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Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE

OBJECTIVES: Nonthyroidal illness syndrome (NTIS), also known as low triiodothyronine (T3) syndrome, frequently affects patients with systemic lupus erythematosus (SLE) and may affect lipid metabolism. Dyslipidemia is highly prevalent and associated with the long-term prognosis of SLE. The aim of the...

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Autores principales: Zhang, Xin, Liu, Lirong, Ma, Xiaolei, Hu, Wei, Xu, Xue, Huang, Saisai, Hua, Bingzhu, Wang, Hong, Chen, Zhiyong, Sun, Lingyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162454/
https://www.ncbi.nlm.nih.gov/pubmed/32298352
http://dx.doi.org/10.1371/journal.pone.0231622
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author Zhang, Xin
Liu, Lirong
Ma, Xiaolei
Hu, Wei
Xu, Xue
Huang, Saisai
Hua, Bingzhu
Wang, Hong
Chen, Zhiyong
Sun, Lingyun
author_facet Zhang, Xin
Liu, Lirong
Ma, Xiaolei
Hu, Wei
Xu, Xue
Huang, Saisai
Hua, Bingzhu
Wang, Hong
Chen, Zhiyong
Sun, Lingyun
author_sort Zhang, Xin
collection PubMed
description OBJECTIVES: Nonthyroidal illness syndrome (NTIS), also known as low triiodothyronine (T3) syndrome, frequently affects patients with systemic lupus erythematosus (SLE) and may affect lipid metabolism. Dyslipidemia is highly prevalent and associated with the long-term prognosis of SLE. The aim of the present study was to explore the clinical significance of NTIS on disease activity and dyslipidemia in patients with SLE. METHODS: Clinical and laboratory data were collected retrospectively from 223 patients with SLE. The correlation between free triiodothyronine (FT3), SLE disease activity, and lipid profiles were estimated. The correlation coefficient (r) was calculated using a Pearson’s regression model. Univariate and multivariate logistic regression analyses were performed to identify the risk factors for dyslipidemia in SLE. RESULTS: Serum FT3 levels were negatively correlated with the levels of 24 h urine protein (UP), blood urea nitrogen (BUN), creatinine (Cr) and SLE disease activity index (SLEDAI) (all p < 0.001) in NTIS patients but not in euthyroid patients. ApoB/ApoA1 was significantly correlated with SLEDAI (p < 0.01) in NTIS patients and CRP (p < 0.001) and ESR (p < 0.01) in euthyroid patients. A multivariate analysis revealed that only FT3 exhibited an independent negative association with dyslipidemia (P = 0.01; OR = 0.48; 95% CI 0.27–0.85). CONCLUSION: NTIS frequently occurs in patients with SLE. Low FT3 is associated with disease activity in SLE patients complicated with NTIS. Low FT3 is an independent risk factor for dyslipidemia in patients with SLE.
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spelling pubmed-71624542020-04-21 Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE Zhang, Xin Liu, Lirong Ma, Xiaolei Hu, Wei Xu, Xue Huang, Saisai Hua, Bingzhu Wang, Hong Chen, Zhiyong Sun, Lingyun PLoS One Research Article OBJECTIVES: Nonthyroidal illness syndrome (NTIS), also known as low triiodothyronine (T3) syndrome, frequently affects patients with systemic lupus erythematosus (SLE) and may affect lipid metabolism. Dyslipidemia is highly prevalent and associated with the long-term prognosis of SLE. The aim of the present study was to explore the clinical significance of NTIS on disease activity and dyslipidemia in patients with SLE. METHODS: Clinical and laboratory data were collected retrospectively from 223 patients with SLE. The correlation between free triiodothyronine (FT3), SLE disease activity, and lipid profiles were estimated. The correlation coefficient (r) was calculated using a Pearson’s regression model. Univariate and multivariate logistic regression analyses were performed to identify the risk factors for dyslipidemia in SLE. RESULTS: Serum FT3 levels were negatively correlated with the levels of 24 h urine protein (UP), blood urea nitrogen (BUN), creatinine (Cr) and SLE disease activity index (SLEDAI) (all p < 0.001) in NTIS patients but not in euthyroid patients. ApoB/ApoA1 was significantly correlated with SLEDAI (p < 0.01) in NTIS patients and CRP (p < 0.001) and ESR (p < 0.01) in euthyroid patients. A multivariate analysis revealed that only FT3 exhibited an independent negative association with dyslipidemia (P = 0.01; OR = 0.48; 95% CI 0.27–0.85). CONCLUSION: NTIS frequently occurs in patients with SLE. Low FT3 is associated with disease activity in SLE patients complicated with NTIS. Low FT3 is an independent risk factor for dyslipidemia in patients with SLE. Public Library of Science 2020-04-16 /pmc/articles/PMC7162454/ /pubmed/32298352 http://dx.doi.org/10.1371/journal.pone.0231622 Text en © 2020 Zhang 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Zhang, Xin
Liu, Lirong
Ma, Xiaolei
Hu, Wei
Xu, Xue
Huang, Saisai
Hua, Bingzhu
Wang, Hong
Chen, Zhiyong
Sun, Lingyun
Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title_full Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title_fullStr Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title_full_unstemmed Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title_short Clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with SLE
title_sort clinical significance of non-thyroidal illness syndrome on disease activity and dyslipidemia in patients with sle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7162454/
https://www.ncbi.nlm.nih.gov/pubmed/32298352
http://dx.doi.org/10.1371/journal.pone.0231622
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