Melatonin suppression by light in euthymic bipolar and unipolar patients

被引:167
作者
Nurnberger, JI
Adkins, S
Lahiri, DK
Mayeda, A
Hu, KL
Lewy, A
Miller, A
Bowman, ES
Miller, MJ
Rau, NL
Smiley, C
Davis-Singh, D
机构
[1] Indiana Univ, Sch Med, Dept Psychiat, Indianapolis, IN 46202 USA
[2] Richard L Roudebush Vet Affairs Med Ctr, Dept Psychiat, Indianapolis, IN 46202 USA
[3] Larue Carter Hosp, Inst Psychiat Res, Indianapolis, IN USA
[4] Wishard Mem Hosp, Dept Psychiat, Indianapolis, IN USA
[5] Oregon Hlth & Sci Univ, Dept Psychiat, Portland, OR 97201 USA
关键词
D O I
10.1001/archpsyc.57.6.572
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Previous studies have suggested that bipolar patients are supersensitive to light suppression of melatonin and that this may be a trait marker for genetic vulnerability. The present study was an attempt to replicate and extend this observation. Propranolol hydrochloride effects were compared with light effects because of the documented influence of beta-adrenergic receptors on melatonin production. Nighttime levels of corticotropin and cortisol were also examined as potential trait vulnerability markers. Methods: Melatonin levels in euthymic bipolar patients (n=29) were tested before and after 500-lux light was administered between 2 and 4 AM and on a separate night in the dark. Results were compared with those of a group of patients with unipolar depression (n=24) and with those of a group of non-psychiatrically ill control subjects (n=50). Lithium effects and propranolol effects were tested in subgroups. Results: No group differences were seen in light suppression among bipolar patients, unipolar patients, and controls; an analysis of the whole group did not reveal differences in propranolol effect, differences in corticotropin or cortisol levels, or evidence for a lithium effect. Holo ever, patients with bipolar I affective disorder showed the following: (1) significantly lower melatonin levels on the light night, at baseline and following light exposure; and (2) a later peak time for melatonin on the dark night. Conclusions: The general hypothesis of increased light sensitivity in bipolar patients was not supported. However, melatonin secretion abnormalities were confirmed in the subgroup with bipolar I disorder. Further assessments of circadian rhythm disruption as a vulnerability marker in bipolar illness are indicated.
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页码:572 / 579
页数:8
相关论文
共 52 条
[1]  
[Anonymous], 1987, DIAGNOSTIC STAT MANU, V4th
[2]   MELATONIN RADIOIMMUNOASSAY [J].
ARENDT, J ;
PAUNIER, L ;
SIZONENKO, PC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1975, 40 (02) :347-350
[3]  
Arendt J., 1985, P15
[4]   LONG-TERM STUDIES ON IMMUNOREACTIVE HUMAN MELATONIN [J].
ARENDT, J ;
WIRZJUSTICE, A ;
BRADTKE, J ;
KORNEMARK, M .
ANNALS OF CLINICAL BIOCHEMISTRY, 1979, 16 (NOV) :307-312
[5]   NOCTURNAL TEMPERATURE IN AFFECTIVE-DISORDER [J].
AVERY, DH ;
WILDSCHIODTZ, G ;
RAFAELSEN, OJ .
JOURNAL OF AFFECTIVE DISORDERS, 1982, 4 (01) :61-71
[6]  
BENCA RM, 1992, ARCH GEN PSYCHIAT, V49, P651
[7]  
BRITTMAN EL, 1983, ENDOCRINOLOGY, V113, P2276
[8]   THE EFFECT OF ORALLY-ADMINISTERED MELATONIN ON THE SEASONALITY OF DEER PELAGE EXCHANGE, ANTLER DEVELOPMENT, LH, FSH, PROLACTIN, TESTOSTERONE, T3, T4, CORTISOL, AND ALKALINE-PHOSPHATASE [J].
BUBENIK, GA ;
SMITH, PS ;
SCHAMS, D .
JOURNAL OF PINEAL RESEARCH, 1986, 3 (04) :331-349
[9]  
CARROLL BJ, 1981, ARCH GEN PSYCHIAT, V38, P15
[10]  
Checkley S, 1992, HDB AFFECTIVE DISORD, P255