Evidence map›Paper›PMID 38961480›Full record

ArticleOrphanet journal of rare diseases2024

Autism spectrum disorder in young patients with congenital central hypoventilation syndrome: role of the autonomic nervous system dysfunction.

Benjamin Dudoignon, Anna Maruani, Richard Delorme, Maxime Patout, Mylene Fefeu, Pierre Ellul, Plamen Bokov, Christophe Delclaux

Abstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Benjamin DudoignonService de Physiologie Pédiatrique-Centre du Sommeil, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, CRMR Maladies respiratoires rares - Hypoventilations alvéolaires rares - Syndrome d'Ondine, INSERM NeuroDiderot, Paris, F-75019, France. benjamin.dudoignon@aphp.fr.ORCID 0000-0003-0827-616X
Anna MaruaniService de psychiatrie de l'enfant et l'adolescent, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, Paris, 75 019, France.
Richard DelormeService de psychiatrie de l'enfant et l'adolescent, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, Paris, 75 019, France.
Maxime PatoutService des Pathologies du Sommeil (Département R3S) - CRMR Hypoventilations centrales congénitales, UMRS1158 Neurophysiologie Respiratoire Expérimentale et Clinique, Sorbonne Université, AP-HP, Hôpital de la Pitié-Salpêtrière, INSERM, Paris, F-75005, France.
Mylene FefeuService de psychiatrie de l'enfant et l'adolescent, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, Paris, 75 019, France.
Pierre EllulService de psychiatrie de l'enfant et l'adolescent, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, Paris, 75 019, France.
Plamen BokovService de Physiologie Pédiatrique-Centre du Sommeil, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, CRMR Maladies respiratoires rares - Hypoventilations alvéolaires rares - Syndrome d'Ondine, INSERM NeuroDiderot, Paris, F-75019, France.
Christophe DelclauxService de Physiologie Pédiatrique-Centre du Sommeil, Université de Paris-Cité, AP-HP, Hôpital Robert Debré, CRMR Maladies respiratoires rares - Hypoventilations alvéolaires rares - Syndrome d'Ondine, INSERM NeuroDiderot, Paris, F-75019, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCongenital central hypoventilation syndrome (CCHS) is a rare condition characterized by alveolar hypoventilation and autonomic nervous system (ANS) dysfunction requiring long-term ventilation. CCHS could constitute a risk factor of autism spectrum disorder (ASD) due to birth injury related to respiratory failure, which remains to be determined. ANS dysfunction has also been described in ASD and there are indications for altered contribution of ANS-central nervous system interaction in processing of social information; thus, CCHS could be a risk factor for ASD based on pathophysiological background also. Our study aimed to determine the prevalence of ASD among CCHS patients, identify risk factors, and explore the relationship between the ANS, evaluated by heart rate variability indices, and adaptative functioning.

resultsOur retrospective study, based on the analysis of records of a French national center of patients with CCHS under 20 years of age, determined that the prevalence of ASD (diagnosed by a psychiatrist, following the criteria of DSM-4 or DSM-5) was 6/69 patients, 8.7% (95% confidence interval: 3.3-18.0%). In a case (CCHS with ASD, n = 6) - control (CCHS without ASD, n = 12) study with matching on sex, longer neonatal hospitalization stay and glycemic dysfunction were associated with ASD. Adaptative functioning was assessed using Vineland Adaptative behavioral scales (VABS) and heart rate variability indices (including daytime RMSSD as an index of parasympathetic modulation) were obtained from ECG Holter performed the same day. In 19 young subjects with CCHS who had both ECG Holter and VABS, significant positive correlations were observed between RMSSD and three of four sub-domains of the VABS (communication: R = 0.50, p = 0.028; daily living skills: R = 0.60, p = 0.006; socialization: R = 0.52, p = 0.021).

conclusionOur study suggests a high prevalence of ASD in patients with CCHS. Glycemic dysfunction and longer initial hospitalization stays were associated with ASD development. A defect in parasympathetic modulation was associated with worse adaptative functioning.

Indexed as

Autism Spectrum DisorderAutonomic Nervous SystemHypoventilationSleep Apnea, CentralAdolescentAutonomic Nervous System DiseasesChildChild, PreschoolFemaleHumansMaleRetrospective StudiesRisk FactorsYoung AdultAutism spectrum disorderAutonomic nervous systemCongenital central hypoventilation syndromeHeart rate variability

Identifiers

PMID38961480
PMCPMC11220943

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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.