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  • 1
    Online-Ressource
    Online-Ressource
    The Endocrine Society ; 2003
    In:  The Journal of Clinical Endocrinology & Metabolism Vol. 88, No. 4 ( 2003-04), p. 1772-1779
    In: The Journal of Clinical Endocrinology & Metabolism, The Endocrine Society, Vol. 88, No. 4 ( 2003-04), p. 1772-1779
    Materialart: Online-Ressource
    ISSN: 0021-972X , 1945-7197
    RVK:
    Sprache: Englisch
    Verlag: The Endocrine Society
    Publikationsdatum: 2003
    ZDB Id: 2026217-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Online-Ressource
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    Oxford University Press (OUP) ; 2005
    In:  Paediatrics & Child Health Vol. 10, No. 1 ( 2005-01), p. 38-40
    In: Paediatrics & Child Health, Oxford University Press (OUP), Vol. 10, No. 1 ( 2005-01), p. 38-40
    Materialart: Online-Ressource
    ISSN: 1205-7088 , 1918-1485
    Sprache: Englisch
    Verlag: Oxford University Press (OUP)
    Publikationsdatum: 2005
    ZDB Id: 2174400-2
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Online-Ressource
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    American Diabetes Association ; 2005
    In:  Diabetes Vol. 54, No. 7 ( 2005-07-01), p. 2060-2069
    In: Diabetes, American Diabetes Association, Vol. 54, No. 7 ( 2005-07-01), p. 2060-2069
    Kurzfassung: Islet transplantation can restore endogenous β-cell function to subjects with type 1 diabetes. Sixty-five patients received an islet transplant in Edmonton as of 1 November 2004. Their mean age was 42.9 ± 1.2 years, their mean duration of diabetes was 27.1 ± 1.3 years, and 57% were women. The main indication was problematic hypoglycemia. Forty-four patients completed the islet transplant as defined by insulin independence, and three further patients received & gt;16,000 islet equivalents (IE)/kg but remained on insulin and are deemed complete. Those who became insulin independent received a total of 799,912 ± 30,220 IE (11,910 ± 469 IE/kg). Five subjects became insulin independent after one transplant. Fifty-two patients had two transplants, and 11 subjects had three transplants. In the completed patients, 5-year follow-up reveals that the majority (∼80%) have C-peptide present post–islet transplant, but only a minority (∼10%) maintain insulin independence. The median duration of insulin independence was 15 months (interquartile range 6.2–25.5). The HbA1c (A1C) level was well controlled in those off insulin (6.4% [6.1–6.7]) and in those back on insulin but C-peptide positive (6.7% [5.9–7.5] ) and higher in those who lost all graft function (9.0% [6.7–9.3]) (P & lt; 0.05). Those who resumed insulin therapy did not appear more insulin resistant compared with those off insulin and required half their pretransplant daily dose of insulin but had a lower increment of C-peptide to a standard meal challenge (0.44 ± 0.06 vs. 0.76 ± 0.06 nmol/l, P & lt; 0.001). The Hypoglycemic score and lability index both improved significantly posttransplant. In the 128 procedures performed, bleeding occurred in 15 and branch portal vein thrombosis in 5 subjects. Complications of immunosuppressive therapy included mouth ulcers, diarrhea, anemia, and ovarian cysts. Of the 47 completed patients, 4 required retinal laser photocoagulation or vitrectomy and 5 patients with microalbuminuria developed macroproteinuria. The need for multiple antihypertensive medications increased from 6% pretransplant to 42% posttransplant, while the use of statin therapy increased from 23 to 83% posttransplant. There was no change in the neurothesiometer scores pre- versus posttransplant. In conclusion, islet transplantation can relieve glucose instability and problems with hypoglycemia. C-peptide secretion was maintained in the majority of subjects for up to 5 years, although most reverted to using some insulin. The results, though promising, still point to the need for further progress in the availability of transplantable islets, improving islet engraftment, preserving islet function, and reducing toxic immunosuppression.
    Materialart: Online-Ressource
    ISSN: 0012-1797 , 1939-327X
    Sprache: Englisch
    Verlag: American Diabetes Association
    Publikationsdatum: 2005
    ZDB Id: 1501252-9
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    In: Diabetes, American Diabetes Association, Vol. 53, No. 4 ( 2004-04-01), p. 955-962
    Kurzfassung: Currently, the major indications for solitary islet transplantation are recurrent severe hypoglycemia and labile glucose control. Quantifying these problems remains subjective. We have developed a scoring system for both hypoglycemia and glycemic lability, established normative data, and used them in patients who have undergone islet transplantation. A composite hypoglycemic score (HYPO score) was devised based on the frequency, severity, and degree of unawareness of the hypoglycemia. In addition, using 4 weeks of glucose records, a lability index (LI) was calculated based on the change in glucose levels over time and compared with a clinical assessment of glycemic lability. A mean amplitude of glycemic excursions (MAGE) was also calculated based on 2 consecutive days of seven readings each day. These scores were determined in 100 randomly selected subjects with type 1 diabetes from our general clinic to serve as a control group and in patients before and after islet transplantation. The mean age of the control diabetic subjects was 38.4 ± 1.3 years (±SE), with a duration of diabetes of 21.5 ± 1.1 years. The median HYPO score in the control subjects was 143 (25th to 75th interquartile range: 46–423). The LI in the diabetic control subjects was 223 (25th to 75th interquartile range: 130–329 mmol/l2/h · week−1). The LI correlated much more closely than the MAGE with the clinical assessment of lability. A HYPO score of ≥1,047 (90th percentile) or an LI ≥433 mmol/l2/h · week−1 (90th percentile) indicated serious problems with hypoglycemia or glycemic lability, respectively. The islet transplant patients (n = 51) were 42.1 ± 1.4 years old, with a duration of diabetes of 25.7 ± 1.4 years. Islet transplant patients had a mean HYPO score of 1,234 ± 184 pretransplant, which was significantly higher than that of the control subjects (P & lt; 0.001), which became negligible posttransplantation with the elimination of hypoglycemia. The median LI pretransplant was 497 mmol/l2/h · week−1 (25th to 75th interquartile range: 330–692), significantly higher than that of control subjects (P & lt; 0.001), and fell to 40 (25th to 75th interquartile range: 14–83) within a month after the final transplant. In those who had lost graft function, the LI rose again. The HYPO score and LI provide measures of the extent of problems with hypoglycemia and glycemic lability, respectively, complement the clinical assessment of the problems with glucose control before islet transplantation, and will allow comparison of selection of subjects for transplants between centers.
    Materialart: Online-Ressource
    ISSN: 0012-1797 , 1939-327X
    Sprache: Englisch
    Verlag: American Diabetes Association
    Publikationsdatum: 2004
    ZDB Id: 1501252-9
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    In: Diabetes Technology & Therapeutics, Mary Ann Liebert Inc, Vol. 8, No. 2 ( 2006-04), p. 165-173
    Materialart: Online-Ressource
    ISSN: 1520-9156 , 1557-8593
    Sprache: Englisch
    Verlag: Mary Ann Liebert Inc
    Publikationsdatum: 2006
    ZDB Id: 2004914-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Online-Ressource
    Online-Ressource
    American Diabetes Association ; 2005
    In:  Diabetes Care Vol. 28, No. 4 ( 2005-04-01), p. 866-872
    In: Diabetes Care, American Diabetes Association, Vol. 28, No. 4 ( 2005-04-01), p. 866-872
    Kurzfassung: OBJECTIVE—Coronary artery disease (CAD) is the most common cause of death in patients with type 1 diabetes. Asymptomatic CAD is common in uremic diabetic patients, but its prevalence in nonuremic type 1 diabetic patients is unknown. The prevalence of CAD was determined by coronary angiography and the performance of noninvasive cardiac investigation evaluated in type 1 diabetic islet transplant (ITX) candidates with preserved renal function. RESEARCH DESIGN AND METHODS—A total of 60 consecutive type 1 diabetic ITX candidates (average age 46 years [mean 24–64], 23 men, and 47% ever smokers) underwent coronary angiography, electrocardiographic stress testing (EST), and myocardial perfusion imaging (MPI) in a prospective cohort study. CAD was indicated on angiography by the presence of stenoses & gt;50%. Models to predict CAD were examined by logistic regression. RESULTS—Most subjects (53 of 60) had no history or symptoms of CAD; 23 (43%) of these asymptomatic subjects had stenoses & gt;50%. CAD was associated with age, duration of diabetes, hypertension, and smoking. Although specific, EST and MPI were not sensitive as predictors of CAD on angiography (specificity 0.97 and 0.93, sensitivity 0.17 and 0.04, respectively) but helped identify two of three subjects requiring revascularization. EST and MPI did not enhance logistic regression models. A clinical algorithm to identify low-risk subjects who may not require angiography was highly sensitive but was applicable only to a minority (n = 8, sensitivity 1.0, specificity 0.27, negative predictive value 1.0). CONCLUSIONS—Nonuremic type 1 diabetic patients with hypoglycemic unawareness and/or metabolic lability referred for ITX are at high risk for asymptomatic CAD despite negative noninvasive investigations. Aggressive management of cardiovascular risk factors and further investigation into optimal cardiac risk stratification in type 1 diabetes are warranted.
    Materialart: Online-Ressource
    ISSN: 0149-5992 , 1935-5548
    Sprache: Englisch
    Verlag: American Diabetes Association
    Publikationsdatum: 2005
    ZDB Id: 1490520-6
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
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    Elsevier BV ; 2013
    In:  Canadian Journal of Diabetes Vol. 37 ( 2013-4), p. S94-S96
    In: Canadian Journal of Diabetes, Elsevier BV, Vol. 37 ( 2013-4), p. S94-S96
    Materialart: Online-Ressource
    ISSN: 1499-2671
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2013
    ZDB Id: 2252861-1
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
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    Elsevier BV ; 2018
    In:  Canadian Journal of Diabetes Vol. 42 ( 2018-04), p. S145-S149
    In: Canadian Journal of Diabetes, Elsevier BV, Vol. 42 ( 2018-04), p. S145-S149
    Materialart: Online-Ressource
    ISSN: 1499-2671
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2018
    ZDB Id: 2252861-1
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
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    Elsevier BV ; 2013
    In:  Canadian Journal of Diabetes Vol. 37 ( 2013-10), p. S468-S470
    In: Canadian Journal of Diabetes, Elsevier BV, Vol. 37 ( 2013-10), p. S468-S470
    Materialart: Online-Ressource
    ISSN: 1499-2671
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2013
    ZDB Id: 2252861-1
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
    Online-Ressource
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    Elsevier BV ; 2015
    In:  Canadian Journal of Diabetes Vol. 39 ( 2015-12), p. S155-S159
    In: Canadian Journal of Diabetes, Elsevier BV, Vol. 39 ( 2015-12), p. S155-S159
    Materialart: Online-Ressource
    ISSN: 1499-2671
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2015
    ZDB Id: 2252861-1
    Standort Signatur Einschränkungen Verfügbarkeit
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