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1.
Immunol Res ; 66(5): 567-576, 2018 10.
Article in English | MEDLINE | ID: mdl-30220011

ABSTRACT

Bullous pemphigoid (BP) following dementia diagnosis has been reported in the elderly. Skin and brain tissues express BP180 and BP230 isoforms. Dementia has been associated with rs6265 (Val66Met) polymorphism of the brain-derived neurotrophic factor (BDNF) gene and low serum BDNF. Here we investigated a possible cross-antigenicity between BP180/BP230 brain and skin isoforms. We assessed antibodies against BP180/BP230 and BDNF levels by ELISA and BDNF Val66Met SNP by PCR in three groups: 50 BP patients, 50 patients with dementia, and 50 elderly controls. Heatmap hierarchical clustering and data mining decision tree were used to analyze the patients' demographic and laboratorial data as predictors of dementia-BP association. Sixteen percent of BP patients with the lowest serological BDNF presented dementia-BP clinical association. Anti-BP180/230 positivity was unexpected observed among dementia patients (10%, 10%) and controls (14%, 1%). Indirect immunofluorescence using healthy human skin showed a BP pattern in two of 10 samples containing antibodies against BP180/BP230 obtained from dementia group but not in the control samples. Neither allelic nor genotypic BDNF Val66Met SNP was associated with dementia or with BP (associated or not with clinical manifestation of dementia). Heatmap analysis was able to differentiate the three studied groups and confirmed the ELISA results. The comprehensive data mining analysis revealed that BP patients and dementia patients shared biological predictors that justified the dementia-BP association. Autoantibodies against the BP180/BP230 brain isoforms produced by dementia patients could cross-react with the BP180/BP230 skin isoforms, which could justify cases of dementia preceding the BP disease.


Subject(s)
Autoantigens/metabolism , Brain/metabolism , Dementia/diagnosis , Dystonin/metabolism , Non-Fibrillar Collagens/metabolism , Pemphigoid, Bullous/diagnosis , Skin/metabolism , Aged , Autoantibodies/blood , Autoantigens/immunology , Biomarkers/blood , Brain-Derived Neurotrophic Factor/blood , Brain-Derived Neurotrophic Factor/genetics , Cross Reactions , Dementia/complications , Dementia/immunology , Dystonin/immunology , Female , Humans , Male , Non-Fibrillar Collagens/immunology , Pemphigoid, Bullous/complications , Pemphigoid, Bullous/immunology , Polymorphism, Single Nucleotide/genetics , Predictive Value of Tests , Prognosis , Collagen Type XVII
2.
Meat Sci ; 123: 192-197, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27750086

ABSTRACT

This study evaluated the effects of growth rate during post-weaning growing phase on carcass traits and beef quality. Thirty-four Nellore young bulls were randomly assigned to one of three treatments: LOW, MEDIUM or HIGH growth rate during post-weaning growing phase followed by high growth rate in the finishing phase. The growth rate affected (P<0.05) all carcass traits evaluated at the end of post-weaning growing phase, except ultimate pH. Carcass dressing was greatest (P<0.05) for the HIGH growth rate group in both phases. Beef from the HIGH group exhibited the greatest (P<0.05) sarcomere length and a* and b* colour values at the end of post-weaning growing phase. However, post-weaning growth rate did not affected (P>0.05) collagen content and solubility, myofibrillar fragmentation index and Warner-Bratzler shear force. Our data suggest that a low post-weaning growth rate produces lighter and leaner carcasses, but it does not affect meat quality traits in Nellore young bulls.


Subject(s)
Cattle/growth & development , Muscle, Skeletal/chemistry , Red Meat , Weaning , Abattoirs , Adipose Tissue/chemistry , Animal Feed/analysis , Animals , Animals, Newborn , Collagen/analysis , Color , Diet/veterinary , Dietary Fats/analysis , Food Quality , Male , Myofibrils/metabolism , Phenotype , Taste
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