Pochat M D, Ferber C, Lemoine P
UCPB, CHS Le Vinatier, 95, boulevard Pinel, 69677 Bron.
Encephale. 1993 Nov-Dec;19(6):601-7.
The sleep apnea syndrome (SAS), which is defined by more than 5 apneas or hypopneas per hour of sleep (9), is quite a frequent affection which concerns 1.4 to 10% of general population (1.7). The major daytime complaints of the SAS are daytime sleepiness, memory and attention disorders, headaches and asthenia especially in the morning, and sexual impotence (9). The nocturnal manifestations are dominated by sonorous and generally long standing snoring, increased by dorsal decubitus and intake of alcohol, with repeated interruptions by respiratory arrests. These manifestations are always noted but rarely spontaneously reported. The sleep, non refreshing, is agitated and perturbed by numerous awakenings. The findings of the clinical examination are poor: obesity is found in 2/3 of the cases and arterial hypertension in 1/2 of the cases (20). Polygraphic recording during sleep only permits an absolute diagnosis. This frequent affection is a real problem of public health because of its numerous complications (3, 10, 12, 13, 18, 21). Symptoms of depression are often found when a patient with a SAS is examined and conversely, symptoms which evoke a SAS can be found in the clinical examination of depressed patients. We decided so to study the thymic and anxious status of 24 patients investigated for a SAS and submitted to a polygraphic recording during sleep. Four clinical parameters were studied: DSM III-R diagnosis criteria, Montgomery and Asberg Depression Rating Scale (MADRS), Hamilton Anxiety Rating Scale (HARS) and thymasthenia rating scale of Lecrubier, Payan and Puech. We also reported Total Sleep Time (TST = 6.5 +/- 1.5), Apnea Hypopnea Index (AHI = 26.7 +/- 21.6), number (2.1 +/- 2.8/h) and duration (174.2 +/- 150.8 s/h) of hypoxic events. Results showed that among 24 patients, 8 were depressed according to DSM III-R diagnosis criteria and had MADRS > 25, 22 were anxious, 11 had a major anxiety (HARS > 15) and 15 presented thymasthenia (SET > 15). Significative correlations existed between anxiety and depression (r = 0.82; p < 0.0001), depression and thymasthenia (r = 0.77; p < 0.0001) and thymasthenia and anxiety (r = 0.75; p < 0.0001). Among the 8 depressed patients a correlation existed between AHI and depression (r = 0.72; p = 0.04), but no correlation was found between depression and hypoxic events. These results were comparable to those of Guilleminault (10), Reynolds (21), Kales (12), Bliwise (3), Klonoff (13) and Millman (18) who studied relations between SAS and depression. The evaluation of thymasthenia gave a more precise typology of the depressive state associated to SAS: the type of the mood disorder is more "blunted" and "anhedonic" than "sorrowful", particularly characterised by asthenia, lack of energy, reduction of interests (leisures, libido, work), loss of initiative, difficulties to organise tasks, fall of performances and reduction of pleasure usually felt in pleasant events (15). The physic symptomatology dominated the psychic one. The sleep disorganization, more than metabolic consequences of apneas, could be involved in this associated depressive state. Other neuropsychiatric troubles can be associated to the SAS. In fact, cognitive troubles (2, 8, 14, 16, 19, 22, 24) and personality disorders (12, 18) have been described. Our data confirm previous observations suggesting a frequent association between SAS, depression, fatigue and anxiety. Clinicians should consequently be aware that a depression with severe complaints of fatigue should deserve an investigation oriented towards SAS. Conversely, when a SAS is diagnosed, it is necessary to look for a possible depression in order to set up the most appropriate treatment. The frequency of SAS, like depression's one, increases with age. Prescription and consummation of sedative psychotropic drugs increase too with age. Since respiratory depressant effects of these drugs have been clearly demonstrated, it is important to evoke SAS when depressive and/or anxious states are diagnosed and not to aggravate it. An efficacious treatment of SAS can also cure the associated depressive state, but this one can persist. It is necessary, in this case, to select a non sedative antidepressant.
睡眠呼吸暂停综合征(SAS)的定义为每小时睡眠中出现5次以上呼吸暂停或呼吸不足(9),这是一种相当常见的病症,在普通人群中的患病率为1.4%至10%(1.7)。SAS患者主要的日间症状包括日间嗜睡、记忆力和注意力障碍、头痛以及尤其是早晨出现的乏力,还有性功能障碍(9)。夜间表现主要为响亮且通常持续时间较长的打鼾,仰卧位及饮酒会加重打鼾,伴有反复的呼吸暂停中断。这些表现虽常被注意到,但患者很少主动报告。睡眠质量不佳,令人无法恢复精力,睡眠中频繁觉醒,睡眠受到干扰。临床检查结果往往不明显:2/3的病例存在肥胖,1/2的病例存在动脉高血压(20)。睡眠期间的多导睡眠图记录仅能做出明确诊断。由于其众多并发症(3, 10, 12, 13, 18, 21),这种常见病症成为了一个真正的公共卫生问题。在对SAS患者进行检查时,常常会发现抑郁症状,反之,在对抑郁症患者进行临床检查时,也可能发现提示SAS的症状。因此,我们决定研究24例因SAS接受检查并在睡眠期间进行多导睡眠图记录的患者的胸腺状态和焦虑状况。研究了四个临床参数:DSM III - R诊断标准、蒙哥马利和阿斯伯格抑郁评定量表(MADRS)、汉密尔顿焦虑评定量表(HARS)以及勒克鲁比耶、帕扬和皮克的胸腺无力评定量表。我们还记录了总睡眠时间(TST = 6.5 +/- 1.5)、呼吸暂停低通气指数(AHI = 26.7 +/- 21.6)、低氧事件的次数(2.1 +/- 2.8/h)和持续时间(174.2 +/- 150.8 s/h)。结果显示,在24例患者中,根据DSM III - R诊断标准,8例为抑郁症患者,MADRS > 25;22例存在焦虑;11例有重度焦虑(HARS > 15);15例表现出胸腺无力(SET > 15)。焦虑与抑郁之间存在显著相关性(r = 0.82;p < 0.0001),抑郁与胸腺无力之间存在显著相关性(r = 0.77;p < 0.0001),胸腺无力与焦虑之间存在显著相关性(r = 0.75;p < 0.0001)。在8例抑郁症患者中,AHI与抑郁之间存在相关性(r = 0.72;p = 0.04),但抑郁与低氧事件之间未发现相关性。这些结果与吉耶尔米诺(10)、雷诺兹(21)、卡莱斯(12)、布利怀斯(3)、克洛诺夫(13)和米尔曼(18)研究SAS与抑郁关系的结果相当。对胸腺无力的评估为与SAS相关的抑郁状态提供了更精确的类型划分:情绪障碍类型更倾向于“迟钝”和“快感缺失”,而非“悲伤”,其特征尤其表现为乏力、缺乏精力、兴趣减退(休闲、性欲、工作方面)、主动性丧失、组织任务困难、表现下降以及在愉快事件中通常感受到的愉悦感降低(15)。躯体症状在心理症状中占主导。睡眠紊乱可能比呼吸暂停的代谢后果更易引发这种相关的抑郁状态。其他神经精神问题也可能与SAS相关。事实上,已有认知障碍(2, 8, 14, 16, 19, 22, 24)和人格障碍(12, 18)的相关描述。我们的数据证实了先前的观察结果,表明SAS、抑郁、疲劳和焦虑之间经常存在关联。因此,临床医生应意识到,对于伴有严重疲劳主诉的抑郁症患者,应进行针对SAS的检查。反之,当诊断出SAS时,有必要排查是否可能存在抑郁症,以便制定最恰当的治疗方案。SAS的患病率与抑郁症一样,随年龄增长而增加。镇静类精神药物的处方量和消费量也随年龄增长而增加。由于这些药物的呼吸抑制作用已得到明确证实,在诊断抑郁和/或焦虑状态时,考虑到SAS并避免加重病情非常重要。有效的SAS治疗也可治愈相关的抑郁状态,但这种抑郁状态可能会持续存在。在这种情况下,有必要选择一种非镇静性抗抑郁药。