Single-donor islet transplantation in type 1 diabetes: patient selection and special considerations

被引:9
|
作者
Tatum, Jacob A. [1 ]
Meneveau, Max O. [1 ]
Brayman, Kenneth L. [1 ]
机构
[1] Univ Virginia Hlth Syst, Dept Surg, Div Transplantat, Charlottesville, VA USA
来源
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY | 2017年 / 10卷
关键词
islet transplantation; diabetes mellitus type 1; brittle diabetes; single donor; patient; INSULIN INDEPENDENCE; HEPATIC STEATOSIS; GRAFT FUNCTION; BETA-SCORE; PREVENTION; MELLITUS; CELLS;
D O I
10.2147/DMSO.S105692
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 1 diabetes mellitus is an autoimmune disorder of the endocrine pancreas that currently affects millions of people in the United States. Although the disease can be managed with exogenous insulin administration, the ultimate cure for the condition lies in restoring a patient's ability to produce their own insulin. Islet cell allotransplantation provides a means of endogenous insulin production. Though far from perfected, islet transplants are now a proven treatment for type 1 diabetics. However, proper patient selection is critical for achieving optimal outcomes. Given the shortage of transplantable organs, selecting appropriate candidates for whom the procedure will be of greatest benefit is essential. Although many of those who receive islets do not retain insulin independence, grafts do play a significant role in preventing hypoglycemic episodes that can be quite detrimental to quality of life and potentially fatal. Additionally, islet transplant requires lifelong immunosuppression. Antibodies, both preformed and following islet infusion, may play important roles in graft outcomes. Finally, no procedure is without inherent risk and islet transfusions can have serious consequences for recipients' livers in the form of both vascular and metabolic complications. Therefore, patient-specific factors that should be taken into account before islet transplantation include aims of therapy, sensitization, and potential increased risk for hepatic and portal-venous sequelae.
引用
收藏
页码:73 / 78
页数:6
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