Evidence map›Paper›PMID 28556830›Full record

ArticleTranslational psychiatry2017

Adolescence is the starting point of sex-dichotomous COMT genetic effects.

S Sannino, M C Padula, F Managò, M Schaer, M Schneider, M Armando, E Scariati, F Sloan-Bena, M Mereu, M Pontillo and 7 more

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
2.2field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 2 syntheses or guidelines pooled it, 36 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Review
  5. Article
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  11. Review
  12. Article
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  15. Article
  16. Inhibition of Catechol-Frontiers in behavioral neuroscience · 2020
    Article
  17. Article
  18. Article
  19. Haplotypic and Genotypic Association of Catechol-Frontiers in pharmacology · 2018
    Article
  20. Making Dopamine Connections in Adolescence.Trends in neurosciences · 2017
    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

17 authors at 7 institutions in 2 countries.

S SanninoDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
M C PadulaOffice Médico-Pédagogique, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
F ManagòDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
M SchaerOffice Médico-Pédagogique, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
M SchneiderOffice Médico-Pédagogique, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
M ArmandoDepartment of Neuroscience, Bambino Gesù Children's Hospital, Piazza Sant'Onofrio, Rome, Italy.
E ScariatiOffice Médico-Pédagogique, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
F Sloan-BenaService of Genetic Medicine, University Geneva Hospitals, Geneva, Switzerland.
M MereuDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
M PontilloDepartment of Neuroscience, Bambino Gesù Children's Hospital, Piazza Sant'Onofrio, Rome, Italy.
S VicariDepartment of Neuroscience, Bambino Gesù Children's Hospital, Piazza Sant'Onofrio, Rome, Italy.
G ContariniDipartimento di Scienze del Farmaco, Universita' degli Studi di Padova, Padova, Italy.
C ChiabreraDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
M PaganiFunctional Neuroimaging Laboratory, Center for Neuroscience and Cognitive Systems, Istituto Italiano di Tecnologia, Rovereto, Italy.
A GozziFunctional Neuroimaging Laboratory, Center for Neuroscience and Cognitive Systems, Istituto Italiano di Tecnologia, Rovereto, Italy.
S EliezOffice Médico-Pédagogique, Department of Psychiatry, University of Geneva, Geneva, Switzerland.
F PapaleoDepartment of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, Genoa, Italy.
Italian Institute of Technology · ITBambino Gesù Children's Hospital · ITUniversity of Geneva · CHOffice Médico Pédagogique · CHCenter for Neuroscience and Cognitive Systems · ITUniversity Hospital of Geneva · CHUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The catechol-o-methyltransferase (COMT) genetic variations produce pleiotropic behavioral/neuroanatomical effects. Some of these effects may vary among sexes. However, the developmental trajectories of COMT-by-sex interactions are unclear. Here we found that extreme COMT reduction, in both humans (22q11.2 deletion syndrome COMT Met) and mice (COMT-/-), was associated to cortical thinning only after puberty and only in females. Molecular biomarkers, such as tyrosine hydroxylase, Akt and neuronal/cellular counting, confirmed that COMT-by-sex divergent effects started to appear at the cortical level during puberty. These biochemical differences were absent in infancy. Finally, developmental cognitive assessment in 22q11DS and COMT knockout mice established that COMT-by-sex-dichotomous effects in executive functions were already apparent in adolescence. These findings uncover that genetic variations severely reducing COMT result in detrimental cortical and cognitive development selectively in females after their sexual maturity. This highlights the importance of taking into account the combined effect of genetics, sex and developmental stage.

Indexed as

Sex CharacteristicsAdolescentAnimalsBiomarkersBrainCatechol O-MethyltransferaseCognitionDiGeorge SyndromeFemaleFrontal LobeGenetic VariationGenotypeHumansMagnetic Resonance ImagingMaleMiceBiomarkersCatechol O-MethyltransferaseCOMT protein, human

Identifiers

PMID28556830
PMCPMC5584523
OpenAlexW2619405979

What OpenQuestion holds

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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.