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1.
BMC Gastroenterol ; 23(1): 106, 2023 Apr 05.
Article in English | MEDLINE | ID: mdl-37020184

ABSTRACT

OBJECTIVE: Comorbid psychiatric disorders negatively affect the survival rate of patients with some physical disorders. In liver transplant recipients, various psychiatric disorders have been identified as worsening prognosis. However, little is known about how the presence of any comorbid (overall) disorders affect the survival rate of transplant recipients. In this study, we examined the effect of overall comorbid psychiatric disorders on survival rate in liver transplant recipients. METHODS: A total of 1006 recipients who underwent liver transplantation between September 1997 and July 2017 across eight transplant facilities with a psychiatric consultation-liaison team were identified consecutively. Recipients were categorized into those with comorbid psychiatric disorders and those without comorbid psychiatric disorders. In the comorbid psychiatric disorder group, psychiatric disorder diagnosis and time of diagnosis were investigated retrospectively. RESULTS: Of the 1006 recipients, 294 (29.2%) had comorbid psychiatric disorders. Comorbid psychiatric disorders in the 1006 recipients were insomnia (N = 107, 10.6%), delirium (N = 103, 10.2%), major depressive disorder (N = 41, 4.1%), adjustment disorder (N = 19, 1.9%), anxiety disorder (N = 17, 1.7%), intellectual disability (N = 11, 1.1%), autism spectrum disorder (N = 7, 0.7%), somatic symptom disorder (N = 4, 0.4%) schizophrenia (N = 4, 0.4%), substance use disorder (N = 24, 2.4%) and personality disorder (N = 2, 0.2%). The most common time of psychiatric disorder diagnosis was within the first 3 months after liver transplantation (51.6%). The final mortality in patients with comorbid psychiatric disorder diagnosis during the five periods (pretransplant, transplant to 3 months, months to 1 year, 1 to 3 years, and over 3 years posttransplant) was 16.2%, 18.8%, 39.1%, 28.6%, and 16.2% respectively, and there were no significant differences between the five periods (χ2 = 8.05, df = 4, p = 0.09). Overall comorbid psychiatric disorders were significantly associated with shorter survival time (log-rank test: p = 0.01, hazard ratio: 1.59 [95% confidence interval: 1.14-2.21], survival rate at the endpoint [%]: 62.0 vs. 83.3). However, after adjusting for confounding variables using Cox proportional hazards regression, there was no significant effect of overall comorbid psychiatric disorders on prognosis. CONCLUSION: Comorbid psychiatric disorders did not affect the survival rate of liver transplant recipients in this study.


Subject(s)
Autism Spectrum Disorder , Depressive Disorder, Major , Liver Transplantation , Mental Disorders , Humans , Retrospective Studies , Referral and Consultation
2.
Nagoya J Med Sci ; 81(2): 249-258, 2019 May.
Article in English | MEDLINE | ID: mdl-31239594

ABSTRACT

Majority of head and neck cancer (HNC) patients are male, and more than 85% of patients with HNC have the habit of smoking and drinking. Due to the specific demographic characteristics, HNC patients are anticipated to have specific coping styles, affecting psychological distress, survival, and quality of life. We explored the subscales of the Mental Adjustment to Cancer (MAC) Scale in male patients with HNC, and then examined the correlation between revised subscales of the MAC scale and anxiety/depression. Participants were 150 male inpatients with HNC, and their demographic and medical data were obtained. Coping style was assessed by MAC scale. Anxiety and depression were assessed using the Hospital Anxiety and Depression Scale. Out of 40 items in the original MAC scale, 19 items were excluded by factor analysis, and the remaining 21 items were divided into three factors: Negative Adjustment, Positive Adjustment, and Abandonment. Negative and Positive Adjustments were similar to the copings of mixed gender patients with heterogeneous cancers, and Abandonment was a new subscale specific to male patients with HNC. This subscale had a weak positive correlation with anxiety and depression. Male HNC patients revealed a specific coping style of Abandonment, related with psychological distress. We believe that an understanding of the Abandonment coping style revealed in our study will improve the psychological support offered to male patients with HNC.


Subject(s)
Head and Neck Neoplasms/psychology , Adult , Aged , Aged, 80 and over , Anxiety/diagnosis , Anxiety/therapy , Cohort Studies , Depression/diagnosis , Depression/therapy , Factor Analysis, Statistical , Humans , Male , Middle Aged , Prospective Studies , Surveys and Questionnaires , Young Adult
3.
Clin Neuropharmacol ; 40(4): 163-168, 2017.
Article in English | MEDLINE | ID: mdl-28622208

ABSTRACT

OBJECTIVE: The purpose of this study was to examine the relationship between the pain-relieving effects of duloxetine and its plasma concentrations in patients with burning mouth syndrome and atypical odontalgia characterized by chronic nonorganic pain in the orofacial region. METHODS: We administered duloxetine to 77 patients diagnosed as having burning mouth syndrome or atypical odontalgia for 12 weeks. The initial dose of duloxetine was established as 20 mg/d and was increased to 40 mg/d after week 2. We evaluated pain using the visual analog scale and depressive symptoms using the Structured Interview Guide for the Hamilton Depression Rating Scale at weeks 0, 2, 4, 6, 8, 10, and 12 and measured plasma concentrations of duloxetine 12 weeks after the start of its administration. RESULTS: Visual analog scale scores were significantly lower 12 weeks after than at the start of the administration of duloxetine (paired t test, t = 6.65, P < 0.0001). We examined the relationship between the rate of decreases in visual analog scale scores and plasma concentrations of duloxetine. There was no significant linear regression or quadratic regression. CONCLUSIONS: Duloxetine significantly relieved pain in patients with chronic nonorganic pain in the orofacial region. However, no relationship was observed between its pain-relieving effects and plasma concentrations.


Subject(s)
Burning Mouth Syndrome/drug therapy , Chronic Pain/drug therapy , Duloxetine Hydrochloride/blood , Duloxetine Hydrochloride/therapeutic use , Facial Pain/drug therapy , Toothache/drug therapy , Aged , Antidepressive Agents/blood , Antidepressive Agents/therapeutic use , Burning Mouth Syndrome/diagnosis , Chronic Pain/diagnosis , Dose-Response Relationship, Drug , Duloxetine Hydrochloride/pharmacology , Facial Pain/diagnosis , Female , Humans , Male , Middle Aged , Pain Measurement/drug effects , Pain Measurement/methods , Toothache/diagnosis , Treatment Outcome
4.
Neuropsychiatr Dis Treat ; 13: 1463-1469, 2017.
Article in English | MEDLINE | ID: mdl-28652746

ABSTRACT

OBJECTIVE: We investigated the association between serotonin- or 5-hydroxytryptamine (5-HT)-related gene polymorphisms and response to antidepressant treatment in a specific symptom cluster of major depression by using the three-factor model of the Montgomery-Åsberg Depression Rating Scale (MADRS), ie, dysphoria (items of sadness, pessimistic thoughts, and suicidal thoughts), retardation (items of lassitude, inability to feel, apparent sadness, and concentration difficulties), and vegetative symptoms (items of reduced sleep, reduced appetite, and inner tension). METHODS: This study was an open-label and nonrandomized trial. A total of 160 patients with baseline MADRS scores of ≥21, who were treated with fluvoxamine or milnacipran for 6 weeks, were included in the statistical analysis. Polymorphisms within a 5-HT transporter (5-HTT) gene-linked polymorphic region (5-HTTLPR), a variable number of tandem repeats in the second intron of the 5-HTT gene (5-HTTVNTR), and 5HT2A receptor (1438G/A) were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). RESULTS: The 5-HTTLPR polymorphisms affected the MADRS score change in dysphoria, but not in retardation, vegetative, or total symptoms. Dysphoria scores significantly decreased in patients with the S/S genotype compared to those in patients with the short (S)/long (L) + L/L genotype. However, 5-HTTVNTR and 1438G/A polymorphisms were not significantly associated with the treatment response to any cluster of depressive symptoms. When a Bonferroni correction was made, however, our results did not reach the criteria for statistical significance. CONCLUSION: The use of a single total depression rating scale may not be sufficient to accurately estimate the clinical response to antidepressants. Analyzing a subset of symptoms in psychological scales could be important when performing pharmacogenetic studies.

5.
J Eat Disord ; 3: 36, 2015.
Article in English | MEDLINE | ID: mdl-26550476

ABSTRACT

The authors investigated the association between personality and physical/mental status in malnourished patients with eating disorders. A total of 45 patients with anorexia nervosa, avoidant/restrictive food intake disorder, and other specified feeding or eating disorders were included and compared with 39 healthy controls. Personality characteristics and severity of depression were assessed using the Temperament and Character Inventory-125 and Beck's Depression Inventory. Depression correlated with harm avoidance and self-directedness in both cases and controls. Body mass index did not correlate with personality in either group. These findings should be verified by longitudinal studies with higher weight/weight recovered patients.

6.
Clin Neuropharmacol ; 38(4): 158-61, 2015.
Article in English | MEDLINE | ID: mdl-26166242

ABSTRACT

Burning mouth syndrome (BMS) causes idiopathic pain or a burning sensation in clinically normal oral mucosa. Burning mouth syndrome is a chronic disease with an unknown etiology. Burning mouth syndrome is also idiopathic, and a consensus regarding diagnosis/treatment has not been reached yet. Recent studies have supported the suggestion that BMS is a neuropathic pain disorder in which both the peripheral and central nervous systems are involved. Tricyclic antidepressants (nortriptyline and amitriptyline), serotonin-noradrenaline reuptake inhibitors (SNRIs) (duloxetine and milnacipran), and antiepileptic drugs, potential-dependent calcium channel α2δ subunit ligands (gabapentine and pregabalin), are currently recommended as the first-choice drugs for neuropathic pain. In this study, we report 5 patients with BMS in whom there was no response to SNRI (milnacipran or duloxetine), or administration was discontinued because of adverse reactions, but in whom pregabalin therapy markedly reduced or led to the disappearance of pain in a short period. Pregabalin, whose mechanism of action differs from that of SNRIs, may become a treatment option for BMS patients who are not responsive to or are resistant to SNRIs.


Subject(s)
Analgesics/therapeutic use , Burning Mouth Syndrome/drug therapy , Pregabalin/therapeutic use , Aged , Antidepressive Agents/therapeutic use , Female , Humans , Male , Middle Aged
7.
J Psychosom Res ; 78(5): 495-498, 2015 May.
Article in English | MEDLINE | ID: mdl-25796514

ABSTRACT

OBJECTIVE: Burning mouth syndrome (BMS) is a chronic disease in which patients feel a burning sensation and pain in the oral cavity. Although personality traits have been suggested to influence the development and course of BMS, they have not yet been examined in detail. We therefore investigated the personality traits of BMS patients. METHODS: Sample consisted of 65 BMS patients presenting to the Aichi-Gakuin Dental School Hospital between May 2005 and April 2009. They were also diagnosed as having pain disorder by a psychiatrist. The control group consisted of 116 healthy subjects. The Temperament and Character Inventory (TCI) was used to evaluate personality traits, while the Beck Depression Inventory (BDI) was used to evaluate the depression rate in both groups. RESULTS: In TCI, we found that, in comparison to the control group, the novelty seeking score was significantly lower (p = 0.009), the harm avoidance score was significantly higher (p < 0.001), and the self-directedness score was significantly lower (p = 0.039) in the BMS group. To remove the influence of depression, we performed an analysis of covariance of each TCI item using the BDI score as a covariate. No significant differences were observed in harm avoidance or self-directedness, whereas the differences noted in novelty seeking were significant (p = 0.008). CONCLUSION: The novelty seeking score was low in BMS patients in comparison to the control group. They also had high harm avoidance and low self-directedness tendencies, but these were attributed to the influence of depression.


Subject(s)
Burning Mouth Syndrome/psychology , Character , Depression/diagnosis , Temperament , Adult , Chronic Disease , Depression/psychology , Exploratory Behavior , Female , Humans , Male , Middle Aged , Personality Inventory , Psychiatric Status Rating Scales
8.
Neuropsychobiology ; 70(3): 173-80, 2014.
Article in English | MEDLINE | ID: mdl-25358426

ABSTRACT

BACKGROUND: Polymorphisms in the glucocorticoid receptors (GRs) have been widely studied with rather less emphasis on relating their differences with possible pharmacological treatment outcomes. The purpose of this study was to investigate whether Bcl1 polymorphisms of GRs are associated with the antidepressant effect of milnacipran, a serotonin noradrenaline reuptake inhibitor (SNRI), and fluvoxamine, a selective serotonin reuptake inhibitor (SSRI), in Japanese patients with depression. METHODS: Patients were prescribed either milnacipran (n = 98) or fluvoxamine (n = 95). The severity of depression was assessed with the Montgomery-Åsberg Depression Rating Scale (MADRS) at 0, 1, 2, 4 and 6 weeks of treatment. RESULTS: Both agents were similarly effective in reducing MADRS scores in 6 weeks. In all subjects receiving milnacipran or fluvoxamine, our data showed no significant interaction between Bcl1 polymorphisms and therapeutic effects. However, when milnacipran- and fluvoxamine-treated subjects were analyzed independently, patients with G allele in Bcl1 polymorphism had a significantly better response to fluvoxamine than those with C/C genotype. On the other hand, no significant relationship was found between treatment response to milnacipran and Bcl1 polymorphism. CONCLUSION: Bcl1 polymorphism may be one of the genetic factors in predicting treatment response to SSRI but not SNRI in Japanese patients with depression.


Subject(s)
Antidepressive Agents/therapeutic use , Cyclin D1/genetics , Cyclopropanes/therapeutic use , Depressive Disorder, Major/drug therapy , Fluvoxamine/therapeutic use , Receptors, Glucocorticoid/genetics , Antidepressive Agents/blood , Asian People , Cyclopropanes/blood , Depressive Disorder, Major/blood , Depressive Disorder, Major/genetics , Female , Fluvoxamine/blood , Genotype , Humans , Male , Middle Aged , Milnacipran , Polymorphism, Single Nucleotide , Selective Serotonin Reuptake Inhibitors/blood , Selective Serotonin Reuptake Inhibitors/therapeutic use , Severity of Illness Index , Treatment Outcome
9.
Jpn J Clin Oncol ; 44(4): 311-7, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24503030

ABSTRACT

OBJECTIVE: Emotional distress is considered to be higher in patients with head and neck cancer than other types of cancer. The present study aimed to identify predictors of the postoperative levels of depression in patients with head and neck cancer who have undergone surgery. METHODS: Postoperative levels of depression were assessed at 3, 6 and 12 months after surgery. The preoperative factors that were significant predictors of the postoperative level of depression at each time point were extracted using multiple regression analyses. RESULTS: The preoperative level of depression was a significant predictor of the postoperative level of depression at the 3rd, 6th and 12th postoperative months. At the sixth postoperative month, negative adjustment to cancer at baseline was also a significant predictor of the postoperative level of depression. CONCLUSION: Evaluating the level of depression and negative adjustment before surgery is considered to be effective for identifying patients who will develop depression after surgery.


Subject(s)
Adaptation, Psychological , Body Image , Depression/etiology , Face , Head and Neck Neoplasms/psychology , Head and Neck Neoplasms/surgery , Postoperative Period , Preoperative Period , Stress Disorders, Post-Traumatic/etiology , Stress, Psychological/etiology , Adult , Aged , Analysis of Variance , Anxiety/etiology , Depression/epidemiology , Female , Humans , Japan/epidemiology , Male , Middle Aged , Patient Selection , Predictive Value of Tests , Prognosis , Prospective Studies , Surveys and Questionnaires , Time Factors
10.
Clin Neuropharmacol ; 35(6): 273-7, 2012.
Article in English | MEDLINE | ID: mdl-23123692

ABSTRACT

OBJECTIVE: We examined the pain-relieving effect of duloxetine on chronic nonorganic orofacial pain (burning mouth syndrome and atypical odontalgia), considering the influence of baseline depressive symptoms. METHODS: In this study of 12 weeks, duloxetine was administered in a fixed-flexible dose of 20 to 40 mg/d to 41 patients with burning mouth syndrome and/or atypical odontalgia. Pain was evaluated using the visual analog scale (VAS) at baseline and at 2, 4, 6, 8, 10, and 12 weeks of treatment. Depressive symptoms were assessed using the Hamilton Depression Rating Scale at baseline and at 12 weeks of treatment. RESULTS: We analyzed the data from 29 patients who completed the study. The VAS score at 12 weeks of treatment was significantly lower than that at baseline. The time course of the VAS scores revealed its significant decrease from 2 weeks of treatment compared to the baseline score. To investigate the influence of baseline depressive symptoms on the pain-relieving effect of duloxetine, the subjects were divided into 2 groups based on the Hamilton Depression Rating Scale score on initial consultation: groups with (≥8) and without (≤7) depressive symptoms. Two-way repeated-measures analysis of variance revealed no significant interaction between time and initial presence or absence of depression. An additional intent-to-treat last-observation-carried-forward analysis including dropped-out patients revealed a similar result. CONCLUSION: Duloxetine significantly relieved chronic nonorganic orofacial pain. Its pain-relieving effect appeared from 2 weeks of treatment. Furthermore, the pain-relieving effects of duloxetine similarly appeared regardless of the presence or absence of baseline depressive symptoms.


Subject(s)
Chronic Pain/drug therapy , Facial Pain/drug therapy , Pain Measurement/drug effects , Thiophenes/therapeutic use , Aged , Antidepressive Agents/therapeutic use , Chronic Pain/diagnosis , Chronic Pain/epidemiology , Duloxetine Hydrochloride , Facial Pain/diagnosis , Facial Pain/epidemiology , Female , Humans , Male , Middle Aged , Pain Measurement/methods , Treatment Outcome
12.
Hum Psychopharmacol ; 27(3): 322-8, 2012 May.
Article in English | MEDLINE | ID: mdl-22585592

ABSTRACT

OBJECTIVES: This study was performed to assess the relationship between plasma levels of milnacipran and its analgesic/antidepressive effect in patients with chronic orofacial pain treated with this drug. METHODS: A total of 44 patients took milnacipran for 12 weeks. Patients were assessed for their pain and depressive symptoms using the visual analog scale (VAS) and Hamilton Depression Rating Scale, respectively. The plasma milnacipran level was also assessed at week 12. RESULTS: Forty patients completed study treatment and were included in the analysis. In these patients, the VAS score at week 12 significantly decreased from the baseline score (t = 5.15, p < 0.0001). The dose of milnacipran was positively correlated in a linear manner with the plasma level of the drug (Y = 44.86 + 0.33X, r = 0.54, R(2) = 0.29, p = 0.0004). A quadratic regression curve was plotted between the percentage of decrease in the VAS score and plasma milnacipran level (Y = 27.39 + 0.76X - 0.008X(2) , p = 0.048, r = 0.40, R(2) = 0.16). On the other hand, no significant relationship was noted between the percentage of decrease in the Hamilton Depression Rating Scale score and plasma milnacipran level. CONCLUSION: The analgesic effect of milnacipran was suppressed in the presence of the plasma level of the drug outside the therapeutic range, whereas its antidepressant effect was not affected by its plasma level.


Subject(s)
Antidepressive Agents/blood , Antidepressive Agents/therapeutic use , Chronic Pain , Cyclopropanes/blood , Cyclopropanes/therapeutic use , Facial Pain , Adult , Aged , Depression/blood , Depression/drug therapy , Depression/etiology , Dose-Response Relationship, Drug , Facial Pain/blood , Facial Pain/complications , Facial Pain/drug therapy , Female , Humans , Male , Middle Aged , Milnacipran , Pain Measurement , Retrospective Studies , Statistics as Topic , Young Adult
13.
BMJ Open ; 2(3)2012.
Article in English | MEDLINE | ID: mdl-22566608

ABSTRACT

OBJECTIVES: The present study aimed to validate screening tools that could be used to identify depression among workers. DESIGN: Diagnostic test study. SETTINGS: Workers from three Japanese companies agreed to participate. PARTICIPANTS: Recruitment for the group 1 occurred between January 2001 and February 2004, and 89 participants (81 men and 8 women with a mean age of 38.4±6.6 years) (98.8%) took part in the study. Recruitment for the group 2 occurred between July 2000 and February 2004, and 1500 participants (1408 men and 92 women with a mean age of 40.9±7.2 years) (94.2%) took part in the study. Demographic data are shown in supplementary table 1. PRIMARY AND SECONDARY OUTCOME MEASURES: the Beck Depression Inventory (BDI) and a two-question case-finding instrument (TQI) were administered to 89 workers and Mini-International Neuropsychiatric Interview was conducted to verify the diagnosis of depression. A second group of 1500 workers completed the BDI and TQI to detect possible sample bias for the distribution of depression. Specificity, sensitivity and positive predictive value were calculated in order to obtain the optimal cut-off scores for BDI and TQI and receiver operating characteristic curves, and Youden Index were applied to further refine the optimal cut-off scores. RESULTS: When paired together, BDI score ≥10 and TQI score of 2 adequately identified workers who had major depressive disorder and those who had other psychiatric disorders that are frequently comorbid with major depressive disorder. CONCLUSIONS: The combination of BDI score ≥10 and TQI score of 2 can adequately screen for current and potential cases of depression among workers. Furthermore, BDI and TQI offer the advantage of being relatively easy to administer to a large number of workers. Early detection of depression could improve treatment outcomes and decrease economic burden. TRIAL REGISTRATION: [corrected]

14.
Prog Neuropsychopharmacol Biol Psychiatry ; 37(1): 26-32, 2012 Apr 27.
Article in English | MEDLINE | ID: mdl-22172534

ABSTRACT

This study aimed to estimate the prevalence of sexual dysfunction, evaluated by the Nagoya Sexual Function Questionnaire (NSFQ), and hyperprolactinemia in patients with schizophrenia and examine a relationship between sexual dysfunction and serum prolactin levels. This cross-sectional, comparative study was performed using a sample comprising 195 Japanese schizophrenic in- and outpatients treated with antipsychotics (117 males and 78 females). Data were collected from October 2009 to January 2010 using single, cross-sectional ratings of sexual function assessed by the NSFQ and concurrent measurement of serum prolactin levels. The prevalence of sexual dysfunction in patients with schizophrenia was high (males 66.7%; females 79.5%). Hyperprolactinemia (>25ng/ml) was highly prevalent among schizophrenia patients, affecting 53.8% of females and 51.3% of males. Among female patients, 16.7% had prolactin levels>100ng/ml. There was no relationship between sexual dysfunction and serum prolactin levels. The present study demonstrated a higher prevalence of sexual dysfunction and hyperprolactinemia in Japanese schizophrenia patients. Clinicians should keep these problems in mind and discuss potential solutions with patients to improve patients' quality of life and adherence to therapy.


Subject(s)
Antipsychotic Agents/therapeutic use , Asian People/ethnology , Hyperprolactinemia/ethnology , Schizophrenia/ethnology , Sexual Dysfunction, Physiological/ethnology , Adult , Asian People/psychology , Cross-Sectional Studies , Data Collection , Female , Humans , Hyperprolactinemia/drug therapy , Hyperprolactinemia/psychology , Male , Middle Aged , Schizophrenia/drug therapy , Sexual Dysfunction, Physiological/drug therapy , Sexual Dysfunction, Physiological/psychology
15.
J Affect Disord ; 135(1-3): 374-6, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21917318

ABSTRACT

BACKGROUND: It has been suggested that the symptoms of major depressive disorder (MDD) are composed of some clusters, which are linked to distinct genetic mechanisms. The purpose of this study was to examine the associations of genetic polymorphisms in the serotonergic system with three factors of the Montgomery-Åsberg Depression Rating Scale (MADRS), i.e., dysphoria, retardation, and vegetative symptoms. METHODS: The subjects were 132 Japanese patients of MDD. The genotypes of tryptophan hydroxylase 218A/C, serotonin transporter gene-linked polymorphic region (5HTTLPR), and 5HT2A receptor -1438G/A polymorphisms were determined by PCR methods. Statistical analyses were performed by the multiple regression analysis. RESULTS: The A allele of 5HT2A polymorphism was associated with higher vegetative scores (p=0.001) and total MADRS scores (p=0.005), while the S allele of 5HTTLPR was related to higher dysphoric scores (p=0.012). The tryptophan hydroxylase genotype was not related to any factor scores or total MADRS scores. LIMITATIONS: The sample size was relatively small, and the subjects were composed of Japanese only. CONCLUSION: This study suggests that the genetic polymorphisms in 5HT2A receptor and serotonin transporter are linked to discrete symptom clusters of MDD.


Subject(s)
Depressive Disorder, Major/genetics , Receptor, Serotonin, 5-HT2A/genetics , Serotonin Plasma Membrane Transport Proteins/genetics , Tryptophan Hydroxylase/genetics , Adult , Alleles , Carrier Proteins/genetics , Depressive Disorder/genetics , Depressive Disorder, Major/diagnosis , Depressive Disorder, Major/psychology , Female , Genotype , Humans , Male , Middle Aged , Polymorphism, Genetic
16.
Hum Psychopharmacol ; 26(4-5): 300-6, 2011.
Article in English | MEDLINE | ID: mdl-21695732

ABSTRACT

OBJECTIVE: This study aims to validate a new user-friendly sexual function questionnaire (Nagoya Sexual Function Questionnaire [NSFQ]) for schizophrenic patients taking antipsychotics. METHODS: Schizophrenic outpatients (men = 30, women = 30) were asked to fill out the NSFQ at initial entry into the research program (Time1) and again 1 to 2 weeks later (Time2). To assess the convergent validity of the NSFQ, at Time1, subjects were asked to fill out the Japanese version of the Udvalg for Kliniske Undersogekser Side Effect Rating Scale (UKU). To assess the discriminant validity of the NSFQ, at Time1, subjects were also asked to fill out the Japanese version of Epworth Sleepiness Scale. RESULTS: Results from Cronbach's alpha analysis indicated that the NSFQ demonstrated excellent internal consistency and scale reliability. The NSFQ also demonstrated strong test-retest reliability. The NSFQ total score was highly correlated with the UKU total score. The NSFQ was shown to have good convergent validity with the UKU. The NSFQ total score was not correlated with the Japanese version of Epworth Sleepiness Scale total score. CONCLUSIONS: This study revealed the internal consistency, test-retest reliability, and convergent and discriminant validities of the NSFQ.


Subject(s)
Antipsychotic Agents/therapeutic use , Galactorrhea/diagnosis , Gynecomastia/diagnosis , Menstruation Disturbances/diagnosis , Schizophrenia/drug therapy , Sexual Dysfunction, Physiological/diagnosis , Sexual Dysfunctions, Psychological/diagnosis , Adolescent , Adult , Antipsychotic Agents/adverse effects , Diagnostic and Statistical Manual of Mental Disorders , Female , Galactorrhea/chemically induced , Galactorrhea/psychology , Gynecomastia/chemically induced , Gynecomastia/complications , Gynecomastia/psychology , Humans , Japan , Male , Menstruation Disturbances/chemically induced , Menstruation Disturbances/complications , Menstruation Disturbances/psychology , Middle Aged , Reproducibility of Results , Schizophrenia/complications , Sexual Dysfunction, Physiological/chemically induced , Sexual Dysfunction, Physiological/complications , Sexual Dysfunction, Physiological/psychology , Sexual Dysfunctions, Psychological/chemically induced , Sexual Dysfunctions, Psychological/complications , Sexual Dysfunctions, Psychological/psychology , Surveys and Questionnaires , Young Adult
17.
J Affect Disord ; 128(1-2): 33-40, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20599274

ABSTRACT

BACKGROUND: Depression influences a worker's productivity and health substantially. Recently, the Japanese society and government reported that working overtime is one of the primary causes of depression and suicide in workers. However, only a few studies have investigated the relation between overtime hours and mental health status, and conclusions vary. In addition, prior findings are inconsistent in terms of the relation between depression and lifestyle factors, including alcohol intake and smoking. Additional studies are required to clarify the relation between possible risk factors and depression in Japanese workers. METHODS: We performed a case-control and a cohort study. Subjects were office workers in four Japanese companies. Diagnosis of depression was made by two psychiatrists who conducted independent clinical interviews using DSM-IV-TR criteria. RESULTS: There was no significant association between working overtime and the onset of depression. The frequency of alcohol intake was significantly related to the onset of depression. We also found a significant relation between younger age and depression onset. Body mass index and physical illness, including diabetes mellitus, had no significant association with depression onset. LIMITATIONS: Data were self-reported and the number of included female workers was small. CONCLUSIONS: Reducing working hours alone is unlikely to be effective in preventing workers' depression. Additional countermeasures are needed, including a reduction in alcohol intake and work stress. Considerations for younger workers are also needed.


Subject(s)
Aging/psychology , Alcohol Drinking/epidemiology , Depression/epidemiology , Depression/psychology , Stress, Psychological/epidemiology , Work/psychology , Workload/psychology , Adult , Age Factors , Age of Onset , Alcohol Drinking/psychology , Case-Control Studies , Cohort Studies , Diagnostic and Statistical Manual of Mental Disorders , Female , Humans , Japan/epidemiology , Life Style , Male , Occupations/statistics & numerical data , Risk Factors , Work/statistics & numerical data , Workforce
18.
Hum Psychopharmacol ; 25(3): 260-7, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20373478

ABSTRACT

OBJECTIVE: To assess the effects of two anxiolytics, diazepam and tandospirone, on driving performance from methodological viewpoints taking frequent rear-end collisions into account. METHODS: In this double-blinded, three-way crossover trial, 18 healthy males received acute doses of 20 mg tandospirone (TSP), 5 mg diazepam (DZP), and placebo (PCB). The subjects were administered three driving tasks-road tracking, car following, and harsh braking-performed using a driving simulator and three cognitive tasks-Wisconsin Card Sorting Test, Continuous Performance Test, and N-back test-at baseline and at 1 and 4 h post-dosing. The Stanford Sleepiness Scale scores were also assessed. RESULTS: DZP nonsignificantly increased the percent change of brake reaction time (BRT) as compared to PCB at 4 h post-dosing. TSP nonsignificantly decreased the percent change of BRT as compared to PCB. Consequently, there was a significant difference in the percent change of BRT between DZP and TSP at 4 h post-dosing. For the remaining tasks, no statistically significant effects of treatment were observed. CONCLUSIONS: Acute doses of DZP significantly impaired the harsh-braking performance as compared to acute doses of TSP. These findings suggest that TSP may be used more safely in patients' driving activities.


Subject(s)
Automobile Driving , Cognition/drug effects , Diazepam/administration & dosage , Isoindoles/administration & dosage , Piperazines/administration & dosage , Psychomotor Performance/drug effects , Pyrimidines/administration & dosage , Adult , Automobile Driving/psychology , Cognition/physiology , Cross-Over Studies , Diazepam/adverse effects , Double-Blind Method , Humans , Isoindoles/adverse effects , Male , Piperazines/adverse effects , Psychomotor Performance/physiology , Pyrimidines/adverse effects , Reaction Time/drug effects , Reaction Time/physiology , Time Factors
19.
Clin Neuropharmacol ; 33(2): 79-83, 2010.
Article in English | MEDLINE | ID: mdl-20375656

ABSTRACT

OBJECTIVES: The effect of milnacipran for the treatment of chronic pain in the orofacial region, including burning mouth syndrome (BMS) and atypical odontalgia (AO), was assessed while accounting for the influence of concurrent depressive symptoms on the pain-relieving effect. METHODS: Milnacipran was administered for 12 weeks to 36 patients with chronic pain in the orofacial region (3 men and 29 women, aged between 22 and 76 years with a mean age of 59 years). Of those patients, 22 and 10 patients had BMS and AO, respectively. The initial dose of milnacipran was 15 mg a day, and the dose was raised up to 100 mg a day. Pain was assessed using the visual analog scale, and symptoms of depression were evaluated using the Hamilton Depression Rating Scale at baseline and at weeks 1, 2, 4, 6, 8, 10, and 12 of the study treatment. RESULTS: Data from 32 patients who completed the study were included in the analysis. The visual analog scale score significantly decreased after the 12-week treatment, and it showed a similar time course of decline irrespective of concurrent depressive symptoms during the 12 weeks. CONCLUSIONS: Treatment with milnacipran resulted in a significant improvement of chronic pain in the orofacial region irrespective of concurrent symptoms of depression. The present results suggested that milnacipran may be an effective agent for treatment of such disorders.


Subject(s)
Adrenergic Uptake Inhibitors/therapeutic use , Burning Mouth Syndrome/drug therapy , Cyclopropanes/therapeutic use , Depression/drug therapy , Facial Pain/drug therapy , Selective Serotonin Reuptake Inhibitors/therapeutic use , Toothache/drug therapy , Adult , Aged , Burning Mouth Syndrome/complications , Chronic Disease , Depression/complications , Dose-Response Relationship, Drug , Facial Pain/complications , Female , Humans , Male , Middle Aged , Milnacipran , Toothache/complications
20.
Psychiatry Clin Neurosci ; 64(1): 62-9, 2010 Feb.
Article in English | MEDLINE | ID: mdl-19968832

ABSTRACT

AIMS: The purpose of the present study was to examine the extent of the effects of psychopathological symptoms and cognitive function on quality of life (QOL) in patients with chronic schizophrenia. METHODS: Data were obtained using the Japanese Schizophrenia Quality of Life Scale (JSQLS), Positive and Negative Syndrome Scale (PANSS), Wisconsin Card-Sorting Test (WCST) Keio version, and Continuous Performance Test (CPT) for 52 schizophrenia patients. RESULTS: Stepwise regression analysis showed that PANSS depression/anxiety factors predicted JSQLS psychosocial conditions and motivation/energy, and that WCST Categories Achieved predicted JSQLS symptoms/side-effects. CONCLUSIONS: Psychopathological symptoms and cognitive function affect subjective QOL in patients with schizophrenia. If the final goal is treatment that improves QOL in a manner that patients themselves are aware of, clinicians probably need to consider a treatment strategy that improves depression/anxiety symptom.


Subject(s)
Cognition/physiology , Quality of Life , Schizophrenic Psychology , Adult , Anxiety/complications , Anxiety/psychology , Attention/physiology , Chronic Disease , Depression/complications , Depression/psychology , Executive Function , Female , Humans , Male , Middle Aged , Motivation , Neuropsychological Tests , Psychiatric Status Rating Scales , Regression Analysis
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