Serum Trypsinogen Levels in Type 1 Diabetes

Author:

Li Xia12,Campbell-Thompson Martha2,Wasserfall Clive H.2,McGrail Kieran2,Posgai Amanda2,Schultz Andrew R.2,Brusko Todd M.2,Shuster Jonathan3,Liang Faming4,Muir Andrew5,Schatz Desmond6,Haller Michael J.6,Atkinson Mark A.26

Affiliation:

1. Institute of Metabolism and Endocrinology, The Second Xiangya Hospital and the Diabetes Center, Metabolic Syndrome Research Center, Central South University, National Clinical Research Center for Metabolic Diseases, Changsha, China

2. Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL

3. Department of Health Outcomes and Policy, University of Florida, Gainesville, FL

4. Department of Biostatistics, University of Florida, Gainesville, FL

5. Department of Pediatrics, Emory University, Atlanta, GA

6. Department of Pediatrics, University of Florida, Gainesville, FL

Abstract

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.

Funder

National Institutes of Health

National Institute of Diabetes and Digestive and Kidney Disease

s

JDRF

American Diabetes Association

Jeffrey Keene Family Professorship

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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