Literature DB >> 29740775

Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease.

Giselli Scaini1, Tássia Tonon2,3, Carolina F Moura de Souza4, Patricia F Schuck5, Gustavo C Ferreira6, João Quevedo7, João Seda Neto8, Tatiana Amorim9, Jose S Camelo10, Ana Vitoria Barban Margutti10, Rafael Hencke Tresbach2,11, Fernanda Sperb-Ludwig2,11, Raquel Boy12, Paula F V de Medeiros13, Ida Vanessa D Schwartz4,11, Emilio Luiz Streck14.   

Abstract

Maple syrup urine disease (MSUD) is an autosomal recessive inherited disorder that affects branched-chain amino acid (BCAA) catabolism and is associated with acute and chronic brain dysfunction. Recent studies have shown that inflammation may be involved in the neuropathology of MSUD. However, these studies have mainly focused on single or small subsets of proteins or molecules. Here we performed a case-control study, including 12 treated-MSUD patients, in order to investigate the plasmatic biomarkers of inflammation, to help to establish a possible relationship between these biomarkers and the disease. Our results showed that MSUD patients in treatment with restricted protein diets have high levels of pro-inflammatory cytokines [IFN-γ, TNF-α, IL-1β and IL-6] and cell adhesion molecules [sICAM-1 and sVCAM-1] compared to the control group. However, no significant alterations were found in the levels of IL-2, IL-4, IL-5, IL-7, IL-8, and IL-10 between healthy controls and MSUD patients. Moreover, we found a positive correlation between number of metabolic crisis and IL-1β levels and sICAM-1 in MSUD patients. In conclusion, our findings in plasma of patients with MSUD suggest that inflammation may play an important role in the pathogenesis of MSUD, although this process is not directly associated with BCAA blood levels. Overall, data reported here are consistent with the working hypothesis that inflammation may be involved in the pathophysiological mechanism underlying the brain damage observed in MSUD patients.

Entities:  

Keywords:  Branched-chain amino acid; Cell adhesion molecules; Inflammation; Maple syrup urine disease; Pro-inflammatory cytokines

Year:  2018        PMID: 29740775     DOI: 10.1007/s10545-018-0188-x

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  77 in total

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Authors:  C G Victora; S R Huttly; S C Fuchs; M T Olinto
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Authors:  Giselli Scaini; Meline O S Morais; Camila B Furlanetto; Luiza W Kist; Talita C B Pereira; Patrícia F Schuck; Gustavo C Ferreira; Matheus A B Pasquali; Daniel P Gelain; José Cláudio F Moreira; Maurício R Bogo; Emilio L Streck
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Review 9.  Neurological damage in MSUD: the role of oxidative stress.

Authors:  Angela Sitta; Graziela S Ribas; Caroline P Mescka; Alethéa G Barschak; Moacir Wajner; Carmen R Vargas
Journal:  Cell Mol Neurobiol       Date:  2013-11-13       Impact factor: 5.046

10.  Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease.

Authors:  Faiqa Imtiaz; Abeer Al-Mostafa; Rabab Allam; Khushnooda Ramzan; Nada Al-Tassan; Asma I Tahir; Nouf S Al-Numair; Mohamed H Al-Hamed; Zuhair Al-Hassnan; Mohammad Al-Owain; Hamad Al-Zaidan; Mohammad Al-Amoudi; Alya Qari; Ameera Balobaid; Moeenaldeen Al-Sayed
Journal:  Mol Genet Metab Rep       Date:  2017-04-07
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3.  Maple syrup urine disease in Brazilian patients: variants and clinical phenotype heterogeneity.

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