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Proteomics in gastroparesis: unique and overlapping protein signatures in diabetic and idiopathic gastroparesis AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY Grover, M., Dasari, S., Bernard, C. E., Chikkamenahalli, L. L., Yates, K. P., Pasricha, P. J., Sarosiek, I., McCallum, R., Koch, K. L., Abell, T. L., Kuo, B., Shulman, R. J., Gibbons, S. J., McKenzie, T. J., Kellogg, T. A., Kendrick, M. L., Tonascia, J., Hamilton, F. A., Parkman, H. P., Farrugia, G., Shulman, R., Chumpitazi, B., Bouette, C., Charron, H., Islam, N., Williams, K., Nurko, S., Varni, J., Pasricha, P., Barat, R., Chen, J., Hernandez, G., Burns, R., McKnight, M., Kuo, B., Mendez, A., Steller, K., Thurler, A., Parkman, H., Mauer, A., Malik, Z., Orthey, P., Palit, A., McCallum, R. W., Connery, S., Ramirez, M., Vega, N., Sigaroodi, S., Abell, T., Stocker, A., Cannon, B., Nowotny, L., Walls, T., Koch, K., Baxter, L., Brown, A., Stuart, P., Abdullah, A., Snape, W., DeVole, N., Earle, K., Kirkeby, K., Lee, C., Lin, M., Troyer, D., von Bakonyi, A., Calles-Escandon, J., Nguyen, L., Adler, E., Orlando, C., Hasler, W., Herman, W., Kraftson, A., Rothberg, A. E., Wootten, S., Belt, P., Donithan, M., Lee, L., Miriel, L., Sharkey, E., Sternberg, A., Van Natta, M., Wilson, L., Yamada, G., Yates, K., Bernard, C., Serrano, J., Hamilton, F., Hall, S., James, S., Torrance, R., NIDDK Gastroparesis Clinical Res C 2019; 317 (5): G716–G726

Abstract

Macrophage-based immune dysregulation plays a critical role in development of delayed gastric emptying in diabetic mice. Loss of anti-inflammatory macrophages and increased expression of genes associated with pro-inflammatory macrophages has been reported in full-thickness gastric biopsies from gastroparesis patients. We aimed to determine broader protein expression (proteomics) and protein-based signaling pathways in gastric biopsies of diabetic (DG) and idiopathic gastroparesis (IG) patients. Additionally, we determined correlations between protein expressions, gastric emptying, and symptoms. Full-thickness gastric antrum biopsies were obtained from nine DG patients, seven IG patients, and five nondiabetic controls. Aptamer-based SomaLogic tissue scan that quantitatively identifies 1,305 human proteins was used. Protein fold changes were computed, and differential expressions were calculated using Limma. Ingenuity pathway analysis and correlations were carried out. Multiple-testing corrected P < 0.05 was considered statistically significant. Seventy-three proteins were differentially expressed in DG, 132 proteins were differentially expressed in IG, and 40 proteins were common to DG and IG. In both DG and IG, "Role of Macrophages, Fibroblasts and Endothelial Cells" was the most statistically significant altered pathway [DG false discovery rate (FDR) = 7.9 × 10-9; IG FDR = 6.3 × 10-12]. In DG, properdin expression correlated with GCSI bloating (r = -0.99, FDR = 0.02) and expressions of prostaglandin G/H synthase 2, protein kinase C-? type, and complement C2 correlated with 4 h gastric retention (r = -0.97, FDR = 0.03 for all). No correlations were found between proteins and symptoms or gastric emptying in IG. Protein expression changes suggest a central role of macrophage-driven immune dysregulation in gastroparesis, specifically, complement activation in diabetic gastroparesis.NEW & NOTEWORTHY This study uses SOMAscan, a novel proteomics assay for determination of altered proteins and associated molecular pathways in human gastroparesis. Seventy-three proteins were changed in diabetic gastroparesis, 132 in idiopathic gastroparesis compared with controls. Forty proteins were common in both. Macrophage-based immune dysregulation pathway was most significantly affected in both diabetic and idiopathic gastroparesis. Proteins involved in the complement and prostaglandin synthesis pathway were associated with symptoms and gastric emptying delay in diabetic gastroparesis.

View details for DOI 10.1152/ajpgi.00115.2019

View details for Web of Science ID 000498403600016

View details for PubMedID 31482734

View details for PubMedCentralID PMC6879892