Cargando…
Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism?
BACKGROUND: Diabetic cardiovascular autonomic neuropathy (CAN) and distal symmetrical polyneuropathy (DSPN) are severe diabetic complications. Collagen type VI (COL6) and III (COL3) have been associated with nerve function. We investigated if markers of COL6 formation (PRO-C6) and COL3 degradation (...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311721/ https://www.ncbi.nlm.nih.gov/pubmed/37386485 http://dx.doi.org/10.1186/s12933-023-01891-8 |
_version_ | 1785066799405989888 |
---|---|
author | Hansen, Christian S. Rasmussen, Daniel G. K. Hansen, Tine W. Nielsen, Signe Holm Theilade, Simone Karsdal, Morten A. Genovese, Federica Rossing, Peter |
author_facet | Hansen, Christian S. Rasmussen, Daniel G. K. Hansen, Tine W. Nielsen, Signe Holm Theilade, Simone Karsdal, Morten A. Genovese, Federica Rossing, Peter |
author_sort | Hansen, Christian S. |
collection | PubMed |
description | BACKGROUND: Diabetic cardiovascular autonomic neuropathy (CAN) and distal symmetrical polyneuropathy (DSPN) are severe diabetic complications. Collagen type VI (COL6) and III (COL3) have been associated with nerve function. We investigated if markers of COL6 formation (PRO-C6) and COL3 degradation (C3M) were associated with neuropathy in people with type 1 diabetes (T1D). METHODS: In a cross-sectional study including 300 people with T1D, serum and urine PRO-C6 and C3M were obtained. CAN was assessed by cardiovascular reflex tests: heart rate response to deep breathing (E/I ratio), to standing (30/15 ratio) and to the Valsalva maneuver (VM). Two or three pathological CARTs constituted CAN. DSPN was assessed by biothesiometry. Symmetrical vibration sensation threshold above 25 V constituted DSPN. RESULTS: Participants were (mean (SD)) 55.7 (9.3) years, 51% were males, diabetes duration was 40.0 (8.9) years, HbA(1c) was 63 (11 mmol/mol, (median (IQR)) serum PRO-C6 was 7.8 (6.2;11.0) ng/ml and C3M 8.3 (7.1;10.0) ng/ml. CAN and DSPN were diagnosed in 34% and 43% of participants, respectively. In models adjusted for relevant confounders a doubling of serum PRO-C6, was significantly associated with odds ratio > 2 for CAN and > 1 for DSPN, respectively. Significance was retained after additional adjustments for eGFR only for CAN. Higher serum C3M was associated with presence of CAN, but not after adjustment for eGFR. C3M was not associated with DSPN. Urine PRO-C6 analyses indicated similar associations. CONCLUSIONS: Results show previously undescribed associations between markers of collagen turnover and risk of CAN and to a lesser degree DSPN in T1D. |
format | Online Article Text |
id | pubmed-10311721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-103117212023-07-01 Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? Hansen, Christian S. Rasmussen, Daniel G. K. Hansen, Tine W. Nielsen, Signe Holm Theilade, Simone Karsdal, Morten A. Genovese, Federica Rossing, Peter Cardiovasc Diabetol Research BACKGROUND: Diabetic cardiovascular autonomic neuropathy (CAN) and distal symmetrical polyneuropathy (DSPN) are severe diabetic complications. Collagen type VI (COL6) and III (COL3) have been associated with nerve function. We investigated if markers of COL6 formation (PRO-C6) and COL3 degradation (C3M) were associated with neuropathy in people with type 1 diabetes (T1D). METHODS: In a cross-sectional study including 300 people with T1D, serum and urine PRO-C6 and C3M were obtained. CAN was assessed by cardiovascular reflex tests: heart rate response to deep breathing (E/I ratio), to standing (30/15 ratio) and to the Valsalva maneuver (VM). Two or three pathological CARTs constituted CAN. DSPN was assessed by biothesiometry. Symmetrical vibration sensation threshold above 25 V constituted DSPN. RESULTS: Participants were (mean (SD)) 55.7 (9.3) years, 51% were males, diabetes duration was 40.0 (8.9) years, HbA(1c) was 63 (11 mmol/mol, (median (IQR)) serum PRO-C6 was 7.8 (6.2;11.0) ng/ml and C3M 8.3 (7.1;10.0) ng/ml. CAN and DSPN were diagnosed in 34% and 43% of participants, respectively. In models adjusted for relevant confounders a doubling of serum PRO-C6, was significantly associated with odds ratio > 2 for CAN and > 1 for DSPN, respectively. Significance was retained after additional adjustments for eGFR only for CAN. Higher serum C3M was associated with presence of CAN, but not after adjustment for eGFR. C3M was not associated with DSPN. Urine PRO-C6 analyses indicated similar associations. CONCLUSIONS: Results show previously undescribed associations between markers of collagen turnover and risk of CAN and to a lesser degree DSPN in T1D. BioMed Central 2023-06-29 /pmc/articles/PMC10311721/ /pubmed/37386485 http://dx.doi.org/10.1186/s12933-023-01891-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hansen, Christian S. Rasmussen, Daniel G. K. Hansen, Tine W. Nielsen, Signe Holm Theilade, Simone Karsdal, Morten A. Genovese, Federica Rossing, Peter Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title | Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title_full | Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title_fullStr | Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title_full_unstemmed | Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title_short | Collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
title_sort | collagen turnover is associated with cardiovascular autonomic and peripheral neuropathy in type 1 diabetes: novel pathophysiological mechanism? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10311721/ https://www.ncbi.nlm.nih.gov/pubmed/37386485 http://dx.doi.org/10.1186/s12933-023-01891-8 |
work_keys_str_mv | AT hansenchristians collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT rasmussendanielgk collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT hansentinew collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT nielsensigneholm collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT theiladesimone collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT karsdalmortena collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT genovesefederica collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism AT rossingpeter collagenturnoverisassociatedwithcardiovascularautonomicandperipheralneuropathyintype1diabetesnovelpathophysiologicalmechanism |