Evidence map›Paper›PMID 24713204›Full record

ArticleBMC research notes2014

Mitochondrial DNA association study of type 2 diabetes with or without ischemic stroke in Taiwan.

Jun-Hun Loo, Jean A Trejaut, Ju-Chen Yen, Zong-Sian Chen, Wai-Mei Ng, Chin-Yuan Huang, Kuang-Nan Hsu, Kuo-Hua Hung, Yachun Hsiao, Yau-Huei Wei and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC research notes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.1field-weighted citation impact, top 45% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Mitochondrial DNA associations with East Asian metabolic syndrome.Biochimica et biophysica acta. Bioenergetics · 2018
    Article
  7. 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

11 authors at 3 institutions in 1 country.

Jun-Hun Loo
Jean A Trejaut
Ju-Chen Yen
Zong-Sian Chen
Wai-Mei Ng
Chin-Yuan Huang
Kuang-Nan Hsu
Kuo-Hua Hung
Yachun Hsiao
Yau-Huei Wei
Marie LinMackay Memorial Hospital, No, 45, Mínshēng Rd, Danshui District, New Taipei City, Taiwan. marilin@ms2.mmh.org.tw.
Mackay Memorial Hospital · TWNational Taipei University · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe importance of mitochondrial DNA (mtDNA) polymorphism in the prediction of type 2 diabetes (T2D) in men and women is not well understood. We questioned whether mtDNA polymorphism, mitochondrial functions, age and gender influenced the occurrence of T2D with or without ischemic stroke (IS).

methodsWe first designed a matched case-control study of 373 T2D patients and 327 healthy unrelated individuals without history of IS. MtDNA haplogroups were determined on all participants using sequencing of the control region and relevant SNPs from the coding region. Mitochondria functional tests, systemic biochemical measurements and complete genomic mtDNA sequencing were further determined on 239 participants (73 healthy controls, 33 T2D with IS, 70 T2D only and 63 IS patients without T2D).

resultsMtDNA haplogroups B4a1a, and E2b1 showed significant association with T2D (P <0.05), and haplogroup D4 indicated resistance (P <0.05). Mitochondrial and systemic functional tests showed significantly less variance within groups bearing the same mtDNA haplotypes. There was a pronounced male excess among all T2D patients and prevalence of IS was seen only in the older population. Finally, nucleotide variant np 15746, a determinant of haplogroup G3 seen in Japanese and of B4a1a prevalent in Taiwanese was associated with T2D in both populations.

conclusionsMen appeared more susceptible to T2D than women. Although the significant association of B4a1a and E2b1 with T2D ceased when corrected for multiple testings, these haplogroups are seen only among Taiwan Aborigines, Southeast Asian and the Pacific Ocean islanders where T2D is predominant. The data further suggested that physiological and biochemical measurements were influenced by the mtDNA genetic profile of the individual. More understanding of the function of the mitochondrion in the development of T2D might indicate ways of influencing the early course of the disease.

Indexed as

Genetic Association StudiesPolymorphism, Single NucleotideAgedAge FactorsBase SequenceBrain IschemiaCase-Control StudiesDiabetes Mellitus, Type 2DNA, MitochondrialFemaleHaplotypesHumansMaleMiddle AgedMolecular Sequence DataSequence Analysis, DNADNA, Mitochondrial

Identifiers

PMID24713204
PMCPMC4108081
OpenAlexW2096215182

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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.