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Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients

In recent studies, much has been discussed about biomarkers used in the evaluation of the transplanted graft function. However, there remains a lack of research regarding the long-term effects of microRNAs (miRNAs) on the different genders for kidney transplant (KTx) patients. In this study, we aim...

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Autores principales: Ko, Sien-Yu, Tsai, Shang-Feng, Hsu, Chia-Tien, Huang, Shih-Ting, Chuang, Ya-Wen, Yu, Tung-Min, Wu, Ming-Ju, Chen, Cheng-Hsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656388/
https://www.ncbi.nlm.nih.gov/pubmed/36361623
http://dx.doi.org/10.3390/ijms232112832
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author Ko, Sien-Yu
Tsai, Shang-Feng
Hsu, Chia-Tien
Huang, Shih-Ting
Chuang, Ya-Wen
Yu, Tung-Min
Wu, Ming-Ju
Chen, Cheng-Hsu
author_facet Ko, Sien-Yu
Tsai, Shang-Feng
Hsu, Chia-Tien
Huang, Shih-Ting
Chuang, Ya-Wen
Yu, Tung-Min
Wu, Ming-Ju
Chen, Cheng-Hsu
author_sort Ko, Sien-Yu
collection PubMed
description In recent studies, much has been discussed about biomarkers used in the evaluation of the transplanted graft function. However, there remains a lack of research regarding the long-term effects of microRNAs (miRNAs) on the different genders for kidney transplant (KTx) patients. In this study, we aim to assess the functions of miRNAs on long term outcomes of KTx patients by extracting differently expressed miRNAs between patients of normal graft function and graft dysfunction, while further analyzing their impact on the different genders. We analyzed the data of 40 patients who had received KTx for a period of more than ten years and included data regarding renal function, immuno-related markers and plasma miRNAs. Data were classified by gender for further studies. Twelve out of 17 females and 8 out of 23 males had undergone graft dysfunction. Renal function analysis showed significantly worse outcomes in the female patients. There were five differently expressed miRNAs between the female control group and female dysfunction group: miR-128-3p, miR-21-5p, miR-150-5p, miR-92a-3p and miR-15a-5p, and five between the male control group and male dysfunction group: miR-23a-3p, miR-126-3p, miR-142-3p, miR-223-3p and miR-26a-5p. Gender differences exist in incidences of kidney graft dysfunction, with male patients displaying better preservation in graft functions. Overall, these differently expressed miRNAs either enhance or suppress host immune responses. They can be predictive markers for graft survival and can also be important factors that lead to worse long term kidney graft function in females when compared to males.
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spelling pubmed-96563882022-11-15 Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients Ko, Sien-Yu Tsai, Shang-Feng Hsu, Chia-Tien Huang, Shih-Ting Chuang, Ya-Wen Yu, Tung-Min Wu, Ming-Ju Chen, Cheng-Hsu Int J Mol Sci Communication In recent studies, much has been discussed about biomarkers used in the evaluation of the transplanted graft function. However, there remains a lack of research regarding the long-term effects of microRNAs (miRNAs) on the different genders for kidney transplant (KTx) patients. In this study, we aim to assess the functions of miRNAs on long term outcomes of KTx patients by extracting differently expressed miRNAs between patients of normal graft function and graft dysfunction, while further analyzing their impact on the different genders. We analyzed the data of 40 patients who had received KTx for a period of more than ten years and included data regarding renal function, immuno-related markers and plasma miRNAs. Data were classified by gender for further studies. Twelve out of 17 females and 8 out of 23 males had undergone graft dysfunction. Renal function analysis showed significantly worse outcomes in the female patients. There were five differently expressed miRNAs between the female control group and female dysfunction group: miR-128-3p, miR-21-5p, miR-150-5p, miR-92a-3p and miR-15a-5p, and five between the male control group and male dysfunction group: miR-23a-3p, miR-126-3p, miR-142-3p, miR-223-3p and miR-26a-5p. Gender differences exist in incidences of kidney graft dysfunction, with male patients displaying better preservation in graft functions. Overall, these differently expressed miRNAs either enhance or suppress host immune responses. They can be predictive markers for graft survival and can also be important factors that lead to worse long term kidney graft function in females when compared to males. MDPI 2022-10-24 /pmc/articles/PMC9656388/ /pubmed/36361623 http://dx.doi.org/10.3390/ijms232112832 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Ko, Sien-Yu
Tsai, Shang-Feng
Hsu, Chia-Tien
Huang, Shih-Ting
Chuang, Ya-Wen
Yu, Tung-Min
Wu, Ming-Ju
Chen, Cheng-Hsu
Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title_full Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title_fullStr Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title_full_unstemmed Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title_short Gender Differences in microRNA Expressions as Related to Long-Term Graft Function in Kidney Transplant Patients
title_sort gender differences in microrna expressions as related to long-term graft function in kidney transplant patients
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9656388/
https://www.ncbi.nlm.nih.gov/pubmed/36361623
http://dx.doi.org/10.3390/ijms232112832
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