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1.
Diabet Med ; 35(5): 583-587, 2018 05.
Article in English | MEDLINE | ID: mdl-29384594

ABSTRACT

AIMS: To document the prevalence of current depressive symptoms and history of depression across the glycaemic spectrum in older adults, and examine if measures of health status and healthcare satisfaction, access and utilization explain differences in the prevalence of current depressive symptoms by diabetes status. METHODS: We conducted a cross-sectional study of 6226 participants aged 67-90 years who attended the 2011-2013 visit of the Atherosclerosis Risk in Communities (ARIC) study. Diabetes was based on self-report, medication use and HbA1c . Current depressive symptoms were defined using the Center for Epidemiologic Studies Depression 11-item questionnaire, and history of depression was assessed via self-report. We examined obesity, history of cardiovascular disease, hypertension, kidney disease, cognitive function, and self-reported health compared with others. Prevalence and prevalence ratios were estimated using age-, race-, and sex-adjusted Poisson regression. RESULTS: The prevalence of current depressive symptoms was 5.4% in people without diabetes and 11.0% in people with diabetes (prevalence ratio 2.04, 95% CI 1.60, 2.48); the prevalence of history of depression was 11% in people without diabetes and 17.7% in people with diabetes (prevalence ratio 1.61, 95% CI 1.28,1.95). Strong correlates of current depressive symptoms were history of depression (prevalence ratio 3.86, 95% CI 3.05, 4.90) and reporting poor health compared with others (prevalence ratio 3.88, 95% CI 2.93, 5.15). No variables had significantly different associations with depressive symptoms across glycaemic categories (P for interaction >0.10). CONCLUSIONS: In older adults, current depressive symptoms were twice as prevalent in people with diabetes compared with those without. Measures of health status and healthcare did not explain differences in depressive symptoms between people with and without diabetes.


Subject(s)
Depression/epidemiology , Diabetes Mellitus/epidemiology , Health Status , Prediabetic State/epidemiology , Aged , Aged, 80 and over , Case-Control Studies , Comorbidity , Cross-Sectional Studies , Depression/psychology , Diabetes Mellitus/metabolism , Diabetes Mellitus/psychology , Female , Glycated Hemoglobin/metabolism , Humans , Male , Prediabetic State/metabolism , Prediabetic State/psychology , Prevalence , Risk Factors , United States/epidemiology
2.
Diabet Med ; 33(12): 1615-1624, 2016 12.
Article in English | MEDLINE | ID: mdl-26997583

ABSTRACT

AIMS: To assess the effect of prediabetes (impaired fasting glucose and/or impaired glucose tolerance) on the incidence of chronic kidney disease. METHODS: PubMed and EMBASE were searched (for studies published up to March 2015). Effects estimated from cohort studies reporting the relationship of prediabetes to incident chronic kidney disease [kidney damage (microalbuminuria, albuminuria or proteinuria) and/or decreased glomerular filtration rate] were pooled using a random-effects model meta-analysis. RESULTS: Nine cohort studies with a total of 185 452, mainly Asian and white, participants were followed for a total of 835 146 person-years. In eight cohort studies defining impaired fasting glucose as fasting glucose 6.1-6.9 mmol/l, the summary relative risk of chronic kidney disease after adjustment for established risk factors was 1.11 (95% CI 1.02-1.21). When a study defining impaired fasting glucose as fasting glucose 5.6-6.9 mmol/dl was added, the overall relative risk of chronic kidney disease was 1.12 (95% CI 1.02-1.21). Exclusion of the only study with information on impaired glucose tolerance did not change the relative risk (1.12; 95% CI 1.02-1.21). There was no evidence of publication bias (P value for Egger test = 0.12). CONCLUSION: Prediabetes is modestly associated with an increase in chronic kidney disease risk, but this remains to be robustly confirmed. Chronic kidney disease screening among people with prediabetes, and aggressive management of prediabetes in those with chronic kidney disease may be warranted.


Subject(s)
Diabetic Nephropathies/complications , Prediabetic State/complications , Renal Insufficiency, Chronic/complications , Adult , Aged , Aged, 80 and over , Albuminuria/etiology , Albuminuria/physiopathology , Blood Glucose/metabolism , Diabetic Nephropathies/physiopathology , Glomerular Filtration Rate/physiology , Humans , Middle Aged , Observational Studies as Topic , Prediabetic State/physiopathology , Renal Insufficiency, Chronic/physiopathology , Risk Factors
3.
Health Place ; 32: 93-8, 2015 Mar.
Article in English | MEDLINE | ID: mdl-25665936

ABSTRACT

Physical and social features of neighborhoods, such as esthetic environments and social cohesion, change over time. The extent to which changes in neighborhood conditions are associated with changes in mental health outcomes has not been well-established. Using data from the MultiEthnic Study of Atherosclerosis, this study investigated the degree to which neighborhood social cohesion, stress, violence, safety and/or the esthetic environment changed between 2002 and 2007 in 103 New York City Census tracts and the associations of these changes with changes in depressive symptoms. Neighborhoods became less stressful, more socially cohesive, safer, and less violent. White, wealthy, highly educated individuals tended to live in neighborhoods with greater decreasing violence and stress and increasing social cohesion. Individuals living in neighborhoods with adverse changes were more likely to have increased CES-D scores, although due to limited sample size associations were imprecisely estimated (P>0.05). Changes in specific features of the neighborhood environment may be associated with changes in level of depressive symptoms among residents.


Subject(s)
Depression/epidemiology , Residence Characteristics/statistics & numerical data , Social Environment , Social Support , Violence/statistics & numerical data , Aged , Aged, 80 and over , Antidepressive Agents/therapeutic use , Atherosclerosis , Depression/drug therapy , Female , Humans , Longitudinal Studies , Male , Middle Aged , New York City/epidemiology , Psychiatric Status Rating Scales , Safety , Socioeconomic Factors , Stress, Psychological/epidemiology , Violence/trends
4.
Int J Obes (Lond) ; 36(12): 1578-84, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22270378

ABSTRACT

OBJECTIVE: Waist-to-hip ratio (WHR) is strongly associated with prevalent atherosclerosis. We analyzed the associations of baseline serum levels of testosterone (T), estradiol (E2), sex-hormone-binding globulin (SHBG) and dehydroepiandrosterone (DHEA) with WHR in the Multi-Ethnic Study of Atherosclerosis (MESA) cohort. SUBJECTS: Baseline data was available for 3144 men and 2038 postmenopausal women, who were non-users of hormone therapy, who were 45-84 years of age, and of White, Chinese, Black or Hispanic racial/ethnic groups. Of these, 2708 men and 1678 women also had longitudinal measurements of WHR measured at the second and/or the third study visits (median follow-up 578 days and 1135 days, respectively). RESULTS: In cross-sectional analyses adjusted for age, race and cardiovascular disease risk factors, T was negatively associated with baseline WHR in men, whereas in both sexes, E2 was positively associated and SHBG was negatively associated with WHR (all P<0.001). In longitudinal analyses, further adjusted for follow-up time and baseline WHR, baseline T was negatively associated with WHR at follow-up (P=0.001) in men, whereas in both sexes, E2 was positively associated (P=0.004) and SHBG was negatively associated with WHR (P<0.001). The longitudinal association of E2, but not T, was independent of SHBG. In cross-sectional or longitudinal analyses, there were no associations between DHEA and WHR in either men or women. CONCLUSION: Sex hormones are associated with WHR at baseline and also during follow-up above and beyond their baseline association. Future research is needed to determine if manipulation of hormones is associated with changes in central obesity.


Subject(s)
Androgens/blood , Estrogens/blood , Obesity/blood , Obesity/ethnology , Testosterone/blood , Waist-Hip Ratio , Black or African American/statistics & numerical data , Aged , Aged, 80 and over , Asian/statistics & numerical data , Body Fat Distribution , Body Mass Index , Cross-Sectional Studies , Female , Hispanic or Latino/statistics & numerical data , Humans , Male , Middle Aged , Obesity/epidemiology , Postmenopause , Risk Assessment , Risk Factors , Sex Hormone-Binding Globulin , Surveys and Questionnaires , United States/epidemiology , White People/statistics & numerical data
5.
Psychoneuroendocrinology ; 37(7): 1009-18, 2012 Jul.
Article in English | MEDLINE | ID: mdl-22178583

ABSTRACT

Socioeconomic and psychosocial factors have been found to be associated with systemic inflammation. Although stress is often proposed as a contributor to these associations, no population studies have investigated the links between inflammation and biomarkers of stress. The current study examines associations between daily cortisol profiles and inflammatory markers interleukin-6 (IL-6), interleukin-10 (IL-10), and tumor necrosis factor (TNF-a) in a population-based sample of 869 adults with repeat measures of cortisol over multiple days. Persons with higher levels of IL-6 had a less pronounced cortisol awakening response, a less steep daily decline, and higher cortisol area under the curve for the day with associations persisting after controls for risk factors and other cytokines. Persons with higher levels of TNF-a had lower cortisol levels upon waking, and flatter daily decline, although associations with decline were attenuated when controlling for inflammatory risk factors. Higher levels of IL-10 were associated with marginally flatter daily cortisol decline (p<.10). This study is the first to identify associations of basal cortisol activity and inflammatory markers in a population based sample. Findings are consistent with the possibility that HPA axis activity may mediate associations between psychosocial stressors and inflammatory processes. Additional prospective data are necessary to clarify the directionality of associations between cortisol and inflammatory markers.


Subject(s)
Atherosclerosis , Biomarkers/blood , Hydrocortisone/metabolism , Inflammation/blood , Saliva/metabolism , Aged , Aged, 80 and over , Atherosclerosis/blood , Atherosclerosis/epidemiology , Atherosclerosis/ethnology , Atherosclerosis/metabolism , Biomarkers/metabolism , Ethnicity/statistics & numerical data , Female , Humans , Hydrocortisone/analysis , Inflammation/epidemiology , Inflammation/ethnology , Inflammation/metabolism , Interleukin-6/analysis , Interleukin-6/blood , Interleukin-6/metabolism , Longitudinal Studies , Male , Middle Aged , Obesity/blood , Obesity/epidemiology , Obesity/ethnology , Obesity/metabolism , Overweight/blood , Overweight/epidemiology , Overweight/ethnology , Overweight/metabolism , Saliva/chemistry
6.
J Clin Endocrinol Metab ; 96(11): 3483-92, 2011 Nov.
Article in English | MEDLINE | ID: mdl-21880797

ABSTRACT

CONTEXT: Prior research has identified associations between social-environmental factors and metabolic syndrome (MetS) components. The physiological mechanisms underlying these associations are not fully understood, but alterations in activity of the hypothalamic-pituitary-adrenal axis, a stress-responsive biological system, have been hypothesized to play a role. OBJECTIVE: The aim of the study was to determine whether MetS diagnosis and specific clusters of MetS components (waist circumference, high-density lipoproteins, glucose, and blood pressure) are associated with cortisol levels. DESIGN AND SETTING: We conducted cross-sectional analyses of data from the Multi-Ethnic Study of Atherosclerosis (MESA) study in the general community. PATIENTS OR OTHER PARTICIPANTS: We studied a population-based sample of 726 adults (ages 48 to 89 yr) who do not have clinical diabetes. INTERVENTION(S): There were no interventions. MAIN OUTCOME MEASURE(S): Cortisol awakening response, cortisol decline across the waking day, and total cortisol output were analyzed (using 18 timed measures of salivary cortisol over 3 d). RESULTS: Overall, we found little evidence that the presence of MetS or its components is related to cortisol output or patterns. Contrary to expectation, the presence of MetS was associated with lower rather than higher area under the curve, and no consistent pattern was observed when MetS components or subsets of components were examined in relation to cortisol. CONCLUSIONS: Our findings do not support the hypothesis that differences in level or diurnal pattern of salivary cortisol output are associated with MetS among persons without clinical diabetes.


Subject(s)
Hydrocortisone/metabolism , Metabolic Syndrome/diagnosis , Metabolic Syndrome/metabolism , Saliva/metabolism , Aged , Aged, 80 and over , Atherosclerosis/ethnology , Atherosclerosis/metabolism , Blood Glucose , Blood Pressure/physiology , Cross-Sectional Studies , Female , Humans , Lipoproteins, HDL/blood , Male , Middle Aged , Risk Factors , Waist Circumference
7.
Osteoporos Int ; 19(1): 1-12, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17763997

ABSTRACT

INTRODUCTION: There have been numerous studies examining the association between depression and bone mineral density (BMD), but the underlying nature of this relationship remains unclear. Independent of this association, there is a growing body of evidence that depression impacts the risk for fracture in older adults. This article reviews the current epidemiological evidence regarding comorbidity of depression, low bone mineral density, and fracture. METHODS: A review of the literature on depression, depressive symptoms, low BMD, osteoporosis, and fracture using electronic databases. RESULTS: We reviewed 20 studies of the association between depression and BMD and five reports of the relationship between depression and fractures. Potential mediating mechanisms (both physiological and behavioral) are discussed, as well as potential confounding influences (e.g., medication use). CONCLUSIONS: Most studies support the finding that depression is associated with increased risk for both low BMD and fractures, but variation in study design, sample composition, and exposure measurement make comparisons across studies difficult. Researchers should be aware of potential confounders, such as medication use, that may influence results. Future research should focus on identifying mediating pathways and targets for intervention in the relationships between depression, low BMD, and fracture.


Subject(s)
Depressive Disorder , Fractures, Bone , Osteoporosis , Adult , Aged , Aged, 80 and over , Asia/epidemiology , Australia/epidemiology , Bone Density , Depressive Disorder/epidemiology , Europe/epidemiology , Female , Fractures, Bone/epidemiology , Fractures, Bone/psychology , Humans , Male , Middle Aged , Osteoporosis/epidemiology , Osteoporosis/psychology , Risk Factors , United States/epidemiology
8.
Am J Epidemiol ; 154(6): 489-94, 2001 Sep 15.
Article in English | MEDLINE | ID: mdl-11549553

ABSTRACT

Many studies have investigated the role of estrogen during menopause; however, less attention has been paid to the role of androgen. Given the possible opposite effects of estrogen and androgen on cardiovascular disease risk, it is suggested that relative androgen excess may better predict the increased risk of cardiovascular disease in women over the age of 50 years than estrogen levels alone. Three phases of hormonal milieu changes are hypothesized as a better way to identify the hormone-cardiovascular disease risk association. A first phase, prepause, occurs before estrogen levels decline (approximately 2 years before menopause). A second phase, interpause, occurs from the end of prepause until approximately age 55. A third phase, postpause, occurs after interpause. The duration of the interpause phase, characterized by relative androgen excess, may be an independent risk factor of cardiovascular disease. This hypothesis could provide a basis for further clinical and epidemiologic research, and it could have important implications for establishing the initiation and duration of estrogen replacement therapy use as a means to prevent cardiovascular disease.


Subject(s)
Androgens/adverse effects , Cardiovascular Diseases/etiology , Postmenopause , Aged , Estrogens/blood , Female , Hormone Replacement Therapy , Humans , Middle Aged , Risk Factors
9.
Diabetes Care ; 22(9): 1408-14, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10480501

ABSTRACT

OBJECTIVE: Although hyperglycemia is hypothesized to increase the short-term risk of infection, this hypothesis has not been well tested in a clinical setting. This study was designed to assess the relationship of perioperative glycemic control to the subsequent risk of infectious complications. RESEARCH DESIGN AND METHODS: A total of 411 adults with diabetes who underwent coronary artery surgery from 1990 to 1995 in the cardiac surgery service of an urban university hospital were included in a nonconcurrent prospective cohort study based on chart review. Perioperative glycemic control was characterized by the mean of six capillary glucose measurements taken during the 36-h interval following surgery. The major outcomes studied were infections of leg and chest wounds, pneumonia, and urinary tract infections. RESULTS: Mean postoperative glucose levels ranged from 121 to 352 mg/dl and were divided into quartiles: quartile 1 (121-206 mg/dl), quartile 2 (207-229 mg/dl), quartile 3 (230-252 mg/dl), and quartile 4 (253352 mg/dl). After simultaneous adjustment for age, sex, race, underlying comorbidity, acute severity of illness, and the length of the stay in the surgical intensive care unit, patients with higher mean capillary glucose readings were at increased risk of developing infections. Compared with people in the lowest quartile of postoperative glucose, those in quartiles 2 (relative odds of infection [95% CI] = 1.17 [0.57-2.40]), 3 (1.86 [0.94-3.68]), and 4 (1.78 [0.86-3.47]) were at progressively higher risk for infection (P = 0.05 for trend). CONCLUSIONS: In patients with diabetes who undergo coronary artery surgery, postoperative hyperglycemia is an independent predictor of short-term infectious complications. Physicians should consider a glucose concentration target of < or =200 mg/dl to reduce the risk of infection.


Subject(s)
Blood Glucose/metabolism , Diabetes Mellitus/metabolism , Intraoperative Care/methods , Opportunistic Infections/metabolism , Postoperative Complications/metabolism , Case-Control Studies , Diabetes Complications , Female , Humans , Male , Middle Aged , Odds Ratio , Risk Factors
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