groups. CONCLUSIONS/SIGNIFICANCE: A higher ε4 allele frequency was observed in Laotian minorities than in the Laotian majority. Furthermore, higher obesity, blood pressure and blood glucose were observed in the middle-aged ethnic majority. Therefore, given these genetic and non-communicable disease risk factors, it seems likely that as the Laotian population ages, elevated rates of non-communicable aging-related diseases, such as dementia, will also become more prevalent.

Indexed as

Minority GroupsAdultAnthropometryApolipoproteins EDiseaseEthnicityFemaleGenotypeHumansLaosMaleMiddle AgedPolymorphism, GeneticRegression AnalysisYoung AdultApolipoproteins E

Identifiers

PMID27168072
PMCPMC4863969
OpenAlexW2371024281

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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.