Evidence map›Paper›PMID 36831752›Full record

ArticleBrain sciences2023

Buffy Coat Score as a Biomarker of Treatment Response in Neuronal Ceroid Lipofuscinosis Type 2.

Siyamini Sivananthan, Laura Lee, Glenn Anderson, Barbara Csanyi, Ruth Williams, Paul Gissen

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

4 citing papers in PubMed, 6 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 2 institutions in 1 country.

Siyamini SivananthanDepartment of Inherited Metabolic Diseases, Great Ormond Street Hospital, London WC1N 1EH, UK.
Laura LeeDepartment of Inherited Metabolic Diseases, Great Ormond Street Hospital, London WC1N 1EH, UK.
Glenn AndersonDepartment of Inherited Metabolic Diseases, Great Ormond Street Hospital, London WC1N 1EH, UK.
Barbara CsanyiDepartment of Inherited Metabolic Diseases, Great Ormond Street Hospital, London WC1N 1EH, UK.
Ruth WilliamsDepartment of Children's Neurosciences, Evelina London Children's Hospital, London SE1 7EH, UK.
Paul GissenDepartment of Inherited Metabolic Diseases, Great Ormond Street Hospital, London WC1N 1EH, UK.ORCID 0000-0002-9712-6122
Great Ormond Street Hospital · GBEvelina London Children's Healthcare · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The introduction of intracerebroventricular (ICV) enzyme replacement therapy (ERT) for treatment of neuronal ceroid lipofuscinosis type 2 (CLN2) disease has produced dramatic improvements in disease management. However, assessments of therapeutic effect for ICV ERT are limited to clinical observational measures, namely the CLN2 Clinical Rating Scale, a subjective measure of motor and language performance. There is a need for an objective biomarker to enable assessments of disease progression and response to treatment. To address this, we investigated whether the proportion of cells with abnormal storage inclusions on electron microscopic examination of peripheral blood buffy coats could act as a biomarker of disease activity in CLN2 disease. We conducted a prospective longitudinal analysis of six patients receiving ICV ERT. We demonstrated a substantial and continuing reduction in the proportion of abnormal cells over the course of treatment, whereas symptomatic scores revealed little or no change over time. Here, we proposed the use of the proportion of cells with abnormal storage as a biomarker of response to therapy in CLN2. In the future, as more tissue-specific biomarkers are developed, the buffy coats may form part of a panel of biomarkers in order to give a more holistic view of a complex disease.

Indexed as

biomarkerblood buffy coatcurvilinear inclusionsdisease progressionelectron microscopyenzyme replacement therapyintracerebroventricularlysosomal storage disorderneurodegenerationneuronal ceroid lipofuscinosis type 2 (CLN2) disease

Identifiers

PMID36831752
PMCPMC9954623
OpenAlexW4318215095

What OpenQuestion holds

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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.