Vitamin k, D-chiro Inositol and α-lactalbumin in Bone Homeostasis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age35-70
SponsorRegina Elena Cancer Institute

About this trial

In women with breast cancer undergoing adjuvant hormone therapy, the marked tissue hypoestrogenism induced by therapy with aromatase inhibitors and/or tamoxifen ± GnRH analogues causes a significant acceleration in bone mass loss, with a consequent increased risk of fracture from the first year of therapy. It is therefore essential to start treatment with antiresorptive drugs and calcium and vitamin D supplementation. It has been hypothesized that vitamin K and α-lactalbumin have an effect in improving the absorption of calcium and vitamin D. In addition, vitamin K promotes gamma-carboxylation of osteocalcin, causing its activation and leading to increased incorporation of hydroxyapatite into the bone, resulting in increased calcium uptake from the blood and other tissues. Studies have reported that a combination of alendronate and vitamin K2 can lead to a decrease in the ratio of uncarboxylated osteocalcin to carboxylated osteocalcin, contributing to an increase in BMD, especially in the femoral neck. α-lactalbumin is able to increase the bioaccessibility of calcium due to its ability to prevent its precipitation at the neutral pH present in the absorptive tracts of the small intestine. Furthermore, α- lactalbumin has a binding site for vitamin D3, and the complexes formed by monomers of this protein and vitamin D have shown good stability in the presence of high vitamin concentrations. Inositol is a carbohydrate structurally similar to glucose which, in its isomeric form D-chiro-inositol, acts on bone remodeling by blocking the activation of osteoclasts through inhibition of the binding of RANK-L to its receptor present on pre-osteoclasts. Our hypothesis is that the use of the combination of vitamin K, α- lactalbumin, and D-chiro-inositol should improve the intestinal absorption of calcium and vitamin D, increasing the percentage of patients able to normalize serum levels of vitamin D and urinary calcium excretion (as a parameter of adequate calcium intake). This aspect, together with the direct effect of these components on bone remodeling, could enhance the anti-resorptive effect of standard therapy with bisphosphonates, improving the quantitative and qualitative parameters of bone. Therefore, we design a prospective randomized pilot study to assess efficacy of the combination of vitamin K, α-lactalbumin, and D-chiro-inositol, comparing patients with standard therapy and patients treated with Synostea®

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

caucasian women aged between 35 and 70;

diagnosed with breast cancer undergoing treatment with aromatase inhibitors or tamoxifen + GnRH analogues or aromatase inhibitors + GnRH analogues not started more than 12 months ago, about to start treatment with oral bone resorption inhibitors (alendronate);

vitamin D levels below 30 ng/ml (test carried out no more than 6 months prior to the baseline/T0 visit)

patients able to comply with the procedures and/or requirements of the study

Disqualifiers

uncontrolled diabetes mellitus (HbA1c 8%), severe CRF (eGFR<30 ml/min);

patients with primary or secondary hyperparathyroidism due to CRF;

baseline vitamin D levels greater than 30 ng/ml;

patients already being treated with anti-resorptive drugs;

Trial population

Adult women (aged between 35 and 70) with breast cancer undergoing treatment with aromatase inhibitors or tamoxifen + GnRH analogues or aromatase inhibitors + GnRH analogues, and about to start treatment with oral bone resorption inhibitors (alendronate), and meeting the other criteria

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Group 1: calcium carbonate/cholecalciferol

    Dietary supplement

    Intake of calcium carbonate 500 mg + cholecalciferol 2000 IU

  • Group 2: Synostea® (calcium carbonate/cholecalciferol/vitamin K/α-lactalbumin/ d-chiro-inositol)

    Dietary supplement

    Intake of Synostea® : calcium carbonate 400 mg + cholecalciferol 2000 IU + vitamin K (menaquinone 50 μg) + α-lactalbumin (30 mg) + d-chiro-inositol (150 mg)

Treatment groups

134 Participants
are divided into 2 treatment groups
Group A: Group 11 intervention
Group B: Group 21 intervention

Trial outcomes

Primary outcomes

1

Evaluation of differences in mean vitamin D levels after six months in patients treated with calcium carbonate + cholecalciferoland patients treated with calcium carbonate + cholecalciferol + vitamin K + α-lactalbumin + d-chiro-inositol

Change in mean vitamin D levels in the two treatment groups after 6 months of therapy

Time frame
6 months

Secondary outcomes

1

Evaluation of the differences in Hip Bone Mineral Density by D-XA between groups

To evaluate difference in the change from baseline in hip BMD (Bone Mineral Density) by dual x ray absorptiometry after 12 months between the 2 groups (standard vitamin d and calcium supplementation vs Synostea®)

Time frame
12 months
2

Evaluation of the differences in lumbar fragility score by Radiofrequency Echographic Multi Spectrometry between groups

To evaluate difference in the change from baseline in lumbar fragility score by Radiofrequency Echographic Multi Spectrometry after 12 months between the 2 groups (standard vitamin d and calcium supplementation vs Synostea®)

Time frame
12 months
3

Evaluation of the differences in serum levels of total calcium betweeeng groups after 12 months

To compare the changes in serum levels of total calcium after 12 months of treatment in the two groups (standard supplementationm with calcium and vitamin d vs Synostea®)

Time frame
12 months
4

Evaluation of the differences in serum levels of parathyroid hormone betweeen groups after 12 months

To compare the changes in serum levels of total calcium after 12 months of treatment in the two groups (standard supplementation with calcium and vitamin d vs Synostea®)

Time frame
12 months

Other outcomes

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