A Dietary Supplement in the Management of Patients with Lumbar Osteochondrosis: A Randomized, Double-Blinded, Placebo-Controlled Study

Author:

Laky Brenda12345,Huemer Daniel16,Eigenschink Martin17,Sagl Benedikt8ORCID,Thell Rainer69,Wagner Karl-Heinz5ORCID,Anderl Werner110,Heuberer Philipp R.11112

Affiliation:

1. Austrian Research Group for Regenerative and Orthopedic Medicine (AURROM), 1050 Vienna, Austria

2. Austrian Society of Regenerative Medicine (RegMed), 1010 Vienna, Austria

3. Faculty of Medicine, Sigmund Freud Private University Medicine, 1020 Vienna, Austria

4. Center for Clinical Research, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria

5. Department of Nutritional Sciences, University of Vienna, 1090 Vienna, Austria

6. Medical University of Vienna, 1090 Vienna, Austria

7. Department for Trauma and Orthopedic Surgery, AUVA Trauma Center Vienna-Meidling, 1100 Vienna, Austria

8. Competence Center Artificial Intelligence, University Clinic of Dentistry, Medical University of Vienna, 1090 Vienna, Austria

9. Emergency Department, Klinik Donaustadt, 1220 Vienna, Austria

10. Momentum Praxis Mödling, 2340 Mödling, Austria

11. OrthoCare, 1100 Vienna, Austria

12. HealthPi Medical Center, 1010 Vienna, Austria

Abstract

Various nutritional supplements are available over the counter, yet few have been investigated in randomized controlled trials. The rationale for using the specific mix of nutritional substances including collagen type II, hyaluronic acid, n-acetyl-glucosamine, bamboo extract, L-lysine, and vitamin C is the assumption that combining naturally occurring ingredients of the intervertebral disc would maintain spine function. This double-blinded, placebo-controlled randomized trial aimed to evaluate the efficacy of a nutraceutical supplement mix in the management of lumbar osteochondrosis. Fifty patients were randomly assigned to either the supplement or placebo group in a 1:1 ratio. Patient-Reported Outcome Measures (PROMs) included the Oswestry Disability Index (ODI), the visual analogue scale for pain (pVAS), short form-12 (SF-12) physical and mental component summary subscale scores (PCS and MCS, respectively), and global physical activity questionnaire (GPAQ). Magnetic resonance imaging (MRI) was used to evaluate degenerative changes of intervertebral discs (IVD) including Pfirrmann grades as well as three-dimensional (3D) volume measurements. Data were collected at baseline and after the 3-month intervention. None of the PROMs were significantly different between the supplement and placebo groups. Disc degeneration according to Pfirrmann classifications remained stable during the 3-month intervention in both groups. Despite no significance regarding the distribution of Pfirrmann grade changes (improvement, no change, worsening; p = 0.259), in the supplement group, one patient achieved a three-grade improvement, and worsening of Pfirrmann grades were only detected in the placebo group (9.1%). Furthermore, in-depth evaluations of MRIs showed significantly higher 3D-measured volume changes (increase) in the supplement (+740.3 ± 796.1 mm3) compared to lower 3D-measured volume changes (decrease) in the placebo group (−417.2 ± 875.0 mm3; p < 0.001). In conclusion, this multi-nutrient supplement might not only stabilize the progression of lumbar osteochondrosis, but it might also potentially even increase IVD volumes as detected on MRIs.

Funder

Natural Products & Drugs GmbH

Publisher

MDPI AG

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