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Published on: October 2, 2019
Childhood Sleepwalking and Sleep Terrors: A Longitudinal Study of Prevalence and Familial Aggregation
Dominique Petit1, Marie-Hélène Pennestri2, Jean Paquet1
1Center for Advanced Research in Sleep Medicine, Hôpital du Sacré-Cœur de Montréal, Montreal, Quebec, Canada2Department of Psychiatry, Université de Montréal, Montreal, Quebec, Canada.
Insights
Childhood sleepwalking and sleep terrors are common parasomnias with a strong genetic link. Parental history of sleepwalking significantly increases a child's risk for both conditions, suggesting a shared origin.
Area of Science:
- Pediatric Neurology
- Sleep Medicine
- Genetics
Background:
- Childhood sleepwalking and sleep terrors are parasomnias that can pose risks of injury.
- Familial aggregation has been previously observed for these sleep disorders.
Purpose of the Study:
- To determine the prevalence of sleepwalking and sleep terrors in children.
- To investigate the association between early sleep terrors and later sleepwalking.
- To evaluate the impact of parental history on the occurrence of these parasomnias.
Main Methods:
- Prospective longitudinal cohort study of 1940 children (Quebec Longitudinal Study of Child Development).
- Yearly assessments from 1.5 years (sleep terrors) and 2.5 years (sleepwalking) up to age 13.
- Mothers completed questionnaires on sleep patterns and parental history of sleepwalking.
Main Results:
- Peak prevalence for sleep terrors was 34.4% at 1.5 years; for sleepwalking, it was 13.4% at 10 years.
- One-third of children with early sleep terrors developed sleepwalking later.
- Parental history of sleepwalking significantly increased the prevalence of childhood sleepwalking and predicted sleep terrors.
Conclusions:
- Strong familial aggregation supports sleepwalking and sleep terrors as manifestations of the same underlying condition.
- Parental history is a significant predictor for both sleepwalking and sleep terrors in children.
- These findings highlight the importance of genetic factors in the pathophysiology of childhood parasomnias.
Importance:
Childhood sleepwalking and sleep terrors are 2 parasomnias with a risk of serious injury for which familial aggregation has been shown.
Objectives:
To assess the prevalence of sleepwalking and sleep terrors during childhood; to investigate the link between early sleep terrors and sleepwalking later in childhood; and to evaluate the degree of association between parental history of sleepwalking and presence of somnambulism and sleep terrors in children.
Design, Setting, And Participants:
Sleep data from a large prospective longitudinal cohort (the Quebec Longitudinal Study of Child Development) of 1940 children born in 1997 and 1998 in the province were studied from March 1999 to March 2011.
Main Outcomes And Measures:
Prevalence of sleep terrors and sleepwalking was assessed yearly from ages 1 1/2 and 2 1/2 years, respectively, to age 13 years through a questionnaire completed by the mother. Parental history of sleepwalking was also queried.
Results:
The peak of prevalence was observed at 1 1/2 years for sleep terrors (34.4% of children; 95% CI, 32.3%-36.5%) and at age 10 years for sleepwalking (13.4%; 95% CI, 11.3%-15.5%). As many as one-third of the children who had early childhood sleep terrors developed sleepwalking later in childhood. The prevalence of childhood sleepwalking increases with the degree of parental history of sleepwalking: 22.5% (95% CI, 19.2%-25.8%) for children without a parental history of sleepwalking, 47.4% (95% CI, 38.9%-55.9%) for children who had 1 parent with a history of sleepwalking, and 61.5% (95% CI, 42.8%-80.2%) for children whose mother and father had a history of sleepwalking. Moreover, parental history of sleepwalking predicted the incidence of sleep terrors in children as well as the persistent nature of sleep terrors.
Conclusions And Relevance:
These findings substantiate the strong familial aggregation for the 2 parasomnias and lend support to the notion that sleepwalking and sleep terrors represent 2 manifestations of the same underlying pathophysiological entity.
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