glycine has been researched along with Diabetes Mellitus, Type 1 in 16 studies
Diabetes Mellitus, Type 1: A subtype of DIABETES MELLITUS that is characterized by INSULIN deficiency. It is manifested by the sudden onset of severe HYPERGLYCEMIA, rapid progression to DIABETIC KETOACIDOSIS, and DEATH unless treated with insulin. The disease may occur at any age, but is most common in childhood or adolescence.
Excerpt | Relevance | Reference |
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"The response of the subjects with IDDM was similar to that of the normal subjects." | 2.70 | Effect of protein restriction on (15)N transfer from dietary [(15)N]alanine and [(15)N]Spirulina platensis into urea. ( Hamadeh, MJ; Hoffer, LJ, 2001) |
"There is substantial evidence for genetic susceptibility to diabetic nephropathy." | 1.32 | Role of alpha-adducin DNA polymorphisms in the genetic predisposition to diabetic nephropathy. ( Brady, HR; Conway, BR; Martin, R; Maxwell, AP; McKnight, AJ; Savage, DA, 2004) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 3 (18.75) | 18.7374 |
1990's | 2 (12.50) | 18.2507 |
2000's | 7 (43.75) | 29.6817 |
2010's | 3 (18.75) | 24.3611 |
2020's | 1 (6.25) | 2.80 |
Authors | Studies |
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Vigers, T | 1 |
Vinovskis, C | 1 |
Li, LP | 1 |
Prasad, P | 1 |
Heerspink, H | 1 |
D'Alessandro, A | 1 |
Reisz, JA | 1 |
Piani, F | 1 |
Cherney, DZ | 1 |
van Raalte, DH | 1 |
Nadeau, KJ | 1 |
Pavkov, ME | 1 |
Nelson, RG | 1 |
Pyle, L | 1 |
Bjornstad, P | 1 |
Stec, DF | 1 |
Wang, S | 1 |
Stothers, C | 1 |
Avance, J | 1 |
Denson, D | 1 |
Harris, R | 1 |
Voziyan, P | 1 |
Chuĭko, MR | 1 |
Efremova, NM | 1 |
Skvortsova, VI | 1 |
Michels, AW | 1 |
Ostrov, DA | 1 |
Zhang, L | 1 |
Nakayama, M | 1 |
Fuse, M | 1 |
McDaniel, K | 1 |
Roep, BO | 1 |
Gottlieb, PA | 1 |
Atkinson, MA | 1 |
Eisenbarth, GS | 2 |
Mauvais-Jarvis, F | 1 |
Boudou, P | 1 |
Sobngwi, E | 1 |
Riveline, JP | 1 |
Kevorkian, JP | 1 |
Villette, JM | 1 |
Porcher, R | 1 |
Vexiau, P | 1 |
Gautier, JF | 1 |
Rudofsky, G | 1 |
Reismann, P | 1 |
Witte, S | 1 |
Humpert, PM | 1 |
Isermann, B | 1 |
Chavakis, T | 1 |
Tafel, J | 1 |
Nosikov, VV | 1 |
Hamann, A | 1 |
Nawroth, P | 1 |
Bierhaus, A | 1 |
Hartemann-Heurtier, A | 1 |
Mars, LT | 1 |
Bercovici, N | 1 |
Desbois, S | 1 |
Cambouris, C | 1 |
Piaggio, E | 1 |
Zappulla, J | 1 |
Saoudi, A | 1 |
Liblau, RS | 1 |
Conway, BR | 1 |
Martin, R | 1 |
McKnight, AJ | 1 |
Savage, DA | 1 |
Brady, HR | 1 |
Maxwell, AP | 1 |
Eller, E | 1 |
Vardi, P | 1 |
Daly, MJ | 1 |
Babu, S | 2 |
Roberts, C | 1 |
Yang, F | 1 |
Fain, PR | 1 |
Prevost, G | 1 |
Fajardy, I | 1 |
Besmond, C | 1 |
Balkau, B | 1 |
Tichet, J | 1 |
Fontaine, P | 1 |
Danze, PM | 1 |
Marre, M | 1 |
Smith, BD | 1 |
Silbert, CK | 1 |
Hart, LM | 1 |
Stolk, RP | 1 |
Jansen, JJ | 1 |
Grobbee, DE | 1 |
Lemkes, HH | 1 |
Maassen, JA | 1 |
Boutin, P | 1 |
Gresh, L | 1 |
Cisse, A | 1 |
Hara, M | 1 |
Bell, G | 1 |
Eisenbarth, G | 1 |
Froguel, P | 1 |
Hamadeh, MJ | 1 |
Hoffer, LJ | 1 |
Beccaria, L | 1 |
Chiumello, G | 1 |
Gianazza, E | 1 |
Luppis, B | 1 |
Righetti, PG | 1 |
Robert, JJ | 1 |
Beaufrere, B | 1 |
Koziet, J | 1 |
Desjeux, JF | 1 |
Bier, DM | 1 |
Young, VR | 1 |
Lestradet, H | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
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CASPER Study: Copeptin in Adolescent Participants With Type 1 Diabetes and Early Renal Hemodynamic Function[NCT03618420] | Phase 1/Phase 2 | 50 participants (Actual) | Interventional | 2018-10-01 | Completed | ||
Renal HEIR Study: Renal Hemodynamics, Energetics and Insulin Resistance in Youth Onset Type 2 Diabetes Study[NCT03584217] | Phase 1/Phase 2 | 100 participants (Actual) | Interventional | 2018-10-01 | Active, not recruiting | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Measured by fasting blood draw; Copeptin will be measured by ultrasensitive assays on KRYPTOR Compact Plus analyzers using the commercial sandwich immunoluminometric assays (Thermo Fisher Scientific, Waltham, MA). The copeptin assay has a lower limit of detection of 0.9 pmol/L, and a sensitivity of <2pmol/L. Elevated copeptin will be defined as >13pmol/L, which is >97.5th percentile for healthy adults (68). (NCT03618420)
Timeframe: 4 hours
Intervention | pmol/L (Mean) |
---|---|
Clinical Investigation | 8.3 |
Measured by para-aminohippurate (PAH) clearance; An intravenous (IV) line was placed, and participants were asked to empty their bladders. Spot plasma and urine samples were collected prior PAH infusion. PAH (2 g/10 mL, prepared at the University of Minnesota, with a dose of [weight in kg]/75 × 4.2 mL; IND #140129) was given slowly over 5 min followed by a continuous infusion of 8 mL of PAH and 42 mL of normal saline at a rate of 24 mL/h for 2 h. After an equilibration period, blood was drawn at 90 and 120 min, and ERPF was calculated as PAH clearance divided by the estimated extraction ratio of PAH, which varies by the level of GFR (13). We report absolute ERPF (mL/min) in the main analyses because the practice of indexing ERPF for body surface underestimates hyperperfusion, and body surface area (BSA) calculations introduce noise into the clearance measurements. (NCT03618420)
Timeframe: 4 hours
Intervention | ml/min (Mean) |
---|---|
Clinical Investigation | 820 |
Measured by iohexol clearance; An intravenous (IV) line was placed, and participants were asked to empty their bladders. Spot plasma and urine samples were collected prior to iohexol infusion. Iohexol was administered through bolus IV injection (5 mL of 300 mg/mL; Omnipaque 300, GE Healthcare). An equilibration period of 120 min was used and blood collections for iohexol plasma disappearance were drawn at +120, +150, +180, +210, +240 min (11). Because the Brøchner-Mortensen equation underestimates high values of GFR, the Jødal-Brøchner-Mortensen equation was used to calculate the GFR (12). We report absolute GFR (mL/min) in the main analyses because the practice of indexing GFR for body surface underestimates hyperfiltration, and body surface area (BSA) calculations introduce noise into the clearance measurements. (NCT03618420)
Timeframe: 4 hours
Intervention | ml/min (Mean) |
---|---|
Clinical Investigation | 189 |
Measured by Blood Oxygen Level Dependent (BOLD) MRI; Regions of interest (ROI) analysis for BOLD MRI will be performed on a Leonardo Workstation (Siemens Medical Systems, Germany). Typically, 1 to 3 regions in each, cortex and medulla, per kidney per slice will be defined leading to a total of about 10 ROIs per region (cortex and medulla) per subject. The mean and standard deviation of these 10 measurements will be used a R2* measurement for the region, for the subject and for that time point. These data are used to calculate kidney oxygen availability (R2*), which is the BOLD-MRI outcome. (NCT03618420)
Timeframe: 60 min
Intervention | s^-1 (Mean) |
---|---|
Clinical Investigation | 22.7 |
Measured by Arterial Spin Labeling (ASL) MRI; ASL MRI: ROI analysis will be used to estimate (delta) M (difference in signal intensity between non-selective and selective inversion images). Using the same ROI, M0 will be estimated from the proton density image. T1 measurements from the same ROI will be obtained by fitting the signal intensity vs. inversion time data as described previously (104) using XLFit (ID Business Solutions Ltd., UK) or T1 maps created using MRI Mapper (Beth Israel Deaconess Medical Center, Boston). Partition coefficient will be assumed to be 0.8 ml/gm (105, 106). These values will then be used to estimate regional blood flow. (NCT03618420)
Timeframe: 10 min
Intervention | ml/min/100g (Mean) |
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Clinical Investigation | 180 |
3 trials available for glycine and Diabetes Mellitus, Type 1
Article | Year |
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Plasma levels of carboxylic acids are markers of early kidney dysfunction in young people with type 1 diabetes.
Topics: Adolescent; Albuminuria; Carboxylic Acids; Diabetes Mellitus, Type 1; Fumarates; Glomerular Filtrati | 2023 |
Plasma levels of carboxylic acids are markers of early kidney dysfunction in young people with type 1 diabetes.
Topics: Adolescent; Albuminuria; Carboxylic Acids; Diabetes Mellitus, Type 1; Fumarates; Glomerular Filtrati | 2023 |
Plasma levels of carboxylic acids are markers of early kidney dysfunction in young people with type 1 diabetes.
Topics: Adolescent; Albuminuria; Carboxylic Acids; Diabetes Mellitus, Type 1; Fumarates; Glomerular Filtrati | 2023 |
Plasma levels of carboxylic acids are markers of early kidney dysfunction in young people with type 1 diabetes.
Topics: Adolescent; Albuminuria; Carboxylic Acids; Diabetes Mellitus, Type 1; Fumarates; Glomerular Filtrati | 2023 |
[Efficacy and safety of glycine and limontar in the complex therapy of discirculatory encephalopathy and encephalopathy in diabetes mellitus type I].
Topics: Cerebrovascular Disorders; Citrates; Diabetes Mellitus, Type 1; Diabetic Angiopathies; Drug Combinat | 2010 |
Effect of protein restriction on (15)N transfer from dietary [(15)N]alanine and [(15)N]Spirulina platensis into urea.
Topics: Alanine; Aspartic Acid; Bacterial Proteins; Diabetes Mellitus, Type 1; Diet, Protein-Restricted; Fem | 2001 |
13 other studies available for glycine and Diabetes Mellitus, Type 1
Article | Year |
---|---|
Alterations of urinary metabolite profile in model diabetic nephropathy.
Topics: Aconitic Acid; Animals; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 1; Diabetes Mellitu | 2015 |
Structure-based selection of small molecules to alter allele-specific MHC class II antigen presentation.
Topics: Alleles; Animals; Antigen Presentation; Autoantigens; Diabetes Mellitus, Type 1; Enzyme-Linked Immun | 2011 |
The polymorphism Gly574Ser in the transcription factor HNF-1alpha is not a marker of adult-onset ketosis-prone atypical diabetes in Afro-Caribbean patients.
Topics: Adult; Africa; Amino Acid Substitution; Black People; Caribbean Region; Diabetes Mellitus, Type 1; D | 2003 |
Asp299Gly and Thr399Ile genotypes of the TLR4 gene are associated with a reduced prevalence of diabetic neuropathy in patients with type 2 diabetes.
Topics: Amino Acid Substitution; Aspartic Acid; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Diabet | 2004 |
An altered self-peptide with superagonist activity blocks a CD8-mediated mouse model of type 1 diabetes.
Topics: Adoptive Transfer; Alanine; Amino Acid Substitution; Animals; Autoantigens; CD8-Positive T-Lymphocyt | 2004 |
Role of alpha-adducin DNA polymorphisms in the genetic predisposition to diabetic nephropathy.
Topics: Adult; Calmodulin-Binding Proteins; Cytoskeletal Proteins; Diabetes Mellitus, Type 1; Diabetic Nephr | 2004 |
IDDM17: polymorphisms in the AMACO gene are associated with dominant protection against type 1A diabetes in a Bedouin Arab family.
Topics: Alleles; Amino Acid Substitution; Arabs; Base Sequence; Biomarkers, Tumor; Calcium-Binding Proteins; | 2004 |
Polymorphisms of the receptor of advanced glycation endproducts (RAGE) and the development of nephropathy in type 1 diabetic patients.
Topics: Amino Acid Substitution; Arginine; Cross-Sectional Studies; Cysteine; Diabetes Mellitus, Type 1; Dia | 2005 |
Fibronectin and collagen of cultured skin fibroblasts in diabetes mellitus.
Topics: Adult; Cells, Cultured; Collagen; Diabetes Mellitus, Type 1; Fibroblasts; Fibronectins; Glycine; Hum | 1981 |
Absence of the Gly40-Ser mutation in the glucagon receptor among diabetic patients in the Netherlands.
Topics: Aged; Cohort Studies; Diabetes Mellitus, Type 1; Diabetes Mellitus, Type 2; Gene Frequency; Glycine; | 1995 |
Missense mutation Gly574Ser in the transcription factor HNF-1alpha is a marker of atypical diabetes mellitus in African-American children.
Topics: Adult; Amino Acid Substitution; Black People; Child; Diabetes Mellitus, Type 1; Diabetes Mellitus, T | 1999 |
Hemoglobin A1C separation by isoelectric focusing.
Topics: Alanine; Aminocaproic Acid; Diabetes Mellitus, Type 1; Glycine; Hemoglobin A; Histidine; Humans; Iso | 1978 |
Whole body de novo amino acid synthesis in type I (insulin-dependent) diabetes studied with stable isotope-labeled leucine, alanine, and glycine.
Topics: Adolescent; Adult; Alanine; Amino Acids; Diabetes Mellitus, Type 1; Glucose; Glycine; Humans; Hyperg | 1985 |