Longitudinal associations between circulating Interleukin-6 and C-Reactive Protein in childhood, and eating disorders and disordered eating in adolescence
by Stacey
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Objective: Few studies have examined the relationship between inflammation and eating disorders, and not using a longitudinal design. We investigated the relationship between serum levels of interleukin-6 (IL-6) and C-reactive protein (CRP) were measured in childhood and eating disorders and related behaviors and cognitions in adolescents in a large sample of the general population.
Method: We used data from the Avon Longitudinal Study of Parents and Children (ALSPAC). our exposure was thirds of IL 6 and CRP derived from serum measurements taken at the age of nine years, and the results were eating disorder diagnosis and self-reported well-eating behavior at ages 14, 16 and 18 years old. We used multilevel logistic regression model univariate and multivariate adjust to a number of potential confounders, including sex, fat mass, and the existing mental health problems.
Results: Our sample included 3,480 children. Those in the top third of CRP have lower chances of binge eating (odds ratio (OR): 0.62, 95% confidence interval (CI): 0.39,1.00, p “is equal to” 0.05) and fasting (OR : 0.63, 95% CI: 0.38,1.07, p “is equal to” 0.09) after adjustment for confounders. We also observed a weak link in proportion to clean, anorexia nervosa and bulimia nervosa. We did not find any association between the levels of IL 6 and one of the outcomes studied.
Conclusion: There is little evidence of an association between CRP and IL-6, and eating disorders result teenager. The inverse relationship was observed between CRP and unexpected dinner party, so caution is required when interpreting it. One possible explanation is that a higher CRP level may have a protective role for organized eat by affecting the appetitive properties. Sishen Pill DSS-Induced Colitis Treatment via Settings Interaction With inflammatory dendritic cells and Gut microbiota Sishen Pill (SSP) is a typical recipe in the pharmacopoeia of traditional Chinese medicine (TCM), and is typically used to treat inflammatory bowel disease (IBD).
Longitudinal associations between circulating Interleukin-6 and C-Reactive Protein in childhood, and eating disorders and disordered eating in adolescence
It is known that inflammatory dendritic cells (DC) and an imbalance of gut microbiota plays an important role in the pathogenesis of IBD. However, it is unclear whether the SSP can treat IBD to regulate the interaction of DC and intestinal microbiota. In this study, the levels of inflammation and intestinal microbiota DC were analyzed by flow cytometry and 16S rDNA analysis. SSP relieved pathological damage to the intestine of mice with colitis induced by dextran sodium sulfate (DSS).
As an indicator of a typical DC inflammation, levels of CD11c + CD103 + E-cadherin + cells and pro-inflammatory cytokines [ interleukin ( IL ) – 1β, -4, -9, and -17A] decreased in mice with colitis treated by the SSP for 10 days. Simultaneously, the composition of the intestinal microbiota is set, and increases beneficial bacteria and pathogenic bacteria is reduced. The results show that the interaction between DC regulated CNS inflammation and intestinal microbiota to treat DSS-induced colitis. cord blood data maternal blood within 24 hours before delivery is available for 158 cases of IL-6 and; 66 diagnosed with FIRS (41.8%; median IL-6, 57.55 pg / mL).
We create value risk (score FIRS) consisting weeks expected delivery (≤30 weeks), the number of white blood cells maternal C-reactive protein (≥1.2 mg / dL), mother (≥13 000 / uL), corticosteroids (no ) and PROM latency period (≥3 days) from multivariate logistic regression models predicting the FIRS.
Description: Quantitativesandwich ELISA kit for measuring Human Interleukin 16, IL-16 in samples from serum, plasma, cell culture supernates, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Human Interleukin 16, IL-16 in samples from serum, plasma, cell culture supernates, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Mouse Interleukin 16, IL-16 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Mouse Interleukin 16, IL-16 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Quantitativesandwich ELISA kit for measuring Rat Interleukin 16, IL-16 in samples from serum, plasma, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Description: Quantitativesandwich ELISA kit for measuring Rat Interleukin 16, IL-16 in samples from serum, plasma, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
Description: Interleukin-16 Mouse Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 127 amino acids and having a molecular mass of 13.2 kDa. ;The Mouse IL-16 is purified by proprietary chromatographic techniques.
Description: Quantitative sandwich ELISA for measuring Human Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: Quantitative sandwich ELISA for measuring Human Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: Quantitative sandwich ELISA for measuring Human Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: Quantitative sandwich ELISA for measuring Mouse Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: Quantitative sandwich ELISA for measuring Mouse Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: Quantitative sandwich ELISA for measuring Mouse Interleukin 16 (IL-16) in samples from cell culture supernatants, serum, whole blood, plasma and other biological fluids.
Description: IL-16 Antibody: IL-16 was initially identified as a chemotactic cytokine, but is now known to possess a wide range of activities. Later studies have more fully characterized IL-16 as an immunomodulatory cytokine that contributes to the regulatory process of CD4+ T cell recruitment and activation at sites of inflammation in association with asthma and several autoimmune diseases. The precursor of IL-16 (pro-IL-16) is thought to be cleaved towards the C-terminal region by Caspase-3, releasing a 20 kDa active form that binds to and signals through CD4. Besides acting as a chemotactic cytokine, IL-16 is thought to also be involved in the regulation of T cell proliferation and multiple infectious, immune-mediated, and autoimmune inflammatory disorders including irritable bowel syndrome, systemic lupus erythematosus, and neurodegenerative disorders. At least two isoforms of IL-16 are known to exist; the longer isoform (also known as NIL-16) is detected only in neurons of the cerebellum and hippocampus.
Description: IL-16 Antibody: IL-16 was initially identified as a chemotactic cytokine, but is now known to possess a wide range of activities. Later studies have more fully characterized IL-16 as an immunomodulatory cytokine that contributes to the regulatory process of CD4+ T cell recruitment and activation at sites of inflammation in association with asthma and several autoimmune diseases. The precursor of IL-16 (pro-IL-16) is thought to be cleaved towards the C-terminal region by Caspase-3, releasing a 20 kDa active form that binds to and signals through CD4. Besides acting as a chemotactic cytokine, IL-16 is thought to also be involved in the regulation of T cell proliferation and multiple infectious, immune-mediated, and autoimmune inflammatory disorders including irritable bowel syndrome, systemic lupus erythematosus, and neurodegenerative disorders. At least two isoforms of IL-16 are known to exist; the longer isoform (also known as NIL-16) is detected only in neurons of the cerebellum and hippocampus.
Description: IL-16 Antibody: IL-16 was initially identified as a chemotactic cytokine, but is now known to possess a wide range of activities. Later studies have more fully characterized IL-16 as an immunomodulatory cytokine that contributes to the regulatory process of CD4+ T cell recruitment and activation at sites of inflammation in association with asthma and several autoimmune diseases. The precursor of IL-16 (pro-IL-16) is thought to be cleaved towards the C-terminal region by Caspase-3, releasing a 20 kDa active form that binds to and signals through CD4. Besides acting as a chemotactic cytokine, IL-16 is thought to also be involved in the regulation of T cell proliferation and multiple infectious, immune-mediated, and autoimmune inflammatory disorders including irritable bowel syndrome, systemic lupus erythematosus, and neurodegenerative disorders. At least two isoforms of IL-16 are known to exist; the longer isoform (also known as NIL-16) is detected only in neurons of the cerebellum and hippocampus.
Description: IL-16 Antibody: IL-16 was initially identified as a chemotactic cytokine, but is now known to possess a wide range of activities. Later studies have more fully characterized IL-16 as an immunomodulatory cytokine that contributes to the regulatory process of CD4+ T cell recruitment and activation at sites of inflammation in association with asthma and several autoimmune diseases. The precursor of IL-16 (pro-IL-16) is thought to be cleaved towards the C-terminal region by Caspase-3, releasing a 20 kDa active form that binds to and signals through CD4. Besides acting as a chemotactic cytokine, IL-16 is thought to also be involved in the regulation of T cell proliferation and multiple infectious, immune-mediated, and autoimmune inflammatory disorders including irritable bowel syndrome, systemic lupus erythematosus, and neurodegenerative disorders. At least two isoforms of IL-16 are known to exist; the longer isoform (also known as NIL-16) is detected only in neurons of the cerebellum and hippocampus.
Description: Interleukin-16 Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 121 amino acids and having a molecular mass of 12.4 kDa. ;The IL-16 is purified by proprietary chromatographic techniques.
IL-16 Interleukin-16 Human Recombinant Protein, (130 a.a.)
Description: Interleukin-16 Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain containing 130 amino acids and having a molecular mass of 13.5 kDa. ;The IL-16 is purified by proprietary chromatographic techniques.
IL-16 Interleukin-16 Human Recombinant Protein, His Tag
Description: Interleukin-16 Human Recombinant produced in E.Coli is a single, non-glycosylated polypeptide chain (502-631 a.a) containing 150 amino acids and having a molecular mass of 15.5kDa. The IL-16 is fused to a 20 a.a His-Tag at N-Terminus.;The IL-16 is purified by proprietary chromatographic techniques.
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human IL-16
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human IL-16
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for WB, IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human IL-16
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human IL-16
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human IL-16
Description: A polyclonal antibody for detection of IL-16 from Human. This IL-16 antibody is for IHC-P, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the N-terminal region of human IL-16
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human IL-16 . This antibody is tested and proven to work in the following applications:
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human IL-16 . This antibody is tested and proven to work in the following applications:
Receiver operating characteristic curve analysis of the scores produced the following results: area under the curve, 0.82; 95% CI, 0.76 to 0.89; Cut-off value, 7.5; sensitivity, 89%; specificity, 63%; positive predictive value, 63% and negative predictive value, 89%.
