Page last updated: 2024-10-16

carbon monoxide and Diffuse Cutaneous Systemic Sclerosis

carbon monoxide has been researched along with Diffuse Cutaneous Systemic Sclerosis in 9 studies

Carbon Monoxide: Carbon monoxide (CO). A poisonous colorless, odorless, tasteless gas. It combines with hemoglobin to form carboxyhemoglobin, which has no oxygen carrying capacity. The resultant oxygen deprivation causes headache, dizziness, decreased pulse and respiratory rates, unconsciousness, and death. (From Merck Index, 11th ed)
carbon monoxide : A one-carbon compound in which the carbon is joined only to a single oxygen. It is a colourless, odourless, tasteless, toxic gas.

Research Excerpts

ExcerptRelevanceReference
" SSc patients with high GDF-15 levels (≥1000 pg/ml) had pulmonary fibrosis, decreased vital capacity, and decreased diffusion capacity for carbon monoxide more often than those with low GDF-15 levels (<1000 pg/ml)."3.78Clinical significance of serum growth differentiation factor-15 levels in systemic sclerosis: association with disease severity. ( Asano, Y; Kadono, T; Sato, S; Sugaya, M; Tada, Y; Yanaba, K, 2012)
"Patients with SSc meeting the ACR/EULAR systemic sclerosis classification criteria with diffuse cutaneous SSc (dcSSc) subset per LeRoy criteria, and a disease duration of less than or equal to 18 months will be randomized to placebo or riociguat 0."2.84RISE-SSc: Riociguat in diffuse cutaneous systemic sclerosis. ( Allanore, Y; de Oliveira Pena, J; Denton, C; Distler, O; Khanna, D; Matucci-Cerinic, M; Pope, J, 2017)
"We investigated in systemic sclerosis (SSc) patients the T cell homeostasis and its relationship with the clinical course of the disease."1.36Analyses of T cell phenotype and function reveal an altered T cell homeostasis in systemic sclerosis. Correlations with disease severity and phenotypes. ( Gambardella, L; Giammarioli, AM; Giovannetti, A; Malorni, W; Maselli, A; Palange, P; Paoletti, P; Pierdominici, M; Pisarri, S; Renzi, C; Rosato, E; Salsano, F, 2010)

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (33.33)29.6817
2010's5 (55.56)24.3611
2020's1 (11.11)2.80

Authors

AuthorsStudies
Wajda, A1
Walczyk, M1
Dudek, E1
Stypińska, B1
Lewandowska, A1
Romanowska-Próchnicka, K1
Chojnowski, M1
Olesińska, M1
Paradowska-Gorycka, A1
Distler, O1
Pope, J1
Denton, C1
Allanore, Y1
Matucci-Cerinic, M1
de Oliveira Pena, J1
Khanna, D1
Iwata, Y1
Yoshizaki, A1
Ogawa, F2
Komura, K1
Hara, T2
Muroi, E2
Takenaka, M1
Shimizu, K2
Hasegawa, M2
Fujimoto, M1
Takehara, K2
Sato, S4
Giovannetti, A1
Rosato, E1
Renzi, C1
Maselli, A1
Gambardella, L1
Giammarioli, AM1
Palange, P1
Paoletti, P1
Pisarri, S1
Salsano, F1
Malorni, W1
Pierdominici, M1
Aozasa, N1
Asano, Y2
Akamata, K1
Noda, S1
Masui, Y1
Tamaki, Z1
Tada, Y2
Sugaya, M2
Kadono, T2
Yanaba, K1
Henes, JC1
Horger, M1
Amberger, C1
Schmalzing, M1
Fierlbeck, G1
Kanz, L1
Koetter, I1
Launay, D1
Mouthon, L1
Hachulla, E1
Pagnoux, C1
de Groote, P1
Remy-Jardin, M1
Matran, R1
Lambert, M1
Queyrel, V1
Morell-Dubois, S1
Guillevin, L1
Hatron, PY1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Randomized, Double-Blind, Placebo-Controlled Phase II Study to Investigate the Efficacy and Safety of Riociguat in Patients With Diffuse Cutaneous Systemic Sclerosis (dcSSc)[NCT02283762]Phase 2121 participants (Actual)Interventional2015-01-15Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

Change From Baseline in Forced Vital Capacity (FVC) Percent Predicted to Week 52

Negative change in FVC percent predicted indicates worsening. (NCT02283762)
Timeframe: Baseline to week 52

InterventionFVC percent predicted (Mean)
Riociguat (Adempas, BAY63-2521)-2.376
Placebo-2.945

Change From Baseline in Modified Rodnan Skin Score (mRSS) to Week 52

The mRSS is a validated physical examination method for estimating skin thickness. It correlates with biopsy measures of collagen in the dermis and reflects prognosis and visceral involvement, especially in early disease. It is scored on 0 (normal) to 3+ (severe induration) ordinal scales over 17 body areas, with a maximum score of 51 (higher score means worse situation) and is used to categorize severity of SSc. A decrease in the mean change of mRSS shows mRSS improved. (NCT02283762)
Timeframe: Baseline to week 52

Interventionscore on a scale (Mean)
Riociguat (Adempas, BAY63-2521)-2.088
Placebo-0.769

Change From Baseline in Health Assessment Questionnaire Disability Index (HAQ-DI) Score to Week 52

The HAQ-DI is a composite measure from which a 'Standard Disability Index' score can be computed to assess a patient's disability level. Generally, a score of 0-1 represents mild to moderate difficulty, 1-2 moderate to severe disability and 2-3 severe to very severe disability. The HAQ-DI comprises 20 items that assess patient abilities across 8 functional activities: dressing, rising, eating, walking, hygiene, reach, grip, and usual activities. Each item is rated on a 4-point scale: 0=Without ANY difficulty, 1=With SOME difficulty, 2=With MUCH difficulty, 3=UNABLE to do. The 8 scores of the 8 sections are summed and divided by 8. In the event that one section is not completed by a subject then the summed score would be divided by 7. The final overall HAQ-DI score ranges from 0 to 3 and positive change indicates worse health-related quality of life (HRQoL). (NCT02283762)
Timeframe: Baseline to week 52

,
Interventionscore on a scale (Mean)
BaselineChange from baseline
Placebo0.6930.127
Riociguat (Adempas, BAY63-2521)0.8880.054

Change From Baseline in Patient's Global Assessment Score to Week 52

The patient's global assessments (a self-report) quantified the overall disease activity or severity of SSc, with scores ranging from 0 (good) to 10 (worse). Positive change in the patient's global assessments score indicates worsening. (NCT02283762)
Timeframe: Baseline to week 52

,
Interventionscore on a scale (Mean)
BaselineChange from baseline
Placebo3.770-0.022
Riociguat (Adempas, BAY63-2521)3.9330.689

Change From Baseline in Physician's Global Assessment Score to Week 52

The physician's global assessments (reported by the physician) quantified the overall disease activity or severity of SSc, with scores ranging from 0 (good) to 10 (worse). Positive change in the physician's global assessments score indicates worsening. (NCT02283762)
Timeframe: Baseline to week 52

,
Interventionscore on a scale (Mean)
BaselineChange from baseline
Placebo4.016-0.745
Riociguat (Adempas, BAY63-2521)4.333-0.067

CRISS (American College of Rheumatology Composite Response Index for Clinical Trials) at Week 52 Reported as Number of Participants With a CRISS Probability >=0.60 or <0.60 From Baseline to Week 52

CRISS forms a composite response index consisting of SSc-related organ involvement and the following five variables: mRSS, FVC percent predicted, physician's and patient's global assessments, and HAQ-DI score (from SHAQ patient-reported outcome). The resulting index is a 2-step process that captures clinically meaningful worsening of internal organ involvement and the core variables that show change. Patients for whom the predicted CRISS probability was ≥ 0.60 were considered improved, while patients for whom the predicted probability was < 0.60 were considered not improved. (NCT02283762)
Timeframe: Week 52

,
InterventionParticipants (Count of Participants)
CRISS probability ≥ 0.60CRISS probability < 0.60
Placebo1150
Riociguat (Adempas, BAY63-2521)1149

Trials

1 trial available for carbon monoxide and Diffuse Cutaneous Systemic Sclerosis

ArticleYear
RISE-SSc: Riociguat in diffuse cutaneous systemic sclerosis.
    Respiratory medicine, 2017, Volume: 122 Suppl 1

    Topics: Carbon Monoxide; Dose-Response Relationship, Drug; Double-Blind Method; Enzyme Activators; Female; H

2017

Other Studies

8 other studies available for carbon monoxide and Diffuse Cutaneous Systemic Sclerosis

ArticleYear
Serum microRNAs in Systemic Sclerosis, Associations with Digital Vasculopathy and Lung Involvement.
    International journal of molecular sciences, 2022, Sep-14, Volume: 23, Issue:18

    Topics: Biomarkers; Carbon Monoxide; Humans; Lung; MicroRNAs; Scleroderma, Diffuse; Scleroderma, Systemic; T

2022
Increased serum pentraxin 3 in patients with systemic sclerosis.
    The Journal of rheumatology, 2009, Volume: 36, Issue:5

    Topics: Acute-Phase Proteins; Biomarkers; C-Reactive Protein; Carbon Monoxide; Cells, Cultured; Enzyme-Linke

2009
Analyses of T cell phenotype and function reveal an altered T cell homeostasis in systemic sclerosis. Correlations with disease severity and phenotypes.
    Clinical immunology (Orlando, Fla.), 2010, Volume: 137, Issue:1

    Topics: Adult; Aged; Aged, 80 and over; Aging; Apoptosis; Carbon Monoxide; CD4 Lymphocyte Count; Cell Prolif

2010
Clinical significance of serum levels of secretory leukocyte protease inhibitor in patients with systemic sclerosis.
    Modern rheumatology, 2012, Volume: 22, Issue:4

    Topics: Biomarkers; Carbon Monoxide; Enzyme-Linked Immunosorbent Assay; Female; Humans; Lung; Lung Diseases,

2012
Clinical significance of serum growth differentiation factor-15 levels in systemic sclerosis: association with disease severity.
    Modern rheumatology, 2012, Volume: 22, Issue:5

    Topics: Adolescent; Adult; Aged; Carbon Monoxide; Child; Disease Progression; Female; Growth Differentiation

2012
Enteric-coated mycophenolate sodium for progressive systemic sclerosis--a prospective open-label study with CT histography for monitoring of pulmonary fibrosis.
    Clinical rheumatology, 2013, Volume: 32, Issue:5

    Topics: Adult; Aged; Carbon Monoxide; Disease Progression; Female; Follow-Up Studies; Humans; Male; Middle A

2013
Serum levels of 8-isoprostane, a marker of oxidative stress, are elevated in patients with systemic sclerosis.
    Rheumatology (Oxford, England), 2006, Volume: 45, Issue:7

    Topics: Adult; Aged; Biomarkers; Carbon Monoxide; Dinoprost; Female; Humans; Male; Middle Aged; Oxidative St

2006
Prevalence and characteristics of moderate to severe pulmonary hypertension in systemic sclerosis with and without interstitial lung disease.
    The Journal of rheumatology, 2007, Volume: 34, Issue:5

    Topics: Adult; Carbon Monoxide; Comorbidity; Dyspnea; Female; Humans; Hypertension, Pulmonary; Lung Diseases

2007