Abstract:Young to middle-aged women usually have notably lower rates of cardiovascular disease (CVD) than their male counterparts, but African American women lack this advantage. Their elevated CVD may be influenced by sex differences in associations between depressed mood and CVD risk factors. This cross-sectional study examined whether relations between scores on the Center for Epidemiologic Studies-Depression (CES-D) scale and a spectrum of CVD risk factors varied by sex among African Americans (n = 1076; ages 30–64… Show more
“…The study conducted by Cooper et al among African Americans showed that the greater the abdominal obesity, the more intensive depressive symptoms are. 76 Our study confirmed a positive correlation between WC and the BDI.…”
Section: Discussionsupporting
confidence: 82%
“…18,[72][73][74][75][76] The EZOP Poland study showed that women more often show symptoms of depression. 67 The present study confirmed this dependence.…”
Background. Chronic non-communicable diseases (CNCDs) are the leading cause of mortality in the world. Identification of risk factors and the implementation of preventive measures can effectively reduce the chance of disease and death due to CNCDs.
“…The study conducted by Cooper et al among African Americans showed that the greater the abdominal obesity, the more intensive depressive symptoms are. 76 Our study confirmed a positive correlation between WC and the BDI.…”
Section: Discussionsupporting
confidence: 82%
“…18,[72][73][74][75][76] The EZOP Poland study showed that women more often show symptoms of depression. 67 The present study confirmed this dependence.…”
Background. Chronic non-communicable diseases (CNCDs) are the leading cause of mortality in the world. Identification of risk factors and the implementation of preventive measures can effectively reduce the chance of disease and death due to CNCDs.
“…[4,7,8] A significant positive association between the Centre for Epidemiologic Studies Depression Scale (CES-D) and hsCRP levels among African-American men with depression was found that was absent in their female counterparts. [13] However, no such gender based variations regarding the association of hsCRP with depression was observed in the present study.…”
BACKGROUNDStudies indicate that along with many other factors, low grade inflammation may play an important contributory role in the development of major depressive psychosis. This may add up as a confounding factor for different complications related to this major psychological disorder. The role of hsCRP as a marker of low grade inflammation has been explored and analysed in the present study.
“…Evidence has suggested, however, that alcohol consumption is associated with early risk markers of cardiometabolic diseases, such as IR and fasting insulin, in a sex-specific manner [10, 36, 37]. It has been suggested that sex differences in the relationship between alcohol intake and metabolic markers are explained by adiposity [12].…”
Purpose
We examined the relation of alcohol consumption to glucose metabolism and insulin resistance (IR) as a function of depressive symptoms, adiposity, and sex.
Method
Healthy adults (aged 18–65 years) provided fasting blood samples and information on lifestyle factors. Alcohol intake was categorized as never, infrequent (1–3 drinks/month), occasional (1–7 drinks/week), and regular (≥2 drinks/day) drinkers. The Beck Depression Inventory (BDI) was used to assess symptom severity. Primary out-comes were fasting insulin, glucose, and IR assessed by the homeostasis model assessment (HOMA).
Results
In univariate analysis, alcohol consumption was negatively associated with HOMA-IR (p = 0.03), insulin (p = 0.007), and body mass index (BMI) (p = 0.04), but not with glucose or BDI. Adjusting for potential confounders including BMI, alcohol consumption was associated with HOMA-IR (p = 0.01) and insulin (p = 0.009) as a function of BDI and sex. For women with minimal depressive symptoms, light-to-moderate alcohol consumption was associated with lower HOMA-IR and insulin. Alcohol consumption was not associated with metabolic markers in women with higher depressive symptoms and in men. In analysis using BMI as a continuous moderator, alcohol consumption was only associated with insulin (p = 0.004). Post-hoc comparisons between BMI groups (<25 vs ≥25 kg/m2) revealed that light-to-moderate alcohol consumption was associated with lower insulin but only in subjects with BMI ≥ 25 kg/m2.
Conclusions
The benefits of light-to-moderate alcohol consumption on fasting insulin and IR are sex dimorphic and appear to be independently moderated by adiposity and depressive symptom severity.
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