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Association of Protein Z with Prediabetes and Type 2 Diabetes
BACKGROUND: Type 2 diabetes mellitus (T2DM) is a progressive metabolic disease. Early detection of prediabetes is important to reduce the risk of T2DM. Some cytokines are known to be associated with T2DM. Therefore, we aimed to identify cytokines as novel biomarkers of glucose dysmetabolism. METHODS...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Endocrine Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258334/ https://www.ncbi.nlm.nih.gov/pubmed/34074095 http://dx.doi.org/10.3803/EnM.2021.962 |
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author | Bae, Yun-Ui You, Ji Hong Cho, Nan Hee Kim, Leah Eunjung Shim, Hye Min Park, Jae-Hyung Cho, Ho Chan |
author_facet | Bae, Yun-Ui You, Ji Hong Cho, Nan Hee Kim, Leah Eunjung Shim, Hye Min Park, Jae-Hyung Cho, Ho Chan |
author_sort | Bae, Yun-Ui |
collection | PubMed |
description | BACKGROUND: Type 2 diabetes mellitus (T2DM) is a progressive metabolic disease. Early detection of prediabetes is important to reduce the risk of T2DM. Some cytokines are known to be associated with T2DM. Therefore, we aimed to identify cytokines as novel biomarkers of glucose dysmetabolism. METHODS: The first stage of the study included 43 subjects (13 subjects with newly diagnosed T2DM, 13 with prediabetes, and 16 with normoglycemia) for cytokine microarray analysis. Blood samples of the subjects were assessed for 310 cytokines to identify potential indicators of prediabetes. The second stage included 142 subjects (36 subjects with T2DM, 35 with prediabetes, and 71 with normoglycemia) to validate the potential cytokines associated with prediabetes. RESULTS: We identified 41 cytokines that differed by 1.5-fold or more in at least one out of the three comparisons (normoglycemia vs. prediabetes, normoglycemia vs. T2DM, and prediabetes vs. T2DM) among 310 cytokines. Finally, we selected protein Z (PROZ) and validated this finding to determine its association with prediabetes. Plasma PROZ levels were found to be decreased in patients with prediabetes (1,490.32±367.19 pg/mL) and T2DM (1,583.34±465.43 pg/mL) compared to those in subjects with normoglycemia (1,864.07±450.83 pg/mL) (P<0.001). There were significantly negative correlations between PROZ and fasting plasma glucose (P=0.001) and hemoglobin A1c (P=0.010). CONCLUSION: PROZ levels were associated with prediabetes and T2DM. We suggest that PROZ may be a promising biomarker for the early detection of prediabetes. Further large-scale studies are needed to evaluate the relationship and mechanism between PROZ and prediabetes and T2DM. |
format | Online Article Text |
id | pubmed-8258334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Korean Endocrine Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82583342021-07-19 Association of Protein Z with Prediabetes and Type 2 Diabetes Bae, Yun-Ui You, Ji Hong Cho, Nan Hee Kim, Leah Eunjung Shim, Hye Min Park, Jae-Hyung Cho, Ho Chan Endocrinol Metab (Seoul) Original Article BACKGROUND: Type 2 diabetes mellitus (T2DM) is a progressive metabolic disease. Early detection of prediabetes is important to reduce the risk of T2DM. Some cytokines are known to be associated with T2DM. Therefore, we aimed to identify cytokines as novel biomarkers of glucose dysmetabolism. METHODS: The first stage of the study included 43 subjects (13 subjects with newly diagnosed T2DM, 13 with prediabetes, and 16 with normoglycemia) for cytokine microarray analysis. Blood samples of the subjects were assessed for 310 cytokines to identify potential indicators of prediabetes. The second stage included 142 subjects (36 subjects with T2DM, 35 with prediabetes, and 71 with normoglycemia) to validate the potential cytokines associated with prediabetes. RESULTS: We identified 41 cytokines that differed by 1.5-fold or more in at least one out of the three comparisons (normoglycemia vs. prediabetes, normoglycemia vs. T2DM, and prediabetes vs. T2DM) among 310 cytokines. Finally, we selected protein Z (PROZ) and validated this finding to determine its association with prediabetes. Plasma PROZ levels were found to be decreased in patients with prediabetes (1,490.32±367.19 pg/mL) and T2DM (1,583.34±465.43 pg/mL) compared to those in subjects with normoglycemia (1,864.07±450.83 pg/mL) (P<0.001). There were significantly negative correlations between PROZ and fasting plasma glucose (P=0.001) and hemoglobin A1c (P=0.010). CONCLUSION: PROZ levels were associated with prediabetes and T2DM. We suggest that PROZ may be a promising biomarker for the early detection of prediabetes. Further large-scale studies are needed to evaluate the relationship and mechanism between PROZ and prediabetes and T2DM. Korean Endocrine Society 2021-06 2021-06-02 /pmc/articles/PMC8258334/ /pubmed/34074095 http://dx.doi.org/10.3803/EnM.2021.962 Text en Copyright © 2021 Korean Endocrine Society https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bae, Yun-Ui You, Ji Hong Cho, Nan Hee Kim, Leah Eunjung Shim, Hye Min Park, Jae-Hyung Cho, Ho Chan Association of Protein Z with Prediabetes and Type 2 Diabetes |
title | Association of Protein Z with Prediabetes and Type 2 Diabetes |
title_full | Association of Protein Z with Prediabetes and Type 2 Diabetes |
title_fullStr | Association of Protein Z with Prediabetes and Type 2 Diabetes |
title_full_unstemmed | Association of Protein Z with Prediabetes and Type 2 Diabetes |
title_short | Association of Protein Z with Prediabetes and Type 2 Diabetes |
title_sort | association of protein z with prediabetes and type 2 diabetes |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8258334/ https://www.ncbi.nlm.nih.gov/pubmed/34074095 http://dx.doi.org/10.3803/EnM.2021.962 |
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