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Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study

INTRODUCTION: Perinatal period is characterized by a broad range of physical, psychological and relational changes. Maternal perinatal depression (PD) is defined as an episode of major depression with the onset from pregnancy to the first year after delivery. Depressive symptoms influence the earlie...

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Autores principales: O. P., M. Caccialupi, Pucci, C., Colaiori, M., Giacchetti, N., Aceti, F., Sogos, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475934/
http://dx.doi.org/10.1192/j.eurpsy.2021.1477
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author O. P., M. Caccialupi
Pucci, C.
Colaiori, M.
Giacchetti, N.
Aceti, F.
Sogos, C.
author_facet O. P., M. Caccialupi
Pucci, C.
Colaiori, M.
Giacchetti, N.
Aceti, F.
Sogos, C.
author_sort O. P., M. Caccialupi
collection PubMed
description INTRODUCTION: Perinatal period is characterized by a broad range of physical, psychological and relational changes. Maternal perinatal depression (PD) is defined as an episode of major depression with the onset from pregnancy to the first year after delivery. Depressive symptoms influence the earlier mother-child interaction and impact on child cognitive, affective and behavioral development. OBJECTIVES: Purpose of our study was to evaluate the consequences of PD on sleep-wake patterns in the early stages of infant development. We aim to investigate the presence of poor sleep in infants/ toddlers and also to identify differences in sleep ecology variables. METHODS: We enrolled, from December 2019 to September 2020, a clinical sample of children born from women with PD (N=19, m.a.=13,7, SD= 7,6) and a healthy control group (N=21, m.a.=15,5, SD=5,43). Infant sleep data were obtained from the Brief Infant Sleep Questionnaire (BISQ). Poor sleepers were defined by the following criteria: >3 night wakings, nocturnal wakefulness >1 hr or total sleep duration <9 hr. Maternal depression was assessed with clinical and psychometric evaluation. T-test was used for comparison between the two samples. RESULTS: Statistical analysis indicates that there were not significant differences between the two groups concerning night wakings (p= .678), nocturnal wakefulness (p= .815), total sleep duration (p= .209) and nocturnal sleep onset time (p= .475). CONCLUSIONS: Our findings suggest that PD is not a risk-factor in the onset of infant sleep problems. Probably negative parentig, affective disengagement, delegation in maternal care and sedative effects of pharmacotherapy may affect mother’s perception of her infant’s sleep.
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spelling pubmed-94759342022-09-29 Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study O. P., M. Caccialupi Pucci, C. Colaiori, M. Giacchetti, N. Aceti, F. Sogos, C. Eur Psychiatry Abstract INTRODUCTION: Perinatal period is characterized by a broad range of physical, psychological and relational changes. Maternal perinatal depression (PD) is defined as an episode of major depression with the onset from pregnancy to the first year after delivery. Depressive symptoms influence the earlier mother-child interaction and impact on child cognitive, affective and behavioral development. OBJECTIVES: Purpose of our study was to evaluate the consequences of PD on sleep-wake patterns in the early stages of infant development. We aim to investigate the presence of poor sleep in infants/ toddlers and also to identify differences in sleep ecology variables. METHODS: We enrolled, from December 2019 to September 2020, a clinical sample of children born from women with PD (N=19, m.a.=13,7, SD= 7,6) and a healthy control group (N=21, m.a.=15,5, SD=5,43). Infant sleep data were obtained from the Brief Infant Sleep Questionnaire (BISQ). Poor sleepers were defined by the following criteria: >3 night wakings, nocturnal wakefulness >1 hr or total sleep duration <9 hr. Maternal depression was assessed with clinical and psychometric evaluation. T-test was used for comparison between the two samples. RESULTS: Statistical analysis indicates that there were not significant differences between the two groups concerning night wakings (p= .678), nocturnal wakefulness (p= .815), total sleep duration (p= .209) and nocturnal sleep onset time (p= .475). CONCLUSIONS: Our findings suggest that PD is not a risk-factor in the onset of infant sleep problems. Probably negative parentig, affective disengagement, delegation in maternal care and sedative effects of pharmacotherapy may affect mother’s perception of her infant’s sleep. Cambridge University Press 2021-08-13 /pmc/articles/PMC9475934/ http://dx.doi.org/10.1192/j.eurpsy.2021.1477 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
O. P., M. Caccialupi
Pucci, C.
Colaiori, M.
Giacchetti, N.
Aceti, F.
Sogos, C.
Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title_full Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title_fullStr Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title_full_unstemmed Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title_short Perinatal depression as a risk-factor for infant sleep disturbances: Subjective data from a case-control study
title_sort perinatal depression as a risk-factor for infant sleep disturbances: subjective data from a case-control study
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9475934/
http://dx.doi.org/10.1192/j.eurpsy.2021.1477
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