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Psychiatry Investig > Volume 7(1); 2010 > Article
An and Chung: A Case of Obstructive Sleep Apnea Syndrome Presenting as Paradoxical Insomnia

Abstract

A 63-year-old female with obstructive sleep apnea syndrome (OSAS) presented with clinical features indistinguishable from paradoxical insomnia (PI). Her main complaint was chronic insomnia. Her subjective sleep latency was 2-3 h, subjective sleep time was less than 3 h, despite spending 8 h in bed, and she reported near constant awareness of her surroundings while lying in bed. Her body mass index (BMI) was 22.67 kg/m2, and her neck circumference was 34.5 cm. Nocturnal polysomnography (NPSG) findings indicated severe OSAS. Her total sleep time (TST) was 359 min, sleep latency 13 min, and her apnea/hypopnea index (AHI) was 74.6/h. The aim of this report is to evaluate the association between PI and OSAS cases confirmed by NPSG.

Introduction

Paradoxical insomnia (PI) is a baffling condition in which the patient complains of almost no sleep for a duration that is physiologically improbable. Furthermore, a large discrepancy between the patient's subjective complaint and a bed partner's objective report may raise doubts about the accuracy of the patient's perception. Most people suffering from insomnia tend to overestimate sleep onset latency (SOL) and underestimate total sleep time (TST)1-4; thus, the reliability of PI as an independent clinical entity has been the subject of much debate.5-8 However, the second edition of the International Classification for Sleep Disorders (ICSD-2) now recognizes PI as a separate disorder and subcategory of insomnia (Table 1).9
The diagnosis of obstructive sleep apnea syndrome (OSAS) is more straightforward. OSAS is characterized by the repeated cessation or a major reduction in upper airway airflow during sleep. It is diagnosed and quantified using the apnea/hypopnea index (AHI), the average number of apnea/hypopnea incidents during an hour as measured by nocturnal polysomnography (NPSG). AHI values of 5, 15, and 30 represent the cut-off values for mild, moderate, and severe OSAS, respectively.10 The risk factors for OSAS are well understood, and snoring is highly associated with the disorder.10 However, recent reports have suggested that the standard diagnostic indicators may not always be applicable to older adults.11-13
We present the case of a female with OSAS who presented with clinical features indistinguishable from PI. The aim of this report is to evaluate the association between PI and OSAS confirmed by NPSG.

Case

A 63-year-old female presented with chronic subjective insomnia. She was 1.51 m tall and weighed 51 kg. Her body mass index (BMI) was 22.67 kg/m2, and her neck circumference was 34.5 cm. She did not have retrognathia, micrognathia, or any other significant abnormality in her craniofacial features. The patient had a psychiatric history of recurrent mild depressive episodes, with full interepisodic recovery, that had started 15 years ago.
Her presenting symptoms began forty days earlier. Her subjective sleep latency was 2-3 h and subjective sleep time was less than 3 h, despite spending 8 h in bed. She reported near constant awareness of her surroundings during most of the time she was lying in bed. She claimed her symptoms were fairly constant and that she was tired all day. She expressed concern about her sleeping problems. Nevertheless, her daughter reported that the patient's observed sleep latency was less than 30 min, her sleep time was over 6 h, and that the patient snored mildly.
In short, the patient fulfilled the ICSD-2 criteria for PI and, as she had no OSAS risk factors, was diagnosed with PI. A 'gold standard' treatment for PI does not yet exist, and the patient was started on a benzodiazepine/nonbenzodiazepine sedative regimen consisting of 3 mg bromazepam, 0.25 mg clonazepam, and 12.5 mg zolpidem. The patient did not respond to these medications. To control underlying depression that may have accompanied her insomnia, we prescribed 15 mg mirtazapine, which has been shown to effectively control insomnia in older patients.14,15 She still showed no response, and we added 25 mg of quetiapine, which has been reported to control insomnia.16 The patient received concurrent cognitive-behavioral therapy (CBT), and despite good compliance, her symptoms were not alleviated. After a month, the patient was admitted to the open ward. During admission, we observed that she slept quite well, though she would not acknowledge this and continued to complain of having less than 3 h of sleep on most nights. She snored continuously, but mildly. A change of her medication regimen to 50 mg chlorpromazine, 200 mg quetiapine, 100 mg trazodone, and 1 mg clonazepam had no effect. We arranged a NPSG to investigate other possible causes for her insomnia.
Although her subjective TST was under 3 h on the night of the test, the objective TST was 359 min, SOL was 13 min, and her wake-time after sleep onset (WASO) was just over 71 min. Her sleep efficiency was 81.0%. She showed almost no slow-wave sleep. Stages N1, N2, and rapid eye movement (REM) occupied 16.2%, 54.9%, and 23.4% of her TST, respectively, and REM sleep latency was 79 min. Her AHI was 74.6/h, indicating severe OSAS. Her minimum SaO2 level was 76.0%, and her average oxygen saturation level was 92.8%. Her oxygen desaturation index, which indicates the average number of oxygen desaturations 4% or more below the baseline level per hour, was 55.1/h (Figure 1, Table 2).
The NPSG results revealed that the patient had severe OSAS, and we concluded that OSAS was the cause of her insomnia. She was informed about the NPSG results and OSAS. We recommended continuous positive airway pressure, but she refused. Her symptoms of PI subsequently improved.

Discussion

PI is a complaint of severe and chronic insomnia with no objective evidence of sleep disturbance or the daytime impairment that would be expected from such an extreme degree of sleep loss.9 Patients often report extensive awareness of the environment while trying to sleep. Associated features include major concerns about sleeping problems and an unwillingness to acknowledge objective evidence indicating normal sleep patterns and duration. NPSG and the multiple sleep latency test rarely detect significant sleep disturbances in these patients. The etiology of PI is unknown, but PI subjects have been demonstrated to consume more oxygen than do normal control subjects. This finding suggests that high levels of physiological activation may be associated with PI.17 Furthermore, a recent study compared cyclic alternating patterns (CAP) in people with PI and normal controls and reported that CAP were more frequent in people with PI, suggesting that repeated arousal may underlie the disorder.18
OSAS is a major cause of daytime sleepiness. Common symptoms include snoring, nocturnal snorting, and gasping.19 OSAS is strongly associated with obesity (≥25 kg/m2)10,20,21 and old age (>65 years)10,20 and less highly associated with male gender,20,21 increased neck circumference (≥39 cm),10,21 a positive family history,10,20 alcohol ingestion,10 and certain craniofacial features such as retrognathia and micrognathia.10,20 Clinical symptoms in conjunction with an AHI ≥5/h are used to diagnose OSAS. The prevalence of OSAS in insomniacs has been reported to be as high as 67%, but reports concerning the characteristics of insomniacs with OSAS are scarce. A few studies have indicated that sleep maintenance insomnia is the most frequent symptom reported by insomniacs with OSAS, possibly caused by repeated apnea during sleep.22 In contrast, physiological hyperarousal has been proposed to explain sleep-onset insomnia in insomniacs with OSAS.23 However, both studies used subjects suspected to have OSAS; thus, their usefulness for diagnostic differentiation between insomnia and OSAS may be limited.
The patient in the present case report fulfilled the diagnostic criteria for PI and had none of the common risk factors for OSAS. She complained of chronic insomnia with a subjective TST of less than 3 h despite contrary observations from family members and medical staff. She claimed she was aware of her surroundings for most of the night. NPSG revealed an AHI of 74.6/h and a respiratory arousal index, the number of arousals due to respiratory incidents per hour, of 57.5/h; thus, she was diagnosed with severe OSAS.
Research during the past decade has demonstrated that the characteristics of OSAS in older adults differ from those of younger people. A previous study that screened a group of older insomniacs using NPSG reported that after excluding all the subjects with OSAS risk factors, the prevalence of OSAS was 29-49%, depending on the cut-off value used (AHI ≥15 or 5 for mild or moderate OSAS, respectively).13 Moreover, a study comparing older people with OSAS and older insomniacs reported that BMI values and the presence of snoring were similar in both groups,12 and a study comparing the clinical features of older men and young and middleaged subjects with OSAS reported that older OSAS subjects snored less, had lower BMI, smaller neck circumference, and milder daytime sleepiness.11
Sleep maintenance insomnia, the most common insomnia symptom experienced by people with OSAS, may be explained by repeated arousal during sleep,22 and repeated arousal indicated by increased CAP is a possible cause of PI.18 Sleep-onset insomnia in patients with OSAS has been hypothesized to be caused by physiological hyperarousal, similar to the increased physiological activation proposed to underlie PI. We suggest that frequent arousal caused by increased respiratory incidents may mimic the repeated arousal that occurs in PI, and physiological hyperarousal may imitate increased physiological activation, thus causing the patient to confuse sleep and wake states.
In conclusion, these findings suggest that it is more difficult to diagnosis OSAS in older people than in younger patients. In some cases, OSAS in older patients may be misdiagnosed as another sleep disorder such as PI. The factors suspected to cause insomnia in people with OSAS are similar to those proposed to cause PI, and this may further hinder differentiation between the two disorders. Currently, the only universally approved diagnostic tool for OSAS is NPSG. Thus, we suggest that older adults presenting with features similar to PI should be examined for signs of OSAS, and a NPSG should be conducted for a definitive diagnosis. Further investigation of the precise indications for NPSG in older adults with complaints of insomnia is necessary.

References

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Figure 1
Hypnogram and sleep architecture of the patient. REM: rapid eye movement stage, S1: sleep stage N1, S2: sleep stage N2, S3: sleep stage N3, LM: limb movement, PLM: periodic limb movement, Desat: oxygen desaturation, SpO2: oxygen saturation, Obstructive: obstructive apnea, Central: central apnea, Mixed: mixed apnea.
pi-7-75-g001.jpg
Table 1
ICSD-2 diagnostic criteria for paradoxical insomnia
pi-7-75-i001.jpg

ICSD-2: International Classification for Sleep Disorders

Table 2
Polysomnographic findings of the patient
pi-7-75-i002.jpg

REM: rapid eye movement, PLM: Periodic Limb Movement, ESS: Epworth Sleepiness Index, PSQI: Pittsburg Sleep Quality Questionnaire



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