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Tulane Sleep Clinic, Department of Psychiatry and Neurology, Tulane Medical Center,
Tulane University, New Orleans, Louisiana, U.S.A,
Summary: Thirty subjects, who were between the ages of 24 and 60 years and
were free of sleep disorders, were evaluated for impotency by use of polysom-
nograms recorded over 2 consecutive nights. No statistical differences between
the first and second nights' recordings were found in latency to rapid eye
movement and stage 4 sleep, sleep efficiency, and movement time with or
without awakening. No differences were noted in times spent in different sleep
stages, nor between the first 3 h and the second 3 h of sleep across both nights
of polysomnography. This confirms previous findings that questioned the effi-
cacy of the first night effect. This study also emphasizes the need to compare
sleep disorder patients with matched normal controls. Key Words: First night
effect-Movement.
Some research findings have encouraged the clinician to disregard data from the first
night of sleep studies because of the longer latencies to stage 4 and rapid eye movement
(REM) sleep on the first night than on subsequent nights (1-4). The first night effect has
influenced the time invested in evaluating sleep disorder patients as well as the expense
of such evaluations (3,5-8). Recently, investigators have obtained controversial results
concerning this adaptation, showing a tendency toward adaptation during the second
night of evaluation, but without statistically significant differences in latencies or in
percentages of time spent in different stages (6-8).
The patient populations providing these various results were paid volunteers, except
that those of Mendels and Hawkins (2) and Kupfer et al. (6) were psychiatric inpatients.
The mean age of these subjects did not exceed the early 20s. Webb and Campbell (4)
compared healthy females in their 20s with those in their 50s; the comparison demon-
strated a longer sleep latency period, less REM and longer REM latency, and more
awakening with increasing age.
Coble et al. (7) maintained that the relative comfort of modern laboratories is respon-
sible for diminishing the first night effect. She is supported by Browman and Cartwright
67
68 G. A. KADER AND P. T. GRIFFIN
(8), who acknowledge that this environment reduces the first night effect in volunteers.
One might question the validity of a generalization based on data provided by normal
volunteers. Patients under stress may require a longer adaptation period than relaxed
volunteers. The present study was done to evaluate the presence of a first night effect in
patients studied for nocturnal penile tumescence (NPT). These patients were free from
known sleep disorders. Unlike the young healthy volunteer subjects of the earlier
studies, these patients were heterogeneous with regard to age and background.
METHODS
Thirty male subjects aged 24- 60 years were evaluated for impotence of 6 months to 5
years. All subjects completed a detailed questionnaire (in part adapted from one used
by Karacan et al. at Baylor University Sleep Center) of sexual history and per-
formance before and after impotence, previous illness, surgery, and history of sleep
disorders and abnormalities. All subjects had a complete examination and a serum
profile.
Subjects were studied for 2 or more successive nights for NPT measurements in the
sleep lab. These studies included three electroencephalogram (EEG) leads (F 4C4'
C40 2 , and T 40 2), eye monitors at outer canthi connected to ipsilateral ears, submental
electromyogram, chest electrocardiogram, respiration monitors from nostril and mouth
air flow and chest movements, and a penile tumescence gauge at the base or tip of the
penis. The records were scored blindly at epochs of 20 s by one observer and reviewed
by a second. Movement time and sleep stage scoring for 20 s were in accordance with
the guidelines of Rechtshaffen and Kales (9). Awakenings of 10 s or longer following
movement were considered an awakening following movement.
Sleep latencies were measured from lights-off to the first 2 min of continuous stage 1
sleep. Stage 4 and REM latency were measured from sleep onset to the respective stage
excluding all intervening periods of wakening. Total time awake included sleep latency
time and total time awake after sleep onset determined by EEG. Sleep efficiency repre-
sented total time asleep divided by total time in bed. All parameters were calculated by
a subject not familiar with the history or diagnosis of the patients. Statistical measures
were performed by an investigator not familiar with the patients' case histories.
No significant difference was found between nights 1 and 2 in sleep efficiency, sleep latency to stage 1, REM latency,
stage 4 latency, or ratio of number of movements followed by awakening to total number of movements.
Night 1
On 22.395 0.553 1.20
Off 5.618 0.472 0.28
Night 2
On 5.634 0.6024 0.02 0.88
RESULTS
A subject x night analysis of variance was performed for each dependent measure.
The latencies for sleep onset (2 min of stage 1), latency to stage 2, REM, and stage 4
were transformed to "speed" measures by taking the inverse of the latency. This was
done to reduce skew, thereby increasing the power of the F test (10).
The means for sleep latency to stage 1, REM latency, stage 4 latency, and the
proportion of movements followed by awakening to the total number of movements
across nights and to age were used as predictors of sleep efficiency in a multiple
regression analysis. Age and sleep latency to stage 1 were significant predictors of sleep
efficiency (F(1,2)4 = 6.12, P < 0.02; F(1,2)4 = 9.54, P < 0.01, respectively). Stage 4
latency, REM latency, and the proportion of movements followed by awakening to the
total number of movements were not significant (Table 1).
Times from lights-off to lights-on were not significantly different between nights 1
and 2 (Table 2). Sleep latencies calculated from lights-off to stage 2 sleep were not
statistically different on the first night as compared with the second night (Table 3).
Moreover, times spent in different stages of sleep were not different between nights in
the majority of subjects (Table 4). When the first 3 h of sleep were compared with the
last 3 h of sleep, no first night effect was noted. Analysis of the same parameters for
blocks of sleep hours across nights and with covariance for night interaction showed no
significant difference. As expected, more stage 4 was noted in the earlier part of the
night and more REM sleep was noted in the second half of the sleep period (Table 5).
The mean of sleep time for all subjects from lights-off to lights-on was an average of 7
h. Thus no sleep deprivation was present in tbese patients during the polysomnographic
evaluation.
DISCUSSION
The present study does not demonstrate a first night effect. However, lower sleep
latency values were noted in the older subjects. These findings emphasize the variation
TABLE 3. Sleep latency to stage 2 analysis for
nights 1 and 2
F Ratio Probability
Night Mean SD latency speed Latency Speed
I 14.4 27.81 0.25 0.26 0.619 0.612
2 11.2 19.13
Subject Total time Total Stage I Stage 2 Stage 3 Stage 4 Stage 3+4 Stage REM
no. Night recorded sleep time time time time time time time
TABLE 5. Analysis of sleep stage data for first 3 h of sleep vs. second 3 h of sleep
for nights 1 and 2
Frequency
of awakening Stage 0 Stage I Stage 2 Stage 3 Stage 4 REM
Night I vs. 2
F ratio 0.68 0.68 0.42 0.03 0.04 0.01 0.14
Probability 0.4177 0.41 0.52 0.85 0.83 0.94 0.711
Both nights
F ratio 0.03 0.03 1.13 1.51 3.86 21.49 11.16
Probability 0.8754 0.87 0.29 0.23 0.06 O.OOOla 0.002a
Night 0.90 0.90 0.25 1.65 3.49 0.46 1.57
Interaction 0.3520 0.35 0.62 0.21 0.07 0.50 0.222
in the sleep parameters of the elderly. Moreover, the study confirms findings of vari-
ability among a heterogeneous population (11) and of variability due to age differ-
ences (4).
The possibility remains that a prolonged adaptation occurs and is evident only after
several successive study nights. The number of polys om no graphic studies necessary to
account for adaptation may have to be assessed for each patient. The guidelines will
certainly depend on age but also may depend on the nature of the sleep disorder to be
evaluated. Further studies should be done to assess the various factors involved in
different diagnostic categories as compared with age-matched normal subjects.
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