Evidence map›Paper›PMID 25902149›Full record

ArticlePloS one2015

Relationship between Adiponectin Gene Polymorphisms and Late-Onset Alzheimer's Disease.

Wei Li, Zhuling Yu, Deren Hou, Lin Zhou, Yanyao Deng, Mi Tian, Xialu Feng

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
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  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Importance of adiponectin activity in the pathogenesis of Alzheimer's disease.Annals of clinical and translational neurology · 2017
    Review
  13. Potential Neuroprotective Effects of Adiponectin in Alzheimer's Disease.International journal of molecular sciences · 2017
    Review
  14. Article
  15. [Correlation between serum adiponectin level and cognitive function in patients with Alzheimer's disease].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2016
    Article
  16. Article
  17. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Wei LiDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Zhuling YuDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China; Department of Nerve medical center, The First Hospital of Changsha, Changsha, China.
Deren HouDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Lin ZhouDepartment of Geriatric Neurology, Xiangya Hospital, Central South University, Changsha, China.
Yanyao DengDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Mi TianDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Xialu FengDepartment of Neurology, The Third Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNThird Xiangya Hospital · CNThe First Hospital of Changsha · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, researchers have found that adiponectin (ANP) plays an important role in the pathogenesis of Alzheimer's disease (AD), and low serum concentrations of ANP are associated with AD. Higher plasma ANP level have a protective effect against the development of cognitive decline, suggesting that ANP may affect AD onset. Meanwhile, accumulating evidence supports the crucial role of ANP in the pathogenesis of AD. To study the relationship between ANP gene polymorphisms (rs266729, -11377C>G and rs1501299, G276T) and late-onset AD (LOAD), we carried out a case-control study that included 201 LOAD patients and 257 healthy control subjects. Statistically significant differences were detected in the genotype and allelotype frequency distributions of rs266729 and rs1501299 between the LOAD group and the control group, with a noticeable increase in the G and T allelotype frequency distributions in the LOAD group (P < 0.05). Logistic regression analysis using recessive model and additive model revealed that the rs266729 GG and rs1501299 TT genotypes are associated with a greater risk of LOAD. Haplotype analysis identified four haplotypes: CG, CT, GG, and GT. The frequencies of the CT and GG haplotypes were not significantly different (P > 0.05) between the LOAD group and control group, whereas the CG and GT haplotypes were significantly different (P < 0.05), suggesting a negative correlation between the CG haplotype and LOAD onset (OR = 0.74, 95% CI = 0.57-0.96, P = 0.022), and a positive correlation between the GT haplotype and LOAD onset (OR = 2.29, 95% CI = 1.42-3.68, P = 0.005). Therefore, we speculated that the rs266729 and rs1501299 of ANP gene polymorphisms and the GT and CG haplotypes were associated with LOAD.

Indexed as

Genetic Predisposition to DiseaseAdiponectinAgedAge of OnsetAlzheimer DiseaseCase-Control StudiesFemaleHaplotypesHumansLogistic ModelsMaleMass SpectrometryPolymorphism, Single NucleotideAdiponectinADIPOQ protein, human

Identifiers

PMID25902149
PMCPMC4406444
OpenAlexW2070871468

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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.