Alpha 1-Antitrypsin Deficiency, Aneurysm, Cystic Fibrosis, Emphysema or COPD
Conditions
Brief summary
Background: Elastin is a unique protein providing elasticity, resilience and deformability to dynamic tissues, such as lungs and vasculature. Elastin fibers are characterized by their high affinity for calcium. However, calcified elastin is more prone to the degrading effects of proteases and, in turn, partially degraded elastin has an even higher affinity for calcium. A disturbed balance between proteases and anti-proteases is a major underlying mechanism in the development of chronic obstructive pulmonary disease (COPD). Virtually the only protein that can protect elastin from calcification is matrix Gla-protein (MGP), which needs vitamin K for its activation. In COPD patients, a lower vitamin K status is found when compared to control subjects and an inverse association exists between vitamin K status and elastin degradation. In addition, vitamin K status is lower and elastin degradation is accelerated in Vitamin K antagonist (VKA) users. VKAs are widely used. Nowadays, an increasing number of patients uses direct oral anticoagulants (DOACs), which do not influence vitamin K status. The hypothesis of this study is that discontinuation of VKAs results in an improved vitamin K status and deceleration of elastin degradation. In order to test this hypothesis, an observational pilot study will be conducted in which the change in elastin degradation- quantified by plasma desmosine concentrations - in patients who discontinue use of VKAs will be used as primary endpoint. Study design: Observational study. Study population: A total of 30 VKA users who will discontinue the use of VKAs. Elastin degradation rate (quantified by plasma desmosine levels) and vitamin K status (quantified by measuring plasma levels of dephosphorylated uncarboxylated (dp-uc)MGP) will be measured during the use of VKAs and approximately 6 months after discontinuation of VKAs. Furthermore, the VKORC1 polymorphisms will be determined. Main study parameters: The primary endpoint is the change in the rate of elastin degradation quantified by the plasma desmosine assay. Secondary endpoints are the change in vitamin K status quantified by measuring plasma levels of dp-ucMGP, the relation between desmosine and dp-ucMGP and differences of desmosine and dp-ucMGP levels among subjects with different polymorphisms of the vitamin K 2,3-epoxide reductase complex 1 (VKORC1) gene.
Interventions
DIAGNOSTIC_TESTVenipuncture
* Approximately 6 months after discontinuation of VKAs one additional venipuncture will be performed for determination of dp-ucMGP and desmosine. * At baseline two additional blood collection tubes will be drawn for determination of dp-ucMGP, desmosine and VKORC1 polymorphisms. Since this is during one of the last regular International Normalized Ratio (INR) testing at the anticoagulation clinic, no additional venipuncture has to be performed at this moment.
Sponsors
Maastricht University Medical Center
Canisius-Wilhelmina Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Use of VKAs for at least 3 months * Stop VKAs at short time * Written informed consent * Age ≥18 years * Ability to comply with all study requirements
Exclusion criteria
* Active malignancy or cured malignancy \<12 months prior to enrollment * Use of maintenance dose oral corticosteroids * Serious mental impairment * Life expectation of less than 6 months on the basis of concurrent disease
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Difference in elastin degradation rate | Plasma desmosine is measured at baseline and 6 months after discontinuation of VKAs | Difference in elastin degradation rate before and after discontinuation of VKAs, quantified by the change in plasma desmosine levels |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Difference in vitamin K status | Plasma dp-ucMGP is measured at baseline and 6 months after discontinuation of VKAs | Difference in vitamin K status before and after discontinuation of VKAs, quantified by the change in dp-ucMGP, discontinuation of VKAs. |
| Association between desmosine and dp-ucMGP | Desmosine and dp-ucMGP are determined before discontinuation of VKAs and 6 months after discontinuation of VKAs | Association between desmosine and dp-ucMGP both in patients who use VKAs and do not use VKAs. |
| Differences in desmosine and dp-ucMGP levels between different VKORC1 polymorphisms | Desmosine and dp-ucMGP are determined, both before discontinuation of VKAs and 6 months after discontinuation of VKAs. VKORC1 polymorphisms are determined before discontinuation of VKAs. | Levels of dp-ucMGP and desmosine levels of subjects with different VKORC1 polymorphisms are compared, both during the use of VKAs and after discontinuation. |
Countries
Netherlands
Contacts
Primary ContactRob Janssen, MD, PhD
Backup ContactIanthe Piscaer, MD
Outcome results
None listed