Rausch J L, Johnson M E, Corley K M, Hobby H M, Shendarkar N, Fei Y, Ganapathy V, Leibach F H
Department of Psychiatry and Health Behavior, Veterans Administration, The Medical College of Georgia, Augusta, GA 30912, USA.
Neuropsychobiology. 2003;47(3):120-7. doi: 10.1159/000070579.
Depression has been associated with a decrease in intracellular serotonin (5-HT) reuptake through its transporter, SERT. The 5-HT transporter long promoter region (5-HTTLPR) deletion in the SERT gene has also been associated with a decrease in 5-HT reuptake. Conversely, increases in extracellular 5-HT have been associated with increased temperature. It has not been established, however, whether body temperature in depressed patients is different from controls. Here, we hypothesized that temperature would be increased in depressed patients as well as in those with the 5-HTTLPR deletion.
A strict oral temperature protocol employed single, cross-sectional, naturalistic time-of-day temperature measures in 125 subjects (46 normal controls, 79 outpatients with major depression). Controls and depressed patients were free of psychotropic medication and classified by the Structured Clinical Interview for Psychiatric Diagnoses. Eighty-one of the subjects (68 depressed, 13 normal) were additionally genotyped for 5-HTTLPR polymorphisms.
Depressed patients had a significantly higher uncorrected body temperature (mean +/- SD 98.38 +/- 0.61 degrees F) than controls (mean +/- SD 98.13 +/- 0.59 degrees F; F = 4.8, p = 0.03). An age (F = 14.09, p < 0.001) and time-of-day (11.4, p = 0.001) correction revealed a more robust (F = 14.02, p < 0.001) difference between depressed patients (mean +/- SD 98.44 +/- 0.55 degrees F) and controls (mean +/- SD 98.02 +/- 0.56 degrees F). When normalized for age and circadian differences between subjects, random, outpatient oral temperatures had a sensitivity of 63% and a specificity of 76% in identifying the depressed subjects from the controls. Independent of depression, subjects with the 5-HTTLPR deletion (short SERT allele) were warmer (mean +/- SD 98.33 +/- 0.65 degrees F) than those lacking the short allele on either chromosome (mean +/- SD 97.91 +/- 0.69 degrees F; F = 7.0, p = 0.01). However, the genotype did not explain the temperature differences between controls and depressed patients.
This is the first demonstration of an increased daytime body temperature in cases with major depression. Subjects with a corrected temperature above 98.3 degrees F were 2.6-fold more likely to be depressed. The results may strengthen the hypothesis of an inflammatory component of depression. In addition, the findings suggest a potential link between genetic differences in 5-HT transport and body temperature.
抑郁症与细胞内血清素(5-羟色胺,5-HT)通过其转运体5-羟色胺转运体(SERT)再摄取减少有关。SERT基因中的5-羟色胺转运体长启动子区域(5-HTTLPR)缺失也与5-羟色胺再摄取减少有关。相反,细胞外5-羟色胺增加与体温升高有关。然而,抑郁症患者的体温是否与对照组不同尚未确定。在此,我们假设抑郁症患者以及5-HTTLPR缺失患者的体温会升高。
采用严格的口腔温度测量方案,对125名受试者(46名正常对照者,79名重度抑郁症门诊患者)进行单一、横断面、自然主义的日间温度测量。对照组和抑郁症患者未服用精神药物,并通过精神疾病诊断结构化临床访谈进行分类。其中81名受试者(68名抑郁症患者,13名正常对照者)还进行了5-HTTLPR多态性基因分型。
抑郁症患者未经校正的体温(平均±标准差98.38±0.61华氏度)显著高于对照组(平均±标准差98.13±0.59华氏度;F = 4.8,p = 0.03)。经年龄(F = 14.09,p < 0.001)和日间时间(11.4,p = 0.001)校正后,抑郁症患者(平均±标准差98.44±0.55华氏度)与对照组(平均±标准差98.02±0.56华氏度)之间的差异更为显著(F = 14.02,p < 0.001)。当对受试者之间的年龄和昼夜差异进行标准化后,随机的门诊口腔温度在从对照组中识别抑郁症患者时,敏感性为63%,特异性为76%。与抑郁症无关,5-HTTLPR缺失的受试者(短SERT等位基因)比两条染色体上均缺乏短等位基因的受试者体温更高(平均±标准差98.33±0.65华氏度)(平均±标准差97.91±0.69华氏度;F = 7.0,p = 0.01)。然而,该基因型并不能解释对照组和抑郁症患者之间的体温差异。
这是首次证明重度抑郁症患者白天体温升高。校正后体温高于98.3华氏度的受试者患抑郁症的可能性高2.6倍。这些结果可能会强化抑郁症存在炎症成分的假说。此外,研究结果表明5-羟色胺转运的基因差异与体温之间可能存在联系。