Knorr Ulla, Simonsen Anja Hviid, Engström Eva Letty Susanne, Zetterberg Henrik, Blennow Kaj, Willkan Mira, Forman Julie, Hasselbalch Steen Gregers, Kessing Lars Vedel
Copenhagen Affective Disorder Research Center (CADIC), Psychiatric Center Copenhagen, Department Rigshospitalet, Copenhagen, Denmark.
Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Neurosci Appl. 2022 Nov 19;2:101011. doi: 10.1016/j.nsa.2022.101011. eCollection 2023.
Disturbed sleep during affective episodes may impact levels of cerebrospinal fluid (CSF)-amyloid-beta (Aβ)42 and other biomarkers of neurodegeneration in patients with bipolar disorder (BD). The study aimed to investigate the correlations between sleep and biomarkers for Alzheimer's disease (AD) and neurodegeneration in BD and healthy controls (HC). We present a prospective, longitudinal case-control study of euthymic patients with BD (N = 86) and HC (N = 44). All participants were evaluated with clinical assessments at baseline, and after a year. The patients' affective states were recorded weekly as euthymic, subthreshold level, major depression, or (hypo)mania. Patients were re-assessed during and after an episode if it occurred during follow-up. Total sleep scores based on three Hamilton-17 Depression Scale items were analyzed in relation to concentrations of CSF-Aβ42, CSF-Aβ40, CSF-Aβ38, CSF-Aβ42/40 and 42/38 ratios, CSF-soluble amyloid-precursor proteins α+β, plasma-Aβ42, plasma-Aβ40, CSF-phosphorylated-tau, CSF-total-tau, plasma-total-tau, CSF-neurofilament-light, plasma-neurofilament-light, CSF-neurogranin, serum-S100B, CSF-8-oxo-7,8-dihydro-guanosine, CSF-8-oxo-7,8-dihydro-2'-deoxyguanosine, urine-8-oxo-7,8-dihydro-guanosine, and urine-8-oxo-7,8-dihydro-2'-deoxyguanosine. The primary outcome was the association between total sleep scores and levels of CSF-Aβ42 at baseline and follow-up estimated by the regression coefficient in a linear mixed model. We found no statistically significant associations between sleep and CSF-Aβ42 (-2.307 pg/ml (95% CI: -9.525-4.911; p = 0.523)) or any other biomarkers. However, higher sleep scores appeared to be associated with higher CSF-Aβ42/40 and CSF-Aβ42/38 ratios, and lower CSF-total-tau concentration, but were not statistically significant after correction for multiple testing. In conclusion attenuated sleep during an affective episode was not associated with changes in biomarkers for AD and neurodegeneration in BD, but larger prospective studies are needed.
情感发作期间睡眠紊乱可能会影响双相情感障碍(BD)患者脑脊液(CSF)中β淀粉样蛋白(Aβ)42水平以及其他神经退行性变生物标志物。本研究旨在调查BD患者及健康对照(HC)中睡眠与阿尔茨海默病(AD)生物标志物及神经退行性变之间的相关性。我们开展了一项针对处于心境正常期的BD患者(N = 86)和HC(N = 44)的前瞻性纵向病例对照研究。所有参与者在基线时以及一年后均接受临床评估。每周记录患者的情感状态,分为心境正常、阈下水平、重度抑郁或(轻)躁狂。如果在随访期间发作,在发作期间及发作后对患者进行重新评估。基于汉密尔顿抑郁量表17项中的三项分析总睡眠得分,并与CSF - Aβ42、CSF - Aβ40、CSF - Aβ38、CSF - Aβ42/40和42/38比值、CSF可溶性淀粉样前体蛋白α + β、血浆 - Aβ42、血浆 - Aβ40、CSF磷酸化tau蛋白、CSF总tau蛋白、血浆总tau蛋白、CSF神经丝轻链、血浆神经丝轻链、CSF神经颗粒素、血清S100B、CSF 8 - 氧代 - 7,8 - 二氢鸟苷、CSF 8 - 氧代 - 7,8 - 二氢 - 2'-脱氧鸟苷、尿8 - 氧代 - 7,8 - 二氢鸟苷以及尿8 - 氧代 - 7,8 - 二氢 - 2'-脱氧鸟苷的浓度进行关联分析。主要结局是通过线性混合模型中的回归系数估计基线和随访时总睡眠得分与CSF - Aβ42水平之间的关联。我们发现睡眠与CSF - Aβ42(-2.307 pg/ml(95%CI:-9.525 - 4.911;p = 0.523))或任何其他生物标志物之间无统计学显著关联。然而,较高的睡眠得分似乎与较高的CSF - Aβ42/40和CSF - Aβ42/38比值以及较低的CSF总tau蛋白浓度相关,但在多重检验校正后无统计学显著性。总之,情感发作期间睡眠减弱与BD患者AD和神经退行性变生物标志物的变化无关,但需要更大规模的前瞻性研究。