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Meeting Abstracts

424-P: Body-Weight Variability and Risk of Cardiovascular Outcomes in Type 1 Diabetes: Results from the DCCT/EDIC Studies

IULIA PETRIA, SAMUEL ALBUQUERQUE, GAEL VAROQUAUX, JILL-JÊNN VIE, GILBERTO VELHO, GIANLUCA PERSEGHIN, RONAN ROUSSEL, LOUIS POTIER

Diabetes 2022;71(Supplement_1):424-P

DOI: https://doi.org/10.2337/db22-424-P

Published: 01 June 2022

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Meeting Abstracts

323-OR: Associations of Leukocyte Telomere Length and Related Allelic Variations with the Risk of Coronary Events in People with Long-Standing Type 1 Diabetes

MANUEL SANCHEZ, LOUIS POTIER, NICOLAS VENTECLEF, FRÉDÉRIC FUMERON, ANDRÉ SCHEEN, JEAN-FRANÇOIS GAUTIER, MICHEL MARRE, RONAN ROUSSEL, KAMEL MOHAMMEDI, GILBERTO VELHO

Diabetes 2022;71(Supplement_1):323-OR

DOI: https://doi.org/10.2337/db22-323-OR

Published: 01 June 2022

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Meeting Abstracts

421-P: Differential Prognostic Burden of Lower-Limb Amputation and Cardiovascular Disease on the Risk of All-Cause Death in People with Type 1 Diabetes

MARION CAMOIN, GILBERTO VELHO, PIERRE-JEAN SAULNIER, LOUIS POTIER, YAWA ABOULEKA, CHARLYNE CARPENTIER, SEVERINE DUBOIS, ALICE LARROUMET, VINCENT RIGALLEAU, OLIVIER BOURRON, ANDRÉ SCHEEN, RONAN ROUSSEL, MICHEL MARRE, KAMEL MOHAMMEDI

Diabetes 2022;71(Supplement_1):421-P

DOI: https://doi.org/10.2337/db22-421-P

Published: 01 June 2022

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Meeting Abstracts

220-OR: Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Risk for Lower Extremity Amputation in People with Type 2 Diabetes

LOUIS POTIER, RONAN ROUSSEL, PIERRE-JEAN SAULNIER, FRÉDÉRIC FUMERON, KAMEL MOHAMMEDI, GILBERTO VELHO

Diabetes 2020;69(Supplement_1):220-OR

DOI: https://doi.org/10.2337/db20-220-OR

Published: 01 June 2020

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Meeting Abstracts

1799-P: Insulin Secretion during a Graded Glucose Infusion Correlates with GPS2 mRNA Expression in Adipocytes

GILBERTO VELHO, KARIMA DRARENI, JEAN-LOUIS NGUEWA, RONAN ROUSSEL, JEAN-PIERRE RIVELINE, NICOLAS VENTECLEF, JEAN-FRANÇOIS GAUTIER

Diabetes 2020;69(Supplement_1):1799-P

DOI: https://doi.org/10.2337/db20-1799-P

Published: 01 June 2020

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Meeting Abstracts

67-OR: Plasma Copeptin and Risk for Lower Extremity Amputation in People with Type 1 and Type 2 Diabetes

LOUIS POTIER, RONAN ROUSSEL, KAMEL MOHAMMEDI, PIERRE SAULNIER, MICHEL MARRE, SAMY HADJADJ, GILBERTO VELHO

Diabetes 2019;68(Supplement_1):67-OR

DOI: https://doi.org/10.2337/db19-67-OR

Published: 01 June 2019

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Meeting Abstracts

431-P: Diabetic Retinopathy and Risk of Lower-Extremity Artery Disease in Type 2 Diabetes

NINON FOUSSARD, PIERRE SAULNIER, CAPUCINE BERTRAND, ELISE GAND, STEPHANIE RAGOT, LOUIS POTIER, GILBERTO VELHO, MICHEL MARRE, RONAN ROUSSEL, VINCENT RIGALLEAU, KAMEL MOHAMMEDI, SAMY HADJADJ

Diabetes 2019;68(Supplement_1):431-P

DOI: https://doi.org/10.2337/db19-431-P

Published: 01 June 2019

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Meeting Abstracts

535-P: Relationship between Renal Capacities to Reabsorb Glucose and Kidney Disease in Patients with Diabetes

ODETTE MATAR, LOUIS POTIER, YAWA ABOULEKA, FRÉDÉRIC FUMERON, KAMEL MOHAMMEDI, SAMY HADJADJ, RONAN ROUSSEL, GILBERTO VELHO, MICHEL MARRE

Diabetes 2019;68(Supplement_1):535-P

DOI: https://doi.org/10.2337/db19-535-P

Published: 01 June 2019

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Meeting Abstracts

550-P: Age at Diabetes Onset and Risk for Diabetic Kidney Disease

CHARLYNE CARPENTIER, SEVERINE DUBOIS, YAWA ABOULEKA, BEATRICE DULY-BOUHANICK, SAMY HADJADJ, REGIS COUTANT, RONAN ROUSSEL, GILBERTO VELHO, MICHEL MARRE

Diabetes 2019;68(Supplement_1):550-P

DOI: https://doi.org/10.2337/db19-550-P

Published: 01 June 2019

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Meeting Abstracts

Association of Diuretics Use and Amputations in Patients with Type 2 Diabetes—A Hypothesis Driven from Canvas Warning?

LOUIS POTIER, KAMEL MOHAMMEDI, ABDUL K. MOUTAIROU, ANISOARA BUMBU, ODETTE MATAR, FABRICE SCHNEIDER, MICHEL MARRE, PIERRE SAULNIER, GILBERTO VELHO, RONAN ROUSSEL, SAMY HADJADJ

Diabetes 2018;67(Supplement_1):2221-PUB

DOI: https://doi.org/10.2337/db18-2221-PUB

Published: 01 July 2018

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Meeting Abstracts

Prognostic Values of Inflammation and Oxidative Stress Biomarkers on the Risk of Peripheral Arterial Disease in Type 2 Diabetes

MATHILDE NATIVEL, FABRICE SCHNEIDER, PIERRE SAULNIER, OLIVIER MEILHAC, PHILIPPE RONDEAU, MAXIME COURNOT, LOUIS POTIER, GILBERTO VELHO, MICHEL MARRE, RONAN ROUSSEL, VINCENT RIGALLEAU, KAMEL MOHAMMEDI, SAMY HADJADJ

Diabetes 2018;67(Supplement_1):2220-PUB

DOI: https://doi.org/10.2337/db18-2220-PUB

Published: 01 July 2018

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Journal Articles

Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Kidney Disease in People With Type 2 Diabetes

Gilberto Velho, Stéphanie Ragot, Kamel Mohammedi, Elise Gand, Mathilde Fraty, Frédéric Fumeron, Pierre-Jean Saulnier, Naima Bellili-Munoz, Nadine Bouby, Louis Potier, François Alhenc-Gelas, Michel Marre, Samy Hadjadj, Ronan Roussel

Diabetes 2015;64(9):3262–3272

DOI: https://doi.org/10.2337/db14-1852

Published: 06 May 2015

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Includes: Supplementary data

Journal Articles

The Common −866G>A Variant in the Promoter of UCP2 Is Associated With Decreased Risk of Coronary Artery Disease in Type 2 Diabetic Men

Nadir Cheurfa, Danièle Dubois-Laforgue, Daniela A.F. Ferrarezi, André F. Reis, Guilherme M. Brenner, Clara Bouché, Claude Le Feuvre, Frédéric Fumeron, José Timsit, Michel Marre, Gilberto Velho

Diabetes 2008;57(4):1063–1068

DOI: https://doi.org/10.2337/db07-1292

Published: 01 April 2008

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Includes: Supplementary data

Journal Articles

The Type and the Position of HNF1A Mutation Modulate Age at Diagnosis of Diabetes in Patients with Maturity-Onset Diabetes of the Young (MODY)-3

Diabetes 2008;57(2):503–508

DOI: https://doi.org/10.2337/db07-0859

Published: 01 February 2008

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Includes: Supplementary data

Journal Articles

Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

Diabetes 2005;54(11):3126–3132

DOI: https://doi.org/10.2337/diabetes.54.11.3126

Published: 01 November 2005

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Includes: Supplementary data

Journal Articles

An Automated Fluorescent Single-Strand Conformation Polymorphism Technique for Screening Mutations in the Hepatocyte Nuclear Factor-1α Gene (Maturity-Onset Diabetes of the Young)

Philippe Boutin, Jean Claude Chévre, El Habib Hani, Ramon Gomis, Victor C Pardini, Pierre-Jean Guillausseau, Martine Vaxillaire, Gilberto Velho, Philippe Froguel

Diabetes 1997;46(12):2108–2109

DOI: https://doi.org/10.2337/diab.46.12.2108

Published: 01 December 1997

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Journal Articles

Genetic Studies of the Sulfonylurea Receptor Gene Locus in NIDDM and in Morbid Obesity Among French Caucasians

El Habib Hani, Karine Clément, Gilberto Velho, Nathalie Vionnet, Jörg Hager, Anne Philippi, Christian Dina, Hiroshi Inoue, M Alan Permutt, Arnaud Basdevant, Michael North, Florence Demenais, Bernard Guy-Grand, Philippe Froguel

Diabetes 1997;46(4):688–694

DOI: https://doi.org/10.2337/diab.46.4.688

Published: 01 April 1997

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Journal Articles

Altered Insulin Secretory Responses to Glucose in Diabetic and Nondiabetic Subjects With Mutations in the Diabetes Susceptibility Gene MODY3 on Chromosome 12

Maria M Byrne, Jeppe Sturis, Stephan Menzel, Kazuya Yamagata, Stefan S Fajans, Mark J Dronsfield, Stephen C Bain, Andrew T Hattersley, Gilberto Velho, Phillipe Froguel, Graeme I Bell, Kenneth S Polonsky

Diabetes 1996;45(11):1503–1510

DOI: https://doi.org/10.2337/diab.45.11.1503

Published: 01 November 1996

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Journal Articles

Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNA^Leu(UUR) Gene Mutation

Gilberto Velho, Maria M Byrne, Karine Clément, Jeppe Sturis, Maria E. Pueyo, Helène Blanché, Nathalie Vionnet, Jean Fiet, Philippe Passa, Jean-Jacques Robert, Kenneth S Polonsky, Philippe Froguel

Diabetes 1996;45(4):478–487

DOI: https://doi.org/10.2337/diab.45.4.478

Published: 01 April 1996

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Journal Articles

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA ^Leu(UUR) gene

Johannes M W van den Ouweland, Herman H P J Lemkes, Richard C Trembath, Richard Ross, Gilberto Velho, Daniel Cohen, Philippe Froguel, J Antonie Maassen

Diabetes 1994;43(6):746–751

DOI: https://doi.org/10.2337/diab.43.6.746

Published: 01 June 1994

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NARROW

424-P: Body-Weight Variability and Risk of Cardiovascular Outcomes in Type 1 Diabetes: Results from the DCCT/EDIC Studies

323-OR: Associations of Leukocyte Telomere Length and Related Allelic Variations with the Risk of Coronary Events in People with Long-Standing Type 1 Diabetes

421-P: Differential Prognostic Burden of Lower-Limb Amputation and Cardiovascular Disease on the Risk of All-Cause Death in People with Type 1 Diabetes

220-OR: Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Risk for Lower Extremity Amputation in People with Type 2 Diabetes

1799-P: Insulin Secretion during a Graded Glucose Infusion Correlates with GPS2 mRNA Expression in Adipocytes

67-OR: Plasma Copeptin and Risk for Lower Extremity Amputation in People with Type 1 and Type 2 Diabetes

431-P: Diabetic Retinopathy and Risk of Lower-Extremity Artery Disease in Type 2 Diabetes

535-P: Relationship between Renal Capacities to Reabsorb Glucose and Kidney Disease in Patients with Diabetes

550-P: Age at Diabetes Onset and Risk for Diabetic Kidney Disease

Association of Diuretics Use and Amputations in Patients with Type 2 Diabetes—A Hypothesis Driven from Canvas Warning?

Prognostic Values of Inflammation and Oxidative Stress Biomarkers on the Risk of Peripheral Arterial Disease in Type 2 Diabetes

Plasma Adrenomedullin and Allelic Variation in the ADM Gene and Kidney Disease in People With Type 2 Diabetes

The Common −866G>A Variant in the Promoter of UCP2 Is Associated With Decreased Risk of Coronary Artery Disease in Type 2 Diabetic Men

The Type and the Position of HNF1A Mutation Modulate Age at Diagnosis of Diabetes in Patients with Maturity-Onset Diabetes of the Young (MODY)-3

Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

An Automated Fluorescent Single-Strand Conformation Polymorphism Technique for Screening Mutations in the Hepatocyte Nuclear Factor-1α Gene (Maturity-Onset Diabetes of the Young)

Genetic Studies of the Sulfonylurea Receptor Gene Locus in NIDDM and in Morbid Obesity Among French Caucasians

Altered Insulin Secretory Responses to Glucose in Diabetic and Nondiabetic Subjects With Mutations in the Diabetes Susceptibility Gene MODY3 on Chromosome 12

Clinical Phenotypes, Insulin Secretion, and Insulin Sensitivity in Kindreds With Maternally Inherited Diabetes and Deafness Due to Mitochondrial tRNA^Leu(UUR) Gene Mutation

Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA ^Leu(UUR) gene

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