Page last updated: 2024-10-17

lactic acid and Glycogenosis

lactic acid has been researched along with Glycogenosis in 26 studies

Lactic Acid: A normal intermediate in the fermentation (oxidation, metabolism) of sugar. The concentrated form is used internally to prevent gastrointestinal fermentation. (From Stedman, 26th ed)
2-hydroxypropanoic acid : A 2-hydroxy monocarboxylic acid that is propanoic acid in which one of the alpha-hydrogens is replaced by a hydroxy group.

Research Excerpts

ExcerptRelevanceReference
"The fasting glucagon test of 40 patients with hepatic glycogen storage disease (type I, 13 patients; type Ib, 5 patients; type III, 12 patients; type IX (phosphorylase kinase deficiency), 10 patients) has been reviewed."7.66Value of the glucagon test in screening for hepatic glycogen storage disease. ( Dunger, DB; Leonard, JV, 1982)
"The plasma glucose, insulin, glucagon, lactate and amino acid response patterns to glucose and protein meals were examined in 11 patients with type III glycogen storage disease (GSD-III)."3.66Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis. ( Bashan, N; Coleman, RA; Moses, S; Mushlin, P; Shipp, E; Slonim, AE, 1983)
"The fasting glucagon test of 40 patients with hepatic glycogen storage disease (type I, 13 patients; type Ib, 5 patients; type III, 12 patients; type IX (phosphorylase kinase deficiency), 10 patients) has been reviewed."3.66Value of the glucagon test in screening for hepatic glycogen storage disease. ( Dunger, DB; Leonard, JV, 1982)
"The ketosis was reversed by glucagon administration."1.27Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency. ( Brown, BI; Burke, BA; Tuchman, M; Ulstrom, RA, 1986)
"Three patients with McArdle's disease exercised for 2 h at 30% VO2max."1.27The second wind phenomenon in McArdle's disease. ( Binkhorst, RA; Braakhekke, JP; de Bruin, MI; Joosten, EM; Stegeman, DF; Wevers, RA, 1986)

Research

Studies (26)

TimeframeStudies, this research(%)All Research%
pre-199017 (65.38)18.7374
1990's2 (7.69)18.2507
2000's3 (11.54)29.6817
2010's2 (7.69)24.3611
2020's2 (7.69)2.80

Authors

AuthorsStudies
Serrano-Lorenzo, P1
Rabasa, M1
Esteban, J1
Hidalgo Mayoral, I1
Domínguez-González, C1
Blanco-Echevarría, A1
Garrido-Moraga, R1
Lucia, A1
Blázquez, A1
Rubio, JC1
Palma-Milla, C1
Arenas, J1
Martín, MA1
Regan, JA1
Golubski, B1
Gilbert, EB1
Sullivan, B1
McCall, SJ1
Sata, SS1
Preisler, N1
Laforêt, P2
Echaniz-Laguna, A1
Ørngreen, MC1
Lonsdorfer-Wolf, E1
Doutreleau, S1
Geny, B1
Stojkovic, T2
Piraud, M2
Petit, FM1
Vissing, J2
Petit, F1
Orngreen, MC1
Andersen, G1
Claeys, KG1
Wary, C1
Hogrel, JY1
Soggia, AP1
Correa-Giannella, ML1
Fortes, MA1
Luna, AM1
Pereira, MA1
Tarnopolsky, M1
Stevens, L1
MacDonald, JR1
Rodriguez, C1
Mahoney, D1
Rush, J1
Maguire, J1
OEI, TL1
Bröjer, JT1
Essén-Gustavsson, B1
Annandale, EJ1
Valberg, SJ1
Mineo, I2
Kono, N2
Shimizu, T2
Sumi, S2
Nonaka, K2
Tarui, S2
Slonim, AE1
Coleman, RA1
Moses, S1
Bashan, N1
Shipp, E1
Mushlin, P1
Greene, HL1
Rumpf, KW1
Wagner, H1
Kaiser, H1
Meinck, HM1
Goebel, HH1
Scheler, F1
Hagberg, JM1
Coyle, EF1
Carroll, JE1
Miller, JM1
Martin, WH1
Brooke, MH1
Dunger, DB1
Leonard, JV1
Clark, DG2
Neville, SD2
Brinkman, M2
Filsell, OH1
de Barsy, T1
Hers, HG1
Nishimura, Y1
Challiss, RA1
Leighton, B1
Wilson, S1
Thurlby, PL1
Arch, JR1
Biggemann, B1
Hilgarth, R1
Wendel, U1
Smit, GP1
Ververs, MT1
Belderok, B1
Van Rijn, M1
Berger, R1
Fernandes, J1
Tuchman, M1
Brown, BI1
Burke, BA1
Ulstrom, RA1
Braakhekke, JP1
de Bruin, MI1
Stegeman, DF1
Wevers, RA1
Binkhorst, RA1
Joosten, EM1
van Riet, W1
de Meirsman, J1
de Saedeleer, J1
Dom, R1
Carton, H1
van den Heede, J1
Bulcke, JA1
Hara, N1
Yamada, Y1
Haynes, WD1
Williams, J1
Hosking, G1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
The Effect of Triheptanoin in Adults With McArdle Disease (Glycogen Storage Disease Type V)[NCT02432768]Phase 222 participants (Actual)Interventional2015-04-30Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

2 reviews available for lactic acid and Glycogenosis

ArticleYear
Glycogen storage disease.
    Seminars in liver disease, 1982, Volume: 2, Issue:4

    Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog

1982
Normal metabolism and disorders of carbohydrate metabolism.
    Bailliere's clinical endocrinology and metabolism, 1990, Volume: 4, Issue:3

    Topics: Carbohydrate Metabolism; Enzymes; Glucose; Glycogen; Glycogen Storage Disease; Glycolysis; Humans; L

1990

Trials

1 trial available for lactic acid and Glycogenosis

ArticleYear
[Type I glycogenosis: extending therapy with uncooked cornstarch].
    Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde, 1986, Volume: 134, Issue:3

    Topics: Adolescent; Blood Glucose; Child; Child, Preschool; Combined Modality Therapy; Creatinine; Enteral N

1986

Other Studies

23 other studies available for lactic acid and Glycogenosis

ArticleYear
Clinical, Biochemical, and Molecular Characterization of Two Families with Novel Mutations in the
    Genes, 2022, 10-11, Volume: 13, Issue:10

    Topics: Codon, Nonsense; Dermatitis; Female; Glycogen Storage Disease; Humans; Isoenzymes; Lactate Dehydroge

2022
Glycogenic Hepatopathy Causing Elevated Lactic Acid and Liver Enzymes.
    The American journal of medicine, 2020, Volume: 133, Issue:2

    Topics: Alanine Transaminase; Alkaline Phosphatase; Aspartate Aminotransferases; Blood Glucose; Diabetes Mel

2020
Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiency.
    The Journal of clinical endocrinology and metabolism, 2013, Volume: 98, Issue:7

    Topics: Adult; Bicycling; Carbohydrate Metabolism; Exercise Test; Exercise Tolerance; Glucose; Glycogen Stor

2013
Muscle glycogenosis due to phosphoglucomutase 1 deficiency.
    The New England journal of medicine, 2009, Jul-23, Volume: 361, Issue:4

    Topics: Adult; Ammonia; Exercise; Glycogen Storage Disease; Humans; Lactic Acid; Male; Muscle, Skeletal; Mut

2009
A novel mutation in the glycogen synthase 2 gene in a child with glycogen storage disease type 0.
    BMC medical genetics, 2010, Jan-05, Volume: 11

    Topics: Base Sequence; Blood Glucose; Child; Codon, Nonsense; Exons; Fasting; Female; Frameshift Mutation; G

2010
Diagnostic utility of a modified forearm ischemic exercise test and technical issues relevant to exercise testing.
    Muscle & nerve, 2003, Volume: 27, Issue:3

    Topics: Adult; Ammonia; Catheterization, Peripheral; Eating; Exercise Test; Forearm; Glycogen Storage Diseas

2003
Hexose monophosphate, pyruvate and lactate in the peripheral blood in glycogen-storage disease type I.
    Clinica chimica acta; international journal of clinical chemistry, 1962, Volume: 7

    Topics: Glycogen; Glycogen Storage Disease; Hexosephosphates; Hexoses; Humans; Lactates; Lactic Acid; Pyruva

1962
Proglycogen, macroglycogen, glucose, and glucose-6-phosphate concentrations in skeletal muscles of horses with polysaccharide storage myopathy performing light exercise.
    American journal of veterinary research, 2006, Volume: 67, Issue:9

    Topics: Animals; Biopsy; Creatine Kinase; Female; Glucose; Glucose-6-Phosphate; Glycogen; Glycogen Storage D

2006
A comparative study on glucagon effect between McArdle disease and Tarui disease.
    Muscle & nerve, 1984, Volume: 7, Issue:7

    Topics: Adult; Female; Glucagon; Glucose; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans;

1984
Amino acid disturbances in type III glycogenosis: differences from type I glycogenosis.
    Metabolism: clinical and experimental, 1983, Volume: 32, Issue:1

    Topics: Adolescent; Adult; Amino Acids; Blood Glucose; Child; Child, Preschool; Diagnosis, Differential; Fem

1983
Increased ammonia production during forearm ischemic work test in McArdle's disease.
    Klinische Wochenschrift, 1981, Dec-01, Volume: 59, Issue:23

    Topics: Ammonia; Forearm; Glycogen; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Ische

1981
Exercise hyperventilation in patients with McArdle's disease.
    Journal of applied physiology: respiratory, environmental and exercise physiology, 1982, Volume: 52, Issue:4

    Topics: Adult; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; Hyperventilation;

1982
Value of the glucagon test in screening for hepatic glycogen storage disease.
    Archives of disease in childhood, 1982, Volume: 57, Issue:5

    Topics: Blood Glucose; Fasting; Glucagon; Glycogen Storage Disease; Humans; Lactates; Lactic Acid; Liver Dis

1982
Glycogen metabolism in the liver of the neonatal gsd/gsd and control (GSD/GSD) rat.
    The Biochemical journal, 1982, Mar-15, Volume: 202, Issue:3

    Topics: Animals; Animals, Newborn; Blood Glucose; Glycogen Storage Disease; Lactates; Lactic Acid; Liver Gly

1982
[Lactate dehydrogenase M subunit deficiency].
    Nihon rinsho. Japanese journal of clinical medicine, 1990, Volume: 48, Issue:7

    Topics: Exercise Test; Glycogen Storage Disease; Glycolysis; Humans; Isoenzymes; L-Lactate Dehydrogenase; La

1990
An investigation of the beta-adrenoceptor that mediates metabolic responses to the novel agonist BRL28410 in rat soleus muscle.
    Biochemical pharmacology, 1988, Mar-01, Volume: 37, Issue:5

    Topics: Animals; Dose-Response Relationship, Drug; Ethanolamines; Female; Glycogen Storage Disease; Heart Ra

1988
Complex carbohydrates in the dietary management of patients with glycogenosis caused by glucose-6-phosphatase deficiency.
    The American journal of clinical nutrition, 1988, Volume: 48, Issue:1

    Topics: Adolescent; Blood Glucose; Child; Dietary Carbohydrates; Glycogen Storage Disease; Glycogen Storage

1988
Clinical and laboratory observations in a child with hepatic phosphorylase kinase deficiency.
    Metabolism: clinical and experimental, 1986, Volume: 35, Issue:7

    Topics: 3-Hydroxybutyric Acid; Alanine; Blood Glucose; Child, Preschool; Glycogen Storage Disease; Histocyto

1986
The second wind phenomenon in McArdle's disease.
    Brain : a journal of neurology, 1986, Volume: 109 ( Pt 6)

    Topics: Adaptation, Physiological; Adult; Ammonia; Blood Glucose; Cardiac Output; Electromyography; Fatigue;

1986
Early onset myophosphorylase deficiency (Mc Ardle's disease) with absence of myophosphorylase protein on SDS electrophoresis. The role of the ischemic forearm test.
    Clinical neurology and neurosurgery, 1985, Volume: 87, Issue:2

    Topics: Adult; Biopsy; Electromyography; Electrophoresis, Polyacrylamide Gel; Exercise Test; Female; Forearm

1985
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
    The Journal of clinical investigation, 1985, Volume: 76, Issue:2

    Topics: Adult; Ammonia; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glycogen Storage

1985
Effects in vivo of food deprivation and 3-mercaptopicolinate in the glycogen-storage-disease (gsd/gsd) rat.
    The Biochemical journal, 1985, Nov-01, Volume: 231, Issue:3

    Topics: Animals; Blood Glucose; Body Weight; Female; Food Deprivation; Glycerol; Glycogen Storage Disease; L

1985
Type V glycogen storage disease.
    Archives of disease in childhood, 1985, Volume: 60, Issue:12

    Topics: Child; Creatine Kinase; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Humans; L

1985