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

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...

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Veröffentlicht in:Journal of inherited metabolic disease 2018-07, Vol.41 (4), p.631-640
Hauptverfasser: Scaini, Giselli, Tonon, Tássia, Moura de Souza, Carolina F., Schuck, Patricia F., Ferreira, Gustavo C., Quevedo, João, Neto, João Seda, Amorim, Tatiana, Camelo, Jose S., Margutti, Ana Vitoria Barban, Hencke Tresbach, Rafael, Sperb-Ludwig, Fernanda, Boy, Raquel, de Medeiros, Paula F. V., Schwartz, Ida Vanessa D., Streck, Emilio Luiz
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container_end_page 640
container_issue 4
container_start_page 631
container_title Journal of inherited metabolic disease
container_volume 41
creator Scaini, Giselli
Tonon, Tássia
Moura de Souza, Carolina F.
Schuck, Patricia F.
Ferreira, Gustavo C.
Quevedo, João
Neto, João Seda
Amorim, Tatiana
Camelo, Jose S.
Margutti, Ana Vitoria Barban
Hencke Tresbach, Rafael
Sperb-Ludwig, Fernanda
Boy, Raquel
de Medeiros, Paula F. V.
Schwartz, Ida Vanessa D.
Streck, Emilio Luiz
description 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.
doi_str_mv 10.1007/s10545-018-0188-x
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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.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>29740775</pmid><doi>10.1007/s10545-018-0188-x</doi><tpages>10</tpages></addata></record>
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source Wiley Online Library Journals Frontfile Complete; Springer Nature - Complete Springer Journals
subjects Biochemistry
Biomarkers
Cell adhesion & migration
Human Genetics
IL-1β
Inflammation
Internal Medicine
Medicine
Medicine & Public Health
Metabolic Diseases
Original Article
Pediatrics
Urine
title Evaluation of plasma biomarkers of inflammation in patients with maple syrup urine disease
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