Evidence map›Paper›PMID 33912759›Full record

ArticleKidney international reports2021

Hepatic Lactate Dehydrogenase A: An RNA Interference Target for the Treatment of All Known Types of Primary Hyperoxaluria.

Gema Ariceta, Kelly Barrios, Bob D Brown, Bernd Hoppe, Ralf Rosskamp, Craig B Langman

Open access · goldAbstract read
In one paragraph

Article in Kidney international reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Gema AricetaDivision of Pediatric Nephrology, Hospital Universitari Vall d'Hebron, Universitat Autonoma de Barcelona, Barcelona, Spain.
Kelly BarriosDicerna Pharmaceuticals, Inc., Lexington, Massachusetts, USA.
Bob D BrownDicerna Pharmaceuticals, Inc., Lexington, Massachusetts, USA.
Bernd HoppeDicerna Pharmaceuticals, Inc., Lexington, Massachusetts, USA.
Ralf RosskampDicerna Pharmaceuticals, Inc., Lexington, Massachusetts, USA.
Craig B LangmanFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Dicerna Pharmaceuticals (United States) · USNorthwestern University · USUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrimary hyperoxaluria (PH) is a family of 3 rare genetic disorders of hepatic glyoxylate metabolism that lead to overproduction and increased renal excretion of oxalate resulting in progressive renal damage.

methodsNonclinical data in mice and nonhuman primates show that

resultsBased on a literature review of human LDHA deficiency, we defined the phenotype as mainly muscle-related with no liver manifestations. Healthy volunteers treated with nedosiran experienced no drug-related musculoskeletal adverse events. There were no significant alterations in plasma lactate, pyruvate, or creatine kinase levels in the nedosiran group compared with the placebo group, signaling the uninterrupted interconversion of lactate and pyruvate and normal muscle function.

conclusionPhase I clinical data on nedosiran and published nonclinical data together provide substantial evidence that

Indexed as

lactate dehydrogenase Anedosiranprimary hyperoxaluriaRNA interferencesmall interfering RNA

Identifiers

PMID33912759
PMCPMC8071644
OpenAlexW3127624578

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.