Jiang Shu-Man, Jia Lin, Liu Jing, Shi Man-Man, Xu Ming-Zhi
Shu-Man Jiang, Lin Jia, Jing Liu, Man-Man Shi, Department of Gastroenterology, Guangzhou First People's Hospital, Guangzhou Medical University, Guangzhou 510180, Guangdong Province, China.
World J Gastroenterol. 2016 Jun 14;22(22):5260-6. doi: 10.3748/wjg.v22.i22.5260.
To explore the effects and mechanism of action of antidepressant mirtazapine in functional dyspepsia (FD) patients with weight loss.
Sixty depressive FD patients with weight loss were randomly divided into a mirtazapine group (MG), a paroxetine group (PG) or a conventional therapy group (CG) for an 8-wk clinical trial. Adverse effects and treatment response were recorded. The Nepean Dyspepsia Index-symptom (NDSI) checklist and the 17-item Hamilton Rating Scale of Depression (HAMD-17) were used to evaluate dyspepsia and depressive symptoms, respectively. The body composition analyzer was used to measure body weight and fat. Serum hormone levels were measured by ELISA.
(1) After 2 wk of treatment, NDSI scores were significantly lower for the MG than for the PG and CG; (2) After 4 or 8 wk of treatment, HAMD-17 scores were significantly lower for the MG and PG than for the CG; (3) After 8 wk of treatment, patients in the MG experienced a weight gain of 3.58 ± 1.57 kg, which was significantly higher than that observed for patients in the PG and CG. Body fat increased by 2.77 ± 0.14 kg, the body fat ratio rose by 4%, and the visceral fat area increased by 7.56 ± 2.25 cm(2); and (4) For the MG, serum hormone levels of ghrelin, neuropeptide Y (NPY), motilin (MTL) and gastrin (GAS) were significantly upregulated; in contrast, those of leptin, 5-hydroxytryptamine (5-HT) and cholecystokinin (CCK) were significantly downregulated.
Mirtazapine not only alleviates symptoms associated with dyspepsia and depression linked to FD in patients with weight loss but also significantly increases body weight (mainly the visceral fat in body fat). The likely mechanism of mirtazapine action is regulation of brain-gut or gastrointestinal hormone levels.
探讨抗抑郁药米氮平对伴有体重减轻的功能性消化不良(FD)患者的作用及作用机制。
将60例伴有体重减轻的抑郁性FD患者随机分为米氮平组(MG)、帕罗西汀组(PG)或常规治疗组(CG),进行为期8周的临床试验。记录不良反应和治疗反应。分别采用内皮消化不良指数症状(NDSI)清单和17项汉密尔顿抑郁评定量表(HAMD-17)评估消化不良和抑郁症状。使用人体成分分析仪测量体重和脂肪。采用酶联免疫吸附测定法(ELISA)检测血清激素水平。
(1)治疗2周后,MG组的NDSI评分显著低于PG组和CG组;(2)治疗4周或8周后,MG组和PG组的HAMD-17评分显著低于CG组;(3)治疗8周后,MG组患者体重增加3.58±1.57 kg,显著高于PG组和CG组患者。体脂增加2.77±0.14 kg,体脂率上升4%,内脏脂肪面积增加7.56±2.25 cm²;(4)MG组血清胃饥饿素、神经肽Y(NPY)、胃动素(MTL)和胃泌素(GAS)水平显著上调;相比之下,瘦素、5-羟色胺(5-HT)和胆囊收缩素(CCK)水平显著下调。
米氮平不仅能缓解伴有体重减轻的FD患者与消化不良和抑郁相关的症状,还能显著增加体重(主要是体脂中的内脏脂肪)。米氮平作用的可能机制是调节脑-肠或胃肠激素水平。