Browsing by Subject "African Americans"
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- ItemOpen AccessAssociation of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon(Public Library of Science, 2014) Wonkam, Ambroise; Bitoungui, Valentina J Ngo; Vorster, Anna A; Ramesar, Raj; Cooper, Richard S; Tayo, Bamidele; Lettre, Guillaume; Ngogang, JeanneBACKGROUND: Genetic variation at loci influencing adult levels of HbF have been shown to modify the clinical course of sickle cell disease (SCD). Data on this important aspect of SCD have not yet been reported from West Africa. We investigated the relationship between HbF levels and the relevant genetic loci in 610 patients with SCD (98% HbSS homozygotes) from Cameroon, and compared the results to a well-characterized African-American cohort. Methods and FINDINGS: Socio-demographic and clinical features were collected and medical records reviewed. Only patients >5 years old, who had not received a blood transfusion or treatment with hydroxyurea were included. Hemoglobin electrophoresis and a full blood count were conducted upon arrival at the hospital. RFLP-PCR was used to describe the HBB gene haplotypes. SNaPshot PCR, Capillary electrophoresis and cycle sequencing were used for the genotyping of 10 selected SNPs. Genetic analysis was performed with PLINK software and statistical models in the statistical package R. Allele frequencies of relevant variants at BCL11A were similar to those detected in African Americans; although the relationships with Hb F were significant (p <.001), they explained substantially less of the variance in HbF than was observed among African Americans (∼ 2% vs 10%). SNPs in HBS1L-MYB region ( HMIP ) likewise had a significant impact on HbF, however, we did not find an association between HbF and the variations in HBB cluster and OR51B5/6 locus on chromosome 11p, due in part to the virtual absence of the Senegal and Indian Arab haplotypes. We also found evidence that selected SNPs in HBS1L-MYB region ( HMIP ) and BCL11A affect both other hematological indices and rates of hospitalization. CONCLUSIONS: This study has confirmed the associations of SNPs in BCL11A and HBS1L-MYB and fetal haemoglobin in Cameroonian SCA patients; hematological indices and hospitalization rates were also associated with specific allelic variants.
- ItemOpen AccessDietary intake and barriers to dietary compliance in black type 2 diabetic patients attending primary health-care services(2002) Nthangeni, Gladys; Steyn, Nelia P; Alberts, Marianne; Steyn, Krisela; Levitt, Naomi S; Laubscher, Ria; Bourne, Lesley; Dick, Judy; Temple, NormanOBJECTIVE: To determine the dietary intake, practices, knowledge and barriers to dietary compliance of black South African type 2 diabetic patients attending primary health-care services in urban and rural areas. DESIGN: A cross-sectional survey. Dietary intake was assessed by three 24-hour recalls, and knowledge and practices by means of a structured questionnaire (n = 133 men, 155 women). In-depth interviews were then conducted with 25 of the patients to explore their underlying beliefs and feelings with respect to their disease. Trained interviewers measured weight, height and blood pressure. A fasting venous blood sample was collected from each participant in order to evaluate glycaemic control. SETTING: An urban area (Sheshego) and rural areas near Pietersburg in the Northern Province of South Africa. SUBJECTS: The sample comprised 59 men and 75 women from urban areas and 74 men and 80 women from rural areas. All were over 40 years of age, diagnosed with type 2 diabetes for at least one year, and attended primary health-care services in the study area over a 3-month period in 1998. RESULTS: Reported dietary results indicate that mean energy intakes were low (< 70% of Recommended Dietary Allowance), 8086-8450 kJ day(-1) and 6967-7382 kJ day(-1) in men and women, respectively. Urban subjects had higher (P < 0.05) intakes of animal protein and lower ratios of polyunsaturated fat to saturated fat than rural subjects. The energy distribution of macronutrients was in line with the recommendations for a prudent diet, with fat intake less than 30%, saturated fat less than 10% and carbohydrate intake greater than 55% of total energy intake. In most respects, nutrient intakes resembled a traditional African diet, although fibre intake was low in terms of the recommended 3-6 g/1000 kJ. More than 90% of patients ate three meals a day, yet only 32-47% had a morning snack and 19-27% had a late evening snack. The majority of patients indicated that they followed a special diet, which had been given to them by a doctor or a nurse. Only 3.4-6.1% were treated by diet alone. Poor glycaemic control was found in both urban and rural participants, with more than half of subjects having fasting plasma glucose above 8 mmol l(-1) and more than 35% having plasma glycosylated haemoglobin level above 8.6%. High triglyceride levels were found in 24 to 25% of men and in 17 to 18% of women. Obesity (body mass index > or = 30 kg m(-2)) was prevalent in 15 to 16% of men compared with 35 to 47% of women; elevated blood pressure (> or = 160/95 mmHg) was least prevalent in rural women (25.9%) and most prevalent in urban men (42.4%). CONCLUSIONS: The majority of black, type 2 diabetic patients studied showed poor glycaemic control. Additionally, many had dyslipidaemia, were obese and/or had an elevated blood pressure. Quantitative and qualitative findings indicated that these patients frequently received incorrect and inappropriate dietary advice from health educators.
- ItemOpen AccessTowards an understanding of the relationship between sleep and cardiovascular disease risk in adults of African descent living in a low socioeconomic status community(2025) Forshaw, Philippa; Rae, Dale; Roden, Laura; Lambert, EstelleBackground: Individuals of African descent, specifically African Americans and those from Sub-Saharan Africa, experience a higher burden of cardiovascular disease (CVD) and its associated risk factors (such as obesity, diabetes and hypertension) as well as shorter, poorer sleep quality, compared to Caucasian American individuals. Blood pressure (BP) non-dipping (i.e. the failure of BP to decrease at night during sleep) and nocturnal hypertension are important markers of CVD risk and are substantially more prevalent in African American, compared to Caucasian American, individuals. Two additional layers that need consideration are socioeconomic status (SES) and sex. In contrast to much of the research in the Global North predominantly demonstrating shorter objective and subjective sleep durations (around 6- 7h per night) among African descended individuals living in low SES environments, South Africans of African descent living in low SES communities report much longer sleep durations, around 8-10h per night. Thus, while on one hand, lower SES has been associated with higher risk for CVD possibly through shorter sleep, the nature of the relationship between long sleep duration and CVD risk in the South African context is not well understood. Given the significant sex-specific differences in both CVD risk and sleep, there is a need for research focused on understanding sex-specific associations between CVD and sleep health. Thus, the purpose of this thesis was to investigate sex-specific relationships between CVD risk, nocturnal BP and sleep health in adults of African descent living in a low SES community in South Africa. This purpose was achieved through the following aims: i) to investigate sex-specific relationships between self-reported sleep characteristics and CVD risk among individuals of African descent living in a low SES community, ii) to investigate sex-specific relationships between actigraphy-derived sleep characteristics and CVD risk in these same individuals, iii) to systematically review the literature on sleep and BP dipping in apparently healthy individuals, iv) to explore sex-specific associations between actigraphy-derived sleep characteristics, nocturnal BP and CVD risk among adults of African descent living in a low SES community and v) to conduct qualitative interviews with these same individuals to explore how external (e.g. environmental barriers to and promoters of good sleep) and internal (e.g. individual knowledge, attitudes, beliefs and perceptions around sleep) factors might impact sleep health. This thesis explored the hypothesis that adverse environmental conditions associated with living in low SES communities are not conducive to healthy sleep, driving BP non-dipping, nocturnal hypertension and higher CVD risk. Methods: For Chapters 2 and 3, individuals of African descent (56% women, 29-51y, 40% employed) living in Khayelitsha (an informal settlement in South Africa characterised by high rates of crime, violence and poverty) were recruited and studied. Sleep characteristics were measured subjectively using self-reported questionnaires (Pittsburgh Sleep Quality Index (PSQI), Epworth Sleepiness Scale (ESS), Insomnia Severity Index (ISI); n=412) and objectively with seven days of wrist-worn actigraphy (n=194). CVD risk was assessed using the body mass index (BMI)-modified Framingham 10-year CVD risk score and clinical measures (BMI, waist circumference, resting BP, fasting glucose). We then conducted a systematic review (Chapter 4) exploring associations between BP dipping and sleep in healthy individuals. In Chapter 5 we measured twenty-four hour ambulatory BP in a sub-set of individuals from the original cohort (n=59) to explore associations between BP dipping, nocturnal hypertension, sleep characteristics and CVD risk scores. Finally, we conducted one-on-one qualitative interviews (Chapter 6) in a further sub-set of participants (n=15) to explore possible external (e.g. environmental barriers to and promoters of good sleep) and internal (e.g. individual knowledge, attitudes, beliefs and perceptions around sleep) factors related to sleep health in this population.Results: When we examined associations between subjectively measured sleep and CVD risk (Chapter 2), found that men (n=178) reporting poor sleep quality (PSQI>5, OR: 1.95, 95%CI: 1.07, 3.51, p=0.025) and earlier bedtimes (OR: 0.54, 95%CI: 0.39, 0.74, p<0.001)were more likely to have higher CVD risk scores. Women (n=234) reporting earlier bedtimes (OR: 0.72, 95%CI: 0.55, 0.95, p=0.020) and wake-up times (OR: 0.30, 95%CI: 0.13, 0.73, p=0.007), longer sleep onset latencies (OR: 1.47, 95%CI: 1.43, 1.88, p=0.003), shorter total sleep times (OR: 0.84, 95%CI: 0.72, 0.98, p=0.029), higher PSQI global scores (OR: 1.93, 95%CI: 1.29, 2.90, p=0.001) and more moderate to severe insomnia symptoms (ISI≥15, OR: 3.24, 95%CI: 1.04, 10.04, p=0.042) were more likely to have higher CVD risk scores. We confirm actigraphy derived long (men: 9.4 ± 1.4h, women: 8.9 ± 1.2h) but disturbed sleep (low sleep efficiencies [men: 81.8 (76.8, 85.7)%), women: 79.9 (72.5, 84.6)%], high sleep fragmentation indices [men: 58.3 (52.5, 65.2)%, women: 63.4 (56.3, 68.2)%] and high wake after sleep onset (WASO) times [men: 103.1 (76.1, 127.0)min, women: 84.9 (68.8, 110.4)min]) in this population, for whom obesity (specifically among women: 60.3%) and hypertension (men: 48%, women: 44%) are prevalent. Associations between actigraphy-derived sleep measures and CVD risk (Chapter 3) found that among men (n=94), earlier midsleep time was associated with higher CVD risk scores (b =–0.17, 95%CI:–0.33, –0.02, p=0.030) while shorter sleep duration was associated with obesity (OR: 0.48, 95%CI: 0.25, 0.90, p=0.023). Among women (n=100), earlier wake-up times (b: –0.24, 95%CI: –0.41, –0.07, p=0.007) and midsleep times (b: – 0.18, 95%CI: –0.39, 0.00, p=0.046) were associated with higher CVD risk scores. Women with earlier bedtimes (OR: 0.53, 95%CI: 0.33, 0.85, p=0.009) and midsleep times (OR: 0.47, 95%CI: 0.26, 0.83, p=0.010) were more likely to have elevated BP, and those with earlier wake-up times (OR: 0.54, 95%CI: 0.35, 0.81, p=0.003) and midsleep times (OR: 0.46, 95%CI: 0.27, 0.77, p=0.003) were also more likely to be obese. Interaction effects revealed that among women, CVD risk scores were higher in those who had shorter sleep combined with later bedtimes or in those who had longer sleep combined with earlier bedtimes (β:–2.38, 95%CI: –0.35, –0.12, p<0.001). A weaker interaction effect was found for WASO such that CVD risk score was higher in women with longer sleep and more WASO or shorter sleep with less WASO (β: 0.004, 95%CI: 0.00, 0.00, p=0.014). The systematic review (Chapter 4) showed that BP non dipping in apparently healthy individuals was associated with short sleep duration, more sleep fragmentation, less sleep depth and increased variability in sleep timing. Measuring 24h ambulatory BP (Chapter 5) found a high proportion of SBP non-dipping (men: 50%, women: 61%), with 48% of men and 72% of women also presenting with nocturnal hypertension. Among the women (n=36), shorter total sleep times (rho: 0.42, p=0.020) and worse sleep efficiencies (rho: 0.51, p=0.003) were correlated with smaller SBP dipping percentages. Similarly, shorter sleep durations (rho: 0.39, p=0.029), shorter total sleep times (rho: 0.44, p=0.014) and worse sleep efficiencies (rho: 0.37, p=0.037) were correlated with smaller DBP dipping percentages. Women with worse sleep efficiencies (rho: –0.39, p=0.016) has higher nocturnal SBP. Among the men (n=23), worse sleep efficiencies (SBP rho: –0.47, p=0.024; DBP rho: – 0.50, p=0.015), greater WASO (SBP rho: 0.59, p=0.003; DBP rho: 0.50, p=0.014) and greater sleep fragmentation indices (SBP rho: 0.59, p=0.003; DBP rho: 0.59, p=0.003) were correlated with higher nocturnal SBP and DBP. Worse sleep duration regularity scores were correlated with lower SBP (rho: – 0.48, p=0.025) and DBP (rho: –0.52, p=0.013) dipping percentages. Men with nocturnal hypertension had higher WASO (116.8 (88.8, 163.3)min vs. 88.1 (65.1, 98.3)min, p=0.031) and sleep fragmentation indices (36.4(33.4, 40.8)% vs. 29.6(25.8, 34.7)%, p=0.019) compared to those without nocturnal hypertension. Insights from the qualitative interviews (Chapter 6) revealed that external factors such as high-density living, noise, crime, violence and excessive alcohol use within the community primarily contributed to disturbing the sleep of participants. Conclusions: This thesis provides new insights, from a Global South lens, to relationships between sleep and cardiovascular health as they relate to adults of African descent living in a low SES environment. 4 Two main features of sleep emerge as important risk factors for CVD in these study participants: mistimed sleep and disturbed sleep, despite adequate sleep opportunities. By considering the lived experiences of individuals in this low SES community, we gained an understanding of the major role that the adverse conditions of the neighbourhood has on impairing sleep health in this population. We speculate that this earlier timed sleep observed predominantly in women, but to some extent in men, might be a direct consequence of environment-related fear, prompting residents to seek refuge in bed at a time which may be too early, potentially contributing to circadian misalignment, which in turn may increase CVD risk. We further hypothesise that when faced with these adverse neighbourhood conditions, some residents may be in a state of hypervigilance at night, resulting in insufficient sympathetic nervous system (SNS) withdrawal, which in turn leads to disturbed sleep. Disturbed sleep may contribute to BP non-dipping or nocturnal hypertension, which may subsequently increase CVD risk, potentially through insufficient cardiovascular system recovery at night. Interestingly, we note that some participants appear to demonstrate resilience through attaining healthy sleep despite living in a challenging neighbourhood environment. Perhaps these are the individuals in whom appropriate SNS withdrawal takes place at night, improving their sleep health and reducing their CVD risk. Considering all the evidence generated though these studies, this thesis proposes the term Sleep Health Insecurity - a lack of regular access to healthy sleep (that which is of sufficient duration, regular, appropriately timed, consolidated, satisfying and refreshing), which is essential for optimal mental and physical health, emotional well-being and cognition. Although we propose that residents of Khayelitsha are experiencing Sleep Health Insecurity, which may increase their CVD risk, these residents likely represent not only a large sector of the South African population but also other similar low SES populations around the world, making this concept a fundamental global health issue.
- ItemOpen AccessWhere does the black population of South Africa stand on the nutrition transition?(2002) Bourne, Lesley T; Lambert, Estelle V; Steyn, KriselaOBJECTIVE: To review data on selected risk factors related to the emergence of noncommunicable diseases (NCDs) in the black population of South Africa. METHODS: Data from existing literature on South African blacks were reviewed with an emphasis placed on changes in diet and the emergence of obesity and related NCDs. DESIGN: Review and analysis of secondary data over time relating to diet, physical activity and obesity and relevant to nutrition-related NCDs. SETTINGS: Urban, peri-urban and rural areas of South Africa. National prevalence data are also included. SUBJECTS: Black adults over the age of 15 years were examined. RESULTS: Shifts in dietary intake, to a less prudent pattern, are occurring with apparent increasing momentum, particularly among blacks, who constitute three-quarters of the population. Data have shown that among urban blacks, fat intakes have increased from 16.4% to 26.2% of total energy (a relative increase of 59.7%), while carbohydrate intakes have decreased from 69.3% to 61.7% of total energy (a relative decrease of 10.9%) in the past 50 years. Shifts towards the Western diet are apparent among rural African dwellers as well. The South African Demographic and Health Survey conducted in 1998 revealed that 31.8% of African women (over the age of 15 years) were obese (body mass index (BMI) > or = 30kg m(-2)) and that a further 26.7% were overweight (BMI > or = 25 to <30 kg m(-2)). The obesity prevalence among men of the same age was 6.0%, with 19.4% being overweight. The national prevalence of hypertension in blacks was 24.4%, using the cut-off point of 140/90 mmHg. There are limited data on the population's physical activity patterns. However, the effects of the HIV/AIDS epidemic will become increasingly important. CONCLUSIONS: The increasing emergence of NCDs in black South Africans, compounded by the HIV/AIDS pandemic, presents a complex picture for health workers and policy makers. Increasing emphasis needs to be placed on healthy lifestyles.