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fructosamine

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Description

Fructosamine is a glycated protein that forms when glucose reacts with the amino group of proteins. It is a measure of average blood glucose levels over the past 2-3 weeks. Fructosamine is synthesized through a non-enzymatic reaction known as the Maillard reaction. It is a byproduct of the glycosylation of proteins, a process that occurs when glucose binds to proteins. Increased fructosamine levels can be an indicator of poor blood glucose control in individuals with diabetes. It is studied because it can help predict the risk of complications associated with diabetes, such as neuropathy, retinopathy, and nephropathy. Fructosamine is also used to monitor the effectiveness of diabetes treatment.'

Fructosamine: An amino sugar formed when glucose non-enzymatically reacts with the N-terminal amino group of proteins. The fructose moiety is derived from glucose by the classical Amadori rearrangement. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID20484
MeSH IDM0028699

Synonyms (9)

Synonym
d-isoglucosamine
fructosamine
4429-04-3
(2r,3s,4r,5r)-2-(aminomethyl)oxane-2,3,4,5-tetrol
d-fructose, 1-amino-1-deoxy-
1-amino-1-deoxy-beta-d-fructopyranose
Q289357
IXZISFNWUWKBOM-ARQDHWQXSA-N
DTXSID901296885

Research Excerpts

Overview

Fructosamine is a glycated protein that reflects blood glucose control over the last 2-3 weeks. It has been suggested as a useful complement to glycated hemoglobin (HbA1c) for the diagnosis and monitoring of diabetes.

ExcerptReferenceRelevance
"Fructosamine is a measure of short-term glycemic control, which has been suggested as a useful complement to glycated hemoglobin (HbA1c) for the diagnosis and monitoring of diabetes. "( An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript.
Barroso, I; Butterworth, AS; Danesh, J; Di Angelantonio, E; Riveros-Mckay, F; Roberts, D; Selvin, E; Soranzo, N; Yu, B, 2022
)
2.42
"Fructosamine is a good predictor of adverse outcomes in patients undergoing THA and should be used routinely to mitigate morbidity and mortality risk."( Fructosamine is a valuable marker for glycemic control and predicting adverse outcomes following total hip arthroplasty: a prospective multi-institutional investigation.
Breckenridge, L; Goswami, K; Held, MB; Malkani, AL; Parvizi, J; Schwarzkopf, R; Shah, RP; Shohat, N, 2021
)
2.79
"Fructosamine measurement is an imperfect surrogate marker for classifying glycaemic control in diabetic dogs and can only complement serial glucose measurements."( Evaluation of fructosamine concentration as an index marker for glycaemic control in diabetic dogs.
Beer, R; Schwendenwein, I; Zeugswetter, FK, 2022
)
2.52
"Fructosamine is a valid and an excellent predictor of complications following TKA. "( 2019 John Insall Award: Fructosamine is a better glycaemic marker compared with glycated haemoglobin (HbA1C) in predicting adverse outcomes following total knee arthroplasty: a prospective multicentre study.
Goswami, K; Kheir, M; Malkani, AL; Parvizi, J; Schwarzkopf, R; Shah, RP; Shohat, N; Tan, TL; Tarabichi, M, 2019
)
2.26
"Fructosamine is a glycemic biomarker which may be useful for indication and control of diabetes respectively."( Fructosamine is a useful indicator of hyperglycaemia and glucose control in clinical and epidemiological studies--cross-sectional and longitudinal experience from the AMORIS cohort.
Grill, V; Gudbjörnsdottir, S; Hammar, N; Jungner, I; Malmström, H; Walldius, G, 2014
)
3.29
"Fructosamine is a marker of glucose control reflecting the average glycaemic level over the preceding 2-3 weeks. "( Fructosamine measurement for diabetes mellitus diagnosis and monitoring: a systematic review and meta-analysis protocol.
Balti, EV; Fokom-Domgue, J; Kengne, AP; Nansseu, JR; Noubiap, JJ; Sobngwi, E, 2015
)
3.3
"Fructosamine is a biomarker of glycation but its associations to macrovascular complications are not well documented."( Fructosamine is a risk factor for myocardial infarction and all-cause mortality - Longitudinal experience from the AMORIS cohort.
Grill, V; Hammar, N; Jungner, I; Malmström, H; Walldius, G, 2015
)
2.58
"Fructosamine is a glycated protein that reflects blood glucose control over the last 2-3 weeks. "( The impact of intra-articular methylprednisolone acetate injection on fructosamine levels in diabetic patients with osteoarthritis of the knee, a case-control study.
Artul, S; Habib, G; Hakim, G; Jabaly-Habib, H; Jabbour, A; Khazin, F; Sakas, F, 2016
)
2.11
"Fructosamine is a short-time marker of blood protein glycation."( UVR protection influences fructosamine level after sun exposure of healthy adults.
Fendler, W; Lesiak, A; Małachowska, B; Mianowska, B; Młynarski, W; Narbutt, J; Young, AR, 2016
)
1.46
"Fructosamine serves as an indicator of overall glycemic control for a 10-14-day time frame versus the 90-day average indicated by the hemoglobin A1c (A1C) test."( A prospective, randomized, multicentered controlled trial to compare the annual outcomes of patients with diabetes mellitus monitored with weekly fructosamine testing versus usual care: a 3-month interim analysis.
Brown, S; Carter, AW; Greene, D; Lindsey, CC; Mangum, S; McCandless, B; Richardson, A, 2002
)
1.24
"Fructosamine is an indicator of overall glycemic control for a 10-14-day time frame, medium-term marker, versus the 90-day average indicated by the hemoglobin A1c (A1C) test. "( A prospective, randomized, multicentered controlled trial to compare the annual glycemic and quality outcomes of patients with diabetes mellitus monitored with weekly fructosamine testing versus usual care.
Brown, SJ; Carter, AW; Essary, JL; Greene, D; Lindsey, CC; Mangum, S; McCandless, B; Richardson, A, 2004
)
1.96
"The fructosamine test is a valuable parameter for the diagnosis and metabolic control of diabetes mellitus in dogs and cats."( Fructosamine. A new parameter for diagnosis and metabolic control in diabetic dogs and cats.
Hoyer, M; Liehs, MR; Reusch, CE; Vochezer, R,
)
2.05
"Fructosamine assay is a new test used in the diagnosis and monitoring of diabetic patients. "( Fructosamine as a possible monitoring parameter in non-insulin dependent diabetes mellitus patients with periodontal disease.
Firatli, E; Meric, H; Oz, H; Sivas, A; Unal, T, 1993
)
3.17
"Fructosamine is a potentially useful post-load glycaemia index."( Diagnostic value of fasting capillary glucose, fructosamine and glycosylated haemoglobin in detecting diabetes and other glucose tolerance abnormalities compared to oral glucose tolerance test.
Ciechanowski, K; Herdzik, E; Safranow, K, 2002
)
1.29
"Fructosamine is thought to be an alternative diabetic long term parameter to HbAlc. "( [The value of fructosamine in hemodialysis patients].
Brunnbauer, M; Graf, H; Küenburg, E; Müller, MM; Prager, R; Watzinger, U; Winter, F, 1990
)
2.08

Effects

Fructosamine has a precise and inexpensive measurement. It is not affected by haemoglobin characteristics. Fructosamines oxidase has a lysine near N5 of its flavin.

Fructosamine has long been considered as a key intermediate of the Maillard reaction, which to a large extent is responsible for specific aroma, taste, and color formation in thermally processed or dehydrated foods. The test has the advantage of accurately reflecting shorter-term changes in glycemia that correspond to the half-life of albumin.

ExcerptReferenceRelevance
"Fructosamine has a precise and inexpensive measurement and it is not affected by haemoglobin characteristics."( Beyond self-monitored plasma glucose and HbA1c: the role of non-traditional glycaemic markers in gestational diabetes mellitus.
Mendes, N; Serrano, F; Tavares Ribeiro, R, 2018
)
1.2
"Fructosamine oxidase has a lysine near N5 of its flavin."( Oxygen reactivity in flavoenzymes: context matters.
Collard, F; Fagan, RL; McDonald, CA; Monnier, VM; Palfey, BA, 2011
)
1.09
"Fructosamine has long been considered as a key intermediate of the Maillard reaction, which to a large extent is responsible for specific aroma, taste, and color formation in thermally processed or dehydrated foods. "( 1-Amino-1-deoxy-d-fructose ("fructosamine") and its derivatives.
Mawhinney, TP; Mossine, VV, 2023
)
2.64
"Fructosamine has a precise and inexpensive measurement and it is not affected by haemoglobin characteristics."( Beyond self-monitored plasma glucose and HbA1c: the role of non-traditional glycaemic markers in gestational diabetes mellitus.
Mendes, N; Serrano, F; Tavares Ribeiro, R, 2018
)
1.2
"Fructosamine has not gained as much popularity as glycated haemoglobin (HbA1c) for diabetes mellitus (DM) control monitoring, and the related underlying reasons remain unclear."( Fructosamine measurement for diabetes mellitus diagnosis and monitoring: a systematic review and meta-analysis protocol.
Balti, EV; Fokom-Domgue, J; Kengne, AP; Nansseu, JR; Noubiap, JJ; Sobngwi, E, 2015
)
2.58
"Fructosamine also has the advantage of accurately reflecting shorter-term changes in glycemia that correspond to the half-life of albumin."( Fructosamine--an underutilized tool in diabetes management: case report and literature review.
El Abbassi, A; Jordan, RM; Peiris, AN; Youssef, D, 2008
)
2.51
"Fructosamine has long been considered as a key intermediate of the Maillard reaction, which to a large extent is responsible for specific aroma, taste, and color formation in thermally processed or dehydrated foods. "( 1-Amino-1-deoxy-D-fructose ("fructosamine") and its derivatives.
Mawhinney, TP; Mossine, VV, 2010
)
2.09
"Fructosamine oxidase has a lysine near N5 of its flavin."( Oxygen reactivity in flavoenzymes: context matters.
Collard, F; Fagan, RL; McDonald, CA; Monnier, VM; Palfey, BA, 2011
)
1.09
"The fructosamine test has got many desirable characteristics, which will give it a role in the assessment of diabetic control."( The use of plasma fructosamine in the assessment of diabetic control.
Atabani, GS; Elmahdi, EM; elWali, NM; Mukhtar, E; Saeed, BO,
)
0.95
"Fructosamine has many advantages over HbA1 measurement such as speed, technical ease, and low cost, and is a reliable alternative to HbA1 estimation as an indication of glycaemic control."( Serum fructosamine and glycated haemoglobin measurements in diabetic control.
Clark, SA; Gatt, JA; Hindle, EJ; Rostron, GM, 1986
)
1.47

Toxicity

ExcerptReferenceRelevance
" The pattern of adverse events and injection site reactions with HOE 901 was similar to that with NPH."( Efficacy and safety of HOE 901 versus NPH insulin in patients with type 1 diabetes. The European Study Group of HOE 901 in type 1 diabetes.
Derobert, E; Eugène-Jolchine, I; Pieber, TR, 2000
)
0.31
" There were no differences between the two insulins in the occurrence of hyperglycemic events (blood glucose >19 mmol/l) or in the number and type of adverse events."( Efficacy, safety, and pump compatibility of insulin aspart used in continuous subcutaneous insulin infusion therapy in patients with type 1 diabetes.
Bode, BW; Strange, P, 2001
)
0.31
" However, alongside this indispensable role for cell survival and growth, glucose is intrinsically toxic by reacting with primary amines such as lysine in proteins in a non-enzymatic glycation process (a."( Intrinsic toxicity of glucose, due to non-enzymatic glycation, is controlled in-vivo by deglycation systems including: FN3K-mediated deglycation of fructosamines and transglycation of aldosamines.
Szwergold, BS, 2005
)
0.53
" The overall incidence of adverse events was similar for all treatment groups, but fewer patients in the extended-release metformin groups discontinued treatment due to nausea during the initial dosing period than in the immediate-release metformin group."( Efficacy, tolerability, and safety of a novel once-daily extended-release metformin in patients with type 2 diabetes.
Berner, B; Chiang, YK; Cramer, M; Fonseca, V; Lewin, A; Schwartz, S, 2006
)
0.33
"Once- or twice-daily extended-release metformin was as safe and effective as twice-daily immediate-release metformin and provided continued glycemic control for up to 24 weeks of treatment."( Efficacy, tolerability, and safety of a novel once-daily extended-release metformin in patients with type 2 diabetes.
Berner, B; Chiang, YK; Cramer, M; Fonseca, V; Lewin, A; Schwartz, S, 2006
)
0.33
"The study objective was to determine if Ramadan fasting was safe in patients with type 2 diabetes mellitus (T2D), based upon a determination of the effect of fasting on a broad range of physiological and clinical parameters, including markers of glycemic control and blood pressure."( Is Ramadan fasting safe in type 2 diabetic patients in view of the lack of significant effect of fasting on clinical and biochemical parameters, blood pressure, and glycemic control?
Chabraoui, L; Chebraoui, L; Chraibi, A; El Guessabi, L; Fellat, S; Israili, ZH; Lyoussi, B; M'guil, M; Ragala, MA, 2008
)
0.35
" plus single-dose insulin glargine regimen was safe for low-risk type 2 diabetic patients who insisted on fasting during Ramadan."( Repaglinide plus single-dose insulin glargine: a safe regimen for low-risk type 2 diabetic patients who insist on fasting in Ramadan.
Bakiner, O; Bozkirli, E; Demirag, NG; Ertorer, ME; Tutuncu, NB, 2009
)
0.35
"The incidence of treatment-emergent adverse events was similar for placebo and ipragliflozin groups."( Safety, pharmacokinetic, and pharmacodynamic profiles of ipragliflozin (ASP1941), a novel and selective inhibitor of sodium-dependent glucose co-transporter 2, in patients with type 2 diabetes mellitus.
Akinlade, B; Klasen, S; Kowalski, D; Schwartz, SL; Wilpshaar, W; Zhang, W, 2011
)
0.37
" Mandatory consideration to the quality and quantity of food offered to patients with T1DM during Ramadan to guard against adverse changes in lipid profile."( Safety and metabolic impact of Ramadan fasting in children and adolescents with type 1 diabetes.
Abo-Elmagd, M; Chalaby, N; El-Gilany, A; El-Hawary, A; El-Ziny, M; Elsharkawy, A; Metwali, A; Salem, N; Wafa, A, 2016
)
0.43
" Commonly observed adverse events included emesis, diarrhea, anorexia, lethargy, and dehydration."( Safety and effectiveness of the sodium-glucose cotransporter inhibitor bexagliflozin in cats newly diagnosed with diabetes mellitus.
Bienhoff, SE; Dupree, TJ; Geller, S; Hadd, MJ; Little, SE; Ogne-Stevenson, J; Scott-Moncrieff, JC,
)
0.13

Pharmacokinetics

ExcerptReferenceRelevance
"For the pharmacokinetic study, a single, 600-mg dose of either controlled-release LA (CRLA) or quick-release LA (QRLA) was administered orally to 12 normal human subjects."( Pharmacokinetics, tolerability, and fructosamine-lowering effect of a novel, controlled-release formulation of alpha-lipoic acid.
Evans, JL; Gavin, LA; Goldfine, ID; Heymann, CJ,
)
0.41
"This study was conducted to evaluate the pharmacokinetic (PK), pharmacodynamic (PD), and tolerability profiles and explore the efficacy of multiple oral doses of alogliptin in patients with T2D."( Pharmacokinetic, pharmacodynamic, and tolerability profiles of the dipeptidyl peptidase-4 inhibitor alogliptin: a randomized, double-blind, placebo-controlled, multiple-dose study in adult patients with type 2 diabetes.
Christopher, R; Covington, P; Davenport, M; Fleck, P; Karim, A; Mekki, QA; Wann, ER, 2008
)
0.35
"This Phase 2, randomized, placebo-controlled study investigated the safety, tolerability, and pharmacokinetic and pharmacodynamic profiles of the novel oral SGLT2 inhibitor ipragliflozin (ASP1941) in T2DM patients."( Safety, pharmacokinetic, and pharmacodynamic profiles of ipragliflozin (ASP1941), a novel and selective inhibitor of sodium-dependent glucose co-transporter 2, in patients with type 2 diabetes mellitus.
Akinlade, B; Klasen, S; Kowalski, D; Schwartz, SL; Wilpshaar, W; Zhang, W, 2011
)
0.37

Compound-Compound Interactions

ExcerptReferenceRelevance
"05) reduced hyperglycemia, glibenclamide or metformin combined with honey produced significantly much lower blood glucose (8."( Glibenclamide or metformin combined with honey improves glycemic control in streptozotocin-induced diabetic rats.
Erejuwa, OO; Gurtu, S; Salleh, MS; Sirajudeen, KN; Sulaiman, SA; Wahab, MS, 2011
)
0.37
" However, the sensitivity of A1C combined with fructosamine was not better than for A1C alone (72% vs."( A1C Combined With Glycated Albumin Improves Detection of Prediabetes in Africans: The Africans in America Study.
Aldana, PC; Chung, ST; Duong, MT; Lozier, JN; Ricks, M; Sacks, DB; Sumner, AE; Tulloch-Reid, MK, 2016
)
0.69

Bioavailability

ExcerptReferenceRelevance
" Provinols enhanced NO bioavailability resulting from increased nitric oxide (NO) production through enhanced endothelial NO-synthase (eNOS) activity and reduced superoxide anion release via decreased expression of NADPH oxidase membrane sub-unit, Nox-1."( Red wine polyphenols prevent metabolic and cardiovascular alterations associated with obesity in Zucker fatty rats (Fa/Fa).
Agouni, A; Andriantsitohaina, R; Desmoulin, F; Heymes, C; Lagrue-Lak-Hal, AH; Martínez, MC; Mostefai, HA; Mulder, P; Rouet, P; Tesse, A, 2009
)
0.35
" This aim of the study is to evaluate the therapeutic potential of CNX-011-67, a highly selective, potent and orally bioavailable GPR40 agonist, in controlling diabetes and other metabolic parameters."( Treatment with CNX-011-67, a novel GPR40 agonist, delays onset and progression of diabetes and improves beta cell preservation and function in male ZDF rats.
Anup, MO; Aparna, K; Biswas, S; Dandu, A; Gowda, N; Jagannath, MR; Lakshmi, MN; Moolemath, Y; Raghav, V; Reddy, A; Sadasivuni, M; Shilpa, PC; Singh, J; Somesh, BP; Sunil, V; Venkataranganna, MV; Verma, MK, 2013
)
0.39
" The occurrence of the MR during the digestion process may reduce the bioavailability of essential amino acids and increase the production of MRPs causing health disorders."( In vitro formation of Maillard reaction products during simulated digestion of meal-resembling systems.
Cai, W; Del Castillo, MD; Fernandez-Gomez, B; Martinez-Saez, N; Uribarri, J, 2019
)
0.51

Dosage Studied

For all cats, a significant increase in mean dosage of PZI and significant decreases in 9-hour mean blood glucose concentration were detected. The first dosage of plasma fructosamine found in 65 medical records was analyzed during prenatal care.

ExcerptRelevanceReference
" The drug was more effective in a dosage of 400 mg than with 200 mg (the rate of efficacy 46% vs 25%) and more effective in obese patients than in lean patients (46% vs 25%)."( A pilot clinical trial of a new oral hypoglycemic agent, CS-045, in patients with non-insulin dependent diabetes mellitus.
Akanuma, Y; Iwamoto, Y; Kajinuma, H; Kasuga, M; Kosaka, K; Kuzuya, T; Shigeta, Y; Takebe, K; Yamanouchi, T; Yoshida, S, 1991
)
0.28
" The aim of the french multicentric study is to estimate the clinical interest of a new insulin-pen (Optipen-Hoechst) with two main characteristics: the ability of a predetermination of the insulin dosage to be administered and the suitability for both regular, intermediate and pre-mixed regular (25%) and intermediate (75%) Hoechst insulin preparations."( [Feasibility and acceptability of insulin therapy using a pen suitable for injecting regular or intermediate insulin. Results of the French multicenter study conducted by the Optipen-France Study Group].
Pasqual, C; Pinget, M; Sandre, D; Vexiau, P; Weisselberg, C, 1990
)
0.28
"To evaluate the possible interest of the dosage of glycated plasma proteins in the diagnosis of glucidic intolerance, OGTT with determination of glycaemia and insulinaemia, HbA1c and fructosamine was determined in 6 normal and 35 obese subjects."( [The importance of glycosylated plasma protein determination in the diagnosis of carbohydrate intolerance in obesity].
Ardizzi, A; Conti, A; Grugni, G; Morabito, F; Moreni, G; Sartorio, A, 1990
)
0.47
" Total insulin dosage was similar (NPH 56."( Double-blind crossover trial of isophane (NPH)- and lente-based insulin regimens.
Alberti, KG; Burrin, JM; Davis, SN; Home, PD; Jensen, I; Murphy, M; Newens, A; Tunbridge, FK, 1989
)
0.28
" Dose-response curves were constructed using sequential euglycaemic (5."( The course and determinants of insulin action in type 1 (insulin-dependent) diabetes mellitus.
Frölich, M; Krans, HM; Nijs, HG; Radder, JK, 1989
)
0.28
" The test indications of the assay could be: situations where the dosage of glycated haemoglobin is not interpretable, diabetic pregnancy follow-up and short term evaluation of a therapeutic change on glycaemic control."( [Assay of fructosamine. Value and limits in diabetology].
Durlach, V; Gillery, P; Gross, A; Leutenegger, M; Ostermann, G; Pasqual, C, 1989
)
0.68
" The selection of serum albumin and the concentration used in the standard solutions is critical since the dose-response curve is affected differently and will therefore influence the estimated values."( The estimation of serum fructosamine: an alternative measurement to glycated haemoglobin.
Gatt, JA; Hindle, EJ; Rostron, GM, 1985
)
0.58
" Therapy was initiated with human insulin 20 IU/day and 500 mg cholopropamide, titrating insulin dosage in order to achieve euglycemia."( [Response of insulin and C-peptide to a mixed meal in non-insulin-dependent diabetics treated with insulin and chlorpropamide].
Alemán-Hoey, DD; García-Rubi, E,
)
0.13
"0 kg m-2, who were poorly controlled on insulin (mean dosage 58."( Obese patients with type 2 diabetes poorly controlled by insulin and metformin: effects of adjunctive dexfenfluramine therapy on glycaemic control.
Molyneaux, LM; Willey, KA; Yue, DK,
)
0.13
" Yet the adequate dosage required for immunomodulation has to be established and the toxicity of high-dose arginine has not been fully elucidated."( Low-dose dietary L-arginine increases plasma interleukin 1 alpha but not interleukin 1 beta in patients with diabetes mellitus.
Hayde, M; Lubec, B; Lubec, G; Popow, C; Vierhapper, H; Weninger, M; Xi, Z, 1994
)
0.29
" The progestogen was administered from day 5 to day 24 of the cycle, over six consecutive cycles, at a dosage (5 mg/d) known to inhibit ovulation."( Effects of nomegestrol acetate on carbohydrate metabolism.
Choisy, H; Dorangeon, P; Hazard, MC; Lumbroso, M; Thomas, JL,
)
0.13
" Over 2 weeks, patients' regimens were titrated to a maximal dosage of 500 mg tid."( Combination of low-dose niacin and pravastatin improves the lipid profile in diabetic patients without compromising glycemic control.
Fonseca, VA; Gardner, SF; Granberry, MC; Marx, MA; Skelton, DR; White, LM, 1997
)
0.3
" Pramlintide was administered subcutaneously prior to meals in four dosing regimens: 30 microg four times per day (breakfast, lunch, dinner, and evening snack), 30 microg three times per day (breakfast, lunch and dinner [BLD]), 30 microg three times per day (breakfast, dinner and evening snack [BDS]), and 60 microg twice per day (breakfast and dinner)."( Effects of 4 weeks' administration of pramlintide, a human amylin analogue, on glycaemia control in patients with IDDM: effects on plasma glucose profiles and serum fructosamine concentrations.
Kolterman, OG; Pearson, L; Thompson, RG, 1997
)
0.49
"To compare glycemic control obtained with the new rapid-acting insulin analog insulin aspart with that obtained with unmodified human insulin using algorithm-driven dosage adjustment."( Improved glycemic control with insulin aspart: a multicenter randomized double-blind crossover trial in type 1 diabetic patients. UK Insulin Aspart Study Group.
Home, PD; Hylleberg, B; Lindholm, A; Round, P, 1998
)
0.3
" Neither dosage nor glucocorticoid employed were modified during the study."( An open comparison of the diabetogenic effect of deflazacort and prednisone at a dosage ratio of 1.5 mg:1 mg.
Blanch Sancho, JJ; Carmona Martín, M; Navarro López, V; Puras Tellaeche, A; Sáez Barcelona, JA, 1999
)
0.3
" Adjustments in dosage of PZI were made as needed to attain control of glycemia."( Efficacy of protamine zinc insulin for treatment of diabetes mellitus in cats.
Lynn, RC; Michels, GM; Nelson, RW; Wagner-Mann, CC, 2001
)
0.31
"For all cats, a significant increase in mean dosage of PZI and significant decreases in 9-hour mean blood glucose concentration, lowest mean blood glucose concentration, and mean serum fructosamine concentration were detected."( Efficacy of protamine zinc insulin for treatment of diabetes mellitus in cats.
Lynn, RC; Michels, GM; Nelson, RW; Wagner-Mann, CC, 2001
)
0.5
"To evaluate the efficacy and safety of two dosage strengths of a single-tablet metformin-glibenclamide (glyburide) combination, compared with the respective monotherapies, in patients with Type 2 diabetes mellitus (DM) inadequately controlled by metformin monotherapy."( Improved glycaemic control with metformin-glibenclamide combined tablet therapy (Glucovance) in Type 2 diabetic patients inadequately controlled on metformin.
Allavoine, T; Howlett, H; Lehert, P; Marre, M, 2002
)
0.31
" After Ramadan, patients resumed their regular meal pattern and treatment dosage for 4 weeks."( Repaglinide versus glibenclamide treatment of Type 2 diabetes during Ramadan fasting.
Mafauzy, M, 2002
)
0.31
"Preprandial dosing (within 5 min before meal) and postprandial dosing (15-20 min after meal onset) of NovoLog Mix 70/30 (BIAsp 30, a biphasic formulation of insulin aspart, 30% soluble and 70% protamine-crystallized) were compared in elderly (> or =65 years) type 2 diabetes patients in this open-label, 12-week, crossover study."( Postprandial versus preprandial dosing of biphasic insulin aspart in elderly type 2 diabetes patients.
Allen, E; Conway, MJ; Klaff, LJ; Rosenstock, J; Warren, ML, 2004
)
0.32
" The overall incidence of adverse events was similar for all treatment groups, but fewer patients in the extended-release metformin groups discontinued treatment due to nausea during the initial dosing period than in the immediate-release metformin group."( Efficacy, tolerability, and safety of a novel once-daily extended-release metformin in patients with type 2 diabetes.
Berner, B; Chiang, YK; Cramer, M; Fonseca, V; Lewin, A; Schwartz, S, 2006
)
0.33
"In a prospective study, were dosed serum leptin level with radioimmunoassay technique, fasting plasma glucose through of the glucoseoxidase-peroxidase reaction, the hemoglobin glycate using the technique microchromatography for ionic exchange resin and insulin through immunoassay system."( [Generalized congenital lipodystrophy: correlation with leptin and other biochemical parameters].
Baracho, Mde F; Brandão-Neto, J; da Silva, AS; de Medeiros, TM; Gurgel, AM; Santos, MG, 2005
)
0.33
" On day 14, mean peak DPP-4 inhibition ranged from 94% to 99%, and mean inhibition at 24 hours after dosing ranged from 82% to 97% across all alogliptin doses."( Pharmacokinetic, pharmacodynamic, and tolerability profiles of the dipeptidyl peptidase-4 inhibitor alogliptin: a randomized, double-blind, placebo-controlled, multiple-dose study in adult patients with type 2 diabetes.
Christopher, R; Covington, P; Davenport, M; Fleck, P; Karim, A; Mekki, QA; Wann, ER, 2008
)
0.35
" The PK and PD profiles of multiple doses of alogliptin in this study supported use of a once-daily dosing regimen."( Pharmacokinetic, pharmacodynamic, and tolerability profiles of the dipeptidyl peptidase-4 inhibitor alogliptin: a randomized, double-blind, placebo-controlled, multiple-dose study in adult patients with type 2 diabetes.
Christopher, R; Covington, P; Davenport, M; Fleck, P; Karim, A; Mekki, QA; Wann, ER, 2008
)
0.35
" The first dosage of plasma fructosamine found in 65 medical records was analyzed during prenatal care (20."( Echocardiographic findings of congenital cardiopathies among fetuses of diabetic pregnant women and their relationship with plasma fructosamine levels.
Bragança, RD; Cabral, AC; Costa, CR; Lage, EM; Miranda, AP; Reis, ZS, 2011
)
0.87
" Adjustments in dosage of rhPZI were made as needed to control glycemia."( Efficacy of protamine zinc recombinant human insulin for controlling hyperglycemia in dogs with diabetes mellitus.
Dennis, J; Johnson, E; Kass, PH; Maggiore, AD; Nelson, RW,
)
0.13
" At time of calving, nine ruminally cannulated Holstein cows were randomly assigned to ruminal dosing of 500 g/d tap water (CON, n = 4) or 500 g/d PG (PPG, n = 5)."( Effect of postpartum propylene glycol allocation to over-conditioned Holstein cows on concentrations of milk metabolites.
Bjerre-Harpøth, V; Larsen, M; Larsen, T; Storm, AC; Vestergaard, M, 2016
)
0.43
" For BBIT, owners were instructed to continue NPH insulin administration at the usual dosage at home (q 12 h, with feeding) and to administer lispro insulin (0."( Effects of treatment with lispro and neutral protamine Hagedorn insulins on serum fructosamine and postprandial blood glucose concentrations in dogs with clinically well-controlled diabetes mellitus and postprandial hyperglycemia.
Bertalan, AV; Drobatz, KJ; Hess, RS, 2020
)
0.78
" Cats were dosed PO with 15 mg bexagliflozin once daily for 56 days, with a 124-day extension to evaluate safety and treatment effect durability."( Safety and effectiveness of the sodium-glucose cotransporter inhibitor bexagliflozin in cats newly diagnosed with diabetes mellitus.
Bienhoff, SE; Dupree, TJ; Geller, S; Hadd, MJ; Little, SE; Ogne-Stevenson, J; Scott-Moncrieff, JC,
)
0.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Pathways (3)

PathwayProteinsCompounds
Selenium micronutrient network095
Vitamin B12 metabolism050
Folate metabolism156

Research

Studies (1,469)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990247 (16.81)18.7374
1990's542 (36.90)18.2507
2000's321 (21.85)29.6817
2010's275 (18.72)24.3611
2020's84 (5.72)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 78.49

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index78.49 (24.57)
Research Supply Index7.49 (2.92)
Research Growth Index4.70 (4.65)
Search Engine Demand Index141.18 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (78.49)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials202 (12.69%)5.53%
Reviews81 (5.09%)6.00%
Case Studies35 (2.20%)4.05%
Observational6 (0.38%)0.25%
Other1,268 (79.65%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]