Page last updated: 2024-10-18

hydrogen and Cystic Fibrosis

hydrogen has been researched along with Cystic Fibrosis in 20 studies

Hydrogen: The first chemical element in the periodic table with atomic symbol H, and atomic number 1. Protium (atomic weight 1) is by far the most common hydrogen isotope. Hydrogen also exists as the stable isotope DEUTERIUM (atomic weight 2) and the radioactive isotope TRITIUM (atomic weight 3). Hydrogen forms into a diatomic molecule at room temperature and appears as a highly flammable colorless and odorless gas.
dihydrogen : An elemental molecule consisting of two hydrogens joined by a single bond.

Cystic Fibrosis: An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.

Research Excerpts

ExcerptRelevanceReference
" It was reported that colonic methane production is far more frequent in cystic fibrosis (CF) patients than in other subjects."7.75Small intestine bacterial overgrowth is frequent in cystic fibrosis: combined hydrogen and methane measurements are required for its detection. ( Lisowska, A; Walkowiak, J; Wójtowicz, J, 2009)
" It was reported that colonic methane production is far more frequent in cystic fibrosis (CF) patients than in other subjects."3.75Small intestine bacterial overgrowth is frequent in cystic fibrosis: combined hydrogen and methane measurements are required for its detection. ( Lisowska, A; Walkowiak, J; Wójtowicz, J, 2009)
"To investigate the prevalence of carbohydrate malabsorption and bacterial overgrowth in children with cystic fibrosis (CF) and abnormal stool pattern referred for breath hydrogen testing."3.70Bowel dysfunction in cystic fibrosis: importance of breath testing. ( Davidson, GP; Lewindon, PJ; Martin, AJ; Moore, DJ; Robb, TA, 1998)
"A lactulose hydrogen breath test was performed on 10 patients with cystic fibrosis and 15 control subjects matched for age and sex."3.66Prolonged small-intestinal transit time in cystic fibrosis. ( Asquith, P; Bali, A; Stableforth, DE, 1983)

Research

Studies (20)

TimeframeStudies, this research(%)All Research%
pre-19907 (35.00)18.7374
1990's4 (20.00)18.2507
2000's6 (30.00)29.6817
2010's2 (10.00)24.3611
2020's1 (5.00)2.80

Authors

AuthorsStudies
Carney, JM1
Gray, AL1
Howell, DN2
Pavlisko, EN1
Fields, TA1
McCall, SJ1
Reams, BD1
Roggli, VL1
Palmer, SM1
Gabel, ME1
Wang, H1
Gelfond, D1
Roach, C1
Rowe, SM1
Clancy, JP1
Sagel, SD1
Borowitz, D1
Schneider, AR1
Klueber, S1
Posselt, HG1
Funk, B1
Murzynski, L1
Caspary, WF1
Stein, J1
Lisowska, A1
Wójtowicz, J1
Walkowiak, J1
Stormon, MO1
Ip, WF1
Ellis, L1
Schibli, S1
Rommens, JM1
Durie, PR1
Casellas, F1
Guarner, L1
Antolín, M1
Malagelada, JR1
Fridge, JL1
Conrad, C1
Gerson, L1
Castillo, RO1
Cox, K1
Bali, A1
Stableforth, DE1
Asquith, P1
Quinton, PM1
O'Brien, S1
Mulcahy, H1
Fenlon, H1
O'Broin, A1
Casey, M1
Burke, A1
FitzGerald, MX1
Hegarty, JE1
Seal, S1
McClean, P1
Walters, M1
Wolfe, SP1
Harding, M1
Coward, W1
Littlewood, JM1
Lewindon, PJ1
Robb, TA1
Moore, DJ1
Davidson, GP1
Martin, AJ1
Coakley, RJ1
Taggart, C1
Canny, G1
Greally, P1
O'Neill, SJ1
McElvaney, NG1
Murphy, MS1
Brunetto, AL1
Pearson, AD1
Ghatei, MA1
Nelson, R1
Eastham, EJ1
Bloom, SR1
Green, AA1
Magazzù, G1
Saccà, MG1
Conti Nibali, S1
Sferlazzas, C1
Tedeschi, A1
Santoro, S1
Fernandes, J1
Kneepkens, CM1
Bijleveld, CM1
Vonk, RJ1
Cleave, AJ1
Kent, PW1
Peacocke, AR1
Slegers, JF1
Stoll, E1
Halter, F1
Gaze, H1
Richterich, R1
Rossi, E1

Other Studies

20 other studies available for hydrogen and Cystic Fibrosis

ArticleYear
Parenteral administration of oral medications in lung transplant recipients: An underrecognized problem.
    American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2019, Volume: 19, Issue:5

    Topics: Administration, Oral; Adolescent; Adult; Biopsy; Cellulose; Cystic Fibrosis; Female; Humans; Infusio

2019
Pulmonary embolization of microcrystalline cellulose in a lung transplant recipient.
    The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation, 2005, Volume: 24, Issue:5

    Topics: Adult; Biopsy; Cellulose; Cystic Fibrosis; Excipients; Female; Humans; Injections, Intravenous; Lung

2005
Changes in Glucose Breath Test in Cystic Fibrosis Patients Treated With 1 Month of Lumacaftor/Ivacaftor.
    Journal of pediatric gastroenterology and nutrition, 2022, 07-01, Volume: 75, Issue:1

    Topics: Adult; Aminophenols; Aminopyridines; Benzodioxoles; Breath Tests; Cystic Fibrosis; Cystic Fibrosis T

2022
Application of the glucose hydrogen breath test for the detection of bacterial overgrowth in patients with cystic fibrosis--a reliable method?
    Digestive diseases and sciences, 2009, Volume: 54, Issue:8

    Topics: Adolescent; Breath Tests; Case-Control Studies; Child; Child, Preschool; Cystic Fibrosis; Female; Ga

2009
Small intestine bacterial overgrowth is frequent in cystic fibrosis: combined hydrogen and methane measurements are required for its detection.
    Acta biochimica Polonica, 2009, Volume: 56, Issue:4

    Topics: Adolescent; Breath Tests; Child; Child, Preschool; Cystic Fibrosis; Gastrointestinal Diseases; Human

2009
Evidence of a generalized defect of acinar cell function in Shwachman-Diamond syndrome.
    Journal of pediatric gastroenterology and nutrition, 2010, Volume: 51, Issue:1

    Topics: Adolescent; Adult; Bone Marrow Diseases; Breath Tests; Case-Control Studies; Child; Child, Preschool

2010
Hydrogen breath test with low-dose rice flour for assessment of exocrine pancreatic insufficiency.
    Pancreas, 2004, Volume: 29, Issue:4

    Topics: Adult; Breath Tests; Cystic Fibrosis; Exocrine Pancreatic Insufficiency; Female; Flour; Humans; Hydr

2004
Risk factors for small bowel bacterial overgrowth in cystic fibrosis.
    Journal of pediatric gastroenterology and nutrition, 2007, Volume: 44, Issue:2

    Topics: Adolescent; Adult; Bacterial Infections; Breath Tests; Child; Child, Preschool; Cystic Fibrosis; Fem

2007
Prolonged small-intestinal transit time in cystic fibrosis.
    British medical journal (Clinical research ed.), 1983, Oct-08, Volume: 287, Issue:6398

    Topics: Adolescent; Adult; Breath Tests; Cystic Fibrosis; Female; Humans; Hydrogen; Intestine, Small; Lactul

1983
Suggestion of an abnormal anion exchange mechanism in sweat glands of cystic fibrosis patients.
    Pediatric research, 1982, Volume: 16, Issue:7

    Topics: Adult; Anions; Chlorides; Cystic Fibrosis; Humans; Hydrogen; Potassium; Sodium; Sweat; Sweat Glands

1982
Intestinal bile acid malabsorption in cystic fibrosis.
    Gut, 1993, Volume: 34, Issue:8

    Topics: Adolescent; Adult; Bile Acids and Salts; Breath Tests; Cystic Fibrosis; Feces; Female; Humans; Hydro

1993
Stable isotope studies of pancreatic enzyme release in vivo.
    Postgraduate medical journal, 1996, Volume: 72 Suppl 2

    Topics: Breath Tests; Carbon Isotopes; Child; Colon; Cystic Fibrosis; Female; Gastrointestinal Transit; Huma

1996
Bowel dysfunction in cystic fibrosis: importance of breath testing.
    Journal of paediatrics and child health, 1998, Volume: 34, Issue:1

    Topics: Breath Tests; Carbohydrate Metabolism; Child; Child, Preschool; Cystic Fibrosis; Digestive System; G

1998
Altered intracellular pH regulation in neutrophils from patients with cystic fibrosis.
    American journal of physiology. Lung cellular and molecular physiology, 2000, Volume: 279, Issue:1

    Topics: 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid; Acids; Adolescent; Adult; Alkalies; Bronchiectasis

2000
Gut hormones and gastrointestinal motility in children with cystic fibrosis.
    Digestive diseases and sciences, 1992, Volume: 37, Issue:2

    Topics: Adolescent; Breath Tests; Child; Cystic Fibrosis; Fasting; Food; Gastrointestinal Motility; Glucagon

1992
Breath hydrogen in celiac disease.
    Gastroenterology, 1989, Volume: 96, Issue:1

    Topics: Adolescent; Bacteria; Breath Tests; Celiac Disease; Child; Child, Preschool; Cystic Fibrosis; Female

1989
General aspects of nutrition, absorption and metabolism in patients with cystic fibrosis.
    Acta paediatrica Scandinavica. Supplement, 1985, Volume: 317

    Topics: Avitaminosis; Breath Tests; Calorimetry; Child; Cystic Fibrosis; Dietary Proteins; Energy Metabolism

1985
The binding of hydrogen and calcium ions by Tamm-Horsfall glycoprotein.
    Biochimica et biophysica acta, 1972, Nov-28, Volume: 285, Issue:1

    Topics: Adult; Calcium; Calcium Isotopes; Carboxylic Acids; Child; Child, Preschool; Clostridium perfringens

1972
Patho-physiological studies of the sweat gland.
    Pflugers Archiv fur die gesamte Physiologie des Menschen und der Tiere, 1966, Volume: 290, Issue:3

    Topics: Adult; Child; Cystic Fibrosis; Humans; Hydrogen; Potassium; Sodium; Sodium Chloride; Sweat Glands

1966
[Acidity and electrolyte concentration in the gastric juice of patients with mucoviscidosis].
    Helvetica paediatrica acta, 1970, Volume: 25, Issue:3

    Topics: Adolescent; Calcium; Child; Chlorides; Cystic Fibrosis; Gastric Acidity Determination; Gastric Juice

1970