Page last updated: 2024-10-20

thiamine and Disease Exacerbation

thiamine has been researched along with Disease Exacerbation in 17 studies

thiamine(1+) : A primary alcohol that is 1,3-thiazol-3-ium substituted by (4-amino-2-methylpyrimidin-5-yl)methyl, methyl and 2-hydroxyethyl groups at positions 3, 4 and 5, respectively.

Research Excerpts

ExcerptRelevanceReference
"Shoshin beriberi is a fulminant form of cardiac beriberi caused by thiamine deficiency."7.80A case of shoshin beriberi presenting as cardiogenic shock with diffuse ST-segment elevation, which dramatically improved after a single dose of thiamine. ( Kang, WC; Kim, J; Kim, JH; Kim, SJ; Kim, SW; Park, S, 2014)
" Although thiamine deficiency is a possible cause of this neuropathy, the pathogenesis still remains to be clarified."7.71Postgastrectomy polyneuropathy with thiamine deficiency. ( Hattori, N; Hirayama, M; Ichimura, M; Ito, H; Ito, S; Koike, H; Misu, K; Nagamatsu, M; Sasaki, I; Sobue, G, 2001)
"Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is the most prevalent encephalopathy in Japanese children."5.51Early administration of vitamins B1 and B6 and l-carnitine prevents a second attack of acute encephalopathy with biphasic seizures and late reduced diffusion: A case control study. ( Fukui, KO; Ishiguro, A; Kashii, H; Kubota, M; Terashima, H, 2019)
"Wernicke encephalopathy is an acute, reversible neuropsychiatric emergency due to thiamine deficiency."4.90Thiamine in the treatment of Wernicke encephalopathy in patients with alcohol use disorders. ( Dore, G; Latt, N, 2014)
"Shoshin beriberi is a fulminant form of cardiac beriberi caused by thiamine deficiency."3.80A case of shoshin beriberi presenting as cardiogenic shock with diffuse ST-segment elevation, which dramatically improved after a single dose of thiamine. ( Kang, WC; Kim, J; Kim, JH; Kim, SJ; Kim, SW; Park, S, 2014)
" Thiamine deficiency (TD) in rats is a model for the study of cellular and molecular mechanisms that lead to selective neuronal loss caused by chronic oxidative deficits."3.76Neurodegeneration in thiamine deficient rats-A longitudinal MRI study. ( Assaf, Y; Biton, IE; Dror, V; Eliash, S; Fattal-Valevski, A; Rehavi, M, 2010)
" Although thiamine deficiency is a possible cause of this neuropathy, the pathogenesis still remains to be clarified."3.71Postgastrectomy polyneuropathy with thiamine deficiency. ( Hattori, N; Hirayama, M; Ichimura, M; Ito, H; Ito, S; Koike, H; Misu, K; Nagamatsu, M; Sasaki, I; Sobue, G, 2001)
"The primary clinical outcome was the Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog)."2.94Benfotiamine and Cognitive Decline in Alzheimer's Disease: Results of a Randomized Placebo-Controlled Phase IIa Clinical Trial. ( Bettendorff, L; Chen, H; Chen, Z; Cirio, R; Flowers, SA; Fonzetti, P; Franchino-Elder, J; Gerber, LM; Gibson, GE; Grandville, T; Habeck, C; Hirsch, JA; Jordan, B; Luchsinger, JA; Schupf, N; Stern, Y; Xu, H, 2020)
"This relation could be modified by genetic susceptibility, particularly related to the C3 genotype."2.82Dietary folate, B vitamins, genetic susceptibility and progression to advanced nonexudative age-related macular degeneration with geographic atrophy: a prospective cohort study. ( Merle, BM; Rosner, B; Seddon, JM; Silver, RE, 2016)
"Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is the most prevalent encephalopathy in Japanese children."1.51Early administration of vitamins B1 and B6 and l-carnitine prevents a second attack of acute encephalopathy with biphasic seizures and late reduced diffusion: A case control study. ( Fukui, KO; Ishiguro, A; Kashii, H; Kubota, M; Terashima, H, 2019)
"A 33-year-old woman with Wernicke's encephalopathy (WE) due to poor oral intake after allogeneic stem cell transplantation for acute myeloid leukemia showed a sequential development of bilateral gaze-evoked nystagmus (GEN), rightward gaze palsy, and upbeat nystagmus."1.38Evolution of abnormal eye movements in Wernicke's encephalopathy: correlation with serial MRI findings. ( Kim, JS; Kim, K; Lee, YB; Park, HM; Park, KH; Shin, DH; Shin, DJ, 2012)
"Thiamine is an essential cofactor for several important enzymes involved in brain oxidative metabolism, such as the alpha-ketoglutarate dehydrogenase complex (KGDHC), pyruvate-dehydrogenase complex (PDHC), and transketolase."1.31Cerebrospinal fluid levels of thiamine in patients with Alzheimer's disease. ( de Bustos, F; Fernández-Vivancos, E; Gómez-Escalonilla, C; Hernánz, A; Jiménez-Jiménez, FJ; Medina, S; Molina, JA; Sayed, Y, 2002)

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (29.41)29.6817
2010's10 (58.82)24.3611
2020's2 (11.76)2.80

Authors

AuthorsStudies
Gibson, GE1
Luchsinger, JA1
Cirio, R1
Chen, H1
Franchino-Elder, J1
Hirsch, JA1
Bettendorff, L1
Chen, Z1
Flowers, SA1
Gerber, LM1
Grandville, T1
Schupf, N1
Xu, H1
Stern, Y1
Habeck, C1
Jordan, B1
Fonzetti, P1
Tsui, E1
Tauber, J1
Barbazetto, I1
Gelman, SK1
Macchione, N1
Bernardini, P1
Piacentini, I1
Mangiarotti, B1
Del Nero, A1
Fukui, KO1
Kubota, M1
Terashima, H1
Ishiguro, A1
Kashii, H1
Latt, N1
Dore, G1
Kim, J1
Park, S1
Kim, JH1
Kim, SW1
Kang, WC1
Kim, SJ1
Merle, BM1
Silver, RE1
Rosner, B1
Seddon, JM1
Freire-Aragón, MD1
Fernández Delgado, E1
Carbajal-Guerrero, J1
Ribera-Rubiales, G1
Flabeau, O1
Foubert-Samier, A1
Meissner, W1
Tison, F1
Helbok, R1
Beer, R1
Engelhardt, K1
Broessner, G1
Lackner, P1
Brenneis, C1
Pfausler, B1
Schmutzhard, E1
Dror, V1
Eliash, S1
Rehavi, M1
Assaf, Y1
Biton, IE1
Fattal-Valevski, A1
Richardson, AD1
Moscow, JA1
Kornienko, AM1
Kornienko, RA1
Kim, K1
Shin, DH1
Lee, YB1
Park, KH1
Park, HM1
Shin, DJ1
Kim, JS1
Molina, JA1
Jiménez-Jiménez, FJ1
Hernánz, A1
Fernández-Vivancos, E1
Medina, S1
de Bustos, F1
Gómez-Escalonilla, C1
Sayed, Y1
Ndiaye, M1
Sène-Diouf, F1
Diop, AG1
Ndao, AK1
Diagne, M1
Thiam, A1
Ndiaye, MM1
Ndiaye, IP1
Koike, H1
Misu, K1
Hattori, N1
Ito, S1
Ichimura, M1
Ito, H1
Hirayama, M1
Nagamatsu, M1
Sasaki, I1
Sobue, G1

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Benfotiamine in Alzheimer's Disease: A Pilot Study[NCT02292238]Phase 271 participants (Actual)Interventional2015-02-15Completed
Age-Related Eye Disease Study (AREDS) and AREDS2 Follow-Up[NCT00594672]110 participants (Actual)Observational2008-06-02Active, not recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in ADAS-Cog Score

"The Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-Cog) is a brief neuropsychological assessment used to assess the severity of cognitive symptoms of dementia. It is one of the most widely used cognitive scales in clinical trials and is considered to be the gold standard for assessing antidementia treatments. The ADAS-Cog range from 0 to 70, where higher scores indicate greater cognitive dysfunction." (NCT02292238)
Timeframe: Baseline, 1 year

Interventionscore on a scale (Mean)
Benfotiamine1.39
Placebo3.26

Change From Baseline in Alzheimer's Disease Cooperative Study-Activities of Daily Living (ADCS-ADL) Score

Alzheimer's Disease Cooperative Study-Activities of Daily Living (ADCS-ADL) is a caregiver-based Activities of Daily Living (ADL) scale composed of 23 items developed for use in dementia clinical studies. It was designed to assess the patient's performance of both basic and instrumental activities of daily living such as those necessary for personal care, communicating and interacting with other people, maintaining a household, conducting hobbies and interests, as well as making judgments and decisions. The range for the total ADCS-ADL score is 0 to 78. Higher scores equate with higher functioning. (NCT02292238)
Timeframe: Baseline, 1 year

Interventionscore on a scale (Mean)
Benfotiamine-1.931
Placebo-3.16129

Change From Baseline in Brain Glucose Utilization

The AAL (Automatic Anatomical Labeling) atlas provides the taxonomy for 116 regions of interest, 90 of which capture non-cerebellar cortical regions. Signal averages from 9 cerebellar regions from each hemisphere were further averaged into one composite cerebellar region for each hemisphere, 'Cerebellum_L' and 'Cerebellum_R', which were comprised of the respective laterality averages of the regions: 'Cerebellum_Crus1 ' 'Cerebellum_Crus2 'Cerebellum_3' 'Cerebellum_4_5' 'Cerebellum_6' 'Cerebellum_7b' 'Cerebellum_8' 'Cerebellum_9' 'Cerebellum_10 '. Subsequently, these two composite regions are further combined with the bilateral paracentral lobules to provide one final composite for reference scaling. Concretely, the values from 'Cerebellum_L', 'Cerebellum_R', 'Paracentral_Lobule_L', and 'Paracentra_Lobule_R' were averaged. This final composite will serve as the denominator for the scaling operation of any ROI value prior to group-level analysis. (NCT02292238)
Timeframe: Baseline, 1 year

Interventionratio (Mean)
Benfotiamine-0.02
Placebo-0.01

Change From Baseline in Buschke Selective Reminding Test (SRT) Score

The SRT is a standard diagnostic tool in the assessment of verbal memory. The Buschke SRT immediate total scores are compared between treated (benfotiamine) and control (placebo) groups. The immediate total score is the sum of correct responses over the 6 learning trials with scores ranging from 0 to 72. A score of 0 means severe impairment in memory. A score of 72 means there is no impairment in memory. For the purpose of determining effect over several trials between groups, the fractional change from the baseline of each group is compared. (NCT02292238)
Timeframe: Baseline, 1 year

Interventionscore on a scale (Mean)
Benfotiamine0.86
Placebo-1.12

Change From Baseline in Clinical Dementia Rating (CDR) Score

The CDR was developed primarily for use in persons with dementia of the Alzheimer type (the equivalent of probable Alzheimer's Disease) and can also be used to stage dementia in other illnesses as well. The scores for the multiple items are summarized in one score. The CDR examines 6 categories of cognitive functioning domains. Each domain is scored on a scale ranging from 0 to 3 (including 0.5). A CDR-SB was generated as the sum of the values in each of the 6 domains. The CDR-SB sum scores range from 0 to 18, with higher scores indicating greater cognitive impairment and a 1 point worsening is considered a clinically significant symptom change. (NCT02292238)
Timeframe: Baseline, 1 year

Interventionscore on a scale (Mean)
Benfotiamine0.05
Placebo0.22

Change From Baseline in Neuropsychiatric Inventory (NPI) Score

The NPI assesses a wide range of behaviors encountered in dementia patients to provide a means of distinguishing frequency and severity of behavioral changes. Ten behavioral and two neuro-vegetative domains are evaluated through an interview with the caregiver. The total score ranges from 0 to 144. Higher scores suggest greater psychiatric impairment. (NCT02292238)
Timeframe: Baseline, 1 year

Interventionscore on a scale (Mean)
Benfotiamine6.69
Placebo9.23

Reviews

1 review available for thiamine and Disease Exacerbation

ArticleYear
Thiamine in the treatment of Wernicke encephalopathy in patients with alcohol use disorders.
    Internal medicine journal, 2014, Volume: 44, Issue:9

    Topics: Alcoholism; Disease Progression; Dose-Response Relationship, Drug; Early Diagnosis; Humans; Korsakof

2014

Trials

3 trials available for thiamine and Disease Exacerbation

ArticleYear
Benfotiamine and Cognitive Decline in Alzheimer's Disease: Results of a Randomized Placebo-Controlled Phase IIa Clinical Trial.
    Journal of Alzheimer's disease : JAD, 2020, Volume: 78, Issue:3

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Aniline Compounds; Apolipoprotein E4; Brain; Cognitive D

2020
Flower Pollen Extract in Association with Vitamins (Deprox 500®) Versus Serenoa repens in Chronic Prostatitis/Chronic Pelvic Pain Syndrome: A Comparative Analysis of Two Different Treatments.
    Anti-inflammatory & anti-allergy agents in medicinal chemistry, 2019, Volume: 18, Issue:2

    Topics: Adult; Aged; Disease Progression; Drug Combinations; Folic Acid; Humans; Hypertension; Male; Middle

2019
Dietary folate, B vitamins, genetic susceptibility and progression to advanced nonexudative age-related macular degeneration with geographic atrophy: a prospective cohort study.
    The American journal of clinical nutrition, 2016, Volume: 103, Issue:4

    Topics: Aged; Body Mass Index; Collagen Type VIII; Complement C2; Complement C3; Complement Factor B; Comple

2016

Other Studies

13 other studies available for thiamine and Disease Exacerbation

ArticleYear
LONG-TERM MULTIMODAL IMAGING OF OCULAR FINDINGS ASSOCIATED WITH THIAMINE-RESPONSIVE MEGALOBLASTIC ANEMIA.
    Retinal cases & brief reports, 2020,Summer, Volume: 14, Issue:3

    Topics: Anemia, Megaloblastic; Disease Progression; Electroretinography; Fluorescein Angiography; Follow-Up

2020
Early administration of vitamins B1 and B6 and l-carnitine prevents a second attack of acute encephalopathy with biphasic seizures and late reduced diffusion: A case control study.
    Brain & development, 2019, Volume: 41, Issue:7

    Topics: Brain Diseases; Carnitine; Case-Control Studies; Child, Preschool; Diagnosis, Differential; Disease

2019
A case of shoshin beriberi presenting as cardiogenic shock with diffuse ST-segment elevation, which dramatically improved after a single dose of thiamine.
    Cardiovascular journal of Africa, 2014, Nov-23, Volume: 25, Issue:6

    Topics: Aged, 80 and over; Beriberi; Disease Progression; Dose-Response Relationship, Drug; Electrocardiogra

2014
Progressive encephalopathy associated with nutritional deficiencies: Identifying patients at high risk for developing thiamine deficiency.
    Medicina intensiva, 2017, Volume: 41, Issue:7

    Topics: Acidosis; Acute Kidney Injury; Delayed Diagnosis; Disease Progression; Duodenitis; Female; Gait Diso

2017
Hearing and seeing: Unusual early signs of Wernicke encephalopathy.
    Neurology, 2008, Aug-26, Volume: 71, Issue:9

    Topics: Adult; Colectomy; Crohn Disease; Disease Progression; Early Diagnosis; Female; Humans; Inferior Coll

2008
Intracerebral haemorrhage in a malnourished patient, related to Wernicke's encephalopathy.
    European journal of neurology, 2008, Volume: 15, Issue:11

    Topics: Adult; Anemia; Black People; Brain; Cerebral Arteries; Cerebral Hemorrhage; Disease Progression; Fem

2008
Neurodegeneration in thiamine deficient rats-A longitudinal MRI study.
    Brain research, 2010, Jan-13, Volume: 1308

    Topics: Analysis of Variance; Animals; Anisotropy; Brain Mapping; Diffusion Tensor Imaging; Disease Progress

2010
Can an enzyme cofactor be a factor in malignant progression?
    Cancer biology & therapy, 2010, Dec-01, Volume: 10, Issue:11

    Topics: Cell Hypoxia; Coenzymes; Disease Progression; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Mem

2010
[Sensorineural hearing loss: New prospects for therapy].
    Vestnik otorinolaringologii, 2011, Issue:2

    Topics: Adjuvants, Immunologic; Administration, Oral; Aged; Audiometry; Disease Progression; Dose-Response R

2011
Evolution of abnormal eye movements in Wernicke's encephalopathy: correlation with serial MRI findings.
    Journal of the neurological sciences, 2012, Dec-15, Volume: 323, Issue:1-2

    Topics: Adult; Ataxia; Disease Progression; Eye Movements; Female; Humans; Leukemia, Myeloid, Acute; Magneti

2012
Cerebrospinal fluid levels of thiamine in patients with Alzheimer's disease.
    Journal of neural transmission (Vienna, Austria : 1996), 2002, Volume: 109, Issue:7-8

    Topics: Aged; Aged, 80 and over; Alzheimer Disease; Chromatography, High Pressure Liquid; Disease Progressio

2002
[Guillain-Barre syndrome in children: experience in the neurology service of Dakar].
    Dakar medical, 2000, Volume: 45, Issue:1

    Topics: Adolescent; Age Distribution; Child; Child, Preschool; Disease Progression; Female; Guillain-Barre S

2000
Postgastrectomy polyneuropathy with thiamine deficiency.
    Journal of neurology, neurosurgery, and psychiatry, 2001, Volume: 71, Issue:3

    Topics: Activities of Daily Living; Adult; Aged; Biopsy; Diagnosis, Differential; Disease Progression; Femal

2001