Human pancreatic islet transplantation: an update and description of the establishment of a pancreatic islet isolation laboratory
Type 1 diabetes mellitus (T1DM) is associated with chronic complications that lead to high morbidity and mortality rates in young adults of productive age. Intensive insulin therapy has been able to reduce the likelihood of the development of chronic diabetes complications. However, this treatment i...
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| Published in: | Archives of Endocrinology and Metabolism Vol. 59; no. 2; pp. 161 - 170 |
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| Main Authors: | , , , , , , , , , , , , , , , , |
| Format: | Journal Article |
| Language: | English |
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Brazil
Brazilian Society of Endocrinology and Metabolism
01.04.2015
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| ISSN: | 2359-3997, 2359-4292, 2359-3997, 2359-4292 |
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| Abstract | Type 1 diabetes mellitus (T1DM) is associated with chronic complications that lead to high morbidity and mortality rates in young adults of productive age. Intensive insulin therapy has been able to reduce the likelihood of the development of chronic diabetes complications. However, this treatment is still associated with an increased incidence of hypoglycemia. In patients with "brittle T1DM", who have severe hypoglycemia without adrenergic symptoms (hypoglycemia unawareness), islet transplantation may be a therapeutic option to restore both insulin secretion and hypoglycemic perception. The Edmonton group demonstrated that most patients who received islet infusions from more than one donor and were treated with steroid-free immunosuppressive drugs displayed a considerable decline in the initial insulin independence rates at eight years following the transplantation, but showed permanent C-peptide secretion, which facilitated glycemic control and protected patients against hypoglycemic episodes. Recently, data published by the Collaborative Islet Transplant Registry (CITR) has revealed that approximately 50% of the patients who undergo islet transplantation are insulin independent after a 3-year follow-up. Therefore, islet transplantation is able to successfully decrease plasma glucose and HbA1c levels, the occurrence of severe hypoglycemia, and improve patient quality of life. The goal of this paper was to review the human islet isolation and transplantation processes, and to describe the establishment of a human islet isolation laboratory at the Endocrine Division of the Hospital de Clínicas de Porto Alegre - Rio Grande do Sul, Brazil. |
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| AbstractList | Type 1 diabetes mellitus (T1DM) is associated with chronic complications that lead to high morbidity and mortality rates in young adults of productive age. Intensive insulin therapy has been able to reduce the likelihood of the development of chronic diabetes complications. However, this treatment is still associated with an increased incidence of hypoglycemia. In patients with "brittle T1DM", who have severe hypoglycemia without adrenergic symptoms (hypoglycemia unawareness), islet transplantation may be a therapeutic option to restore both insulin secretion and hypoglycemic perception. The Edmonton group demonstrated that most patients who received islet infusions from more than one donor and were treated with steroid-free immunosuppressive drugs displayed a considerable decline in the initial insulin independence rates at eight years following the transplantation, but showed permanent C-peptide secretion, which facilitated glycemic control and protected patients against hypoglycemic episodes. Recently, data published by the Collaborative Islet Transplant Registry (CITR) has revealed that approximately 50% of the patients who undergo islet transplantation are insulin independent after a 3-year follow-up. Therefore, islet transplantation is able to successfully decrease plasma glucose and HbA1c levels, the occurrence of severe hypoglycemia, and improve patient quality of life. The goal of this paper was to review the human islet isolation and transplantation processes, and to describe the establishment of a human islet isolation laboratory at the Endocrine Division of the Hospital de Clínicas de Porto Alegre - Rio Grande do Sul, Brazil. Type 1 diabetes mellitus (T1DM) is associated with chronic complications that lead to high morbidity and mortality rates in young adults of productive age. Intensive insulin therapy has been able to reduce the likelihood of the development of chronic diabetes complications. However, this treatment is still associated with an increased incidence of hypoglycemia. In patients with "brittle T1DM", who have severe hypoglycemia without adrenergic symptoms (hypoglycemia unawareness), islet transplantation may be a therapeutic option to restore both insulin secretion and hypoglycemic perception. The Edmonton group demonstrated that most patients who received islet infusions from more than one donor and were treated with steroid-free immunosuppressive drugs displayed a considerable decline in the initial insulin independence rates at eight years following the transplantation, but showed permanent C-peptide secretion, which facilitated glycemic control and protected patients against hypoglycemic episodes. Recently, data published by the Collaborative Islet Transplant Registry (CITR) has revealed that approximately 50% of the patients who undergo islet transplantation are insulin independent after a 3-year follow-up. Therefore, islet transplantation is able to successfully decrease plasma glucose and HbA1c levels, the occurrence of severe hypoglycemia, and improve patient quality of life. The goal of this paper was to review the human islet isolation and transplantation processes, and to describe the establishment of a human islet isolation laboratory at the Endocrine Division of the Hospital de Clínicas de Porto Alegre - Rio Grande do Sul, Brazil.Type 1 diabetes mellitus (T1DM) is associated with chronic complications that lead to high morbidity and mortality rates in young adults of productive age. Intensive insulin therapy has been able to reduce the likelihood of the development of chronic diabetes complications. However, this treatment is still associated with an increased incidence of hypoglycemia. In patients with "brittle T1DM", who have severe hypoglycemia without adrenergic symptoms (hypoglycemia unawareness), islet transplantation may be a therapeutic option to restore both insulin secretion and hypoglycemic perception. The Edmonton group demonstrated that most patients who received islet infusions from more than one donor and were treated with steroid-free immunosuppressive drugs displayed a considerable decline in the initial insulin independence rates at eight years following the transplantation, but showed permanent C-peptide secretion, which facilitated glycemic control and protected patients against hypoglycemic episodes. Recently, data published by the Collaborative Islet Transplant Registry (CITR) has revealed that approximately 50% of the patients who undergo islet transplantation are insulin independent after a 3-year follow-up. Therefore, islet transplantation is able to successfully decrease plasma glucose and HbA1c levels, the occurrence of severe hypoglycemia, and improve patient quality of life. The goal of this paper was to review the human islet isolation and transplantation processes, and to describe the establishment of a human islet isolation laboratory at the Endocrine Division of the Hospital de Clínicas de Porto Alegre - Rio Grande do Sul, Brazil. |
| Author | Rosa, Annelise R. Brondani, Letícia A. Oliveira, Fernanda S. de Bauer, Andrea C. Azevedo, Mirela J. Crispim, Daisy Lemos, Natália E. Estivalet, Aline A. F. Bouças, Ana P. Silveiro, Sandra P. Carlessi, Rodrigo Cruz, Lavínia A. Assmann, Taís S. Souza, Bianca M. de Rheinheimer, Jakeline Gross, Jorge L. Leitão, Cristiane B. |
| Author_xml | – sequence: 1 givenname: Jakeline surname: Rheinheimer fullname: Rheinheimer, Jakeline organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 2 givenname: Andrea C. surname: Bauer fullname: Bauer, Andrea C. organization: Hospital de Clínicas de Porto Alegre, Brazil – sequence: 3 givenname: Sandra P. surname: Silveiro fullname: Silveiro, Sandra P. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 4 givenname: Aline A. F. surname: Estivalet fullname: Estivalet, Aline A. F. organization: Hospital de Clínicas de Porto Alegre, Brazil – sequence: 5 givenname: Ana P. surname: Bouças fullname: Bouças, Ana P. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 6 givenname: Annelise R. surname: Rosa fullname: Rosa, Annelise R. organization: Hospital de Clínicas de Porto Alegre, Brazil – sequence: 7 givenname: Bianca M. de surname: Souza fullname: Souza, Bianca M. de organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 8 givenname: Fernanda S. de surname: Oliveira fullname: Oliveira, Fernanda S. de organization: Hospital de Clínicas de Porto Alegre, Brazil – sequence: 9 givenname: Lavínia A. surname: Cruz fullname: Cruz, Lavínia A. organization: Hospital de Clínicas de Porto Alegre, Brazil – sequence: 10 givenname: Letícia A. surname: Brondani fullname: Brondani, Letícia A. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 11 givenname: Mirela J. surname: Azevedo fullname: Azevedo, Mirela J. organization: Universidade Federal do Rio Grande do Sul, Brazil – sequence: 12 givenname: Natália E. surname: Lemos fullname: Lemos, Natália E. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 13 givenname: Rodrigo surname: Carlessi fullname: Carlessi, Rodrigo organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 14 givenname: Taís S. surname: Assmann fullname: Assmann, Taís S. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 15 givenname: Jorge L. surname: Gross fullname: Gross, Jorge L. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 16 givenname: Cristiane B. surname: Leitão fullname: Leitão, Cristiane B. organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil – sequence: 17 givenname: Daisy surname: Crispim fullname: Crispim, Daisy organization: Hospital de Clínicas de Porto Alegre, Brazil; Universidade Federal do Rio Grande do Sul, Brazil |
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| CitedBy_id | crossref_primary_10_1016_j_mce_2020_110729 crossref_primary_10_3389_fendo_2017_00382 crossref_primary_10_1080_19382014_2017_1335842 crossref_primary_10_1186_s13098_023_01089_8 crossref_primary_10_1515_chem_2020_0153 crossref_primary_10_3390_mi12030304 crossref_primary_10_1097_TP_0000000000001292 crossref_primary_10_1016_j_lpm_2022_104139 crossref_primary_10_1080_19382014_2020_1856618 crossref_primary_10_1088_1758_5090_ac23ac crossref_primary_10_1016_j_mce_2018_02_016 crossref_primary_10_1007_s11892_019_1166_x crossref_primary_10_1007_s40200_020_00674_2 crossref_primary_10_1080_19382014_2017_1286434 |
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| Title | Human pancreatic islet transplantation: an update and description of the establishment of a pancreatic islet isolation laboratory |
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