Evidence map›Paper›PMID 22359560›Full record

ArticlePloS one2012

Characterization of the poly-T variant in the TOMM40 gene in diverse populations.

Colton Linnertz, Ann M Saunders, Michael W Lutz, Donna M Crenshaw, Iris Grossman, Daniel K Burns, Keith E Whitfield, Michael A Hauser, Jeanette J McCarthy, Megan Ulmer and 4 more

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. TOMM40-APOE haplotypes are associated with cognitive decline in non-demented Blacks.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2021
    Article
  8. Article
  9. Article
  10. Use of local genetic ancestry to assessNeurology. Genetics · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Characterization ofAlzheimer's & dementia (New York, N. Y.) · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. New Genetic Approaches to AD: Lessons from APOE-TOMM40 Phylogenetics.Current neurology and neuroscience reports · 2016
    Review
  19. APOE/TOMM40 genetic loci, white matter hyperintensities, and cerebral microbleeds.International journal of stroke : official journal of the International Stroke Society · 2015
    Article
  20. The Broad Impact of TOM40 on Neurodegenerative Diseases in Aging.Journal of Parkinson's disease and Alzheimer's disease · 2014
    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

14 authors.

Colton LinnertzInstitute for Genome Sciences & Policy, Duke University, Durham, North Carolina, United States of America.
Ann M Saunders
Michael W Lutz
Donna M Crenshaw
Iris Grossman
Daniel K Burns
Keith E Whitfield
Michael A Hauser
Jeanette J McCarthy
Megan Ulmer
Rand Allingham
Kathleen A Welsh-Bohmer
Allen D Roses
Ornit Chiba-Falek

Funding

Genetic Factors that Impact the Risk of Alzheimer's DiseaseRC1AG035635 · NIA · DUKE UNIVERSITY · PI ROSES, ALLEN D · 2009 to 2010
$820k
NIA NIH HHS 1RC1AG035635-01NIA NIH HHS RC1 AG035635
6 · The paper itself

Abstract

We previously discovered that a polymorphic, deoxythymidine-homopolymer (poly-T, rs10524523) in intron 6 of the TOMM40 gene is associated with age-of-onset of Alzheimer's disease and with cognitive performance in elderly. Three allele groups were defined for rs10524523, hereafter '523', based on the number of 'T'-residues: 'Short' (S, T≤19), 'Long' (L, 20≤T≤29) and 'Very Long' (VL, T≥30). Homopolymers, particularly long homopolymers like '523', are difficult to genotype because 'slippage' occurs during PCR-amplification. We initially genotyped this locus by PCR-amplification followed by Sanger-sequencing. However, we recognized the need to develop a higher-throughput genotyping method that is also accurate and reliable. Here we describe a new '523' genotyping assay that is simple and inexpensive to perform in a standard molecular genetics laboratory. The assay is based on the detection of differences in PCR-fragment length using capillary electrophoresis. We discuss technical problems, solutions, and the steps taken for validation. We employed the novel assay to investigate the '523' allele frequencies in different ethnicities. Whites and Hispanics have similar frequencies of S/L/VL alleles (0.45/0.11/0.44 and 0.43/0.09/0.48, respectively). In African-Americans, the frequency of the L-allele (0.10) is similar to Whites and Hispanics; however, the S-allele is more prevalent (0.65) and the VL-allele is concomitantly less frequent (0.25). The allele frequencies determined using the new methodology are compared to previous reports for Ghanaian, Japanese, Korean and Han Chinese cohorts. Finally, we studied the linkage pattern between TOMM40-'523' and APOE alleles. In Whites and Hispanics, consistent with previous reports, the L is primarily linked to ε4, while the majority of the VL and S are linked to ε3. Interestingly, in African-Americans, Ghanaians and Japanese, there is an increased frequency of the '523'S-APOEε4 haplotype. These data may be used as references for '523' allele and '523'-APOE haplotype frequencies in diverse populations for the design of research studies and clinical trials.

Indexed as

Alzheimer DiseaseApolipoproteins EEthnicityGene FrequencyGenotypeHaplotypesHumansIntronsMembrane Transport ProteinsMethodsMitochondrial Precursor Protein Import Complex ProteinsPoly TPopulation GroupsApolipoproteins EMembrane Transport ProteinsMitochondrial Precursor Protein Import Complex ProteinsPoly TTOMM40 protein, human

Identifiers

PMID22359560
PMCPMC3281049

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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.