Urine Proteomics Reveals Sex-Specific Response to Total Pancreatectomy With Islet Autotransplantation

被引:1
作者
Bennike, Tue Bjerg [1 ,2 ,3 ]
Templeton, Kate [4 ]
Fujimura, Kimino [2 ,5 ]
Bellin, Melena D. [6 ,7 ,8 ]
Ahmed, Saima [1 ,2 ]
Schlaffner, Christoph N. [1 ,2 ,5 ,9 ,10 ]
Arora, Rohit [2 ,11 ]
Cruz-Monserrate, Zobeida [12 ]
Arnaout, Ramy [2 ,11 ]
Beilman, Gregory J. [8 ]
Grover, Amit S. [4 ,13 ]
Conwell, Darwin L. [12 ]
Steen, Hanno [1 ,2 ]
机构
[1] Boston Childrens Hosp, Dept Pathol, 300 Longwood Ave, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Aalborg Univ, Dept Hlth Sci & Technol, Aalborg, Denmark
[4] Boston Childrens Hosp, Div Gastroenterol Hepatol & Nutr, Boston, MA USA
[5] Boston Childrens Hosp, FM Kirby Neurobiol Ctr, Boston, MA 02115 USA
[6] Univ Minnesota, Med Ctr, Dept Pediat, Minneapolis, MN 55455 USA
[7] Masonic Childrens Hosp, Minneapolis, MN 55455 USA
[8] Univ Minnesota, Sch Med, Dept Surg, Minneapolis, MN 55455 USA
[9] Hasso Plattner Inst Digital Engn, Data Analyt & Computat Stat, Potsdam, Germany
[10] Univ Potsdam, Digital Engn Fac, Potsdam, Germany
[11] Beth Israel Deaconess Med Ctr, Dept Pathol, 330 Brookline Ave, Boston, MA 02215 USA
[12] Ohio State Univ, Comprehens Canc Ctr, Div Gastroenterol Hepatol & Nutr, Wexner Med Ctr, Columbus, OH 43210 USA
[13] Harvard Med Sch, Dept Pediat, Boston, MA 02115 USA
基金
日本学术振兴会;
关键词
TPIAT; pancreatectomy; diabetes; autoislet; pancreatitis; nephropathy; CHRONIC-PANCREATITIS; COMPREHENSIVE ANALYSIS; RENAL-DISEASE; RISK-FACTORS; BIOMARKERS; DIAGNOSIS; ETIOLOGY; STAGE;
D O I
10.1097/MPA.0000000000002063
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives Total pancreatectomy with islet autotransplantation (TPIAT) is a surgical option for refractory chronic pancreatitis-related pain. Despite the known clinical implications of TPIAT, the molecular effects remain poorly investigated. We performed the first hypothesis-generating study of the urinary proteome before and after TPIAT. Methods Twenty-two patients eligible for TPIAT were prospectively enrolled. Urine samples were collected the week before and 12 to 18 months after TPIAT. The urine samples were prepared for bottom-up label-free quantitative proteomics using the "MStern" protocol. Results Using 17 paired samples, we identified 2477 urinary proteins, of which 301 were significantly changed post-TPIAT versus pre-TPIAT. Our quantitative analysis revealed that the molecular response to TPIAT was highly sex-specific, with pronounced sex differences pre-TPIAT but minimal differences afterward. Comparing post-TPIAT versus pre-TPIAT, we found changes in cell-cell adhesion, intracellular vacuoles, and immune response proteins. After surgery, immunoglobulins, complement proteins, and cathepsins were increased, findings that may reflect glomerular damage. Finally, we identified both known and novel markers for immunoglobulin A nephropathy after 1 patient developed the disease 2 years after TPIAT. Conclusions We found distinct changes in the urinary proteomic profile after TPIAT and the response to TPIAT is highly sex-specific.
引用
收藏
页码:435 / 444
页数:10
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