51 research outputs found
The Relationship Among Morningness-Eveningness, Sleep Duration, Social Jetlag, and Body Mass Index in Asian Patients With Prediabetes
Background: Circadian system is known to influence energy metabolism. Recent evidence suggested that evening preference could be associated with higher body mass index (BMI). Moreover, evening preference is known to be associated with insufficient sleep duration and greater social jetlag, both described to be associated with obesity. This study aimed to explore whether morningness-eveningness was directly associated with BMI or its effect was transmitted through sleep duration or social jetlag in patients with prediabetes.Methods: A total 2,133 patients with prediabetes were enrolled. Morningness-eveningness was assessed using a Composite Scale of Morningness (CSM). Average weekly sleep duration and sleep timing were obtained, and social jetlag was calculated. BMI was calculated by weight (kg)/height2 (m2). A mediation analysis was performed based on two pathways, i.e. CSMāsleepādurationāBMI and CSMāsocial jetlagāBMI. A sequential equation model was used to estimate the direct and indirect effects of CSM on BMI.Results: Mean (SD) age and BMI were 63.6 (9.2) years and 25.8 (4.0) kg/m2. For CSMāsleep durationāBMI pathway, every one point decrease in CSM (more evening preference) was associated with a decrease in sleep duration by 0.054 h (95% CI 0.043ā0.066), whereas sleep duration was negatively associated with BMI (coefficient = ā0.156, 95%CI ā0.288, ā0.024). Mediation analysis indicated that a change in CSM (from 90th to 10th percentile, more evening preference) was associated with a decrease in sleep duration and an increase in BMI by 0.102 kg/m2 (95% CI 0.015, 0.207). In addition, this change in CSM was directly associated with an increase in BMI by 0.511 kg/m2 (95%CI 0.030, 0.952). The CSMāsocial jetlagāBMI pathway analysis revealed that social jetlag was not significantly associated with BMI. A subgroup analysis in those aged ā¤60 years (n = 784) revealed that each hour increase in social jetlag was associated with an increase in BMI by 0.56 kg/m2 (p = 0.026) while CSM and sleep duration were not.Conclusion: In patients with prediabetes, more evening preference was directly associated with higher BMI and indirectly through insufficient sleep duration, while social jetlag did not mediate the relationship between CSM and BMI. In those ā¤60 years, only greater social jetlag was associated with higher BMI. These data could inform further interventional studies to reduce BMI in this high risk group
Sex-specific associations between self-reported sleep characteristics and 10-year cardiovascular disease risk in men and women of African descent living in a low socioeconomic status environment
BackgroundRisk factors for cardiovascular disease (CVD) and sleep health are well-known to be sex- and race-specific. To build on the established relationship between sleep duration and CVD risk, this cross-sectional study aimed to describe sex-specific associations between CVD risk and other sleep characteristics (sleep quality, sleep timing and sleep onset latency) in low-income adults of African descent.MethodsSelf-reported sleep (Pittsburgh Sleep Quality Index [PSQI], Epworth Sleepiness Scale [ESS], Insomnia Severity Index [ISI]), demographic and lifestyle data were collected in 412 adults (56% women, 35.0Ā±7.6y, 40% employed) living in an informal settlement in South Africa. CVD risk was determined using the BMI-modified Framingham 10-year CVD risk formula.ResultsLogistic regression analyses, adjusted for employment, alcohol use and physical activity, indicated that men reporting poor sleep quality (OR: 1.9[95%CI: 1.1-3.5],p=0.025) and earlier bedtimes (0.54[0.39-0.74],p<0.001) were more likely to belong to a higher 10-year CVD risk score quintile. Women reporting earlier bedtimes (0.72[0.55-0.95],p=0.020) and wake-up times (0.30[0.1-0.7],p=0.007), longer sleep-onset latency (1.5[1.4-1.9],p=0.003), shorter total sleep times (0.84[0.7-0.9],p=0.029), higher PSQI global scores (1.9[1.3-2.9],p=0.001) and more moderate to severe symptoms of insomnia (ISIā„15)(3.24[1.04-10.04],p=0.016) were more likely to belong to higher 10-year CVD risk score quintile.ConclusionIn addition to sleep duration, we found that sleep quality, sleep timing and sleep onset latency are additional risk factors for CVD in adults of African descent. Sex-specific differences in the sleep-CVD-risk relationship observed suggests that future studies and recommendations about sleep health in relation to CVD should take sex into account.<br/
Associations between self-reported sleep duration and cardiometabolic risk factors in young African-origin adults from the five-country Modeling the Epidemiologic Transition Study (METS)
To investigate associations between self-reported sleep duration and cardiometabolic (CM) risk factors in African-origin adults residing in five countries spanning the epidemiologic transition.
Cross-sectional.
Ghanaian (nāÆ=āÆ491), South African (nāÆ=āÆ503), Jamaican (nāÆ=āÆ508), Seychellois (nāÆ=āÆ501) and American (nāÆ=āÆ480) men and women.
Self-reported sleep duration was obtained using questionnaires. Sex- and site-stratified logistic regression analyses investigated relationships between sleep duration, individual CM risk factors and a binary CM risk variable (presence of ā„3 CM risk factors), adjusting for age, physical activity and education.
Sleep duration distributions varied by cohort: 44.5%, 41.4%, 35.9%, 16.8% and 2.5% of American, Jamaican, Seychellois, Ghanaian and South African men reported <7āÆh sleep per night respectively (pāÆ<āÆ0.001). Similarly, 42.6%, 28.6%, 25.2%, 12.8% and 1.5% of American, Jamaican, Seychellois, Ghanaian and South African women reported <7āÆh sleep respectively (pāÆ<āÆ0.001). American men reporting ā¤6āÆh sleep were more likely to be in the elevated CM risk group (OR: 2.52, 95%CI: 1.02, 6.22, pāÆ=āÆ0.045) and to have a high waist circumference (OR: 2.44, 95%CI: 1.07, 5.57, pāÆ=āÆ0.034) compared to those reporting 8āÆh sleep. Jamaican women reporting ā¤6āÆh sleep (OR: 2.53, 95%CI: 1.19, 5.36, pāÆ=āÆ0.016) and American women reporting 7āÆh sleep (OR: 2.71, 95%CI: 1.17, 6.26, pāÆ=āÆ0.002) were more likely to be obese than those reporting 8āÆh sleep.
Associations between short sleep and CM risk factors were only evident in the American men and women and Jamaican women. Future interventions to address CM risk and sleep health may need to be country-specific when targeting high-risk populations
Associations between fears related to safety during sleep and self-reported sleep in men and women living in a low-socioeconomic status setting
South Africans living in low socioeconomic areas have self-reported unusually long sleep durations (approximately 9ā10 h). One hypothesis is that these long durations may be a compensatory response to poor sleep quality as a result of stressful environments. This study aimed to investigate whether fear of not being safe during sleep is associated with markers of sleep quality or duration in men and women. South Africans (n = 411, 25ā50 y, 57% women) of African-origin living in an urban township, characterised by high crime and poverty rates, participated in this study. Participants are part of a larger longitudinal cohort study: Modelling the Epidemiologic Transition Study (METS)āMicrobiome. Customised questions were used to assess the presence or absence of fears related to feeling safe during sleep, and the Epworth Sleepiness Scale, Pittsburgh Sleep Quality Index (PSQI) and Insomnia Severity Index were used to assess daytime sleepiness, sleep quality and insomnia symptom severity respectively. Adjusted logistic regression models indicated that participants who reported fears related to safety during sleep were more likely to report poor sleep quality (PSQI > 5) compared to participants not reporting such fears and that this relationship was stronger among men than women. This is one of the first studies outside American or European populations to suggest that poor quality sleep is associated with fear of personal safety in low-SES South African adults
Sleep characteristics in type 1 diabetes and associations with glycemic control: systematic review and meta-analysis
AbstractObjectivesThe association between inadequate sleep and type 2 diabetes has garnered much attention, but little is known about sleep and type 1 diabetes (T1D). Our objectives were to conduct a systematic review and meta-analysis comparing sleep in persons with and without T1D, and to explore relationships between sleep and glycemic control in T1D.MethodsStudies were identified from Medline and Scopus. Studies reporting measures of sleep in T1D patients and controls, and/or associations between sleep and glycemic control, were selected.ResultsA total of 22 studies were eligible for the meta-analysis. Children with T1D had shorter sleep duration (mean difference [MD]ā=āā26.4 minutes; 95% confidence interval [CI]ā=āā35.4, ā17.7) than controls. Adults with T1D reported poorer sleep quality (MD in standardized sleep quality scoreā=ā0.51; 95% CIā=ā0.33, 0.70), with higher scores reflecting worse sleep quality) than controls, but there was no difference in self-reported sleep duration. Adults with TID who reported sleeping >6 hours had lower hemoglobin A1c (HbA1c) levels than those sleeping ā¤6 hours (MDā=āā0.24%; 95% CIā=āā0.47, ā0.02), and participants reporting good sleep quality had lower HbA1c than those with poor sleep quality (MDā=āā0.19%; 95% CIā=āā0.30, ā0.08). The estimated prevalence of obstructive sleep apnea (OSA) in adults with TID was 51.9% (95% CIā=ā31.2, 72.6). Patients with moderate-to-severe OSA had a trend toward higher HbA1c (MDā=ā0.39%, 95% CIā=āā0.08, 0.87).ConclusionT1D was associated with poorer sleep and high prevalence of OSA. Poor sleep quality, shorter sleep duration, and OSA were associated with suboptimal glycemic control in T1D patients
Dietary Factors and Risks of Cardiovascular Diseases: An Umbrella Review
Unhealthy diet is a significant risk factor for cardiovascular diseases (CVD). Therefore, this umbrella review aims to comprehensively review the effects of dietary factors, including dietary patterns, food groups, and nutrients on CVD risks. Medline and Scopus databases were searched through March 2020. Systematic reviews with meta-analyses (SRMA) of randomized controlled trials (RCTs) or observational studies measuring the effects of dietary factors on CVD risks were eligible. Fifty-four SRMAs, including 35 SRMAs of observational studies, 10 SRMAs of RCTs, and 9 SRMAs of combined RCT and observational studies, were included for review. Findings from the SRMAs of RCTs suggest the significant benefit of Mediterranean and high-quality diets for lowering CVD risk, with pooled risk ratios (RRs) ranging from 0.55 (95%CI: 0.39–0.76) to 0.64 (95%CI: 0.53–0.79) and 0.70 (95%CI: 0.57–0.87), respectively. For food nutrients, two SRMAs of RCTs found that high intake of n-3 polyunsaturated fatty acid (PUFA) significantly reduced CVD risks, with pooled RRs ranging from 0.89 (95%CI: 0.82, 0.98) to 0.90 (95%CI: 0.85–0.96), while evidence of efficacy of n-6 PUFA and combined n-3 and n-6 PUFA were inconsistent. Moreover, results from the SRMAs of RCTs did not find a significant benefit of a low-salt diet and low total fat intake for CVD prevention. For food groups, results from the SRMAs of cohort studies suggest that high intakes of legumes, nuts, and chocolate, as well as a vegetarian diet significantly reduced the risk of coronary heart disease, with pooled RRs of 0.90 (95%CI: 0.84–0.97), 0.68 (95%CI: 0.59–0.78), 0.90 (95%CI: 0.82–0.97), and 0.71 (95%CI: 0.57–0.87), respectively. Healthy dietary patterns had a significant benefit for CVD prevention. With the substitutional and synergistic interactions between different food groups and nutrients, dietary recommendations for CVD prevention should be focused more on healthy dietary patterns than single food groups or nutrients
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Resistance to thyroid hormone in the absence of mutations in the thyroid hormone receptor genes
Most people with resistance to thyroid hormone have mutant thyroid hormone receptors that interfere with the function of the normal receptor and produce a dominant mode of inheritance. Conversely, thyroid hormone receptor Ī² gene deletion is inherited as a recessive trait. In about 10% of cases, resistance to thyroid hormone manifests in the absence of thyroid hormone receptor gene abnormalities. The clinical manifestations and laboratory abnormalities found in these individuals are not significantly different than those found in patients with thyroid hormone receptor Ī² defects. We propose that the defect must be elsewhere in the pathway of thyroid hormone action
Effects of probiotic supplements on insulin resistance in gestational diabetes mellitus: A doubleāblind randomized controlled trial
Abstract Aims/Introduction To evaluate the effect of probiotic supplements on insulin resistance in pregnant women with dietācontrolled gestational diabetes mellitus. Materials and Methods A randomized, doubleāblind, placeboācontrolled trial was carried out between June 2016 and February 2017. Pregnant women with dietācontrolled gestational diabetes mellitus were enrolled in the study at 24ā28Ā weeksāofāgestation and randomized to receive either probiotic supplements containing Bifidobacterium and Lactobacillus or a placebo daily for four consecutive weeks. Primary outcomes were mean differences in insulin resistance (homeostatic model assessment for insulin resistance), fasting insulin and fasting plasma glucose between the two groups. Secondary outcomes were changes in maternal weight after the intervention. Results Data from 28 patients in the probiotic group and 29 in the placebo group were analyzed. The changes in metabolic parameters after randomization showed significant improvement in glucose metabolism in the probiotic group compared with the placebo group, including fasting plasma glucose (0.68Ā Ā±Ā 5.88 vs 4.620Ā Ā±Ā 7.78Ā mg/dL, mean difference ā3.94Ā mg/dL, 95% confidence interval ā7.62, ā0.27, PĀ =Ā 0.034), fasting plasma insulin (1.11Ā Ā±Ā 1.71 vs 3.77Ā Ā±Ā 1.70Ā mIU/L, mean difference ā2.67Ā mIU/L, 95% confidence interval ā3.57, ā1.76, PĀ =Ā 0.001) and homeostatic model assessment for insulin resistance (0.25Ā Ā±Ā 0.37 vs 0.89Ā Ā±Ā 0.46, mean difference ā0.63, 95% confidence interval ā0.86, ā0.41, PĀ =Ā 0.001). Weight gain during randomization was similar between the two groups. Conclusions Four weeks of probiotic supplements in women with dietācontrolled gestational diabetes in the late second and early third trimester lowered fasting glucose and increased insulin sensitivity. Probiotic supplements may be considered as an adjunct treatment for glycemic control in these patients
Associations between Timing and Duration of Eating and Glucose Metabolism: A Nationally Representative Study in the U.S.
Diabetes is highly prevalent and is associated with dietary behaviors. Time-restricted eating, which consolidates caloric intake to a shortened eating duration, has demonstrated improvement in metabolic health. Timing of eating could also impact metabolism. Our objective was to examine whether the timing of eating was associated with metabolic health independently of eating duration. Data (n = 7619) are from four cycles (2005–2012) of the National Health and Nutrition Examination Survey (NHANES), a nationally representative U.S. survey that included surveys, physical examinations, and dietary recalls. The primary exposures are eating duration and eating start time estimated from two non-consecutive dietary recalls. Primary outcomes were fasting glucose and estimated insulin resistance using the homeostatic model assessment method (HOMA-IR). The mean (95% CI) eating duration was 12.0 h (11.9–12.0) and the mean (95% CI) start time was 8:21 (8:15–8:26). Earlier eating start time was significantly associated with lower fasting glucose and estimated insulin resistance but eating interval duration was not. Every hour later that eating commenced was associated with approximately 0.6% higher glucose level and 3% higher HOMA-IR (both p < 0.001). In this cross-sectional study, earlier eating start time was associated with more favorable metabolic measures, indicating that meal timing is another important characteristic of dietary patterns that may influence metabolism
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