Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/107463
DC Field | Value | Language |
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dc.contributor | School of Optometry | - |
dc.creator | Yang, S | - |
dc.creator | Zhu, Z | - |
dc.creator | Chen, S | - |
dc.creator | Yuan, Y | - |
dc.creator | He, M | - |
dc.creator | Wang, W | - |
dc.date.accessioned | 2024-06-25T04:31:08Z | - |
dc.date.available | 2024-06-25T04:31:08Z | - |
dc.identifier.uri | http://hdl.handle.net/10397/107463 | - |
dc.language.iso | en | en_US |
dc.publisher | Nature Publishing Group | en_US |
dc.rights | © The Author(s) 2023 | en_US |
dc.rights | 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. | en_US |
dc.rights | The following publication Yang, S., Zhu, Z., Chen, S. et al. Metabolic fingerprinting on retinal pigment epithelium thickness for individualized risk stratification of type 2 diabetes mellitus. Nat Commun 14, 6573 (2023) is available at https://doi.org/10.1038/s41467-023-42404-1. | en_US |
dc.title | Metabolic fingerprinting on retinal pigment epithelium thickness for individualized risk stratification of type 2 diabetes mellitus | en_US |
dc.type | Journal/Magazine Article | en_US |
dc.identifier.volume | 14 | - |
dc.identifier.doi | 10.1038/s41467-023-42404-1 | - |
dcterms.abstract | The retina is an important target organ of diabetes mellitus, with increasing evidence from patients and animal models suggesting that retinal pigment epithelium (RPE) may serve as an early marker for diabetes-related damages. However, their longitudinal relationship and the biological underpinnings remain less well understood. Here, we demonstrate that reduced in vivo measurements of RPE thickness (RPET) represents a significant risk factor for future type 2 diabetes mellitus (T2DM) and its microvascular phenotypes. After performing systematic analyses of circulating plasma metabolites using two complementary approaches, we identify a wide range of RPET metabolic fingerprints that are independently associated with reduced RPET. These fingerprints hold their potential to improve predictability and clinical utility for stratifying future T2DM and related microvascular phenotypes beyond traditional clinical indicators, providing insights into the promising role of retinas as a window to systemic health. | - |
dcterms.accessRights | open access | en_US |
dcterms.bibliographicCitation | Nature communications, 2023, v. 14, 6573 | - |
dcterms.isPartOf | Nature communications | - |
dcterms.issued | 2023 | - |
dc.identifier.scopus | 2-s2.0-85174455400 | - |
dc.identifier.eissn | 2041-1723 | - |
dc.identifier.artn | 6573 | - |
dc.description.validate | 202406 bcch | - |
dc.description.oa | Version of Record | en_US |
dc.identifier.FolderNumber | a2877a | en_US |
dc.identifier.SubFormID | 48619 | en_US |
dc.description.fundingSource | Others | en_US |
dc.description.fundingText | Hainan Province Clinical Medical Center; National Natural Science Foundation of China; Natural Science Foundation of Guangdong Province; Global STEM Professorship Scheme | en_US |
dc.description.pubStatus | Published | en_US |
dc.description.oaCategory | CC | en_US |
Appears in Collections: | Journal/Magazine Article |
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File | Description | Size | Format | |
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48619_s41467-023-42404-1.pdf | 2.23 MB | Adobe PDF | View/Open |
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