Evidence map›Paper›PMID 25486118›Full record

ArticlePloS one2014

Association between NME8 locus polymorphism and cognitive decline, cerebrospinal fluid and neuroimaging biomarkers in Alzheimer's disease.

Ying Liu, Jin-Tai Yu, Hui-Fu Wang, Xiao-Ke Hao, Yu-Fen Yang, Teng Jiang, Xi-Chen Zhu, Lei Cao, Dao-Qiang Zhang, Lan Tan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Functional Diversity and Emerging Roles of Human NME/NDPK Group II Proteins.International journal of molecular sciences · 2026
    Review
  3. Review
  4. Review
  5. Article
  6. Association of the top 20 Alzheimer's disease risk genes with [Alzheimer's & dementia (Amsterdam, Netherlands) · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Frontiers in neuroscience · 2019
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 5 institutions in 1 country.

Ying LiuDepartment of Neurology, Dalian Medical University, Qingdao Municipal Hospital, Qingdao, China.
Jin-Tai YuDepartment of Neurology, Dalian Medical University, Qingdao Municipal Hospital, Qingdao, China; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China; Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.
Hui-Fu WangDepartment of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.
Xiao-Ke HaoDepartment of Computer Science and Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing, China.
Yu-Fen YangAir Beijing Dongjiao Lane Community Health, Beijing, China.
Teng JiangDepartment of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
Xi-Chen ZhuDepartment of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.
Lei CaoDepartment of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.
Dao-Qiang ZhangDepartment of Computer Science and Engineering, Nanjing University of Aeronautics and Astronautics, Nanjing, China.
Lan TanDepartment of Neurology, Dalian Medical University, Qingdao Municipal Hospital, Qingdao, China; Department of Neurology, Qingdao Municipal Hospital, School of Medicine, Qingdao University, China; Department of Neurology, Qingdao Municipal Hospital, Nanjing Medical University, Nanjing, China.
Nanjing Medical University · CNNanjing University of Aeronautics and Astronautics · CNQingdao University · CNDalian Medical University · CNQingdao Municipal Hospital · CN

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
Canadian Institutes of Health ResearchNIA NIH HHS U01 AG024904NIA NIH HHS U24 AG021886
6 · The paper itself

Abstract

Recently, a large meta-analysis of five genome wide association studies (GWAS) identified a novel locus (rs2718058) adjacent to NME8 that played a preventive role in Alzheimer's disease (AD). However, this link between the single nucleotide polymorphism (SNP) rs2718058 and the pathology of AD have not been mentioned yet. Therefore, this study assessed the strength of association between the NME8 rs2718058 genotypes and AD-related measures including the cerebrospinal fluid (CSF) amyloid beta, tau, P-tau concentrations, neuroimaging biomarkers and cognitive performance, in a large cohort from Alzheimer's Disease Neuroimaging Initiative (ADNI) database. We used information of a total of 719 individuals, including 211 normal cognition (NC), 346 mild cognitive impairment (MCI) and 162 AD. Although we didn't observe a positive relationship between rs2718058 and AD, it was significantly associated with several AD related endophenotypes. Among the normal cognitively normal participants, the minor allele G carriers showed significantly associated with higher CDRSB score than A allele carriers (P = 0.021). Occipital gyrus atrophy were significantly associated with NME8 genotype status (P = 0.002), with A allele carriers has more atrophy than the minor allele G carriers in AD patients; lateral ventricle (both right and left) cerebral metabolic rate for glucose (CMRgl) were significantly associated with NME8 genotype (P < 0.05), with GA genotype had higher metabolism than GG and AA genotypes in MCI group; the atrophic right hippocampus in 18 months is significantly different between the three group, with GG and AA genotypes had more hippocampus atrophy than GA genotypes in the whole group. Together, our results are consistent with the direction of previous research, suggesting that NME8 rs2718058 appears to play a role in lowering the brain neurodegeneration.

Indexed as

NeuroimagingAgedAlzheimer DiseaseBiomarkersCognition DisordersFemaleGenome-Wide Association StudyGenotypeHumansMaleNeuropsychological TestsPolymorphism, GeneticThioredoxinsBiomarkersNME8 protein, humanThioredoxins

Identifiers

PMID25486118
PMCPMC4259473
OpenAlexW1995695796

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.