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Involvement of Plasmatic Factors in the Peripheral Muscle Dysfunction of COPD Patients - In Vitro Study

Involvement of Plasmatic Factors in the Peripheral Muscle Dysfunction of COPD Patients - In Vitro Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03197909
Enrollment
18
Registered
2017-06-23
Start date
2017-07-06
Completion date
2019-01-31
Last updated
2019-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Obstructive Pulmonary

Keywords

COPD (Chronic Obstructive Pulmonary Patients), Atrophy, cell cultur, systemic inflammation, Catabolism

Brief summary

Chronic Obstructive Pulmonary Patients is a defined by persistent airflow limitation that is usually progressive and associated with an enhanced chronic inflammatory response in the airways and the lung to noxious particles or gases. It is associated with an atrophy of the skeletal muscle that impairs the patient's prognosis. The biological mechanisms of this muscle atrophy have not been elucidated, and the spill-over theory has recently emerged. Indeed, in COPD patients, the pulmonary inflammation is associated with a systemic low-grade inflammation, and the increased pro-inflamatory molelcules in the blood - which constitute the cellular micro-environement of the muscle fibre - could activate the mechanisms of the cell atrophy.

Interventions

OTHERDetermination of pro-inflammatory plasma factors

Determination of pro-inflammatory plasma factors at COPD patients aged from 35 to 85 years old and Healthy subjects aged from 35 to 85 years old

Sponsors

University Hospital, Montpellier
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
35 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

35 to 85 years old * COPD patients: association of symtoms (breathlessness, cough, sputum) and chronic exposure to inhalated risk factors (like tobacco smoke) and a FEV1/VC ratio \<70% assessed by a spirometry * Healthy subjects: A sedentariness assessed by a Voorrips score \<9.4 and/or a report of \<150 min/week of moderate-to-vigorous physical activity

Exclusion criteria

* A recent COPD exacerbation (\< 4weeks) * The decompensation of a comorbidity * An antioxidant supplementation or medication * A long-term systemic corticosteroid medication

Design outcomes

Primary

MeasureTime frameDescription
Myotube diameter of in vitro cultured myotubes6 daysMyotube diameter of in vitro cultured myotubes from healthy subjects, exposed to the serum of healthy controls and COPD patients

Secondary

MeasureTime frameDescription
Expression and translation of markers of6 daysExpression and translation of markers of anabolic and catabolic pathways

Other

MeasureTime frameDescription
Level of pro-Inflamatory markers6 daysLevel of pro-Inflamatory markers in the serum

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026