2Ankara Social Sciences University, Faculty of Social and Humanities, Department of Psychology
Objective: Neurological soft signs (NSS) and sleep disorders are quite common in schizophrenia.Both symptom clusters have been proposed as candidate endophenotypes for the disorder. This study aimed to investigate the relationships between NSS, chronotype and sleep quality among patients with schizophrenia.
Method: Positive and Negative Syndrome Scale (PANSS), The Neurological Evaluation Scale (NES), Morningness-Eveningness Questionnaire (MEQ), Pittsburgh Sleep Quality Index (PSQI), Beck Depression Inventory (BDI), and Beck AnxietyInventory (BAI) were administered to 50 patients with schizophrenia and 50 age- and gender-matched healthy control participants. Group differences were assessed using multivariate covariance models. We used stepwise multiple regression analysis to evaluate the potential relationships between NSS and clinical characteristics, diurnal preferences, sleep quality, anxiety, and depression in patients with schizophrenia.
Results: Patients with schizophrenia were more likely to reveal severe impairments in NSS than healthy control participants even after controlling for demographic characteristics and the MEQ, PSQI, BAI, and BDI scores. In addition, patients were more prone to report evening-type characteristics than healthy individuals. Sleep disturbances were significant correlates of deficits in total NES, motor coordination, and other NSS. PSQI global and poor habitual sleep efficiency were associated with sequencing of complex motor acts. No relationships were found between NSS and chronotype. However, general psychopathology significantly contributed to NSS.
Conclusion: The data showed that evening-type diurnal preferences and sleep quality as well as NSS seem to have complex implications in schizophrenia.
Neurological soft signs (NSS) are minor abnormal signs on clinical neurological examination that are mostly concentrated in the areas of sensory integrity, motor coordination, and sequential motor actions (1-3). Collectively, they may suggest the existence of an organic pathology (4).
In almost all studies, NSS were found to be significantly higher in patients with schizophrenia than in control participants (5). Moreover, NSS have been shown to be more common in first-degree relatives of patients with schizophrenia than control participants (6-7). According to previous studies, the presence of a high rate of NSS in schizophrenia patients is associated with early neurodevelopmental abnormalities (8-9) and is not associated with prognosis or treatment (10). However, NSS do not show the same homogeneity in all schizophrenia patient groups. In patients with negative symptoms, chronic progression, resistance to treatment, and impaired cognitive functions, NSS were found to be more common than other patients (11-13). NSS are, therefore, an endophenotype candidate that can be used for research on the genetic origin of schizophrenia.
In humans, the sleep-wake cycle, body temperature, hormone levels, affect, and certain cognitive functions have a daily rhythm called circadian rhythm (14-15). Advance, delay, or deterioration in the circadian rhythm is strongly associated with psychiatric disorders, particularly, mood disorders, such as bipolar depression, major depression, and seasonal affective disorders (16). Humans have different chronotypes called morningness and eveningness in terms of differences in biological and behavioral rhythms, including sleep-wake cycles, body temperature fluctuation, cortisol release, and melatonin release time. Morningness-type individuals go to sleep early, wake up early, and perform better in the morning. Eveningness-type individuals go to sleep late and prefer evening hours for activities (17, 18). There is a phase difference of about 2 h between the two types. This phase difference is also approximately 2 h in terms of the periods of release of hormones, such as body temperature hormones, cortisol, and melatonin (18). In addition,a relationship between depression and chronotypes due to circadian rhythm differences has beendefined. While being an evening-typeindividual is considered a risk for the development of depression in healthy individuals (19), eveningness-type depressive patients have more suicidal ideation and higher depression scores and lower sleep quality than morningness-type depressive patients(20, 21). Features such as neuroticism, impulsivity, stressful lifestyle, and sleep disturbances (i.e., irregular sleep-wake cycles, decreased sleep activity, and decreased slow-wave sleep) are associated with circadian rhythm in the relationship between eveningness and depression (21-23). Unlike morningness-type individuals, eveningness-type individuals have a delayed phase, incompatible internal and external rhythm determinants, and, thus, a disturbed relationship between circadian rhythm and homeostasis (24).
Schizophrenia has long been associated with sleep abnormalities; however, only a few studies have been conducted on circadian rhythms and chronotypes (25). These studies indicated that patients with schizophrenia have severe circadian sleep-wake disturbances, and schizophrenia may be associated with the eveningness chronotype (26-28). A complex interaction of wake and sleep mechanisms, neurotransmitter systems, multiple brain regions, and modulatory hormones is thought to be responsible for the generation of sleep and circadian rhythm disturbances in patients with schizophrenia (26, 29). Variations in multiple genes have been shown to be associated with rhythm-related sleep disorders, sleep homeostasis, phenotypic differences between morning and evening preferences (30), midbrain dopamine regulation, and reward processing (31). These findings suggest that sleep-wake disturbances in patients with schizophrenia may have a genetic basis (32). The demonstration that circadian rhythm disorders predict poor prognosis at a 1-year follow-up in adolescents at clinically high risk for psychosis (33) and a strong association between circadian rhythm integrity and cognitive performance (34) also support that sleep-wake disturbances in patients with schizophrenia may provide an endophenotypic dimension.
Concerning both NSS and chronotype in schizophrenia, the presence of common features, such as those observed before onset of the disease, thoserelated to cognitive impairment, and those providing evidence of a genetic basis, suggest that these dimensions may be related. In this study, we aimed to investigate NSS and chronotype and to examine the comparative relationship between these variables in patients with schizophrenia and healthy control participants. We explored whether NSS was significantly associated with diurnal preferences and sleep quality. We investigated whether schizophrenia patients differenced in their NSS symptoms from health controls after adjusting for diurnal preferences, sleep quality, anxiety, depression, and demographics. We also investigated group differences in diurnal preferences and sleep quality after controlling for demographic characteristics. Finally, we identified the predictive values of demographic and clinical variables, diurnal preferences, sleep quality, anxiety, and depression on NSS.
Fifty outpatients who had consecutively applied to the Izmir KâtipCelebi University Education and Research Hospital, Psychiatry Outpatient Clinic within the specified 20 days and met the inclusion criteria were included in the study. Patients with clinically significant and/or considerable depressive symptoms and patients with severe cognitive impairment were excluded from the study. Outpatients were preferred because hospitalization was thought to adversely affect sleep patterns and comparison with healthy control participants. All patients were taking antipsychotics. The patients who used antiparkinsonian medications, benzodiazepines, antihistaminic medications, minor tranquilizers, and other psychotropics and patients who had extrapyramidal side effects were excluded because all these factors were thought to affect NSS. Fifty healthy age- and gender-matched controls were used forstatistical analysis (Table 1). The mean age of the patients and healthy control participants was 37.73 years [standard deviation (SD)12.42, range 20-67].
All participants gave written and informed consent to participate in accordance with the Declaration of Helsinki after the institutional review board approval. The study was approved by the local ethics committee.
Two examiners who were also qualified psychiatrists confirmed the diagnoses using the fourth edition of “Structural Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders” (SCID-IV) (35).
We assessed NSS with the Neurological Evaluation Scale (NES). The NES scale yields a total and four neurological subscale scores of sensory integration, motor coordination, sequencing of complex motor acts, and other NSS” (36). The Turkish version of the NES had adequate reliability and validity (37).
Positive and Negative Syndrome Scale (PANSS) was used to evaluate the psychotic symptoms, which contains three subscales ofpositive, negative, and general psychopathology.The PANNS consists of 30 items (38). The Turkish version of the PANNS was demonstrated to have good psychometric properties(39).
Chronotype was evaluated by using the Morningness-Eveningness Questionnaire (MEQ) (40). The MEQ is a self-assessment questionnaire that measures the peak and nadir of one’s day-to-day activities. Horne and Ostberg confirmed this scale against daily temperature rhythms. The Turkish MEQ had good reliability and reliability (41).
The Pittsburgh Sleep Quality Index (PSQI) was used to assess quality of sleep among participants (42). This PSQI contains 19 items examining seven components of subjective sleep quality, habitual sleep efficiency, sleep latency, sleep disturbances, sleep duration, use of sleeping medication, and daytime dysfunction. The validity and reliability of the Turkish PSQI was demonstrated by Agargun et al. (43).
Examination of depressive symptoms was based on the Beck Depression Inventory (BDI). BDI is a21-item self-report instrument designed to evaluate the presence and severity of symptoms of depression. Each item is asked to be rated on a 4-point scale, ranging from 0 and 3. A total score is obtainedby summingup the item responses,yieldinga total score ranging from 0 to 63 (44).
The Beck Anxiety Inventory (BAI) was devised to examine anxiety arousal symptomsover the past week. Participants are asked to rate each item on a 4-point scale, ranging from 0 and 3. The greater the scores, the higher the symptom severity. The BAI is the gold standard in evaluating physiological anxious arousal (45). Both the BDI and the BAI were translated into Turkish, and good validity and reliability wasreported for the Turkish versions (46, 47).
We began with computing descriptive statistics for socio-demographic and clinical features of the patients and healthy controls. Using nonparametric χ-squared test, we compared gender and marital status between groups. We used independent sample t-test in order to compare age and duration of education between patients with psychosis and healthy controls. We performed Pearson product moment correlation coefficients of total and subscale scores on the NES with psychological variables.
Using general linear modeling approach, we assessed group differences in NSS, diurnal preferences and sleep quality. For the total scores of the NES, we used analysis of covariance (ANCOVA) after controlling for age, gender, marital status, education (yrs), and scores on the BAI, BDI, MEQ, and PSQI to compare groups. Next, to explore significance of multivariate variation on NSS between groups, we carried out multivariate analysis of covariance (MANCOVA) for the four subscales of the NES (sensory integration, motor coordination, sequencing of complex motor acts, and other neurological soft signs) after controlling for age, gender, marital status, education (yrs), and scores on the BAI, BDI, MEQ, and PSQI. Then, each subscale of the NES was compared between groups using ANCOVA.
A body of evidence has well-documented in the literature that depression and anxiety have substantial shared variances with diurnal preferences and sleep quality (48-51). Therefore, we carried out two ANCOVAs after adjusting for only demographic variables (age, gender, marital status, education), in which the MEQ and PSQI total scores were dependent variables. Next, seven components of the PSQI (subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication and daytime dysfunction) were subjected to MANCOVA together after controlling for demographics. Finally, group difference for each component of the PSQI was evaluated using ANCOVA.
We carried out four stepwise multiple regression analyses among patients with schizophrenia. The total and subscale scores on the NES were dependent variables in theregression analyses. Socio-demographic variables (age, gender, education, and marital status), clinical features (age at the onset, duration of the illness (yrs), and number of hospitalization), subscale scores of the PANSS (positive and negative symptom severity, and general psychopathology),the PSQI components (subjective sleep quality, habitual sleep efficiency, sleep latency, sleep disturbances, sleep duration, use of sleeping medication, and daytime dysfunction), and total scores on the MEQ, BAI and BDI regressed onto neurological symptoms as measured by total and subscales the NES.
The sociodemographic and clinical characteristics of the patients and healthy control participants are presented in Table 1. Gender (χ(1)=361, p=0.548) and age (t=0.377, p=0.707) did not statistically significantly differ between schizophrenia patients and healthy control participants. Patients with schizophrenia were more likely to be single than healthy control participants (χ(1)=9.180, p=0.002).
Using Pearson product moments correlation coefficients, we evaluated the associations between scale scores and NSS by groups. Schizophrenia patients with high NSS as indexed by the NES reported significantly greater scores of general psychopathology (r=0.28, p<0.05). Impairment in sensory integration was significantly correlated with general psychopathology (r=0.28, p<0.05), poor subjective sleep quality (r=0.30, p<0.05), and longer sleep latency (r=0.30, p<0.05) among patients with schizophrenia. In the healthy control group, anxiety (r=0.33 p<0.05), depression (r=0.33, p<0.05), and sleep disturbance (r=0.41, p<0.01) were significantly correlated with the total NES score. Difficulties in motor coordination were significantly associated with sleep disturbances (r=0.55, p<0.01). Deterioration in the sequencing of complex motor acts was significantly correlated with anxiety (r=0.48, p<0.01), depression (r=0.45, p<0.01), poor sleep quality (r=0.34, p<0.05), and disturbance in habitual sleep efficiency (r=0.33, p<0.05) among control participants. Anxiety (r=0.31, p<0.05), depression (r=0.31, p<0.05), and sleep disturbances (r=0.40, p<0.01) were significantly correlated with other NSS in healthy participants. These findings are presented in Table 2.
To explore the individual differences on scale scores between the patients and healthy control participants, we conducted a series of general linear analyses. First, we conducted an ANCOVA between patients and healthy control participants, in which the unique variance of dependent variables of the NES total scores were controlled for sociodemographic variables (i.e., age, gender, marital status, and education) and the total BAI, BDI, MEQ, and PUKI scores. Patients demonstrated significantly greater total NES scores than the control participants (F [1, 90]=15.312, p<0.001, η2=0.145). Next, we conducted a MANCOVA, in which differences between the patient group and control group in the four subscales of the NES (sensory integration, motor coordination, sequencing of complex motor acts, and other neurological soft signs) were assessed after controlling for sociodemographic variables and the total BAI, BDI, MEQ, and PUKI scores. The MANCOVA yielded a significant Wilk’s λ value of 0.812 (F [4, 87]=5.043, p=0.01, η2=0.188). Therefore, to explore the group differences between patients and healthy controls on each subscale of the NES, we carried out four ANCOVAs. Each subscale of the NES (sensory integration, motor coordination, sequencing of complex motor acts, and other neurological soft signs) was subjected to ANCOVA separately. Compared to control participants, schizophrenia patients had marked deficits in sensory integration (F [1, 90]=14.484, p<0.001, η2=0.139), motor coordination (F [1, 90]=4.105, p<0.05, η2=0.044), the sequencing of complex motor acts (F [1, 90]=11.288, p<0.01, η2=0.111), and other NSS (F [1, 90]=8.657, p<0.01, η2=0.088), even after adjusting for sociodemographic characteristics (age, gender, marital status, and education) and other scale scores (BAI, BDI, MEQ, and PUKI). Findings are presented in Table 3.
We conducted an ANCOVA between the groups for the total MEQ scores after adjusting for sociodemographic features(age, gender, marital status, and education). ANCOVA showed that schizophrenia patients were more prone to evening-type diurnal preferences than healthy participants (F [1, 94]=6.694, p<0.05, η2=0.066). In a similar vein, we conducted another ANCOVA between the groups for the PSQI global scores after controlling for sociodemographic features (age, gender, marital status, and education). The ANCOVA analysis result with the PSQI total score as the dependent variable was not statistically significant (F [1, 94]=0.118, p=0.732, η2=0.001). Then, we carried out a MANCOVA between groups in which the PSQI subscales were treated as the dependent variables set. MANCOVA between the patient and control groups with the seven components of the PSQI as the dependent variables revealed significant multivariate group difference (Wilk’s λ=0.815, F [7, 88]=5.002 p=0.010, η2=0.185). Therefore, we carried out seven ANCOVAs to explore the differences in the PSQI components between patients and healthy controls. The ANOVA for use of sleep medication subscale revealed that patients were more likely to use sleep medications than control participants (F [1, 94]=10.649, p<0.01, η2=0.102). However, group differences in subjective sleep quality (F [1, 94]=3.751, p=0.056, η2=0.038), sleep latency (F [1, 94]=0.522, p=0.472, η2=0.006),sleep duration (F [1, 94]=1.284, p=0.260, η2=0.013),habitual sleep efficiency (F [1, 94]=0.161, p=0.689, η2=0.002), sleep disturbances (F [1, 94]=1.009, p=0.318, η2=0.011), and daytime dysfunction (F [1, 94]=0.522, p=0.472, η2=0.006) were not significant. These findings are presented in Table 4.
Using stepwise multiple regression analysis in the patient group (n=50), we investigated the predictive value of positive symptoms, negative symptoms, general psychopathology, diurnal preferences, anxiety, depression, the seven components of the PSQI, and sociodemographic (i.e., age, gender, marital status and levels of education) and clinical features (i.e., duration of the illness and number of hospitalizations) on the total and subscale NES scoresseperately. To this end, we run five multiple stepwise regression analyses.In the first regression analysis, in which the total NES score was the dependent variable, the final model converged at the second step. Increased levels of general psychopathology (β=0.30, t=2.205, p<0.05) and lower levels of education (β=-0.274, t=-2.041, p<0.05) were significantly related to NSS, explaining 15.5% of the variance in the total NES scores. The second multiple regression model converged at the first step that being male (β=0.40, t=3.031, p<0.01) was significantly associated with impairment in sensory integration. The third stepwise multiple regression analysis showed that the number of hospitalizations (β=0.40, t=2.975, p<0.01) was significantly associated with impairment in motor coordination. In the fourth stepwise regression analysis, we identified that patients with lower levels of education (β=-0.42, t=-3.247, p<0.01) reported significant deterioration in the sequencing of complex motor acts. In the final stepwise regression analysis, we found that neither of the independent variables significantly contributed to other soft neurological signs.The results of these analyses are presented in Table 5.
The most salient finding of this study was that NSS was prominent among schizophrenia patients in comparison to controls after controlling for anxiety, depression, sleep quality, diurnal preferences and sleep quality as well as demographic features. Evening-type diurnal preferences were more likely among psychotic patients than controls. Even though group differences were not significant, sleep disturbance was tied to the NES total and motor coordination deficits among patients. Sequencing of complex motor acts was a substantial correlate of the PSQI global and poor habitual sleep efficiency.General psychopathology was predictive of NSS.
Our findings suggested a correlation between general psychopathology and total NES, especially sensory integration. In general, negative symptoms were found to be the most relevant factors correlated with NSS (52-57), but motor signs were especially correlated with negative symptoms (58). Few studies have found significant associations with positive symptoms (59-61). While our study differs from other studies in terms of these results, a strong correlation between general symptoms of schizophrenia and NSS was reported in a meta-analysis (5). This notion has been confirmed by longitudinal studies addressing that the associations between psychotic symptomatology and NSS increase over time (4). In addition, differences in the strength of these associations may be a function of age, duration of the disease, and symptom severity in our outpatient group.
In healthy controls, anxiety and depression were correlated with the sequencing of complex motor acts, other NSS, and the total NES score.The presence of NSS is thought to help distinguish bipolar disorder from diseases that are less likely to have a neurodevelopmental component, such as unipolar depression (62-67). However, there are studies showing the presence of NSS in depression (65) and a correlation between NSS and anxiety-depressive symptomatology and childhood maltreatment (66).
Our study revealed a chronotype difference between patients with schizophrenia and healthy control participants and suggested an association with the eveningness chronotype in patients with schizophrenia, as was suggested in previous studies (26, 33, 67, 68). However, no correlation was found between NSS and chronotype. The hypothesis that NSS and chronotype may have a relationship due to the common phenotypic characteristics was not confirmed in our study. Since our study is the first study on this relationship, this hypothesis can be tested in future studies.
On the other hand, relationships including impairment in sensory integration and poor subjective sleep quality, andimpairment in sensory integration and longer sleep latency were substantial in patients with schizophrenia. Sleep and circadian rhythm impairment in schizophrenia have been reported as hallmarks of the disorder (69, 70). Patients with schizophrenia have been reported to experience “a wide range of sleep disruption phenotypes” that may have substantial suggestions for understanding the underlying pathophysiology of the disorder (71). Difficulties with sleep continuity and increased sleep onset latency are also among these phenotypes (72-75), which are also observed in the prodromal phase (67, 68). The finding that deterioration in sensory integration is associated with sleep disturbance in our study also contributes to the hypothesis that disruption of sleep and atypical brain functioning may be interlaced (76). Similarly, the finding that deterioration in NSS was also associated with sleep-related parameters in healthy control participants in our study supports these notions. So much so that we found an association between NSS, especially difficulties in motor coordination and sleep disturbances and an association between the sequencing of complex motor acts and poor sleep quality in healthy controls.
In addition, our study demonstrated impairments in sensory integration, the sequencing complex motor acts, and other NSS in patients with schizophrenia, even after adjusting for sociodemographic characteristics and other scale scores. The fact that NSS weresignificantly higher in patients even if other variables were fixed shows that NSS are a part of the persistent condition of the disease. In our study, we also found that NSS emerged with affective changes in healthy controls but were not influenced by affective changes in the patient group. These results indicate that NSS can be considered as a marker in schizophrenia. Evidence suggesting that deteriorations in neurodevelopmental processes are an important risk factor in schizophrenia is increasing (77-81). NSS were independently related to obstetric complications, genetic liability toschizophrenia, impairment in pre-morbid functioning, neurodevelopmental delay, and motor disorders (9). A study suggested a polygenic overlap between schizophrenia and NSS scores (82). Only a study that evaluated NSS in subjects without a family history of any mental disorders reported the presence of frequent silent neurodevelopmental deterioration in the general population and suggested that NSS are “possibly a weak generic rather than specific risk factor” (83).
Finally, our study showed that general psychopathology and lower levels of education were significantly correlated with NSS. In addition, lower levels of education were significantly associated with significant deterioration in the sequencing of complex motor acts. Unlike the general literature that suggests NSS are associated with negative symptoms, we found that general psychopathology predicts NSS. As we have previously discussed, this difference may be due to differences in variables such as age, duration of disease, and symptom severity in our outpatient group. However, most previous studies have also reported a negative relationship between NSS and education level (52, 57, 84). In our study, male gender was significantly associated with impairment in sensory integration. The literature suggests NSS are more common and more permanent in men than in women; this difference may be due to the timing of brain maturation and higher birth complications in males (85-87). An association was also found between the number of hospitalizations and impairment in motor coordination. This finding may be associated with the duration and the severity of the disease, and it is also possible that neuroleptics may contribute to the emergence of NSS (88).
Some limitations of the present study should be considered while interpreting our results. First, our study was a cross-sectional study, and motor abnormalities may vary during the long-term follow-up of the disease. Second, the effect of the type and dose of antipsychotic were not clarified. In addition, the measurement of sleep disorders in this study was based solely on self-report questionnaires, without further objective evaluation, such as actigraphy or polysomnography. Finally, to date, although the NES has been instrumental in evaluating NSS in Turkish samples, psychometric properties of the Turkish version have not been addressed adequately.Psychometric features of the Turkish version should be warranted in further studies.
There are many studies investigating NSS in schizophrenia and investigating chronotypes in affective disorders, but our study is crucial in terms of the fact that the chronotype in schizophrenia is a less researched area and that it also evaluated NSS. We determined a relationship between sensory integration and sleep quality, yet we could not find any relationships between NSS and chronotype in our study. However, we did not have the opportunity to compare our results with similar studies, since we were unable to find any studies on this subject in the literature.Although the possible effect of chronotype on psychosis is not as clear as NSS, our data suggests a circadian disruption involvement in the sleep-wake phenotypes in patients with schizophrenia. To improve the prevention and treatment of related disorders, future research should demonstrate a mechanical connection and improve biological understanding by examining the possible antipsychotic drug effects on circadian rhythms and molecular processes underlying NSS in a longitudinal perspective.
Ethics Committee Approval: The study was approved by the local Ethics Committee.
Informed Consent: All participants gave written and informed consent to participate in accordance with the Declaration of Helsinki after the institutional review board approval.
Peer-review: Externally peer-reviewed.
Conflict of Interest: The authors declare no conflict of interest.
Financial Disclosure: The authors declare that the current study was not financially supported by any institution or organization.
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2Ankara Sosyal Bilimler Üniversitesi, Sosyal ve Beşeri Bilimler Fakültesi, Psikoloji Bölümü
Amaç: Nörolojik silik belirtiler (NSB) ve uyku bozuklukları şizofrenide oldukça yaygındır ve her iki belirti grubu da hastalık için aday endofenotipler olarak önerilmiştir. Bu çalışma, şizofreni hastalarında NSB, uyku kalitesi ve uyku kronotipini araştırmayı ve sağlıklı kontrollerle aralarındaki karşılaştırmalı ilişkiyi incelemeyi amaçlamaktadır.
Yöntem: Elli şizofreni hastası ve yaş ve cinsiyet açısından eşleştirilmiş 50 sağlıklı kontrole Sosyodemografik Veri Formu, Sabahlılık- Akşamlılık Envanteri (SAE), Nörolojik Değerlendirme Ölçeği (NDÖ), Beck Anksiyete Envanteri (BAE), Beck Depresyon Envanteri (BDE), Pittsburg Uyku Kalitesi ölçeği (PUKÖ) ve Pozitif ve Negatif Sendrom Ölçeği (PANSS) uygulandı. Grup farklılıkları çok değişkenli kovaryans modelleri kullanılarak değerlendirildi. Hastalarda NSS'nin klinik özellikler, günlük tercihler, uyku kalitesi, anksiyete ve depresyon ile potansiyel ilişkilerini değerlendirmek için ise aşamalı çoklu regresyon analizi kullanıldı.
Bulgular: Şizofreni hastalarında, MEQ, PSQI, BAI ve BDI üzerindeki demografik ve klinik özellikleri ve skorları kontrol ettikten sonra bile NSB'de ciddi bozulmaların olduğu saptanmıştır. Şizofreni hastaları sağlıklı bireylere kıyasla akşamcıl tip kronotip özellikleri bildirmeye daha yatkınlardı. Buna ek olarak, şizofreni hastalarında NDÖ’nün alt ölçeklerinden duyusal entegrasyonda bozulma ile zayıf subjektif uyku kalitesi ve uyku latansı arasında bir ilişki saptanmış; ancak, NSS ve kronotip arasında ilişki bulunamamıştır. Bununla birlikte, genel psikopatolojideki bozulmaların NSB'ye önemli ölçüde katkıda bulunduğu saptanmıştır.
Sonuç: Bulgularımız, NSB'nin yanı sıra akşam tipi günlük tercihlerin ve uyku kalitesinin de şizofrenide karmaşık çıkarımlara sahip olduğunu göstermiştir.