<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>97(11)</volume><submitter>Vantyghem MC</submitter><pubmed_abstract>&lt;h4>Context&lt;/h4>For the last 10 yr, continuous glucose monitoring (CGM) has brought up new insights into the accuracy of blood glucose analysis.&lt;h4>Objective&lt;/h4>Our objective was to determine how islet graft function was able to influence the various components of dysglycemia after islet transplantation (IT).&lt;h4>Design and setting&lt;/h4>We conducted a single-arm open-labeled study with a 3-yr follow-up in a referral center (ClinicalTrial.gov identifiers NCT00446264 and NCT01123187).&lt;h4>Patients&lt;/h4>Twenty-three consecutive patients with type 1 diabetes (14 islet alone, nine islet after kidney) received IT within 3 months using the Edmonton protocol.&lt;h4>Intervention&lt;/h4>INTERVENTION included 72-h CGM before and 3, 6, 9, 12, 24, and 36 months after transplantation.&lt;h4>Main outcome measure&lt;/h4</pubmed_abstract><journal>The Journal of clinical endocrinology and metabolism</journal><pagination>E2078-83</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3485599</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Continuous glucose monitoring after islet transplantation in type 1 diabetes: an excellent graft function (β-score greater than 7) Is required to abrogate hyperglycemia, whereas a minimal function is necessary to suppress severe hypoglycemia (β-score greater than 3).</pubmed_title><pmcid>PMC3485599</pmcid><pubmed_authors>Defrance F</pubmed_authors><pubmed_authors>Kerr-Conte J</pubmed_authors><pubmed_authors>Raverdy V</pubmed_authors><pubmed_authors>Caiazzo R</pubmed_authors><pubmed_authors>Gmyr V</pubmed_authors><pubmed_authors>Hazzan M</pubmed_authors><pubmed_authors>Vantyghem MC</pubmed_authors><pubmed_authors>Balavoine AS</pubmed_authors><pubmed_authors>Arnalsteen L</pubmed_authors><pubmed_authors>Noel C</pubmed_authors><pubmed_authors>Pattou F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Continuous glucose monitoring after islet transplantation in type 1 diabetes: an excellent graft function (β-score greater than 7) Is required to abrogate hyperglycemia, whereas a minimal function is necessary to suppress severe hypoglycemia (β-score greater than 3).</name><description>&lt;h4>Context&lt;/h4>For the last 10 yr, continuous glucose monitoring (CGM) has brought up new insights into the accuracy of blood glucose analysis.&lt;h4>Objective&lt;/h4>Our objective was to determine how islet graft function was able to influence the various components of dysglycemia after islet transplantation (IT).&lt;h4>Design and setting&lt;/h4>We conducted a single-arm open-labeled study with a 3-yr follow-up in a referral center (ClinicalTrial.gov identifiers NCT00446264 and NCT01123187).&lt;h4>Patients&lt;/h4>Twenty-three consecutive patients with type 1 diabetes (14 islet alone, nine islet after kidney) received IT within 3 months using the Edmonton protocol.&lt;h4>Intervention&lt;/h4>INTERVENTION included 72-h CGM before and 3, 6, 9, 12, 24, and 36 months after transplantation.&lt;h4>Main outcome measure&lt;/h4</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012 Nov</publication><modification>2025-06-01T00:11:17.836Z</modification><creation>2025-06-01T00:11:17.836Z</creation></dates><accession>S-EPMC3485599</accession><cross_references><pubmed>22996144</pubmed><doi>10.1210/jc.2012-2115</doi></cross_references></HashMap>