Evidence map›Paper›PMID 27847291›Full record

ReviewInternational journal of surgery (London, England)2016

RNA interference in the treatment of renal stone disease: Current status and future potentials.

Kyle D Wood, Ross P Holmes, John Knight

Open access · greenAbstract readReview
In one paragraph

Review in International journal of surgery (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Breaking the Cycle of Recurrent Calcium Stone Disease.Advances in kidney disease and health · 2023
    Review
  4. Effect of alanine supplementation on oxalate synthesis.Biochimica et biophysica acta. Molecular basis of disease · 2021
    Article
  5. Article
  6. Combined and sequential liver-kidney transplantation in children.Pediatric nephrology (Berlin, Germany) · 2018
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Kyle D WoodDepartment of Urology, 816 KAUL Building, 720 20th Street South, The University of Alabama at Birmingham, Birmingham, AL, 35294-3411, USA. Electronic address: kwood2@uabmc.edu.
Ross P HolmesDepartment of Urology, 816 KAUL Building, 720 20th Street South, The University of Alabama at Birmingham, Birmingham, AL, 35294-3411, USA. Electronic address: rholmes@uab.edu.
John KnightDepartment of Urology, 816 KAUL Building, 720 20th Street South, The University of Alabama at Birmingham, Birmingham, AL, 35294-3411, USA. Electronic address: knight74@uab.edu.
University of Alabama at Birmingham · US

Funding

Mitochondrial Metabolism in Primary HyperoxaluriaR01DK054468 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOLMES, ROSS P · 1999 to 2017
$4.1M
Endogenous Oxalate SynthesisR01DK073732 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOLMES, ROSS P · 2006 to 2014
$2.4M
Hydroxproline Catabolism and HyperoxaluriaR01DK083527 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI HOLMES, ROSS P, LOWTHER, W TODD · 2010 to 2012
$753k
NIDDK NIH HHS R01 DK054468NIDDK NIH HHS R01 DK073732NIDDK NIH HHS R01 DK083527
6 · The paper itself

Abstract

Recent advances in RNA interference (RNAi) delivery and chemistry have resulted in the development of more than 20 RNAi-based therapeutics, several of which are now in Phase III trials. The most advanced clinical trials have utilized modifications such as lipid nanoparticles and conjugation to N-acetyl galactosamine to treat liver specific diseases. Recent reports have suggested that reducing endogenous oxalate synthesis by RNAi may be a safe and effective therapy for patients with the rare disease, Primary Hyperoxaluria (PH). Our current understanding of endogenous oxalate synthesis indicates that two enzymes, hydroxyproline dehydrogenase and glycolate oxidase (GO), are suitable targets for oxalate reduction therapy. Our studies in a mouse model of PH type 1 have demonstrated that reducing the expression of either of these enzymes in the liver with RNAi significantly reduces urinary oxalate excretion. Early human phase clinical trials are now under way in PH1 patients with RNAi targeting GO. Future elaboration of other contributors of stone disease and improvement in tissue specific targeting with RNAi may lead to further therapies that target idiopathic stone disease.

Indexed as

RNA InterferenceAnimalsGenetic TherapyHumansKidney CalculiPrognosisEndogenous oxalateGlycolate oxidaseHydroxyprolineHydroxyproline dehydrogenaseIdiopathic calcium oxalateKidney stoneNephrolithiasisOxalatePrimary hyperoxaluriaRNAiRNA interference

Identifiers

PMID27847291
PMCPMC5218583
OpenAlexW2557173648

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.