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1.
Braz. j. med. biol. res ; 53(12): e10279, 2020. tab, graf
Article in English | LILACS, ColecionaSUS | ID: biblio-1132507

ABSTRACT

Obesity affects the respiratory system through various mechanisms, including systemic inflammation and direct mechanical hindrance due to fat deposition in the chest and abdomen. In addition, changes in the neural control of respiration and increases in thoracic blood volume can promote abnormalities in lung function. Thus, determining relationships between the distance covered in the 6-min walk test (6MWT) and demographic and lung function variables may help us better understand the mechanisms involved in reduced functional exercise capacity in obesity. To explore the determinants of the 6-min walking distance (6MWD) and evaluate the influence of lung function on the distance covered, 263 obese Brazilian women performed the 6MWT and underwent spirometry and respiratory muscle strength measurement. The mean age was 41.8±11.1 years. The mean body mass index (BMI) was 45±8 kg/m2. The 6MWD showed correlations with height (r=0.319), age (r=-0.281), weight (r=-0.370), BMI (r=-0.561), forced vital capacity (FVC, r=0.443), expiratory peak flow (r=0.278), maximal inspiratory pressure (MIP, r=0.326), and maximal expiratory pressure (r=0.259), all with P<0.0001. In the stepwise forward regression analysis, BMI, FVC, age, and MIP were the independent predictive variables for 6MWD, explaining 41% of its variability. The reference equation including lung function was as follows: 6MWD (m) = 513.6 - (4.439 × BMIkg/m2) + (1.136 × FVC%predicted) - (1.048 × ageyrs) + (0.544 × MIP%predicted). Thus, the inclusion of lung function in a reference equation for 6MWD contributes to a better prediction of the distance covered in this population.


Subject(s)
Humans , Female , Adult , Middle Aged , Obesity/therapy , Brazil , Walking , Exercise Tolerance , Diabetes Mellitus, Type 2 , Walk Test , Lung
2.
Braz. j. med. biol. res ; 40(12): 1671-1679, Dec. 2007. graf, tab
Article in English | LILACS | ID: lil-466737

ABSTRACT

Costimulatory and antigen-presenting molecules are essential to the initiation of T cell immunity to mycobacteria. The present study analyzed by immunocytochemistry, using monoclonal antibodies and alkaline phosphatase-anti-alkaline phosphatase method, the frequency of costimulatory (CD86, CD40, CD40L, CD28, and CD152) and antigen-presenting (MHC class II and CD1) molecules expression on human lung cells recovered by sputum induction from tuberculosis (TB) patients (N = 22) and non-TB controls (N = 17). TB cases showed a statistically significant lower percentage of HLA-DR+ cells than control subjects (21.9 ± 4.2 vs 50.0 ± 7.2 percent, P < 0.001), even though similar proportions of TB cases (18/22) and control subjects (16/17, P = 0.36) had HLA-DR-positive-stained cells. In addition, fewer TB cases (10/22) compared to control subjects (16/17) possessed CD86-expressing cells (P = 0.04; OR: 0.05; 95 percentCI = 0.00-0.51), and TB cases expressed a lower percentage of CD86+ cells (P = 0.04). Moreover, TB patients with clinically limited disease (£1 lobe) on chest X-ray exhibited a lower percentage of CD86-bearing cells compared to patients with more extensive lung disease (>1 lobe) (P = 0.02). The lower expression by lung cells from TB patients of HLA-DR and CD86, molecules involved in antigen presentation and activation of T cells, may minimize T cell recognition of Mycobacterium tuberculosis, fostering an immune dysfunctional state and active TB.


Subject(s)
Adult , Female , Humans , Male , Antigen-Presenting Cells/immunology , Antigens, CD/immunology , HLA-DR Antigens/immunology , Histocompatibility Antigens Class II/immunology , T-Lymphocytes/immunology , Tuberculosis, Pulmonary/immunology , Alkaline Phosphatase/immunology , Antibodies, Monoclonal/immunology , Antigen-Presenting Cells/metabolism , Antigens, CD/metabolism , Case-Control Studies , HLA-DR Antigens/metabolism , Histocompatibility Antigens Class II/metabolism , Immunity, Cellular , Immunohistochemistry , Lymphocyte Activation/immunology , Mycobacterium tuberculosis/immunology , Sputum/microbiology
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