Evidence map›Paper›PMID 30352621›Full record

ArticleClinical epigenetics2018

Prediction of smoking by multiplex bisulfite PCR with long amplicons considering allele-specific effects on DNA methylation.

Nikolay Kondratyev, Arkady Golov, Margarita Alfimova, Tatiana Lezheiko, Vera Golimbet

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Clinical epigenetics, 2018. 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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Ten Years of EWAS.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2021
    Review
  3. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Nikolay KondratyevClinical Genetics Laboratory, Mental Health Research Center, Moscow, Russia. nikolay.quadrat@gmail.com.ORCID 0000-0002-5134-6007
Arkady GolovClinical Genetics Laboratory, Mental Health Research Center, Moscow, Russia.
Margarita AlfimovaClinical Genetics Laboratory, Mental Health Research Center, Moscow, Russia.
Tatiana LezheikoClinical Genetics Laboratory, Mental Health Research Center, Moscow, Russia.
Vera GolimbetClinical Genetics Laboratory, Mental Health Research Center, Moscow, Russia.
Mental Health Research Center of Russian Academy of Medical Sciences · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethylation of DNA is associated with a variety of biological processes. With whole-genome studies of DNA methylation, it became possible to determine a set of genomic sites where DNA methylation is associated with a specific phenotype. A method is needed that allows detailed follow-up studies of the sites, including taking into account genetic information. Bisulfite PCR is a natural choice for this kind of task, but multiplexing is one of the most important problems impeding its implementation. To address this task, we took advantage of a recently published method based on Pacbio sequencing of long bisulfite PCR products (single-molecule real-time bisulfite sequencing, SMRT-BS) and tested the validity of the improved methodology with a smoking phenotype.

resultsHerein, we describe the "panhandle" modification of the method, which permits a more robust PCR with multiple targets. We applied this technique to determine smoking by DNA methylation in 71 healthy people and 83 schizophrenia patients (n = 50 smokers and n = 104 non-smokers, Russians of the Moscow region). We used five targets known to be influenced by smoking (regions of genes AHRR, ALPPL2, IER3, GNG12, and GFI1). We discovered significant allele-specific methylation effects in the AHRR and IER3 regions and assessed how this information could be exploited to improve the prediction of smoking based on the collected DNA methylation data. We found no significant difference in the methylation profiles of selected targets in relation to schizophrenia suggesting that smoking affects methylation at the studied genomic sites in healthy people and schizophrenia patients in a similar way.

conclusionsWe determined that SMRT-BS with "panhandle" modification performs well in the described setting. Additional information regarding methylation and allele-specific effects could improve the predictive accuracy of DNA methylation-based models, which could be valuable for both basic research and clinical applications.

Indexed as

DNA MethylationApoptosis Regulatory ProteinsBasic Helix-Loop-Helix ProteinsCpG IslandsFemaleHigh-Throughput Nucleotide SequencingHumansMaleMembrane ProteinsMultiplex Polymerase Chain ReactionRepressor ProteinsSchizophreniaSequence Analysis, DNASmokingYoung AdultAHRR protein, humanApoptosis Regulatory ProteinsBasic Helix-Loop-Helix ProteinsIER3 protein, humanMembrane ProteinsRepressor ProteinsAllele-specific methylationClinical sequencingDNA methylationSchizophreniaSingle-molecule sequencingSmokingTargeted sequencing

Identifiers

PMID30352621
PMCPMC6199807
OpenAlexW2896409264

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.