A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes
Clinical parameters used in type 2 diabetes mellitus (T2D) diagnosis and monitoring such as glycosylated haemoglobin (HbA1c) are often unable to capture important information related to diabetic control and chronic complications. In order to search for additional biomarkers, we performed a pilot stu...
| Autores: | , , , , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:252632 |
| Acceso en línea: | https://ddd.uab.cat/record/252632 https://dx.doi.org/urn:doi:10.3390/jcm9061619 |
| Access Level: | acceso abierto |
| Palabra clave: | Erythrocytes Type 2 diabetes mellitus NMR Metabolomics Biomarker |
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A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 DiabetesPalomino-Schätzlein, MartinaLamas-Domingo, RubénCiudin, Andreea|||0000-0001-5622-0203Gutiérrez-Carcedo, Patricia|||0000-0001-8903-2380Marés, Roso|||0000-0002-7339-0172Aparicio-Gómez, Carolina|||0000-0002-0845-2365Hernández, Cristina|||0000-0002-3109-1721Simó Canonge, Rafael|||0000-0003-0475-3096Herance, José Raul|||0000-0001-7178-3290ErythrocytesType 2 diabetes mellitusNMRMetabolomicsBiomarkerClinical parameters used in type 2 diabetes mellitus (T2D) diagnosis and monitoring such as glycosylated haemoglobin (HbA1c) are often unable to capture important information related to diabetic control and chronic complications. In order to search for additional biomarkers, we performed a pilot study comparing T2D patients with healthy controls matched by age, gender, and weight. By using 1 H-nuclear magnetic resonance (NMR) based metabolomics profiling of red blood cells (RBCs), we found that the metabolic signature of RBCs in T2D subjects differed significantly from non-diabetic controls. Affected metabolites included glutathione, 2,3-bisphophoglycerate, inosinic acid, lactate, 6-phosphogluconate, creatine and adenosine triphosphate (ATP) and several amino acids such as leucine, glycine, alanine, lysine, aspartate, phenylalanine and tyrosine. These results were validated by an independent cohort of T2D and control patients. An analysis of the pathways in which these metabolites were involved showed that energetic and redox metabolism in RBCs were altered in T2D, as well as metabolites transported by RBCs. Taken together, our results revealed that the metabolic profile of RBCs can discriminate healthy controls from T2D patients. Further research is needed to determine whether metabolic fingerprint in RBC could be useful to complement the information obtained from HbA1c and glycemic variability as well as its potential role in the diabetes managementUniversitat Autònoma de Barcelona 22020-01-0120202020-01-01Articlehttp://purl.org/coar/resource_type/c_6501VoRhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleapplication/pdfhttps://ddd.uab.cat/record/252632https://dx.doi.org/urn:doi:10.3390/jcm9061619reponame:Dipòsit Digital de Documents de la UABinstname:Universitat Autònoma de BarcelonaInglésengInstituto de Salud Carlos III https://doi.org/10.13039/501100004587 PI16/0206Agència de Gestió d'Ajuts Universitaris i de Recerca https://doi.org/10.13039/501100003030 2017/SGR-130open accesshttp://purl.org/coar/access_right/c_abf2Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessoai:ddd.uab.cat:2526322026-06-06T12:50:31Z |
| dc.title.none.fl_str_mv |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| title |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| spellingShingle |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes Palomino-Schätzlein, Martina Erythrocytes Type 2 diabetes mellitus NMR Metabolomics Biomarker |
| title_short |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| title_full |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| title_fullStr |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| title_full_unstemmed |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| title_sort |
A Translational In Vivo and In Vitro Metabolomic Study Reveals Altered Metabolic Pathways in Red Blood Cells of Type 2 Diabetes |
| dc.creator.none.fl_str_mv |
Palomino-Schätzlein, Martina Lamas-Domingo, Rubén Ciudin, Andreea|||0000-0001-5622-0203 Gutiérrez-Carcedo, Patricia|||0000-0001-8903-2380 Marés, Roso|||0000-0002-7339-0172 Aparicio-Gómez, Carolina|||0000-0002-0845-2365 Hernández, Cristina|||0000-0002-3109-1721 Simó Canonge, Rafael|||0000-0003-0475-3096 Herance, José Raul|||0000-0001-7178-3290 |
| author |
Palomino-Schätzlein, Martina |
| author_facet |
Palomino-Schätzlein, Martina Lamas-Domingo, Rubén Ciudin, Andreea|||0000-0001-5622-0203 Gutiérrez-Carcedo, Patricia|||0000-0001-8903-2380 Marés, Roso|||0000-0002-7339-0172 Aparicio-Gómez, Carolina|||0000-0002-0845-2365 Hernández, Cristina|||0000-0002-3109-1721 Simó Canonge, Rafael|||0000-0003-0475-3096 Herance, José Raul|||0000-0001-7178-3290 |
| author_role |
author |
| author2 |
Lamas-Domingo, Rubén Ciudin, Andreea|||0000-0001-5622-0203 Gutiérrez-Carcedo, Patricia|||0000-0001-8903-2380 Marés, Roso|||0000-0002-7339-0172 Aparicio-Gómez, Carolina|||0000-0002-0845-2365 Hernández, Cristina|||0000-0002-3109-1721 Simó Canonge, Rafael|||0000-0003-0475-3096 Herance, José Raul|||0000-0001-7178-3290 |
| author2_role |
author author author author author author author author |
| dc.contributor.none.fl_str_mv |
Universitat Autònoma de Barcelona |
| dc.subject.none.fl_str_mv |
Erythrocytes Type 2 diabetes mellitus NMR Metabolomics Biomarker |
| topic |
Erythrocytes Type 2 diabetes mellitus NMR Metabolomics Biomarker |
| description |
Clinical parameters used in type 2 diabetes mellitus (T2D) diagnosis and monitoring such as glycosylated haemoglobin (HbA1c) are often unable to capture important information related to diabetic control and chronic complications. In order to search for additional biomarkers, we performed a pilot study comparing T2D patients with healthy controls matched by age, gender, and weight. By using 1 H-nuclear magnetic resonance (NMR) based metabolomics profiling of red blood cells (RBCs), we found that the metabolic signature of RBCs in T2D subjects differed significantly from non-diabetic controls. Affected metabolites included glutathione, 2,3-bisphophoglycerate, inosinic acid, lactate, 6-phosphogluconate, creatine and adenosine triphosphate (ATP) and several amino acids such as leucine, glycine, alanine, lysine, aspartate, phenylalanine and tyrosine. These results were validated by an independent cohort of T2D and control patients. An analysis of the pathways in which these metabolites were involved showed that energetic and redox metabolism in RBCs were altered in T2D, as well as metabolites transported by RBCs. Taken together, our results revealed that the metabolic profile of RBCs can discriminate healthy controls from T2D patients. Further research is needed to determine whether metabolic fingerprint in RBC could be useful to complement the information obtained from HbA1c and glycemic variability as well as its potential role in the diabetes management |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2 2020-01-01 2020 2020-01-01 |
| dc.type.none.fl_str_mv |
Article http://purl.org/coar/resource_type/c_6501 VoR http://purl.org/coar/version/c_970fb48d4fbd8a85 |
| dc.type.openaire.fl_str_mv |
info:eu-repo/semantics/article |
| format |
article |
| dc.identifier.none.fl_str_mv |
https://ddd.uab.cat/record/252632 https://dx.doi.org/urn:doi:10.3390/jcm9061619 |
| url |
https://ddd.uab.cat/record/252632 https://dx.doi.org/urn:doi:10.3390/jcm9061619 |
| dc.language.none.fl_str_mv |
Inglés eng |
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Inglés |
| language |
eng |
| dc.relation.none.fl_str_mv |
Instituto de Salud Carlos III https://doi.org/10.13039/501100004587 PI16/0206 Agència de Gestió d'Ajuts Universitaris i de Recerca https://doi.org/10.13039/501100003030 2017/SGR-130 |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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info:eu-repo/semantics/openAccess |
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open access http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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openAccess |
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application/pdf |
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