Cargando…
Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation
Over half of patients with type 2 diabetes (T2D) are unable to achieve blood glucose targets despite therapeutic compliance, significantly increasing their risk of long-term complications. Discovering ways to identify and properly treat these individuals is a critical problem in the field. The arach...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783643/ https://www.ncbi.nlm.nih.gov/pubmed/36557272 http://dx.doi.org/10.3390/metabo12121234 |
_version_ | 1784857626139426816 |
---|---|
author | Fenske, Rachel J. Weeks, Alicia M. Daniels, Michael Nall, Randall Pabich, Samantha Brill, Allison L. Peter, Darby C. Punt, Margaret Cox, Elizabeth D. Davis, Dawn Belt Kimple, Michelle E. |
author_facet | Fenske, Rachel J. Weeks, Alicia M. Daniels, Michael Nall, Randall Pabich, Samantha Brill, Allison L. Peter, Darby C. Punt, Margaret Cox, Elizabeth D. Davis, Dawn Belt Kimple, Michelle E. |
author_sort | Fenske, Rachel J. |
collection | PubMed |
description | Over half of patients with type 2 diabetes (T2D) are unable to achieve blood glucose targets despite therapeutic compliance, significantly increasing their risk of long-term complications. Discovering ways to identify and properly treat these individuals is a critical problem in the field. The arachidonic acid metabolite, prostaglandin E(2) (PGE(2)), has shown great promise as a biomarker of β-cell dysfunction in T2D. PGE(2) synthesis, secretion, and downstream signaling are all upregulated in pancreatic islets isolated from T2D mice and human organ donors. In these islets, preventing β-cell PGE(2) signaling via a prostaglandin EP3 receptor antagonist significantly improves their glucose-stimulated and hormone-potentiated insulin secretion response. In this clinical cohort study, 167 participants, 35 non-diabetic, and 132 with T2D, were recruited from the University of Wisconsin Hospital and Clinics. At enrollment, a standard set of demographic, biometric, and clinical measurements were performed to quantify obesity status and glucose control. C reactive protein was measured to exclude acute inflammation/illness, and white cell count (WBC), erythrocyte sedimentation rate (ESR), and fasting triglycerides were used as markers of systemic inflammation. Finally, a plasma sample for research was used to determine circulating PGE(2) metabolite (PGEM) levels. At baseline, PGEM levels were not correlated with WBC and triglycerides, only weakly correlated with ESR, and were the strongest predictor of T2D disease status. One year after enrollment, blood glucose management was assessed by chart review, with a clinically-relevant change in hemoglobin A1c (HbA1c) defined as ≥0.5%. PGEM levels were strongly predictive of therapeutic response, independent of age, obesity, glucose control, and systemic inflammation at enrollment. Our results provide strong support for future research in this area. |
format | Online Article Text |
id | pubmed-9783643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97836432022-12-24 Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation Fenske, Rachel J. Weeks, Alicia M. Daniels, Michael Nall, Randall Pabich, Samantha Brill, Allison L. Peter, Darby C. Punt, Margaret Cox, Elizabeth D. Davis, Dawn Belt Kimple, Michelle E. Metabolites Article Over half of patients with type 2 diabetes (T2D) are unable to achieve blood glucose targets despite therapeutic compliance, significantly increasing their risk of long-term complications. Discovering ways to identify and properly treat these individuals is a critical problem in the field. The arachidonic acid metabolite, prostaglandin E(2) (PGE(2)), has shown great promise as a biomarker of β-cell dysfunction in T2D. PGE(2) synthesis, secretion, and downstream signaling are all upregulated in pancreatic islets isolated from T2D mice and human organ donors. In these islets, preventing β-cell PGE(2) signaling via a prostaglandin EP3 receptor antagonist significantly improves their glucose-stimulated and hormone-potentiated insulin secretion response. In this clinical cohort study, 167 participants, 35 non-diabetic, and 132 with T2D, were recruited from the University of Wisconsin Hospital and Clinics. At enrollment, a standard set of demographic, biometric, and clinical measurements were performed to quantify obesity status and glucose control. C reactive protein was measured to exclude acute inflammation/illness, and white cell count (WBC), erythrocyte sedimentation rate (ESR), and fasting triglycerides were used as markers of systemic inflammation. Finally, a plasma sample for research was used to determine circulating PGE(2) metabolite (PGEM) levels. At baseline, PGEM levels were not correlated with WBC and triglycerides, only weakly correlated with ESR, and were the strongest predictor of T2D disease status. One year after enrollment, blood glucose management was assessed by chart review, with a clinically-relevant change in hemoglobin A1c (HbA1c) defined as ≥0.5%. PGEM levels were strongly predictive of therapeutic response, independent of age, obesity, glucose control, and systemic inflammation at enrollment. Our results provide strong support for future research in this area. MDPI 2022-12-08 /pmc/articles/PMC9783643/ /pubmed/36557272 http://dx.doi.org/10.3390/metabo12121234 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 | Article Fenske, Rachel J. Weeks, Alicia M. Daniels, Michael Nall, Randall Pabich, Samantha Brill, Allison L. Peter, Darby C. Punt, Margaret Cox, Elizabeth D. Davis, Dawn Belt Kimple, Michelle E. Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title | Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title_full | Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title_fullStr | Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title_full_unstemmed | Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title_short | Plasma Prostaglandin E(2) Metabolite Levels Predict Type 2 Diabetes Status and One-Year Therapeutic Response Independent of Clinical Markers of Inflammation |
title_sort | plasma prostaglandin e(2) metabolite levels predict type 2 diabetes status and one-year therapeutic response independent of clinical markers of inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9783643/ https://www.ncbi.nlm.nih.gov/pubmed/36557272 http://dx.doi.org/10.3390/metabo12121234 |
work_keys_str_mv | AT fenskerachelj plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT weeksaliciam plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT danielsmichael plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT nallrandall plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT pabichsamantha plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT brillallisonl plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT peterdarbyc plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT puntmargaret plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT coxelizabethd plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT davisdawnbelt plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation AT kimplemichellee plasmaprostaglandine2metabolitelevelspredicttype2diabetesstatusandoneyeartherapeuticresponseindependentofclinicalmarkersofinflammation |