Chronotyping glaucoma patients with the Munich Chrono Type Questionnaire: A case-control study

被引:2
作者
Bierings, Ronald A. J. M. [1 ]
Gordijn, Marijke C. M. [2 ,3 ]
Jansonius, Nomdo M. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Ophthalmol, Groningen, Netherlands
[2] Univ Groningen, Groningen Inst Evolutionary Life Sci, Chronobiol Unit, Groningen, Netherlands
[3] Chrono Work BV, Groningen, Netherlands
关键词
RETINAL GANGLION-CELLS; QUALITY-OF-LIFE; PUPILLARY LIGHT REFLEX; HUMAN CIRCADIAN SYSTEM; VISUAL-FIELD LOSS; MORNINGNESS-EVENINGNESS; SLEEP; MELATONIN; RHYTHMS; PERIOD;
D O I
10.1371/journal.pone.0214046
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Purpose The circadian clock is entrained to light by the intrinsically photosensitive retinal ganglion cells. Loss of these cells in glaucoma, an eye disease with loss of retinal ganglion cells as its key feature, might thus result in a change in chronotype. We aimed to compare the chrono-type between glaucoma patients and healthy subjects. Methods We sent the Munich Chrono Type Questionnaire to 221 glaucoma patients (response rate 81%); controls (primary control group) were primarily their spouses. After exclusion of shift workers and participants who woke-up due to an alarm clock on days off, 159 glaucoma patients (88 early, 21 moderate, 23 severe) and 163 controls remained. We calculated chronotype as the mid-sleep on days off, corrected for workweek accumulated sleep debt (MSFsc). We compared means and variances between groups using Welch's tests and F-tests, respectively. A secondary control group was recruited from participants in a citizen-science project (n = 17073) who completed an online questionnaire. A resampling method was applied to enable an age- and gender- matched comparison with the glaucoma patients. Results Compared to the primary control group, glaucoma did not affect the mean MSFsc (controls 3:47; early, moderate, and severe glaucoma 3:40, 3:45, and 3:33, respectively [P = 0.62]). Chrono type variability seemed to increase with increasing disease severity (severe glaucoma versus controls: P = 0.023). The mean MSFsc of the secondary control group was 3:50 (95% confidence interval 3:48 to 3:52); significantly later than that of the glaucoma patients (3:40; P = 0.024). Mean MSFsc did not differ significantly between the control groups (P = 0.42). Conclusions No clear changes were found in the chronotype as determined by sleep phase in patients with glaucoma, especially not in early and moderate glaucoma. In severe glaucoma, chrono-type variability seems to increase, possibly alongside a small advancement.
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