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Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease
BACKGROUND: L-ficolin (encoded by FCN2) binds to acetylated sugar moieties of many pathogens, including Trypanosoma cruzi, promoting their phagocytosis and lysis by the complement system. METHODS: We investigated L-ficolin levels in 160 T. cruzi infected patients with chronic Chagas disease and 71 h...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617223/ https://www.ncbi.nlm.nih.gov/pubmed/23593180 http://dx.doi.org/10.1371/journal.pone.0060237 |
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author | Luz, Paola R. Boldt, Angelica B. W. Grisbach, Caroline Kun, Jürgen F. J. Velavan, Thirumalaisamy P. Messias-Reason, Iara J. T. |
author_facet | Luz, Paola R. Boldt, Angelica B. W. Grisbach, Caroline Kun, Jürgen F. J. Velavan, Thirumalaisamy P. Messias-Reason, Iara J. T. |
author_sort | Luz, Paola R. |
collection | PubMed |
description | BACKGROUND: L-ficolin (encoded by FCN2) binds to acetylated sugar moieties of many pathogens, including Trypanosoma cruzi, promoting their phagocytosis and lysis by the complement system. METHODS: We investigated L-ficolin levels in 160 T. cruzi infected patients with chronic Chagas disease and 71 healthy individuals, and FCN2 polymorphisms (−986 G>A, −602 G>A, and −4 A>G in the promoter and A258S in exon 8) in 243 patients, being 88 indeterminate (asymptomatic), 96 with cardiac, 23 with digestive and 33 with cardiodigestive manifestations (two were unspecified) and 305 controls (135 for A258S). RESULTS: Patients presented lower L-ficolin plasma levels than controls (p<0.0001). Among the different groups of cardiac commitment, individuals with moderate forms had higher L-ficolin levels than the severe forms (P = 0.039). Lower L-ficolin levels were found associated with the 258S variant in the patients (P = 0.034). We found less −4A/G heterozygotes in the cardiac patients, than in the controls (OR = 0.56 [95% CI = 0.33–0.94], P = 0.034). Heterozygote −4A/G genotypes with the 258S variant and 258SS homozygotes were nevertheless more frequent among cardiodigestive patients than in controls (OR = 14.1 [95% CI = 3.5–56.8], P = 0.0001) and in indeterminate patients (OR = 3.2 [95% CI = 1.1–9.4], P = 0.037). We also found an association of the allelic frequency of the 258S variant with cardiodigestive Chagas disease compared to controls (OR = 2.24 [95% CI = 1.1–4.5], P = 0.037). Thus, decreased patient levels of L-ficolin reflect not only protein consumption due to the disease process, but also the higher frequency of the 258S variant in patients with cardiodigestive symptoms. CONCLUSION: The very first study on Brazilian cohort associates both L-ficolin plasma levels and FCN2 variants to Chagas disease and subsequent disease progression. The prognostic value of L-ficolin levels and the FCN2*A258S polymorphism should be further evaluated in other settings. |
format | Online Article Text |
id | pubmed-3617223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-36172232013-04-16 Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease Luz, Paola R. Boldt, Angelica B. W. Grisbach, Caroline Kun, Jürgen F. J. Velavan, Thirumalaisamy P. Messias-Reason, Iara J. T. PLoS One Research Article BACKGROUND: L-ficolin (encoded by FCN2) binds to acetylated sugar moieties of many pathogens, including Trypanosoma cruzi, promoting their phagocytosis and lysis by the complement system. METHODS: We investigated L-ficolin levels in 160 T. cruzi infected patients with chronic Chagas disease and 71 healthy individuals, and FCN2 polymorphisms (−986 G>A, −602 G>A, and −4 A>G in the promoter and A258S in exon 8) in 243 patients, being 88 indeterminate (asymptomatic), 96 with cardiac, 23 with digestive and 33 with cardiodigestive manifestations (two were unspecified) and 305 controls (135 for A258S). RESULTS: Patients presented lower L-ficolin plasma levels than controls (p<0.0001). Among the different groups of cardiac commitment, individuals with moderate forms had higher L-ficolin levels than the severe forms (P = 0.039). Lower L-ficolin levels were found associated with the 258S variant in the patients (P = 0.034). We found less −4A/G heterozygotes in the cardiac patients, than in the controls (OR = 0.56 [95% CI = 0.33–0.94], P = 0.034). Heterozygote −4A/G genotypes with the 258S variant and 258SS homozygotes were nevertheless more frequent among cardiodigestive patients than in controls (OR = 14.1 [95% CI = 3.5–56.8], P = 0.0001) and in indeterminate patients (OR = 3.2 [95% CI = 1.1–9.4], P = 0.037). We also found an association of the allelic frequency of the 258S variant with cardiodigestive Chagas disease compared to controls (OR = 2.24 [95% CI = 1.1–4.5], P = 0.037). Thus, decreased patient levels of L-ficolin reflect not only protein consumption due to the disease process, but also the higher frequency of the 258S variant in patients with cardiodigestive symptoms. CONCLUSION: The very first study on Brazilian cohort associates both L-ficolin plasma levels and FCN2 variants to Chagas disease and subsequent disease progression. The prognostic value of L-ficolin levels and the FCN2*A258S polymorphism should be further evaluated in other settings. Public Library of Science 2013-04-04 /pmc/articles/PMC3617223/ /pubmed/23593180 http://dx.doi.org/10.1371/journal.pone.0060237 Text en © 2013 Luz et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Luz, Paola R. Boldt, Angelica B. W. Grisbach, Caroline Kun, Jürgen F. J. Velavan, Thirumalaisamy P. Messias-Reason, Iara J. T. Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title | Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title_full | Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title_fullStr | Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title_full_unstemmed | Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title_short | Association of L-Ficolin Levels and FCN2 Genotypes with Chronic Chagas Disease |
title_sort | association of l-ficolin levels and fcn2 genotypes with chronic chagas disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617223/ https://www.ncbi.nlm.nih.gov/pubmed/23593180 http://dx.doi.org/10.1371/journal.pone.0060237 |
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