Evidence map›Paper›PMID 29808448›Full record

ArticleInternational urology and nephrology2018

Transcriptome analysis supports viral infection and fluoride toxicity as contributors to chronic kidney disease of unknown etiology (CKDu) in Sri Lanka.

Saravanabavan Sayanthooran, Lishanthe Gunerathne, Tilak D J Abeysekera, Dhammika N Magana-Arachchi

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In one paragraph

Article in International urology and nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Selenium attenuates apoptosis and p-AMPK expressions in fluoride-induced NRK-52E cells.Environmental science and pollution research international · 2019
    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

4 authors at 2 institutions in 1 country.

Saravanabavan SayanthooranMolecular Microbiology and Human Diseases, National Institute of Fundamental Studies, Kandy, 20000, Sri Lanka.ORCID http://orcid.org/0000-0002-1334-6364
Lishanthe GunerathneRenal Research Centre, District Hospital, Girandurukotte, 90750, Sri Lanka.ORCID http://orcid.org/0000-0001-8184-0252
Tilak D J AbeysekeraCentre for Education, Research and Training on Kidney Diseases (CERTKID), Faculty of Medicine, University of Peradeniya, Peradeniya, 20400, Sri Lanka.ORCID http://orcid.org/0000-0002-8802-6832
Dhammika N Magana-ArachchiMolecular Microbiology and Human Diseases, National Institute of Fundamental Studies, Kandy, 20000, Sri Lanka. cellbio@ifs.ac.lk.ORCID http://orcid.org/0000-0001-5825-4626
National Institute of Fundamental Studies · LKUniversity of Peradeniya · LK

Funding

National Research Council Sri Lanka 11-059
6 · The paper itself

Abstract

purposeChronic kidney disease of unknown etiology (CKDu), having epidemic characteristics, is being diagnosed increasingly in certain tropical regions of the world, mainly Latin America and Sri Lanka. They have been observed primarily in farming communities and current hypotheses point toward many environmental and occupational triggers. CKDu does not have common etiologies of chronic kidney disease (CKD) such as hypertension, diabetes, or autoimmune disease. We aimed to understand the molecular processes underlying CKDu in Sri Lanka using transcriptome analysis.

methodsRNA extracted from whole blood was reverse transcribed and used for microarray analysis using the Human HT-12 v.4 array (Illumina). Pathway analysis was carried out using ingenuity pathway analysis (IPA-Qiagen). Microarray results were validated using real-time PCR of five selected genes.

resultsPathways related to innate immune response, including interferon signaling, inflammasome signaling and TREM1 signaling had the most significant positive activation z scores, where as EIF2 signaling and mTOR signaling had the most significant negative activation z scores. Pathways previously linked to fluoride toxicity; G-protein activation, Cdc42 signaling, Rac signaling and RhoA signaling were activated in CKDu patients. The most significantly activated biological functions were cell death, cell movement and antimicrobial response. Significant toxicological functions were mitochondrial dysfunction, oxidative stress and apoptosis.

conclusionsBased on the molecular pathway analysis in CKDu patients and review of literature, viral infections and fluoride toxicity appear to be contributing to the molecular mechanisms underlying CKDu.

Indexed as

Adultcdc42 GTP-Binding ProteinEukaryotic Initiation Factor-2FluoridesGene Expression ProfilingGTP-Binding ProteinsHumansImmunity, InnateInflammasomesInterferonsMiddle AgedOligonucleotide Array Sequence Analysisrac GTP-Binding ProteinsRenal Insufficiency, ChronicrhoA GTP-Binding ProteinRNAcdc42 GTP-Binding ProteinCDC42 protein, humanEukaryotic Initiation Factor-2FluoridesGTP-Binding ProteinsInflammasomesInterferonsMTOR protein, humanrac GTP-Binding ProteinsrhoA GTP-Binding ProteinRNATOR Serine-Threonine KinasesTREM1 protein, humanTriggering Receptor Expressed on Myeloid Cells-1EIF2 signalingInnate immunityInterferon signalingMicroarraymTOR signalingRT-qPCR

Identifiers

PMID29808448
OpenAlexW2805546155

What OpenQuestion holds

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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.