Single Cell Sequencing of Tonsillar Tissue in Children With OSA

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age6-11
SponsorChinese University of Hong Kong

About this trial

Obstructive sleep apnoea (OSA) in children is a prevalent sleep disorder, and is characterised by repetitive complete or partial upper airway obstruction during sleep. It is an important disease as it is associated with a large spectrum of end-organ morbidities.

Adenotonsillar hypertrophy is the commonest cause of OSA in children, however, the cause of the lymphoid tissue hypertrophy in some individuals but not the others remains unknown. To address the cellular heterogeneity and immune cell involvement in adenotonsillar hypertrophy, here, we propose to employ single-cell sequencing analysis to identify the cell-specific expression patterns associated with the disease, which will enhance our understanding of the pathogenesis of tonsillar hypertrophy in children with OSA and may provide directions for development of novel therapy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Case: Chinese children aged 6-11 years old with habitual snoring (≥3 nights per week) and polysomnography (PSG) confirmed OSA (obstructive apnoea hypopnoea index (OAHI) of ≥1/hour), with adenotonsillar hypertrophy and clinical indications for adenotonsillectomy will be recruited as cases. Control: Non-OSA subjects (with PSG OAHI \<1/hour) who undergo adenotonsillectomy for other reasons such as recurrent tonsillitis.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • Tonsillectomy

    Procedure/Surgery

    Subjects who are diagnosed to have OSA with adeontonsillar enlargement will undergo adenotonsillectomy if it is clinically indicated. Adenotonsillar tissue will be obtained for single cell sequencing. Controls will be non-OSA subjects (with PSG OAHI \<1/hour) who undergo adenotonsillectomy for other reasons such as recurrent tonsillitis.

Treatment groups

15 Participants
are divided into 2 treatment groups
Group A: OSA case1 intervention
Group B: Control1 intervention

Trial outcomes

Primary outcomes

1

Tonsil cell characteristics

Cells characteristics by single-cell sequencing of the adenotonsillar tissue in children with OSA.

Time frame
Through study completion, an average of 2 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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