Evidence map›Paper›PMID 40525315›Full record

ArticleBrain and behavior2025

22q11.2 Deletion Syndrome: Cognitive, Visuomotor, and Adaptive Functioning Followed Longitudinally.

L Wallin, C Gillberg, J Knutsson, E Fernell, I C Gillberg, E Billstedt

Abstract read
In one paragraph

Article in Brain and behavior, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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.

L WallinGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0009-0009-2519-8811
C GillbergGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
J KnutssonGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
E FernellGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
I C GillbergGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
E BillstedtGillberg Neuropsychiatry Centre, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID https://orcid.org/0000-0002-4200-2149

Funding

AnnMari och Per Ahlqvists StiftelseKurt and Ingrid Dahréns foundationQueen Silvia Children's hospital research fundthe Swedish state under the agreement between the Swedish government and the county councils, the ALF-agreement State (ALFGBG-721321)Willhelm and Martina Lundgren Foundation
6 · The paper itself

Abstract

backgroundLongitudinal studies on cognitive, visuomotor, and adaptive function and their relation to outcomes in adults with the 22q11.2 deletion syndrome (22q11.2DS) are limited.

methodsThis study involved 79 participants (43 females, 36 males) from an original cohort of 100 individuals (58 females, 42 males) with 22q11.2DS, assessed at ages 1-35 years between 1997 and 2006 (T1) and followed up in 2017-2022 (T2), when they were aged 18-50. Clinical, neuropsychological, and adaptive functioning assessments were performed.

resultsAt the group level, overall Full-Scale Intelligence Quotient (FSIQ) remained stable; however, females displayed a significant decline in FSIQ and visuomotor integration (Beery VMI) from T1 to T2. At follow-up, 19 of 56 (34%) participants had an uneven intelligence quotient (IQ) profile, with most (15/56; 27%) showing a higher Verbal Function Index (VFI) than Perceptual Function Index (PFI). At T1, 10 of 49 participants (20%) had this "uneven IQ profile," defined as having a higher VFI than PFI (Verbal Comprehension Index [VCI] ≥15 IQ points higher than Perceptual Reasoning Index [PRI]), compared to 14 of 49 (29%) at T2. In the psychosis subgroup (n = 8), FSIQ and Verbal Intelligence Quotient (VIQ) showed significant decreases; however, the small sample size limits the validity of these findings. Severe to moderate adaptive function impairments, as measured by the Global Assessment of Functioning (GAF) scale, were observed at T2, with T1 FSIQ predicting GAF at T2.

conclusionsWhile group-level intellectual functioning appeared stable, individual declines were noted. Long-term follow-up is essential for personalized support to mitigate severe psychiatric risks, including psychosis with declines in FSIQ, particularly VIQ, potentially indicating or resulting from psychosis in this population.

Indexed as

Adaptation, PsychologicalCognitionDiGeorge SyndromePsychomotor PerformanceAdolescentAdultChildChild, PreschoolFemaleHumansInfantIntelligenceIntelligence TestsLongitudinal StudiesMaleMiddle Aged

Identifiers

PMID40525315
PMCPMC12171631

What Socratic 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 Socratic graph.