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1.
Clin Nutr ESPEN ; 27: 38-43, 2018 10.
Article in English | MEDLINE | ID: mdl-30144891

ABSTRACT

BACKGROUND: There is little information about serum phosphate levels among patients with pulmonary tuberculosis (TB) and HIV infection. OBJECTIVE: We aimed to assess the role of TB, HIV, inflammation and other correlates on serum phosphate levels. METHODS: A cross-sectional study was conducted among TB patients and age- and sex-matched non-TB controls. Pulmonary TB patients were categorized as sputum -negative and -positive, based on culture. Age- and sex-matched non-TB controls were randomly selected among neighbours to sputum-positive TB patients. Data on age, sex, alcohol and smoking habits were obtained. HIV status, serum phosphate, and the acute phase reactants C-reactive protein (serum CRP) and α1-acid glycoprotein (serum AGP) were determined. Linear regression analysis was used to identify correlates of serum phosphate. RESULTS: Of 1605 participants, 355 (22.1%) were controls and 1250 (77.9%) TB patients, of which 9.9% and 50.4% were HIV-infected. Serum phosphate was determined before start of TB treatment in 44%, and 1-14 days after start of treatment in 56%. Serum phosphate was up to 0.10 mmol/L higher 1-3 days after start of TB treatment, and lowest 4 days after treatment, after which it increased. In multivariable analysis, TB patients had 0.09 (95% CI: 0.05; 0.13) mmol/L higher serum phosphate than controls, and those with HIV had 0.05 (95% CI: 0.01; 0.08) mmol/L higher levels than those without. Smoking was also a positive correlate of serum phosphate, whereas male sex and age were negative correlates. CONCLUSION: While HIV and TB are associated with higher serum phosphate, our data suggest that TB treatment is followed by transient reductions in serum phosphate, which may reflect hypophosphataemia in some patients.


Subject(s)
HIV Infections/blood , Inflammation/blood , Phosphates/blood , Tuberculosis, Pulmonary/blood , Acute-Phase Proteins/metabolism , Adult , C-Reactive Protein/metabolism , Cross-Sectional Studies , Female , HIV Infections/epidemiology , Humans , Inflammation/epidemiology , Male , Middle Aged , Nutritional Status , Risk Factors , Sputum/microbiology , Tanzania/epidemiology , Tuberculosis, Pulmonary/drug therapy , Tuberculosis, Pulmonary/epidemiology , Young Adult
2.
Trop Med Int Health ; 22(10): 1302-1313, 2017 10.
Article in English | MEDLINE | ID: mdl-28712113

ABSTRACT

OBJECTIVES: Low grip strength is a marker of frailty and a risk factor for mortality among HIV patients and other populations. We investigated factors associated with grip strength in malnourished HIV patients at referral to ART, and at 12 weeks and 2-3 years after starting ART. METHODS: The study involved HIV-infected Zambian and Tanzanian participants recruited to the NUSTART trial when malnourished (body mass index <18.5 kg/m2 ) and requiring ART. The relationship of grip strength to nutritional, infectious and demographic factors was assessed by multivariable linear regression at referral for ART (n = 1742) and after 12 weeks (n = 778) and 2-3 years of ART (n = 273). RESULTS: In analyses controlled only for sex, age and height, most nutrition and infection-related variables were associated with grip strength. However, in multivariable analyses, consistent associations were seen for fat-free mass index, mid-upper arm circumference, haemoglobin and systolic blood pressure, and a variable association with fat mass index in men. C-reactive protein and CD4 count had limited independent effects on grip strength, while receiving tuberculosis treatment was associated with weaker grip strength. CONCLUSIONS: In this population of originally malnourished HIV patients, poor grip strength was more strongly and independently associated with nutritional than with infection and inflammation variables. Programmes to improve health and survival of HIV patients should incorporate nutritional assessment and management and could use grip strength as a functional indicator of improving nutrition.


Subject(s)
Anti-HIV Agents/therapeutic use , HIV Infections/complications , Hand Strength/physiology , Nutritional Status/physiology , Adolescent , Adult , Anti-HIV Agents/pharmacology , Body Mass Index , C-Reactive Protein/analysis , CD4 Lymphocyte Count , Female , HIV Infections/physiopathology , HIV Wasting Syndrome/complications , HIV Wasting Syndrome/diagnosis , HIV Wasting Syndrome/etiology , Humans , Linear Models , Male , Middle Aged , Multicenter Studies as Topic , Muscle Strength Dynamometer , Prognosis , Randomized Controlled Trials as Topic , Risk Factors , Tanzania , Young Adult , Zambia
4.
Eur J Clin Nutr ; 70(4): 499-504, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26785764

ABSTRACT

BACKGROUND/OBJECTIVES: The effects of inflammation on nutritional rehabilitation after starting antiretroviral therapy (ART) are not well understood. We assessed the relationship between inflammation and body composition among patients enrolled in the Nutritional Support for African Adults Starting Antiretroviral therapy (NUSTART) trial in Tanzania and Zambia from 2011 to 2013. SUBJECTS/METHODS: HIV-infected, ART-eligible adults with body mass index (BMI) of <18.5 kg/m(2) enrolled in the NUSTART trial were eligible for this study. Anthropometric and body composition data were collected at recruitment and 6 and 12 weeks post ART and C-reactive protein (CRP) was measured at recruitment and 6 weeks. The relationships between CRP and body composition were assessed using multiple regression. RESULTS: Of the 1815 trial participants, 838 (46%) had baseline and 6-week CRP measurements. Median age was 36 years, 55% were females and median CD4 count was 135 cells/µl. A one-log reduction in CRP at 6 weeks was associated with increased mid-upper arm circumference (0.45 cm; 95% CI: 0.30, 0.61), calf circumference (0.38 cm; 0.23, 0.54), waist circumference (0.98 cm; 0.59, 1.37), BMI (0.37 kg/m(2); 0.24, 0.50) and fat-free mass (0.58 kg; 0.26, 0.91), but not with fat mass (0.09 kg; -0.17, 0.34). Fat-free mass gains persisted at 12 weeks and were more closely associated with 6-week CRP values than with baseline values. CONCLUSIONS: Reduction in CRP shortly after ART initiation was associated with higher fat-free mass gains. Further studies are warranted to determine whether interventions to reduce systemic inflammation will enhance gains in fat-free mass.


Subject(s)
Anti-HIV Agents/administration & dosage , Body Composition , HIV Infections/drug therapy , Inflammation/therapy , Malnutrition/therapy , Adult , Body Mass Index , C-Reactive Protein/metabolism , CD4 Lymphocyte Count , Double-Blind Method , Female , HIV Infections/complications , Humans , Inflammation/drug therapy , Inflammation/etiology , Longitudinal Studies , Male , Malnutrition/etiology , Nutritional Support , Prospective Studies , Tanzania , Waist Circumference , Zambia
5.
Eur J Clin Nutr ; 69(10): 1125-32, 2015 Oct.
Article in English | MEDLINE | ID: mdl-25828630

ABSTRACT

BACKGROUND/OBJECTIVES: Gains in fat mass and lean mass during tuberculosis (TB) treatment may determine functional recovery and survival; yet, data are scarce. We aimed to assess predictors of fat and fat-free mass during 2 months of intensive TB treatment in a cohort in Mwanza, Tanzania. SUBJECTS/METHODS: Fat and fat-free mass were determined at the start of TB treatment and repeated after 2 months using the deuterium dilution technique. Gains in fat and fat-free mass were determined and predictors assessed using regression analysis. RESULTS: Data for 116 patients were available at baseline and during follow-up. Of these, 38.8% were females, mean age was 37.3 (s.d. 13.5) years, 69% (81) had sputum-positive TB, 45.7% (53) were HIV infected and 25% (29) were current smokers. The mean weight gain was 3.3 kg (95% confidence interval: 2.7; 3.8), and it did not differ by sex. However, compared with females, males had 1.0 (0.4; 1.6) kg/m(2) lower fat mass but 0.7 (0.2; 1.3) kg/m(2) higher fat-free mass gain. Current smoking was associated with higher fat mass (0.7 kg/m(2), 0.04; 1.4) but lower fat-free mass (-0.5 kg/m(2), -1.2; 0.07) gain. Among HIV-infected patients, antiretroviral therapy (ART) led to a lower fat gain (-1.2 kg/m(2), -2.2; -0.2) but to a higher fat-free mass among sputum-negative (2.9 kg/m(2), 0.8; 5.1) but not sputum-positive patients. CONCLUSIONS: During intensive phase of TB treatment, sex, smoking and ART were predictors of body composition. Larger studies are needed to further understand predictors of body composition during recovery, to help design interventions to improve treatment outcomes.


Subject(s)
Adipose Tissue/metabolism , Anti-HIV Agents/adverse effects , Body Composition , Body Fluid Compartments/metabolism , HIV Infections/complications , Smoking/adverse effects , Tuberculosis/complications , Adult , Female , HIV Infections/drug therapy , Humans , Male , Middle Aged , Sex Factors , Sputum , Tanzania , Tuberculosis/therapy , Young Adult
6.
Int J Tuberc Lung Dis ; 18(7): 810-7, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24902557

ABSTRACT

OBJECTIVE: To estimate the costs incurred by patients during the intensive and continuation phases of the current 6-month tuberculosis (TB) regimen in Bangladesh and Tanzania, and thus identify potential benefits to patients of a shorter, 4-month treatment regimen. DESIGN: The validated Stop TB patient cost questionnaire was adapted and used in interviews with 190 patients in the continuation phase of treatment with current regimens. RESULTS: In both countries, overall patient costs were lower during 2 months of the continuation phase (US$74 in Tanzania and US$56 in Bangladesh) than during the 2 months of the intensive phase of treatment (US$150 and US$111, respectively). However, continuation phase patient costs still represented 89% and 77% of the 2-month average national income in the respective countries. Direct travel costs in some settings were kept low by local delivery system features such as community treatment observation. Lost productivity and costs for supplementary foods remained significant. CONCLUSIONS: Although it is not a straightforward exercise to determine the exact magnitude of likely savings, a shorter regimen would reduce out-of-pocket expenses incurred by patients in the most recent 2 months of the continuation phase and allow an earlier return to productive activities.


Subject(s)
Antitubercular Agents/therapeutic use , Financing, Personal/economics , Travel/economics , Tuberculosis/drug therapy , Adult , Antitubercular Agents/administration & dosage , Antitubercular Agents/economics , Bangladesh , Cross-Sectional Studies , Drug Administration Schedule , Drug Costs , Efficiency , Female , Humans , Male , Surveys and Questionnaires , Tanzania , Time Factors , Tuberculosis/economics
7.
Epidemiol Infect ; 142(6): 1334-42, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24007696

ABSTRACT

SUMMARY: We assessed the role of tuberculosis (TB) disease and HIV infection on the level of physical activity. A combined heart rate and movement sensor was used to assess habitual physical activity in TB patients and non-TB controls. The association between sputum-negative TB, sputum-positive TB, HIV and physical activity estimates were assessed in multivariable linear regression models adjusted for age, sex, haemoglobin and alpha-1-acid glycoprotein (AGP). Sputum-positive [eB 0·43, 95% confidence interval (CI) 0·29-0·64] and sputum-negative (eB 0·67, 95% CI 0·47-0·94) TB as well as HIV infection (eB 0·59, 95% CI 0·46-0·75) were associated with reduced activity compared to controls. Anaemia accounted for a substantial part of the effects of HIV, while elevated AGP primarily mediated the TB effect. The level of physical activity is highly influenced by TB and HIV, and mainly mediated through anaemia of infection and associated with elevated acute phase response.


Subject(s)
Accelerometry , Heart Rate/physiology , Monitoring, Physiologic , Motor Activity , Tuberculosis/epidemiology , Tuberculosis/metabolism , Adult , Female , Humans , Male , Tanzania
8.
Int J Tuberc Lung Dis ; 16(12): 1680-5, 2012 Dec.
Article in English | MEDLINE | ID: mdl-23131269

ABSTRACT

BACKGROUND: As diabetes impairs tuberculosis (TB) treatment outcomes, it is essential to identify diabetes among TB patients. While little is known about predictors of diabetes among healthy individuals in Africa, predictors among TB patients are almost non-existent. OBJECTIVE: To assess potential predictors for diabetes among newly diagnosed pulmonary TB patients in Tanzania. METHODS: TB patients were tested for diabetes using an oral glucose tolerance test, demographic information was collected and anthropometric measurements taken. The association between diabetes and possible predictors were examined using logistic regression analyses. RESULTS: Of 1205 TB patients, 16.4% (n = 197) had diabetes, 9.0% (n = 108) were aged ≥55 years, 3.3% (n = 40) were overweight (body mass index [BMI] ≥ 25 kg/m(2)) and 12.7% (n = 152) severely underweight (BMI < 16 kg/m(2)). Diabetes was most prevalent in the 45-55 year age group, and increasing weight, BMI and waist circumference were associated with diabetes. Severe underweight (BMI < 16 kg/m(2)) among male TB patients (sex-BMI interaction, P = 0.02) was associated with diabetes (OR 2.52, P = 0.004). CONCLUSION: Diabetes is a common comorbidity among TB patients. Although diabetes was associated with obesity and was more prevalent among the middle-aged, the majority of TB patients with diabetes comorbidity were young and lean. With diabetes as a major risk factor for TB, and with the lack of strong predictors for diabetes, universal diabetes screening should be implemented in the TB programme.


Subject(s)
Diabetes Mellitus/epidemiology , Overweight/epidemiology , Thinness/epidemiology , Tuberculosis, Pulmonary/epidemiology , Urban Health , Adult , Body Mass Index , Chi-Square Distribution , Comorbidity , Diabetes Mellitus/diagnosis , Female , Glucose Tolerance Test , Humans , Linear Models , Logistic Models , Male , Middle Aged , Odds Ratio , Overweight/diagnosis , Predictive Value of Tests , Prevalence , Risk Factors , Sex Factors , Tanzania/epidemiology , Thinness/diagnosis , Tuberculosis, Pulmonary/diagnosis , Waist Circumference , Weight Gain , Young Adult
9.
Int J Tuberc Lung Dis ; 16(11): 1455-60, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23006814

ABSTRACT

SETTING: Data on pediatric tuberculosis (TB) from TB-endemic, resource-constrained regions are limited, impacting awareness of disease burden and influencing diagnostic actions. OBJECTIVE: To obtain recorded incidence of childhood (age <5 years) TB in Mwanza Municipality, Tanzania, to estimate true incidence and to explore setting-specific reasons for differences. DESIGN: Recorded incidence of pediatric TB (2006-2010) was obtained from Mwanzan TB registries. Incident smear-positive pulmonary TB cases recruited from four TB clinics were used to estimate children exposed and the theoretical incidence of disease, assuming that either 10% or 23% of children would progress to disease following exposure. Reasons for underestimation were evaluated in the medical records of children who died at a secondary hospital. RESULTS: Between 2006 and 2010, 279 early childhood TB cases were recorded (TB incidence 63/100,000/year). Over a 3-month period in 2011, 44% of smear-positive TB patients being treated in Mwanza were living with a total of 139 children. From census data, we estimated that 1279 children were exposed in Mwanza in 2011. Using estimates of the likelihood of disease progression, the theoretical incidence of early childhood TB ranged from 134.2 to 308.5/100,000/year. CONCLUSIONS: The true burden of early childhood TB is likely much higher than recorded. Age-specific reporting, increasing clinical awareness and screening may reduce the magnitude of underdiagnosis in this vulnerable population.


Subject(s)
Mass Screening/methods , Models, Statistical , Tuberculosis, Pulmonary/epidemiology , Age Factors , Child, Preschool , Disease Progression , Female , Humans , Incidence , Infant , Infant, Newborn , Likelihood Functions , Male , Prospective Studies , Registries , Retrospective Studies , Sputum/microbiology , Tanzania/epidemiology , Tuberculosis, Pulmonary/diagnosis
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