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1.
Neurosurg Focus ; 56(6): E17, 2024 06.
Article in English | MEDLINE | ID: mdl-38823060

ABSTRACT

OBJECTIVE: Dystonia is among the most common pediatric movement disorders and can manifest with a range of debilitating symptoms, including sleep disruptions. The duration and quality of sleep are strongly associated with quality of life in these individuals and could serve as biomarkers of dystonia severity and the efficacy of interventions such as deep brain stimulation (DBS). Thus, this study investigated sleep duration and its relationship to disease severity and DBS response in pediatric dystonia. METHODS: Actigraphs (wearable three-axis accelerometers) were used to record multiday sleep data in 22 children with dystonia, including 6 patients before and after DBS implantation, and age- and sex- matched healthy controls. Data were preprocessed, and metrics of sleep duration and quality were extracted. Repeated-measures statistical analyses were used. RESULTS: Children with dystonia slept less than typically developing children (p = 0.009), and shorter sleep duration showed trending correlation with worse dystonia severity (r = -0.421, p = 0.073). Of 4 patients who underwent DBS and had good-quality data, 1 demonstrated significantly improved sleep (p < 0.001) postoperatively. Reduction in dystonia severity strongly correlated with increased sleep duration after DBS implantation (r = -0.965, p = 0.035). CONCLUSIONS: Sleep disturbances are an underrecognized marker of pediatric dystonia severity, as well as the effectiveness of interventions such as DBS. They can serve as objective biomarkers of disease burden and symptom progression after treatment.


Subject(s)
Actigraphy , Deep Brain Stimulation , Dystonia , Sleep , Humans , Deep Brain Stimulation/methods , Male , Female , Child , Dystonia/therapy , Adolescent , Actigraphy/methods , Sleep/physiology , Quality of Life , Dystonic Disorders/therapy , Sleep Wake Disorders/therapy , Sleep Wake Disorders/etiology , Sleep Wake Disorders/diagnosis , Severity of Illness Index , Treatment Outcome
2.
Aust J Gen Pract ; 53(6): 389-393, 2024 06.
Article in English | MEDLINE | ID: mdl-38840377

ABSTRACT

BACKGROUND: Shift work is characterised by displaced sleep opportunities and associated sleep disturbance. Shift workers often report sleepiness and other wake time symptoms associated with poor sleep. However, clinical sleep disorders are also prevalent in shift workers. Although prevalence rates are similar or higher in shift workers compared with the general population, help seeking in shift workers with sleep disorders is low. OBJECTIVE: This article aims to provide general practitioners with a contemporary overview of the prevalence rates for sleep disorders in shift workers, to clarify the existing evidence relating to mental and physical health consequences of sleep disorders in shift workers and to highlight the need to consider undiagnosed sleep disorders before attributing sleep-related symptoms solely to work schedules. DISCUSSION: Symptoms of sleep loss associated with shift work overlap with symptoms experienced by individuals living with sleep disorders. Although >40% of middle-aged Australians live with a sleep disorder that requires investigation and management, symptoms in shift workers are often attributed to the work schedule and, as a result, might not be investigated for appropriate diagnosis and treatment. We argue that screening for sleep disorders in shift workers with sleep complaints should be a priority.


Subject(s)
General Practice , Sleep Wake Disorders , Humans , Sleep Wake Disorders/therapy , Sleep Wake Disorders/physiopathology , Sleep Wake Disorders/diagnosis , Australia/epidemiology , General Practice/methods , Sleep Disorders, Circadian Rhythm/therapy , Sleep Disorders, Circadian Rhythm/physiopathology , Sleep Disorders, Circadian Rhythm/diagnosis , Sleep Disorders, Circadian Rhythm/complications , Prevalence , Shift Work Schedule/adverse effects , Work Schedule Tolerance/physiology
3.
Can Fam Physician ; 70(6): 388-390, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38886082

ABSTRACT

QUESTION: I continue to hear concerns from parents in my practice about the frequent use of light-emitting devices by their children. I have also found that many children suffer from sleep disturbances. What are the effects of screen time on sleep, and what are some best practices for sleep hygiene and screen use among children? ANSWER: Screen time is higher now than before the onset of the COVID-19 pandemic, and knowledge about the effects of screen time is evolving. Spending time in front of a screen may replace sleep time or sleep-promoting activities such as exercise, and the engaging content and social interactions on screens interfere with falling asleep. Evidence exists on the disruption of the circadian rhythm by light emitted by screens. Advice to families should include sleep hygiene activities as well as elimination of screen use at least 1 hour before sleep.


Subject(s)
COVID-19 , Screen Time , Sleep , Humans , Child , Sleep/physiology , Sleep Hygiene , Sleep Wake Disorders/diagnosis , SARS-CoV-2
4.
Int J Rheum Dis ; 27(6): e15181, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38831523

ABSTRACT

OBJECTIVES: Sleep disturbance is common in autoimmune rheumatism diseases (ARD) and it plays an important role in activating disease and affects the quality of life. This study aims to evaluate the efficacy and acceptability of the novel electrical therapy on sleep disturbance in ARD patients and its effect on immunologic factors. METHODS: A total of 51 ARD patients (26 treatment group and 25 control group) with sleep disturbance were enrolled in this study. Sleep parameters and immunological indicators (serum level of 12 cytokines and immune function) were collected. The novel electrical therapy was prescribed for 15-30 min 3-6 times a day. The Pittsburg Sleep Index (PSQI) was assessed before and after 3 months' treatment by Mi Energy equipment. Immune function and serum levels of cytokines of all participants at baseline and after treatment were tested with flow cytometry and flow immunofluorescence, respectively. Correlation analysis was used to analyze the relationship between sleep disturbance and immunologic factors. Multiple linear regression analysis was employed to investigate the risk of sleep disturbance in ARD. RESULTS: The global score of PSQI (Baseline: 12.81 ± 4.07, After novel electrical therapy: 4.88 ± 2.76) was effectively improved after 3 months of adjuvant therapy by electrical therapy. We also found that serum levels of IL-8 and IL-1ß statistically significantly decreased after novel electrical therapy. This adjuvant therapy can also significantly decrease the percentage of CD4 + CD8 + T cell, effector memory CD8 + T cell, Memory CD8 + T cell, Th17 cell, and plasma cell and significantly can increase the percentage of naïve CD8 + T cell, Th2 cell, and Tfh2 cell. Nevertheless, all serum level of 12 cytokines and the percentage of immune cells did not correlate with the PSQI global score except the Tc17 cell. Furthermore, age is an independent risk factor influencing PSQI scores (OR = 1.15, p < 0.05) in patients with autoimmune diseases through multiple linear regression analysis. CONCLUSIONS: Novel electrical therapy can effectively improve sleep disturbance in patients with ARD. It can also change the serum level of some cytokines (IL-8 and IL-1ß) and percentage of immune cells (CD4 + CD8 + T cell, effector memory CD8 + T cell, Memory CD8 + T cell, Th17 cell, naïve CD8 + T cell, Th2 cell, Tfh2 cell, and plasma cell).


Subject(s)
Autoimmune Diseases , Rheumatic Diseases , Sleep Wake Disorders , Humans , Female , Male , Rheumatic Diseases/therapy , Rheumatic Diseases/immunology , Rheumatic Diseases/blood , Rheumatic Diseases/complications , Middle Aged , Sleep Wake Disorders/etiology , Sleep Wake Disorders/blood , Sleep Wake Disorders/therapy , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/physiopathology , Autoimmune Diseases/blood , Autoimmune Diseases/therapy , Autoimmune Diseases/diagnosis , Autoimmune Diseases/complications , Autoimmune Diseases/immunology , Adult , Treatment Outcome , Time Factors , Electric Stimulation Therapy/methods , Biomarkers/blood , Sleep , Cytokines/blood , Case-Control Studies , Sleep Quality
5.
Zh Nevrol Psikhiatr Im S S Korsakova ; 124(5. Vyp. 2): 132-134, 2024.
Article in Russian | MEDLINE | ID: mdl-38934678

ABSTRACT

On November 17-18, 2023, the VII Scientific and Practical Conference "Clinical Somnology" was held in Moscow. The conference was organized by the all-Russian public organization "Russian Society of Somnologists" (ROS). The forum discussed the issues of diagnostics and treatment of sleep disorders, also presented the topics of fundamental research, discussed new ways of studying sleep and the prospects of development of somnology as a science. The conference was attended by more than 250 participants from 38 regions. Broadcasting of the sessions of the first day of the event was watched by more than 270 listeners. Within 2 days of the conference 14 symposiums were held and 52 reports were presented.


Subject(s)
Sleep Wake Disorders , Humans , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/therapy , Russia , Sleep/physiology , Moscow , Congresses as Topic
6.
J Paediatr Child Health ; 60(6): 212-221, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38726707

ABSTRACT

AIM: This study examined the outcomes of a telehealth model for sleep health assessment among Indigenous and non-Indigenous children residing in remote and regional communities at the Top End Northern Territory (NT) of Australia. METHODS: Video telehealth consultation, that included clinical history and relevant physical findings assessed virtually with an interstate paediatric sleep physician was conducted remotely. Polysomnography (PSG) and therapeutic interventions were carried out locally at Darwin, NT. The study participants were children referred between 2015 and 2020. RESULTS: Of the total 812 children referred for sleep assessment, 699 underwent a diagnostic PSG. The majority of patients were female (63%), non-Indigenous (81%) and resided in outer regional areas (88%). Indigenous children were significantly older and resided in remote or very remote locations (22% vs. 10%). Referral patterns differed according to locality and Indigenous status - (non-Indigenous via private (53%), Indigenous via public system (35%)). Receipt of referrals to initial consultation was a median of 16 days and 4 weeks from consult to PSG. Remote children had slightly longer time delay between the referral and initial consult (32 vs. 15 days). Fifty one percent were diagnosed to have OSA, 27% underwent adenotonsillectomy and 2% were prescribed with CPAP therapy. CONCLUSIONS: This study has demonstrated that a telehealth model can be an effective way in overcoming logistical barriers and in providing sleep health services to children in remote and regional Australia. Further innovative efforts are needed to improve the service model and expand the reach for vulnerable children in very remote communities.


Subject(s)
Telemedicine , Humans , Female , Northern Territory , Male , Child , Child, Preschool , Rural Population , Polysomnography , Referral and Consultation , Health Services Accessibility , Adolescent , Rural Health Services/organization & administration , Sleep Wake Disorders/therapy , Sleep Wake Disorders/diagnosis , Infant , Remote Consultation , Native Hawaiian or Other Pacific Islander
8.
Tunis Med ; 102(5): 278-283, 2024 May 05.
Article in French | MEDLINE | ID: mdl-38801285

ABSTRACT

INTRODUCTION: Sleep quality is a complex phenomenon with quantitative and subjective aspects that vary during adolescence. The prevalence of sleep disorders is not known in Tunisia due to the lack of validated tools. AIM: To translate and validate the questionnaire Pittsburgh Sleep Quality Index (PSQI) into Tunisian Arabic in middle school students. METHODS: We translated the PSQI into Tunisian Arabic based on the translation back-translation method. We conducted a cross-sectional study on a sample of 560 adolescents. Exploratory factor analysis was performed to study construct validity. To test reliability, the global internal consistency of the scale was computed. RESULTS: The construct validity was verified by factor analysis, proving that a single factor explained 30.3% of the overall variance. This model produced a good factor load for all the components. The analysis of the reliability showed an acceptable internal consistency (Cronbach's alpha=0.6). CONCLUSION: The Arabic Tunisian version of the PSQI is a psychometrically valid measure. The PSQI could be useful for the detection and evaluation of symptoms of sleep disorders, as well as for further studies and researches about associated factors with poor sleep quality in adolescent and youth.


Subject(s)
Psychometrics , Sleep Quality , Sleep Wake Disorders , Translations , Humans , Adolescent , Tunisia/epidemiology , Female , Male , Cross-Sectional Studies , Reproducibility of Results , Surveys and Questionnaires/standards , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/epidemiology , Psychometrics/standards , Psychometrics/methods , Translating , Child , Students/statistics & numerical data , Students/psychology
9.
BMC Pediatr ; 24(1): 378, 2024 May 31.
Article in English | MEDLINE | ID: mdl-38822278

ABSTRACT

BACKGROUND: To translate and culturally adapt the Children's Sleep Habits Questionnaire (CSHQ) to a Swedish version, CSHQ-SWE, and to assess its validity and reliability for use with children with attention deficit hyperactivity disorder (ADHD). METHODS: A total of 84 children with ADHD (51 boys and 33 girls; 6-12 years) and parents (7 men and 77 women; 28-51 years) were included in the study. CSHQ was translated and culturally adapted to Swedish, and assessed for concurrent validity with sleep actigraphy (analyzed by Kendall's Tau) and for reliability by internal consistency (analyzed by McDonald's Omega H). Face and content validity was evaluated by parents (n = 4) and healthcare professionals (n = 6) qualitatively (comprehensiveness, relevance, and comprehensibility assessed by interviews and analyzed by thematic analysis) and quantitatively (analyzed by content validity ratio and content validity index for 33 items and four non-scored inquiries). RESULTS: Parent-reported sleep problems (CSHQ-SWE total score) were moderately correlated with less "Sleep Efficiency" (Tau = -0.305; p < 0.001) measured by sleep actigraphy. Parent-reported problems with "Sleep Onset Delay" was moderately correlated with measured time for "Sleep Onset Latency" (Tau = 0.433; p < 0.001). Parent-reported problems with "Night Wakings" were weakly correlated with measured time for "Wake After Sleep Onset" (Tau = 0.282; p < 0.001). Parents estimation of "Total daily sleep duration" was moderately correlated with measured "Total Sleep Time" (Tau = 0.386; p < 0.001). Five of the seven subscales reached an acceptable level for internal consistency (McDonald's Omega H > 0.700). Comprehensiveness, relevance, and comprehensibility of CSHQ-SWE were satisfactory overall. Content validity ratio was 0.80 to 1.00 for six items, 0.00 to 0.60 for 22 items, and < 0.00 for nine items. Content validity index was 0.22. CONCLUSIONS: CSHQ-SWE demonstrated acceptable concurrent validity with objectively measured sleep and internal consistency, whereas the overall results of face and content validity assessment varied. The instrument needs to be further evaluated regarding construct validity, responsiveness, test-retest reliability, and its generalization to other populations.


Subject(s)
Actigraphy , Attention Deficit Disorder with Hyperactivity , Parents , Humans , Male , Female , Child , Reproducibility of Results , Sweden , Surveys and Questionnaires/standards , Attention Deficit Disorder with Hyperactivity/diagnosis , Adult , Middle Aged , Translations , Sleep , Habits , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/etiology
10.
BMC Neurol ; 24(1): 147, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38693483

ABSTRACT

BACKGROUND: Sleep disorders are a prevalent non-motor symptom of Parkinson's disease (PD), although reliable biological markers are presently lacking. OBJECTIVES: To explore the associations between sleep disorders and serum neurofilament light chain (NfL) levels in individuals with prodromal and early PD. METHODS: The study contained 1113 participants, including 585 early PD individuals, 353 prodromal PD individuals, and 175 healthy controls (HCs). The correlations between sleep disorders (including rapid eye movement sleep behavior disorder (RBD) and excessive daytime sleepiness (EDS)) and serum NfL levels were researched using multiple linear regression models and linear mixed-effects models. We further investigated the correlations between the rates of changes in daytime sleepiness and serum NfL levels using multiple linear regression models. RESULTS: In baseline analysis, early and prodromal PD individuals who manifested specific behaviors of RBD showed significantly higher levels of serum NfL. Specifically, early PD individuals who experienced nocturnal dream behaviors (ß = 0.033; P = 0.042) and movements of arms or legs during sleep (ß = 0.027; P = 0.049) showed significantly higher serum NfL levels. For prodromal PD individuals, serum NfL levels were significantly higher in individuals suffering from disturbed sleep (ß = 0.038; P = 0.026). Our longitudinal findings support these baseline associations. Serum NfL levels showed an upward trend in early PD individuals who had a higher total RBDSQ score (ß = 0.002; P = 0.011) or who were considered as probable RBD (ß = 0.012; P = 0.009) or who exhibited behaviors on several sub-items of the RBDSQ. In addition, early PD individuals who had a high total ESS score (ß = 0.001; P = 0.012) or who were regarded to have EDS (ß = 0.013; P = 0.007) or who exhibited daytime sleepiness in several conditions had a trend toward higher serum NfL levels. CONCLUSION: Sleep disorders correlate with higher serum NfL, suggesting a link to PD neuronal damage. Early identification of sleep disorders and NfL monitoring are pivotal in detecting at-risk PD patients promptly, allowing for timely intervention. Regular monitoring of NfL levels holds promise for tracking both sleep disorders and disease progression, potentially emerging as a biomarker for evaluating treatment outcomes.


Subject(s)
Biomarkers , Neurofilament Proteins , Parkinson Disease , Sleep Wake Disorders , Humans , Parkinson Disease/blood , Parkinson Disease/diagnosis , Parkinson Disease/complications , Male , Female , Neurofilament Proteins/blood , Middle Aged , Aged , Sleep Wake Disorders/blood , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/epidemiology , Biomarkers/blood , REM Sleep Behavior Disorder/blood , REM Sleep Behavior Disorder/diagnosis , Prodromal Symptoms
11.
Vet Q ; 44(1): 1-9, 2024 Dec.
Article in English | MEDLINE | ID: mdl-38698657

ABSTRACT

Neurodegenerative diseases are characterised by neuronal loss and abnormal deposition of pathological proteins in the nervous system. Among the most common neurodegenerative diseases are Alzheimer's disease (AD), Parkinson's disease (PD), Huntington's disease and transmissible spongiform encephalopathies (TSEs). Sleep and circadian rhythm disturbances are one of the most common symptoms in patients with neurodegenerative diseases. Currently, one of the main objectives in the study of TSEs is to try to establish an early diagnosis, as clinical signs do not appear until the damage to the central nervous system is very advanced, which prevents any therapeutic approach. In this paper, we provide the first description of sleep disturbance caused by classical scrapie in clinical and preclinical sheep using polysomnography compared to healthy controls. Fifteen sheep classified into three groups, clinical, preclinical and negative control, were analysed. The results show a decrease in total sleep time as the disease progresses, with significant changes between control, clinical and pre-clinical animals. The results also show an increase in sleep fragmentation in clinical animals compared to preclinical and control animals. In addition, sheep with clinical scrapie show a total loss of Rapid Eye Movement sleep (REM) and alterations in Non Rapid Eyes Movement sleep (NREM) compared to control sheep, demonstrating more shallow sleep. Although further research is needed, these results suggest that prion diseases also produce sleep disturbances in animals and that polysomnography could be a diagnostic tool of interest in clinical and preclinical cases of prion diseases.


Subject(s)
Polysomnography , Scrapie , Sleep Wake Disorders , Animals , Scrapie/diagnosis , Sheep , Polysomnography/veterinary , Sleep Wake Disorders/veterinary , Sleep Wake Disorders/diagnosis , Female
12.
Nutr Metab Cardiovasc Dis ; 34(7): 1703-1711, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38644079

ABSTRACT

BACKGROUND AND AIMS: Sleep disorders are bidirectionally linked with eating behaviors and glucose metabolism, which could be clinically relevant in type 1 diabetes (T1D). We investigated the relationship between dietary habits and sleep quality in individuals with T1D on insulin pumps and continuous glucose monitoring (CGM). METHODS AND RESULTS: In a cross-sectional study, dietary habits (7-day food diary, EPIC questionnaire) and sleep quality (Pittsburgh Sleep Quality Index questionnaire) were assessed in 59 men and 58 women with T1D, aged 19-79 years, using CGM and insulin pump. Differences in dietary habits and blood glucose after dinner (6 h) between participants differing in sleep quality, sleep duration, and sleep onset latency were evaluated. Bad Sleepers (n = 81) were twice as prevalent as Good Sleepers (n = 36) and had a significantly higher intake of fat than Good Sleepers (dinner: 30.7 ± 10.7 vs. 24.0 ± 10.5 g, p = 0.004). Short sleepers had a significantly higher usual intake (g/1000 kcal) of coffee and tea (90.4 ± 71.7 vs. 62.0 ± 35.6), alcoholic (47.8 ± 51.1 vs. 28.9 ± 31.5) and carbonated beverages (21.8 ± 38.1 vs. 9.3 ± 17.2) (p < 0.05 for all) than Long Sleepers. Long Sleep Onset Latency was associated with a significantly higher fat intake at dinner (41.8 ± 7.4 vs. 38.1 ± 9.1 % total energy, p = 0.029) than Short Sleep Onset Latency. No significant differences in post-dinner blood glucose levels were detected between participants with good or bad sleep quality. CONCLUSION: Sleep disruption is common in T1D and is associated with unhealthy dietary choices, especially at dinner, independently of post-dinner blood glucose control.


Subject(s)
Blood Glucose Self-Monitoring , Blood Glucose , Diabetes Mellitus, Type 1 , Feeding Behavior , Glycemic Control , Hypoglycemic Agents , Insulin Infusion Systems , Insulin , Sleep Quality , Humans , Male , Female , Diabetes Mellitus, Type 1/blood , Diabetes Mellitus, Type 1/diagnosis , Diabetes Mellitus, Type 1/physiopathology , Diabetes Mellitus, Type 1/drug therapy , Middle Aged , Cross-Sectional Studies , Adult , Blood Glucose/metabolism , Aged , Blood Glucose Self-Monitoring/instrumentation , Young Adult , Insulin/blood , Time Factors , Hypoglycemic Agents/administration & dosage , Biomarkers/blood , Sleep , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/physiopathology , Sleep Wake Disorders/blood , Risk Factors , Treatment Outcome , Postprandial Period , Continuous Glucose Monitoring
13.
J Clin Immunol ; 44(5): 109, 2024 Apr 27.
Article in English | MEDLINE | ID: mdl-38676767

ABSTRACT

Inborn errors of immunity have been associated with reduced health-related quality of life and increased fatigue. Sleep disorders, which have been shown to contribute to fatigue and other health concerns, are prevalent in the general population, but there are limited studies evaluating these conditions in patients with common variable immunodeficiency (CVID). Our aim was to evaluate the prevalence of fatigue, sleep disturbances, and sleep-disordered breathing in adults with CVID. Patients completed 4 validated, self-administered questionnaires and a 1-night disposable home sleep apnea test. Our results demonstrated increased median Patient-Reported Outcomes Measurement Information System fatigue scores of 58.7 in patients with CVID in addition to clinically significant fatigue as measured by Fatigue Severity Scale score (median, 5.2) and overall poor sleep quality based on global Pittsburgh Sleep Quality Index score (median, 9.0). For CVID patients who completed the home sleep apnea test, 76.9% met criteria for sleep-disordered breathing with an Apnea-Hypopnea Index score of 5 or greater. The results of our study indicate that patients with CVID may have increased rates of undiagnosed sleep disorders that may contribute to increased fatigue and reduced health-related quality of life.


Subject(s)
Common Variable Immunodeficiency , Fatigue , Quality of Life , Sleep Wake Disorders , Humans , Male , Female , Common Variable Immunodeficiency/complications , Common Variable Immunodeficiency/epidemiology , Common Variable Immunodeficiency/diagnosis , Middle Aged , Adult , Surveys and Questionnaires , Fatigue/epidemiology , Fatigue/etiology , Fatigue/diagnosis , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/etiology , Sleep Wake Disorders/diagnosis , Severity of Illness Index , Prevalence , Aged , Sleep Apnea Syndromes/epidemiology , Sleep Apnea Syndromes/diagnosis
14.
Sleep Med ; 119: 80-87, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38657437

ABSTRACT

OBJECTIVES: Sleep disorders impact at least 10 % of children, pose risks to overall wellbeing, and are key targets of preventive interventions. The objectives of this study were to describe the prevalence of pediatric sleep disorder diagnoses across sociodemographic characteristics and co-occurring conditions, and to explore potential sociodemographic disparities. METHODS: Cross-sectional analysis of 12,394,902 children (0-17 years; 50.9 % Medicaid-insured) in the 2017 MarketScan database. Prevalence was assessed utilizing ICD-10 codes, with multivariate logistic regressions examining disparities (insurance coverage; race and ethnicity in Medicaid-insured) for diagnoses in ≥0.10 % of children. RESULTS: The prevalence of sleep disorder diagnoses was 2.36 %. The most common diagnoses were obstructive sleep disordered breathing (oSDB, 1.17 %), unspecified sleep disorders (0.64 %), insomnia (0.52 %), and other SDB (0.10 %), with <0.10 % for all other diagnoses. Insomnia and parasomnias diagnoses were much lower than diagnostic estimates. Sleep diagnoses were more prevalent in Medicaid versus commercially insured youth, 2-5-year-olds, and in children with co-occurring medical, neurodevelopmental, or behavioral health conditions. Girls and boys were generally equally likely to be diagnosed with any sleep disorder. In Medicaid-insured children, white children were more likely to have any sleep diagnosis compared to all other racial and ethnic groups. Black/African American children were more likely than white children to have oSDB. CONCLUSIONS: Compared to diagnostic estimates, claims data suggest sleep disorders are under-diagnosed, with notable sociodemographic disparities. Findings suggest a need for clinical resources to identify and address sleep disorders and to understand biases potentially driving disparities, given that sleep is a modifiable determinant of child wellbeing.


Subject(s)
Medicaid , Sleep Wake Disorders , Humans , Male , Female , Child , Child, Preschool , Cross-Sectional Studies , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/diagnosis , United States/epidemiology , Adolescent , Infant , Prevalence , Medicaid/statistics & numerical data , Infant, Newborn
15.
Physiol Meas ; 45(5)2024 May 15.
Article in English | MEDLINE | ID: mdl-38653318

ABSTRACT

Objective.Sleep staging based on full polysomnography is the gold standard in the diagnosis of many sleep disorders. It is however costly, complex, and obtrusive due to the use of multiple electrodes. Automatic sleep staging based on single-channel electro-oculography (EOG) is a promising alternative, requiring fewer electrodes which could be self-applied below the hairline. EOG sleep staging algorithms are however yet to be validated in clinical populations with sleep disorders.Approach.We utilized the SOMNIA dataset, comprising 774 recordings from subjects with various sleep disorders, including insomnia, sleep-disordered breathing, hypersomnolence, circadian rhythm disorders, parasomnias, and movement disorders. The recordings were divided into train (574), validation (100), and test (100) groups. We trained a neural network that integrated transformers within a U-Net backbone. This design facilitated learning of arbitrary-distance temporal relationships within and between the EOG and hypnogram.Main results.For 5-class sleep staging, we achieved median accuracies of 85.0% and 85.2% and Cohen's kappas of 0.781 and 0.796 for left and right EOG, respectively. The performance using the right EOG was significantly better than using the left EOG, possibly because in the recommended AASM setup, this electrode is located closer to the scalp. The proposed model is robust to the presence of a variety of sleep disorders, displaying no significant difference in performance for subjects with a certain sleep disorder compared to those without.Significance.The results show that accurate sleep staging using single-channel EOG can be done reliably for subjects with a variety of sleep disorders.


Subject(s)
Electrooculography , Sleep Stages , Sleep Wake Disorders , Humans , Sleep Stages/physiology , Electrooculography/methods , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/physiopathology , Male , Female , Adult , Cohort Studies , Middle Aged , Signal Processing, Computer-Assisted , Neural Networks, Computer , Young Adult , Polysomnography
16.
Neurology ; 102(10): e209302, 2024 May.
Article in English | MEDLINE | ID: mdl-38662978

ABSTRACT

BACKGROUND AND OBJECTIVES: Sleep disorders are a common and important clinical feature in patients with autoimmune encephalitis (AE); however, they are poorly understood. We aimed to evaluate whether cardiopulmonary coupling (CPC), an electrocardiogram-based portable sleep monitoring technology, can be used to assess sleep disorders in patients with AE. METHODS: Patients fulfilling the diagnostic criteria of AE were age- and sex-matched with recruited healthy control subjects. All patients and subjects received CPC testing between August 2020 and December 2022. Demographic data, clinical information, and Pittsburgh Sleep Quality Index (PSQI) scores were collected from the medical records. Data analysis was performed using R language programming software. RESULTS: There were 60 patients with AE (age 26.0 [19.8-37.5] years, male 55%) and 66 healthy control subjects (age 30.0 [25.8-32.0] years, male 53%) included in this study. Compared with healthy subjects, patients with AE had higher PSQI scores (7.00 [6.00-8.00] vs 3.00 [2.00-4.00], p < 0.001), lower sleep efficiency (SE 80% [71%-87%] vs 92% [84%-95%], p < 0.001), lower percentage of high-frequency coupling (25% [14%-43%] vs 45% [38%-53%], p < 0.001), higher percentage of REM sleep (19% ± 9% vs 15% ± 7%, p < 0.001), higher percentage of wakefulness (W% 16% [11%-25%] vs 8% [5%-16%], p = 0.074), higher low-frequency to high-frequency ratio (LF/HF 1.29 [0.82-2.40] vs 0.91 [0.67-1.29], p = 0.001), and a higher CPC-derived respiratory disturbance index (9.78 [0.50-22.2] vs 2.95 [0.40-6.53], p < 0.001). Follow-up evaluation of 14 patients showed a decrease in the PSQI score (8.00 [6.00-9.00] vs 6.00 [5.00-7.00], p = 0.008), an increased SE (79% [69%-86%] vs 89% [76%-91%], p = 0.030), and a decreased W% (20% [11%-30%] vs 11% [8%-24], p = 0.035). Multiple linear regression indicated that SE (-7.49 [-9.77 to -5.21], p < 0.001) and LF/HF ratio (0.37 [0.13-0.6], p = 0.004) were independent factors affecting PSQI scores in patients with AE. DISCUSSION: Sleep disorders with autonomic dysfunction are common in patients with AE. Improvements in the PSQI score and SE precede the restoration of sleep microstructural disruption in the remission stage. CPC parameters may be useful in predicting sleep disorders in patients with AE.


Subject(s)
Encephalitis , Sleep Wake Disorders , Humans , Male , Female , Adult , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/physiopathology , Young Adult , Encephalitis/diagnosis , Encephalitis/complications , Encephalitis/physiopathology , Hashimoto Disease/complications , Hashimoto Disease/physiopathology , Hashimoto Disease/diagnosis , Electrocardiography/methods , Polysomnography/methods
17.
Sleep Med ; 117: 9-17, 2024 May.
Article in English | MEDLINE | ID: mdl-38479041

ABSTRACT

BACKGROUND: Angelman Syndrome (AS) is a rare genetic disorder characterised by hyperactivity, overexcitability, developmental delays, and lack of speech. METHODS: This study used secondary data analysis to investigate sleep disturbances in children and adolescents (n = 212) who are enrolled in the Global Angelman Syndrome Registry. Participants were divided into two groups based on the presence or absence of sleep disturbance. The cut-off score of 40 on the Sleep Disturbance Scale for Children was used to indicate the presence or absence of sleep disturbances. Sleep disturbances and their association with co-occurring conditions were examined regarding challenging behaviour, language and communication, infancy history, gastrointestinal symptoms, and epilepsy. Multiple regression was then conducted to investigate possible predictors for sleep disturbances. RESULTS: Children and adolescents with AS, with and without sleep disturbances, differed considerably regarding anxiety. Sleep disturbances were significantly associated with an ability to use spoken words and computerised communication devices, and anxiety was a predictor of sleep disturbances. CONCLUSION: Future research is necessary to replicate this novel research, and to advance the clinical treatment of sleep disturbances in children and adolescents with AS.


Subject(s)
Angelman Syndrome , Epilepsy , Sleep Wake Disorders , Child , Humans , Adolescent , Angelman Syndrome/complications , Sleep Wake Disorders/complications , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/diagnosis , Epilepsy/complications , Anxiety , Sleep
19.
Neurourol Urodyn ; 43(5): 1127-1133, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38511613

ABSTRACT

INTRODUCTION: Nocturia is a complex and multifactorial condition, associated with several genitourinary abnormalities as well as a host of conditions beyond the urinary tract, and thus often poses a significant diagnostic challenge in real-world practice. Sleep Disorders, Comorbidities, Actions, Lower Urinary Tract Dysfunction, and Medications, the so-called "Sleep C.A.L.M." factors, are five common causes of nocturia requiring judicious evaluation according to current consensus guidelines. This study aims to assess the prevalence of the Sleep C.A.L.M. factors in a nocturia clinical population. METHODS: Retrospective analysis of frequency-volume charts from men with ≥2 nocturnal voids as well as concurrent demographic, clinical, and medical history data to identify patients with each of the Sleep C.A.L.M. FACTORS: Comorbidities and medications were classified as a single group. RESULTS: A total of 213 subjects met the criteria for inclusion (median age 68.0 [63.5-75.5] years). The prevalence of 1) sleep disorders, 2) comorbidities and/or medication use, 3) actions (i.e., modifiable behaviors/lifestyle factors), and 4) lower urinary tract dysfunction was 31%, 31%, 19%, and 41%, respectively. Among included participants, 73% were found to have at least 1 Sleep C.A.L.M. factor, and 33% had multiple Sleep C.A.L.M. FACTORS: Results were similar upon stratification by age and nocturnal polyuria status. CONCLUSIONS: The Sleep C.A.L.M. factors are highly common among nocturia patients in the clinical urology setting. Although many of these factors are strongly associated with advanced age in community-based nocturia study samples, they appear common even among younger men in a nocturia patient population; the differential effect of age and individual Sleep C.A.L.M. factors on nocturia pathophysiology requires further investigation.


Subject(s)
Nocturia , Sleep Wake Disorders , Humans , Nocturia/epidemiology , Nocturia/physiopathology , Nocturia/diagnosis , Male , Aged , Middle Aged , Retrospective Studies , Prevalence , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/physiopathology , Sleep Wake Disorders/diagnosis , Veterans , Comorbidity , Risk Factors , Sleep
20.
Alzheimers Dement ; 20(5): 3270-3280, 2024 May.
Article in English | MEDLINE | ID: mdl-38506627

ABSTRACT

INTRODUCTION: People with Down syndrome (DS) have high risk of developing Alzheimer's disease (AD). This study examined mean ages of AD diagnosis and associations with co-occurring conditions among adults with DS from five European countries. METHODS: Data from 1335 people with DS from the Horizon 21 European DS Consortium were used for the analysis. RESULTS: Mean ages of AD diagnosis ranged between 51.4 (SD 7.0) years (United Kingdom) and 55.6 (SD 6.8) years (France). Sleep-related and mental health problems were associated with earlier age of AD diagnosis. The higher number of co-occurring conditions the more likely the person with DS is diagnosed with AD at an earlier age. DISCUSSION: Mean age of AD diagnosis in DS was relatively consistent across countries. However, co-occurring conditions varied and impacted on age of diagnosis, suggesting that improvements can be made in diagnosing and managing these conditions to delay onset of AD in DS. HIGHLIGHTS: Mean age of AD diagnosis was relatively consistent between countries Sleep problems and mental health problems were associated with earlier age of AD diagnosis APOE ε4 carriers were diagnosed with AD at an earlier age compared to non-carriers Number of co-occurring conditions was associated with earlier age of AD diagnosis No differences between level of intellectual disability and mean age of AD diagnosis.


Subject(s)
Alzheimer Disease , Down Syndrome , Humans , Down Syndrome/epidemiology , Down Syndrome/diagnosis , Down Syndrome/complications , Alzheimer Disease/diagnosis , Alzheimer Disease/epidemiology , Male , Female , Middle Aged , Europe/epidemiology , Adult , United Kingdom/epidemiology , Sleep Wake Disorders/epidemiology , Sleep Wake Disorders/diagnosis , Age Factors , Age of Onset , France/epidemiology , Aged , Comorbidity , Apolipoprotein E4/genetics
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