Amélie Doussau

Mrs. Amélie Doussau

orcid

Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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11 September 2023 in European Journal of Paediatric Neurology
Verified
Journal Article
Open access
SPSarah Provost
Sarah Provost
SFSolène Fourdain
Solène Fourdain
PVPhetsamone Vannasing
Phetsamone Vannasing
JTJulie Tremblay
Julie Tremblay
KRKassandra Roger
Kassandra Roger
AGAnne Gallagher
Anne Gallagher
Survivors of complex forms of congenital heart disease (CHD)∗ are at high risk of neurodevelopmental disabilities. Neuroimaging studies have pointed to brain anomalies and immature networks in infants with CHD, yet less is known about their functional network topology and associations with neurodevelopment. To characterize the functional network topology in 4-month-old infants with repaired CHD, we compared graph theory metrics measured using resting-state functional near-infrared spectroscopy (rs-fNIRS) between infants with CHD (n = 22) and healthy controls (n = 30). We also investigated the moderating effect of graph theory metrics on the relationship between group (CHD vs. Controls) and developmental outcomes at 24 months. At 4 months, both groups presented similar functional brain network topology. At 24 months, children with CHD had lower scores on the language scale and the expressive communication subscale of the Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III), as well as lower scores on the Grammatical Form scale of the MacArthur-Bates Communicative Development Inventory (MBCDI). The relationship between group and expressive language was moderated by the normalized characteristic path length (λ) and the degree (k). Although infants with CHD have functional brain topology similar to that of healthy controls, our findings suggest that they do not benefit from an optimal functional brain organization in comparison with healthy infants.

23 August 2019 in Preprints.org
Verified
Preprint
Open access
PDF file
SFSolène Fourdain
Solène Fourdain
MSMarie-Noelle Simard
Marie-Noelle Simard
LDLynn Dagenais
Lynn Dagenais
MMManuela Materassi
Manuela Materassi
ADAmélie Doussau
Amélie Doussau
AGAnne Gallagher
Anne Gallagher
Objective: In this pilot study, we described the gross motor development of infants aged 4 to 24 months with congenital heart disease (CHD) and assessed through a systematic develop­mental screening programme, with individualised motor interventions. Methods: Thirty infants who had cardiac repair underwent gross motor evaluations using the AIMS at 4 months, and the Bayley-III at 12 and 24 months. Results: Based on AIMS, 80% of 4-month-old infants had a delay in gross motor development and required physical therapy. Gross motor abilities significantly improved by 24 months. Infants who benefited from regular physiotherapy tended to show better improvement in motor scores. Conclusion: Our study highlights the importance of early motor screening in infants with CHD and suggests a potential benefit of early physical therapy in those at-risk. Further research is needed to assess the effectiveness of systematic developmental screening and individualized inter­vention programmes at identifying at risk patients, and their impact on developmental outcomes.

8 September 2026 in Preprints.org
Verified
Preprint
Open access
PDF file
Charlotte SavardCharlotte Savard
Charlotte Savard
JTJulie Tremblay
Julie Tremblay
SPSarah Provost
Sarah Provost
NPNatacha Paquette
Natacha Paquette
SKSarah Kessouri
Sarah Kessouri
AGAnne Gallagher
Anne Gallagher
Background/Objectives: Congenital heart disease (CHD) is associated with altered brain development and an increased risk of neurodevelopmental difficulties, particularly in more severe forms of the condition. Although alterations in functional brain connectivity have been reported before and after the first corrective surgery in early infancy, as well as in adulthood, little is known about their presentation in early childhood and their association with neurodevelopmental outcomes. This study aimed to characterize resting-state functional connectivity in 3-year-old children with moderate-to-severe CHD and to examine its associations with neurodevelopmental outcomes, including cognitive, language, and motor abilities. Methods: Twenty-five 3-year-old children with moderate-to-severe CHD and 28 age-matched healthy controls completed resting-state functional near-infrared spectroscopy (fNIRS) and a standardized neurodevelopmental assessment. Functional brain connectivity was examined across frontal, fronto-parietal, left and right fronto-temporal, and inter-hemispheric networks. Group differences were analyzed using ANCOVAs controlling for socioeconomic status (maternal SES) and with sex as a factor. Associations between functional brain connectivity and neurodevelopmental measures were examined using hierarchical linear regression models adjusted for diagnostic group, sex, and socioeconomic status, with connectivity-by-group interactions tested to assess group differences in these associations. Results: Children with moderate-to-severe CHD showed overall lower resting-state functional connectivity and poorer language performance than controls. Greater interhemispheric functional connectivity was associated with fewer executive function difficulties across participants, with no significant differences in these associations between groups. Conclusions: Preschool-aged children with CHD show altered functional connectivity and language vulnerabilities, while the association between interhemispheric connectivity and executive functioning appears to extend across both CHD and typically developing children.

1 October 2026 in Biomedicines
Verified
Journal Article
Open access
PDF file
Charlotte SavardCharlotte Savard
Charlotte Savard
JTJulie Tremblay
Julie Tremblay
SPSarah Provost
Sarah Provost
NPNatacha Paquette
Natacha Paquette
SKSarah Kessouri
Sarah Kessouri
AGAnne Gallagher
Anne Gallagher
Background/Objectives: Congenital heart disease (CHD) is associated with altered brain development and an increased risk of neurodevelopmental difficulties, particularly in more severe forms of the condition. Although alterations in functional brain connectivity have been reported before and after the first corrective surgery in early infancy, as well as in adulthood, little is known about their presentation in early childhood and their association with neurodevelopmental outcomes. This study aimed to characterize resting-state functional connectivity in 3-year-old children with moderate-to-severe CHD and to examine its associations with neurodevelopmental outcomes, including cognitive, language, and motor abilities. Methods: Twenty-five 3-year-old children with moderate-to-severe CHD and 28 age-matched healthy controls completed resting-state functional near-infrared spectroscopy (fNIRS) analysis and a standardized neurodevelopmental assessment. Connectivity was compared across networks using a repeated-measures analysis of covariance (ANCOVA), then within each network separately, controlling for maternal socioeconomic status and with sex as a factor. Associations with neurodevelopmental measures were examined using hierarchical linear regressions adjusted for group, sex, and socioeconomic status, with connectivity-by-group interactions tested. Results: Children with moderate-to-severe CHD showed lower resting-state functional connectivity than controls specifically within the right fronto-temporal network, with no group differences in the four remaining networks, as well as poorer language performance. Greater inter-hemispheric functional connectivity was associated with fewer executive function difficulties and better overall motor performance across participants, and greater frontal connectivity with better motor coordination, with no significant differences in these associations between groups. Conclusions: Preschool-aged children with CHD show regionally circumscribed alterations in functional connectivity and language vulnerabilities, while the associations between connectivity and executive and motor functioning appear to extend across both CHD and typically developing children.