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Published on: October 2, 2019
Sleep in children from northeastern Brazil with congenital Zika syndrome: assessment using polysomnography
Valéria Brandão Marquis1,2, Adriana de Oliveira Melo1,2, Márcia Pradella-Hallinan3
1Federal University of Campina Grande, Campina Grande, Paraíba, Brazil.
Insights
Sleep disorders are common in children with congenital Zika syndrome, with central sleep apnea being the most frequent issue. This study highlights the need for sleep assessments in these children.
Area of Science:
- Neurology
- Pediatrics
- Sleep Medicine
Background:
- Congenital Zika syndrome (CZS) is a condition resulting from prenatal Zika virus infection.
- Sleep disturbances are increasingly recognized in children with neurological conditions.
Purpose of the Study:
- To characterize sleep patterns in children diagnosed with congenital Zika syndrome.
- To identify the prevalence and types of sleep disorders in this population.
Main Methods:
- Polysomnography (PSG) with neurological setup and capnography was conducted.
- Children were classified based on neuroclinical and neuroradiological findings.
- Respiratory events were scored using American Academy of Sleep Medicine criteria.
Main Results:
- Sleep apnea was present in 35.4% of children, with central sleep apnea being the most common type (65.2%).
- Periodic leg movements were observed in 73.8% of participants.
- Ventriculomegaly and calcifications were frequent neuroimaging findings.
Conclusions:
- Sleep disorders are prevalent in children with congenital Zika syndrome.
- Central sleep apnea is a significant finding in this population.
- Further research into the management of sleep disorders in CZS is warranted.
Study Objectives:
We performed this study to describe the characteristics of sleep in children with congenital Zika syndrome through polysomnographic assessment.
Methods:
Polysomnography with neurological setup and capnography was performed. Respiratory events were scored according to American Academy of Sleep Medicine criteria. Children were classified based on neuroclinical examination as having corticospinal plus neuromuscular abnormalities or exclusively corticospinal abnormalities. Neuroradiological classification was based on imaging exams, with children classed as having supratentorial plus infratentorial abnormalities or exclusively supratentorial abnormalities.
Results:
Of 65 children diagnosed with congenital Zika syndrome, sleep apnea was present in 23 children (35.4%), desaturation in 26 (40%), and snoring in 13 (20%). The most prevalent apnea type was central in 15 children (65.2%), followed by obstructive apnea in 5 (21.7%) and mixed type in 3 (13%). The average of the lowest saturation recorded was slightly below normal (89.1 ± 4.9%) and the mean partial pressure of end-tidal carbon dioxide value was normal. Periodic leg movements were present in 48 of 65 children. Lower ferritin levels were observed in 84.6% of children. Palatine and pharyngeal tonsils (adenoids) were small in most children and not associated with the presence of obstructive apnea. Ventriculomegaly and subcortical and nucleus calcification were the most frequent neuroimaging findings. Supratentorial and infratentorial anomalies were present in 26.7% (16 of 60) and exclusively supratentorial changes in 73.3% (44 of 60). In the neuroclinical classification, isolated corticospinal changes were more frequent and the mean peak in capnography was lower in this group. There was no difference regarding the presence of apnea for children in the neuroclinical and neuroradiological classification groups.
Conclusions:
Sleep disorders were frequent in children with congenital Zika syndrome, with central sleep apnea being the main finding.
Citation:
Brandão Marquis V, de Oliveira Melo A, Pradella-Hallinan M, et al. Sleep in children from northeastern Brazil with congenital Zika syndrome: assessment using polysomnography. J Clin Sleep Med. 2023;19(10):1759-1767.
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