Evidence map›Paper›PMID 36738194›Full record

ReviewAnnals of clinical and translational neurology2023

Linking autism spectrum disorders and parkinsonism: clinical and genetic association.

Aaron Shengting Mai, Chun En Yau, Fan Shuen Tseng, Qi Xuan Joel Foo, Dennis Qing Wang, Eng-King Tan

Open access · goldAbstract readReview
In one paragraph

Review in Annals of clinical and translational neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Cognitive Aging Patterns in Autism: Parallel, Accelerated, or Safeguarded?Journal of autism and developmental disorders · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Review of Elevated Para-Cresol in Autism and Possible Impact on Symptoms.International journal of molecular sciences · 2025
    Review
  8. Article
  9. Article
  10. Review
  11. Review
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.

Aaron Shengting MaiYong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Chun En YauYong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Fan Shuen TsengDepartment of Neurology, Singapore General Hospital Campus, National Neuroscience Institute, Singapore, Singapore.
Qi Xuan Joel FooDepartment of Neurology, Singapore General Hospital Campus, National Neuroscience Institute, Singapore, Singapore.
Dennis Qing WangDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Southern Medical University, Guangzhou, China.ORCID 0000-0002-3882-6540
Eng-King TanDepartment of Neurology, Singapore General Hospital Campus, National Neuroscience Institute, Singapore, Singapore.ORCID 0000-0002-8807-1529
Singapore General Hospital · SGNational University of Singapore · SGZhujiang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutism spectrum disorders (ASD) comprise many complex and clinically distinct neurodevelopmental conditions, with increasing evidence linking them to parkinsonism.

methodsWe searched Medline and Embase from inception to 21 March 2022 and reviewed the bibliographies of relevant articles. Studies were screened and reviewed comprehensively by two independent authors.

resultsOf 863 references from our search, we included eight clinical studies, nine genetic studies, and five case reports. Regardless of age group, Parkinson's disease (PD) and parkinsonian syndromes were more frequently observed in patients with ASD, though the evidence for increased rates of parkinsonism is less clear for children and adolescents. Parkinsonian features and hypokinetic behavior were common in Rett syndrome, with prevalence estimates ranging from 40% to 80%. Frequently observed parkinsonian features include bradykinesia, rigidity, hypomimia, and gait freezing. PD gene PARK2 copy number variations appear more frequently in ASD cases than controls. Evidence suggests that RIT2 and CD157/BST1 are implicated in ASD and PD, while the evidence for other PD-related genes (DRD2, GPCR37, the SLC gene family, and SMPD1) is less clear. Rare mutations, such as ATP13A2, CLN3, and WDR45, could result in autistic behavior and concomitant parkinsonism.

conclusionThe prevalence of parkinsonism in ASD is substantially greater than in the general population or matched controls. Various PD-associated gene loci, especially PARK2, could confer susceptibility to ASD as well. Important future directions include conducting prospective cohort studies to understand how parkinsonian symptoms may progress, genetic studies to reveal relevant gene loci, and pathophysiologic studies to identify potential therapeutic targets.

Indexed as

Autism Spectrum DisorderParkinson DiseaseParkinsonian DisordersAdolescentCarrier ProteinsChildDNA Copy Number VariationsHumansMembrane GlycoproteinsMolecular ChaperonesProspective StudiesCarrier ProteinsCLN3 protein, humanMembrane GlycoproteinsMolecular ChaperonesWDR45 protein, human

Identifiers

PMID36738194
PMCPMC10109258
OpenAlexW4319163243

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.