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1.
Braz. j. med. biol. res ; 48(11): 1032-1038, Nov. 2015. tab, graf
Article in English | LILACS | ID: lil-762904

ABSTRACT

Milk fat globule epidermal growth factor 8 (MFG-E8) is an opsonin involved in the phagocytosis of apoptotic cells. In patients with chronic obstructive pulmonary disease (COPD), apoptotic cell clearance is defective. However, whether aberrant MFG-E8 expression is involved in this defect is unknown. In this study, we examined the expression of MFG-E8 in COPD patients. MFG-E8, interleukin (IL)-1β and transforming growth factor (TGF)-β levels were measured in the plasma of 96 COPD patients (93 males, 3 females; age range: 62.12±10.39) and 87 age-matched healthy controls (85 males, 2 females; age range: 64.81±10.11 years) using an enzyme-linked immunosorbent assay. Compared with controls, COPD patients had a significantly lower plasma MFG-E8 levels (P<0.01) and significantly higher plasma TGF-β levels (P=0.002), whereas there was no difference in plasma IL-1β levels between the two groups. Moreover, plasma MFG-E8 levels decreased progressively between Global Initiative for Chronic Obstructive Lung Disease (GOLD) I and GOLD IV stage COPD. Multiple regression analysis showed that the forced expiratory volume in 1 s (FEV1 % predicted) and smoking habit were powerful predictors of MFG-E8 in COPD (P<0.01 and P=0.026, respectively). MFG-E8 was positively associated with the FEV1 % predicted and negatively associated with smoking habit. The area under the receiver operating characteristic curve was 0.874 (95% confidence interval: 0.798-0.95; P<0.01). Our findings demonstrated the utility of MFG-E8 as a marker of disease severity in COPD and that cigarette smoke impaired MFG-E8 expression in these patients.


Subject(s)
Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Antigens, Surface/blood , Apoptosis/physiology , Milk Proteins/blood , Pulmonary Disease, Chronic Obstructive/blood , Biomarkers/blood , Case-Control Studies , Enzyme-Linked Immunosorbent Assay , Forced Expiratory Volume , Interleukin-1beta/blood , Predictive Value of Tests , Pulmonary Disease, Chronic Obstructive/epidemiology , Regression Analysis , ROC Curve , Severity of Illness Index , Smoking/blood , Transforming Growth Factor beta/blood
2.
J Genet ; 2001 Dec; 80(3): 137-40
Article in English | IMSEAR | ID: sea-114234

ABSTRACT

Polymorphic allelic variants of chemokine receptors CCR2 and CCR5, as well as of stromal-derived factor-1 SDF-1, the ligand for the chemokine receptor CXCR4, are known to have protective effects against HIV-1 infection and to be involved with delay in disease progression. We have studied the DNA polymorphisms at the loci that encode these proteins in 525 healthy individuals without any history of HIV-1 infection from 11 diverse populations of Andhra Pradesh, South India. The two protective alleles SDF-1-3'A and CCR2-64I at the SDF-1 and CCR2 loci, respectively, are present in all populations studied, although their frequencies differ considerably across populations (from 17% to 35% for the SDF-1-3'A allele, and from 3% to 17% for CCR2-64I). In contrast the CCR5-Delta32 allele is observed only in three populations (Yamani, Pathan and Kamma), all in low frequencies (i.e. 1% to 3%). The mean number of mutant alleles (for the three loci together) carried by each individual varies from 0.475 (in Vizag Brahmins) to 0.959 (in Bohra Muslims). The estimated relative hazard values for the populations, computed from the three-locus genotype data, are comparable to those from Africa and Southeast Asia, where AIDS is known to be widespread.


Subject(s)
Acquired Immunodeficiency Syndrome/genetics , Alleles , Chemokine CXCL12 , Chemokines, CXC/genetics , Disease Progression , Gene Frequency , Genetic Predisposition to Disease , Genetic Variation , Genotype , HIV Infections/genetics , HIV-1 , Humans , India/ethnology , Mutation , Polymorphism, Genetic , Receptors, CCR2 , Receptors, CCR5/genetics , Receptors, Chemokine/genetics
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