Evidence map›Paper›PMID 39062702›Full record

ArticleGenes2024

Intellectual Disabilities and Neurocognitive Impairment in Adult Patients with Inherited Metabolic Diseases: A UK Single Centre Experience.

John Warner-Levy, Adrian H Heald, Daniel Hand, Reena Sharma, Rachel Thomasson, Karolina M Stepien

Abstract read
In one paragraph

Article in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

John Warner-LevyDepartment of Diabetes and Endocrinology, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.ORCID 0000-0003-2632-7266
Adrian H HealdDepartment of Diabetes and Endocrinology, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.
Daniel HandAdult Inherited Metabolic Disorders, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.
Reena SharmaAdult Inherited Metabolic Disorders, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.
Rachel ThomassonNeurology and Neuropsychiatry Department, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.
Karolina M StepienAdult Inherited Metabolic Disorders, Salford Royal Organisation, Northern Care Alliance NHS Foundation Trust, Salford M6 8HD, UK.ORCID 0000-0003-0148-6332

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited metabolic diseases (IMDs) are a group of heterogeneous genetic disorders resulting in substrate accumulation, energy deficiency, or complex molecular defects due to the failure of specific molecules to act as enzymes, cofactors, transporters, or receptors in specific metabolic pathways. The pathophysiological changes seen in IMDs are sometimes associated with intellectual disability (ID) or neurocognitive decline, necessitating multidisciplinary input. We here describe our experience at one tertiary metabolic centre in the UK. We reviewed the case prevalence and existing service provision in one adult IMD service covering a multi-ethnic population of 10 million in North England. In our cohort of 2268 IMD patients, 1598 patients had general metabolic conditions (70.5%), and 670 had lysosomal storage disease/disorders (LSD)s (29.5%). The overall prevalence of ID and neurocognitive decline was found to be 15.7% (

Indexed as

Intellectual DisabilityAdolescentAdultAgedCognitive DysfunctionFemaleHumansLysosomal Storage DiseasesMaleMetabolic DiseasesMetabolism, Inborn ErrorsMiddle AgedNeurocognitive DisordersPrevalenceUnited KingdomYoung Adultinherited metabolic diseasesintellectual disabilityneurocognitive assessmentneurocognitive dysfunctionrare disease

Identifiers

PMID39062702
PMCPMC11276493

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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.