Evidence map›Paper›PMID 35474244›Full record

ArticleGene therapy2023

Adeno-associated virus serotype 9 antibody titers in patients with SMA pre-screened for treatment with onasemnogene abeparvovec -routine care evidence.

Sharon Aharoni, Jacob Bistritzer, Hagit Levine, Liora Sagi, Aviva Fattal-Valevski, Mira Ginzberg, Iris Noyman, Rony Cohen, Yoram Nevo

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Gene therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. The impact of threeFrontiers in neurology · 2024
    Pooled it
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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

9 authors at 3 institutions in 1 country.

Sharon AharoniInstitute of Pediatric Neurology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel. sharonah@clalit.org.il.ORCID http://orcid.org/0000-0001-7255-6276
Jacob BistritzerInstitute of Pediatric Neurology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Hagit LevineSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Liora SagiSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Aviva Fattal-ValevskiSackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Mira GinzbergPediatric Neurology Unit, Wolfson Medical Center, Holon, Israel.
Iris NoymanPediatric Neurology Unit, Soroka University Medical Center, Ben Gurion University, Beer Sheva, Israel.
Rony CohenInstitute of Pediatric Neurology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Yoram NevoInstitute of Pediatric Neurology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.
Tel Aviv University · ILSchneider Children's Medical Center · ILWolfson Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal muscular atrophy (SMA) is characterized by progressive weakness of skeletal and respiratory muscles. This study aimed to evaluate the prevalence of pre-existing anti adeno-associated virus serotype 9 antibody (AAV9-Ab) titers among infantile-onset SMA diagnosed infants pre-screened for treatment with AAV9-based onasemnogene abeparvovec, and to explore whether clinical and/or demographic characteristics are correlated with AAV9 Ab test results. This is a retrospective multicenter study of children diagnosed with 5q SMA younger than two years of age. The obtained data included demographic data, SMA type, SMN2 gene copy number, onset date, and results of AAV9-Ab test and of SMA prior treatments. Thirty-four patients were enrolled; six patients had positive results of AAV9-Ab (titer > 1:50) in the initial screening, 15 patients were re-tested for AAV9-Abs, of whom, three patients had seroreverted [1.5-4.5 months] between the two AAV9-Abs tests. One patient had seroconverted (5.5 months after the first AAV9-Abs test). The remaining 11 patients presented matching titer results in the two tests. No demographic/clinical factors were correlated to high AAV9-Abs titers (P > 0.05).We recommend AAV9-Ab re-tests to be performed until the age of 8 months, or, if 1.5 months or more have passed after the initial AAV9-Abs test.

Indexed as

Muscular Atrophy, SpinalSpinal Muscular Atrophies of ChildhoodChildDependovirusGenetic TherapyHumansInfantSerogroup

Identifiers

PMID35474244
OpenAlexW4224943464

What OpenQuestion holds

Textmetadata
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.