Melatonin rhythms in renal transplant recipients with sleep–wake disturbances

ABSTRACT

We assessed salivary melatonin levels in renal transplant (RTx) recipients who participated in a randomised, multicentre wait-list controlled trial on the effect of bright light therapy on their sleep and circadian rhythms. A large proportion of RTx recipients in our cohort had unexpectedly low melatonin values, which precluded calculation of the dim-light melatonin onset (DLMO) as a circadian marker. Thus, the aim of this post hoc analysis was to describe the melatonin profile of home-dwelling RTx recipients diagnosed with sleep–wake disturbances (SWDs). The participants were characterised by means of sleep questionnaires, validated psychometric instruments [Pittsburgh sleep quality Index (PSQI), Epworth sleepiness scale (ESS), Morningness-Eveningness Questionnaire (MEQ) and Depression, Anxiety and Stress Scale (DASS)] in addition to melatonin assay in saliva. Data were analysed with descriptive statistics and group comparisons made with appropriate post hoc tests. RTx recipients [n = 29 (aged 54.83 ± 13.73, transplanted 10.62 ± 6.84 years ago)] were retrospectively grouped into two groups: RTx recipients whose dim light melatonin onset (DLMO) could be calculated (n = 11) and those whose DLMO could not be calculated (n = 18). RTx recipients having a measurable DLMO had a number of differences from those without DLMO: they were younger [46.4 ± 14.9 compared to 60.0 ± 10.3 (p = .007)], had higher haemoglobin values [135.36 ± 12.01 versus 122.82 ± 11.56 (p = .01)], less anxiety [4 (0;8) versus 12 (6.5;14) (p = .021)] and a better overall sense of coherence [SOC Score: 71.09 ± 12.78 versus 56.28 ± 15.48 (p = 0.013)]. These results suggest that RTx recipients whose DLMO could be calculated have less health impairments, underlying the relevance of a stable circadian system.

KEYWORDS:

• Adults
• chronobiology
• kidney transplantation
• melatonin profile
• rental transplant recipients
• sleep-wake disturbances
• salivary melatonin

Acknowledgments

This study was funded by a research grant from the Swiss Renal Foundation (Alfred and Erika Baer-Spycher Foundation). We thank Claudia Renz, Centre for Chronobiology, University Psychiatric Clinics Basel and Bühlmann AG for the melatonin assays.

Declaration of interest

The results presented in this study have not been published elsewhere. The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

Supplemental material

Supplemental data for this article can be accessed on the online at http://www.tandfonline.com/icbi.