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Serum Trypsinogen Levels in Type 1 Diabetes

OBJECTIVE: The pancreas in type 1 diabetes exhibits decreased size (weight/volume) and abnormal exocrine morphology. Serum trypsinogen levels are an established marker of pancreatic exocrine function. As such, we hypothesized that trypsinogen levels may be reduced in patients with pre–type 1 diabete...

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Autores principales: Li, Xia, Campbell-Thompson, Martha, Wasserfall, Clive H., McGrail, Kieran, Posgai, Amanda, Schultz, Andrew R., Brusko, Todd M., Shuster, Jonathan, Liang, Faming, Muir, Andrew, Schatz, Desmond, Haller, Michael J., Atkinson, Mark A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Diabetes Association 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360284/
https://www.ncbi.nlm.nih.gov/pubmed/28115475
http://dx.doi.org/10.2337/dc16-1774
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author Li, Xia
Campbell-Thompson, Martha
Wasserfall, Clive H.
McGrail, Kieran
Posgai, Amanda
Schultz, Andrew R.
Brusko, Todd M.
Shuster, Jonathan
Liang, Faming
Muir, Andrew
Schatz, Desmond
Haller, Michael J.
Atkinson, Mark A.
author_facet Li, Xia
Campbell-Thompson, Martha
Wasserfall, Clive H.
McGrail, Kieran
Posgai, Amanda
Schultz, Andrew R.
Brusko, Todd M.
Shuster, Jonathan
Liang, Faming
Muir, Andrew
Schatz, Desmond
Haller, Michael J.
Atkinson, Mark A.
author_sort Li, Xia
collection PubMed
description OBJECTIVE: The pancreas in type 1 diabetes exhibits decreased size (weight/volume) and abnormal exocrine morphology. Serum trypsinogen levels are an established marker of pancreatic exocrine function. As such, we hypothesized that trypsinogen levels may be reduced in patients with pre–type 1 diabetes and type 1 diabetes compared with healthy control subjects. RESEARCH DESIGN AND METHODS: Serum trypsinogen levels were determined in 100 persons with type 1 diabetes (72 new-onset, 28 established), 99 autoantibody-positive (AAb(+)) subjects at varying levels of risk for developing this disease, 87 AAb-negative (AAb(−)) control subjects, 91 AAb(−) relatives with type 1 diabetes, and 18 patients with type 2 diabetes. RESULTS: Trypsinogen levels increased significantly with age in control subjects (r = 0.71; P < 0.0001) and were significantly lower in patients with new-onset (mean ± SD 14.5 ± 6.1 ng/mL; P < 0.0001) and established type 1 diabetes (16.7 ± 6.9 ng/mL; P < 0.05) versus AAb(−) control subjects (25.3 ± 11.2 ng/mL), AAb(−) relatives (29.3 ± 15.0 ng/mL), AAb(+) subjects (26.5 ± 12.1 ng/mL), and patients with type 2 diabetes (31.5 ± 17.3 ng/mL). Multivariate analysis revealed reduced trypsinogen in multiple-AAb(+) subjects (P < 0.05) and patients with type 1 diabetes (P < 0.0001) compared with AAb(−) subjects (control subjects and relatives combined) and single-AAb(+) (P < 0.01) subjects when considering age and BMI. CONCLUSIONS: These findings further support the interplay between pancreatic endocrine and exocrine dysfunction. Longitudinal studies are warranted to validate trypsinogen as a predictive biomarker of type 1 diabetes progression.
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spelling pubmed-53602842018-04-01 Serum Trypsinogen Levels in Type 1 Diabetes Li, Xia Campbell-Thompson, Martha Wasserfall, Clive H. McGrail, Kieran Posgai, Amanda Schultz, Andrew R. Brusko, Todd M. Shuster, Jonathan Liang, Faming Muir, Andrew Schatz, Desmond Haller, Michael J. Atkinson, Mark A. Diabetes Care Pathophysiology/Complications OBJECTIVE: The pancreas in type 1 diabetes exhibits decreased size (weight/volume) and abnormal exocrine morphology. Serum trypsinogen levels are an established marker of pancreatic exocrine function. As such, we hypothesized that trypsinogen levels may be reduced in patients with pre–type 1 diabetes and type 1 diabetes compared with healthy control subjects. RESEARCH DESIGN AND METHODS: Serum trypsinogen levels were determined in 100 persons with type 1 diabetes (72 new-onset, 28 established), 99 autoantibody-positive (AAb(+)) subjects at varying levels of risk for developing this disease, 87 AAb-negative (AAb(−)) control subjects, 91 AAb(−) relatives with type 1 diabetes, and 18 patients with type 2 diabetes. RESULTS: Trypsinogen levels increased significantly with age in control subjects (r = 0.71; P < 0.0001) and were significantly lower in patients with new-onset (mean ± SD 14.5 ± 6.1 ng/mL; P < 0.0001) and established type 1 diabetes (16.7 ± 6.9 ng/mL; P < 0.05) versus AAb(−) control subjects (25.3 ± 11.2 ng/mL), AAb(−) relatives (29.3 ± 15.0 ng/mL), AAb(+) subjects (26.5 ± 12.1 ng/mL), and patients with type 2 diabetes (31.5 ± 17.3 ng/mL). Multivariate analysis revealed reduced trypsinogen in multiple-AAb(+) subjects (P < 0.05) and patients with type 1 diabetes (P < 0.0001) compared with AAb(−) subjects (control subjects and relatives combined) and single-AAb(+) (P < 0.01) subjects when considering age and BMI. CONCLUSIONS: These findings further support the interplay between pancreatic endocrine and exocrine dysfunction. Longitudinal studies are warranted to validate trypsinogen as a predictive biomarker of type 1 diabetes progression. American Diabetes Association 2017-04 2017-01-23 /pmc/articles/PMC5360284/ /pubmed/28115475 http://dx.doi.org/10.2337/dc16-1774 Text en © 2017 by the American Diabetes Association. http://www.diabetesjournals.org/content/licenseReaders may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.
spellingShingle Pathophysiology/Complications
Li, Xia
Campbell-Thompson, Martha
Wasserfall, Clive H.
McGrail, Kieran
Posgai, Amanda
Schultz, Andrew R.
Brusko, Todd M.
Shuster, Jonathan
Liang, Faming
Muir, Andrew
Schatz, Desmond
Haller, Michael J.
Atkinson, Mark A.
Serum Trypsinogen Levels in Type 1 Diabetes
title Serum Trypsinogen Levels in Type 1 Diabetes
title_full Serum Trypsinogen Levels in Type 1 Diabetes
title_fullStr Serum Trypsinogen Levels in Type 1 Diabetes
title_full_unstemmed Serum Trypsinogen Levels in Type 1 Diabetes
title_short Serum Trypsinogen Levels in Type 1 Diabetes
title_sort serum trypsinogen levels in type 1 diabetes
topic Pathophysiology/Complications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360284/
https://www.ncbi.nlm.nih.gov/pubmed/28115475
http://dx.doi.org/10.2337/dc16-1774
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