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The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study

Abnormalities of thyroid function are common in patients with nephrotic syndrome (NS). However, a limited number of studies have reported on the association between clinicopathologic features and thyroid dysfunction in patients with NS. We retrospectively studied 317 patients who had been definitive...

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Autores principales: Li, Ling-Zhi, Hu, Yao, Ai, Shuang-Lan, Cheng, Lu, Liu, Jing, Morris, Emily, Li, Yi, Gou, Shen-Ju, Fu, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478922/
https://www.ncbi.nlm.nih.gov/pubmed/31015507
http://dx.doi.org/10.1038/s41598-019-42905-4
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author Li, Ling-Zhi
Hu, Yao
Ai, Shuang-Lan
Cheng, Lu
Liu, Jing
Morris, Emily
Li, Yi
Gou, Shen-Ju
Fu, Ping
author_facet Li, Ling-Zhi
Hu, Yao
Ai, Shuang-Lan
Cheng, Lu
Liu, Jing
Morris, Emily
Li, Yi
Gou, Shen-Ju
Fu, Ping
author_sort Li, Ling-Zhi
collection PubMed
description Abnormalities of thyroid function are common in patients with nephrotic syndrome (NS). However, a limited number of studies have reported on the association between clinicopathologic features and thyroid dysfunction in patients with NS. We retrospectively studied 317 patients who had been definitively diagnosed with NS. The NS patients with thyroid dysfunction showed higher urine protein, creatinine and lipid levels and lower albumin and hemoglobin than those with normal thyroid function, with no significant differences of pathological types. After dividing thyroid dysfunction groups into five subgroups, interestingly, membranous nephropathy was the most common pathologic type, both in normal thyroid group and in subclinical hypothyroidism group (40.4% and 46.7%, respectively), followed by minimal change disease (28.1% and 21.7%, respectively); while in the hypothyroid, low T3, and low T3T4 groups minimal change disease is now the leading type (48.8%, 33.3% and 38.6%, respectively). High levels of urinary protein, creatinine, cholesterol, and platelets were independent risk factors predicting thyroid dysfunction, while higher albumin and hemoglobin were protective factors. We demonstrated that the type of renal pathology was different among NS patients in different thyroid dysfunction subgroups. Interpretation of the interactions between thyroid and renal function is a challenge for clinicians involved in the treatment of patients with NS.
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spelling pubmed-64789222019-05-03 The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study Li, Ling-Zhi Hu, Yao Ai, Shuang-Lan Cheng, Lu Liu, Jing Morris, Emily Li, Yi Gou, Shen-Ju Fu, Ping Sci Rep Article Abnormalities of thyroid function are common in patients with nephrotic syndrome (NS). However, a limited number of studies have reported on the association between clinicopathologic features and thyroid dysfunction in patients with NS. We retrospectively studied 317 patients who had been definitively diagnosed with NS. The NS patients with thyroid dysfunction showed higher urine protein, creatinine and lipid levels and lower albumin and hemoglobin than those with normal thyroid function, with no significant differences of pathological types. After dividing thyroid dysfunction groups into five subgroups, interestingly, membranous nephropathy was the most common pathologic type, both in normal thyroid group and in subclinical hypothyroidism group (40.4% and 46.7%, respectively), followed by minimal change disease (28.1% and 21.7%, respectively); while in the hypothyroid, low T3, and low T3T4 groups minimal change disease is now the leading type (48.8%, 33.3% and 38.6%, respectively). High levels of urinary protein, creatinine, cholesterol, and platelets were independent risk factors predicting thyroid dysfunction, while higher albumin and hemoglobin were protective factors. We demonstrated that the type of renal pathology was different among NS patients in different thyroid dysfunction subgroups. Interpretation of the interactions between thyroid and renal function is a challenge for clinicians involved in the treatment of patients with NS. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478922/ /pubmed/31015507 http://dx.doi.org/10.1038/s41598-019-42905-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Li, Ling-Zhi
Hu, Yao
Ai, Shuang-Lan
Cheng, Lu
Liu, Jing
Morris, Emily
Li, Yi
Gou, Shen-Ju
Fu, Ping
The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title_full The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title_fullStr The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title_full_unstemmed The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title_short The relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
title_sort relationship between thyroid dysfunction and nephrotic syndrome: a clinicopathological study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478922/
https://www.ncbi.nlm.nih.gov/pubmed/31015507
http://dx.doi.org/10.1038/s41598-019-42905-4
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