The melanopsin-mediated pupil response is reduced in idiopathic hypersomnia with long sleep time

• Published in: Scientific reports Vol. 12; no. 1; pp. 9018 - 10
• Main Authors: Rach, Héloïse, Kilic-Huck, Ulker, Reynaud, Eve, Hugueny, Laurence, Peiffer, Emilie, Roy de Belleplaine, Virginie, Fuchs, Fanny, Bourgin, Patrice, Geoffroy, Pierre A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 30.05.2022; Nature Publishing Group; Nature Portfolio
• Subjects: 631/378; 631/378/1385; 692/617/375/1816; Human health and pathology; Humanities and Social Sciences; Latency; Life Sciences; Melanopsin; multidisciplinary; Neurons and Cognition; Phototransduction; Science; Science (multidisciplinary); Sleep; Sleep and wakefulness; Sleep disorders; Tissues and Organs
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-022-13041-3

Idiopathic hypersomnia (IH), characterized by an excessive day-time sleepiness, a prolonged total sleep time on 24 h and/or a reduced sleep latency, affects 1 in 2000 individuals from the general population. However, IH remains underdiagnosed and inaccurately treated despite colossal social, professional and personal impacts. The pathogenesis of IH is poorly known, but recent works have suggested possible alterations of phototransduction. In this context, to identify biomarkers of IH, we studied the Post-Illumination Pupil Response (PIPR) using a specific pupillometry protocol reflecting the melanopsin-mediated pupil response in IH patients with prolonged total sleep time (TST > 660 min) and in healthy subjects. Twenty-eight patients with IH (women 86%, 25.4 year-old ± 4.9) and 29 controls (women 52%, 27.1 year-old ± 3.9) were included. After correction on baseline pupil diameter, the PIPR was compared between groups and correlated to sociodemographic and sleep parameters. We found that patients with IH had a lower relative PIPR compared to controls (32.6 ± 9.9% vs 38.5 ± 10.2%, p = 0.037) suggesting a reduced melanopsin response. In addition, the PIPR was not correlated to age, chronotype, TST, nor depressive symptoms. The melanopsin-specific PIPR may be an innovative trait marker of IH and the pupillometry might be a promising tool to better characterize hypersomnia.