Evidence map›Paper›PMID 20864813›Full record

ArticleEpigenetics2011

Epigenetic investigation of variably X chromosome inactivated genes in monozygotic female twins discordant for primary biliary cirrhosis.

Michelle M Mitchell, Ana Lleo, Luca Zammataro, Marlyn J Mayo, Pietro Invernizzi, Nancy Bach, Shinji Shimoda, Stuart Gordon, Mauro Podda, M Eric Gershwin and 2 more

Open access · bronzeAbstract readTwin Study
In one paragraph

Article in Epigenetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.3field-weighted citation impact, top 3% 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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 78 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Impact of Menopause on Autoimmune and Rheumatic Diseases.Clinical reviews in allergy & immunology · 2025
    Review
  4. Review
  5. Article
  6. Review
  7. PIN1 and PIN4 inhibitionFrontiers in microbiology · 2023
    Article
  8. The Role of Epigenetics in Primary Biliary Cholangitis.International journal of molecular sciences · 2022
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Animal models of primary biliary cirrhosis.Clinical reviews in allergy & immunology · 2015
    Review
  18. Article
  19. Review
  20. 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

12 authors at 9 institutions in 5 countries.

Michelle M MitchellMedical Microbiology and Immunology, University of California at Davis, CA, USA.
Ana Lleo
Luca Zammataro
Marlyn J Mayo
Pietro Invernizzi
Nancy Bach
Shinji Shimoda
Stuart Gordon
Mauro Podda
M Eric Gershwin
Carlo Selmi
Janine M LaSalle
University of California, Davis · USBipar · FRENT and Allergy · USFondazione Humanitas per la Ricerca · ITHenry Ford Hospital · USIRCCS Humanitas Research Hospital · ITKyushu University · JPMount Sinai Medical Center · USThe University of Texas Southwestern Medical Center · US

Funding

Epigenetic Interaction of MECP2 and Organic Pollutants in NeurodevelopmentR01ES015171 · NIEHS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LASALLE, JANINE M · 2006 to 2009
$1.8M
EPIGENETICS X-LINKED GENES IN PBC: DOES X MARK THE SPOT?R21DK075400 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI SELMI, CARLO FRANCESCO · 2006 to 2007
$374k
NIDDK NIH HHS R21 DK075400NIDDK NIH HHS R21DK075400NIEHS NIH HHS R01 ES015171NIEHS NIH HHS R01ES015171
6 · The paper itself

Abstract

Primary biliary cirrhosis (PBC) is an autoimmune chronic cholestatic liver disease with a strong genetic susceptibility due to the high concordance in monozygotic (MZ) twins and a striking female predominance. Women with PBC manifest an enhanced X monosomy rate in peripheral lymphocytes and we thus hypothesized an X chromosome epigenetic component to explain PBC female prevalence. While most genes on the female inactive X chromosome are silenced by promoter methylation following X chromosome inactivation (XCI), approximately 10% of X- linked genes exhibit variable escape from XCI in healthy females. This study was designed to test the hypothesis that susceptibility to PBC is modified by one or more X-linked gene with variable XCI status. Peripheral blood mRNA and DNA samples were obtained from a unique cohort of MZ twin sets discordant and concordant for PBC. Transcript levels of the 125 variable XCI status genes was determined by quantitative RT-PCR analysis and two genes (CLIC2 and PIN4) were identified as consistently downregulated in the affected twin of discordant pairs. Both CLIC2 and PIN4 demonstrated partial and variable methylation of CpG sites within 300 bp of the transcription start site that did not predict the XCI status. Promoter methylation of CLIC2 manifested no significant difference between samples and no significant correlation with transcript levels. PIN4 methylation showed a positive trend with transcription in all samples but no differential methylation was observed between discordant twins. A genetic polymorphism affecting the number of CpG sites in the PIN4 promoter did not impact methylation or transcript levels in a heterozygous twin pair and showed a similar frequency in independent series of unrelated PBC cases and controls. Our results suggest that epigenetic factors influencing PBC onset are more complex than methylation differences at X-linked promoters and variably 3 inactivated X-linked genes may be characterized by partial promoter methylation and biallelic transcription.

Indexed as

DNA MethylationX Chromosome InactivationChloride ChannelsChromosomes, Human, XCohort StudiesCpG IslandsFemaleGenetic Diseases, X-LinkedHumansLiver Cirrhosis, BiliaryLymphocytesNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePolymorphism, GeneticRNA, MessengerTranscription, GeneticChloride ChannelsCLIC2 protein, humanNIMA-Interacting Peptidylprolyl IsomerasePeptidylprolyl IsomerasePIN1 protein, humanPIN4 protein, humanRNA, Messenger

Identifiers

PMID20864813
PMCPMC3029486
OpenAlexW2160286936

What OpenQuestion holds

Textmetadata
LicenceTDM
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.