Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

A 12-week randomized, double-blind, placebo-controlled multicenter study of choline-stabilized orthosilicic acid in patients with symptomatic knee osteoarthritis

P. Geusens, K. Pavelka, J. Rovensky, J. Vanhoof, N. Demeester, M. Calomme, D. Vanden Berghe,

. 2017 ; 18 (1) : 2. [pub] 20170105

Jazyk angličtina Země Anglie, Velká Británie

Typ dokumentu časopisecké články, multicentrická studie, randomizované kontrolované studie

Perzistentní odkaz   https://www.medvik.cz/link/bmc17031161

BACKGROUND: The aim of this study was to assess the efficacy of choline-stabilized orthosilicic acid (ch-OSA) in patients with symptomatic knee osteoarthritis (OA). METHODS: In a multicenter, double-blind, placebo-controlled study, 211 patients with knee OA (Kellgren and Lawrence grade II or III) and moderate to moderately severe pain were randomly allocated to ch-OSA or placebo for 12 weeks. The primary outcome was the change in the WOMAC pain subscale from baseline to week 12. Secondary outcomes were changes from baseline to week 12 in WOMAC total, WOMAC stiffness, WOMAC physical function, Subject Global Assessment and levels of cartilage degradation biomarkers C-terminal telopeptide of collagen type II (CTX-II) and cartilage oligomeric matrix protein (COMP). Pre-specified subgroup analyses included the effect of gender. RESULTS: A total of 166 (120 women, 46 men) patients were included in the analysis (87 and 79 in the ch-OSA and placebo group, respectively). In the total study population, no differences were observed between the two treatment groups for the different outcomes but significant treatment x gender interactions were found. In men taking ch-OSA, a significant improvement in WOMAC total, WOMAC stiffness and WOMAC physical function as well as a lower increase in biomarker levels of cartilage degradation was observed, but not in women. The change in WOMAC pain showed a similar positive trend in men taking ch-OSA. CONCLUSION: After 12 weeks of treatment, no effect was found of ch-OSA in the total study population on clinical parameters and biomarkers, but a gender interaction was observed. In men, ch-OSA was found effective in reducing symptoms of knee OA, which was associated with a slight but significant reduction of biomarkers that are related to cartilage degradation. TRIAL REGISTRATION: The study was registered retrospectively: ISRCTN88583133 . Registration date: 2015-10-07.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc17031161
003      
CZ-PrNML
005      
20171030124227.0
007      
ta
008      
171025s2017 enk f 000 0|eng||
009      
AR
024    7_
$a 10.1186/s12891-016-1370-7 $2 doi
035    __
$a (PubMed)28056936
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a enk
100    1_
$a Geusens, Piet $u Biomedical Research Institute (BIOMED), Hasselt University, Diepenbeek, Belgium. drpgeusens@gmail.com. Rheumatology, Maastricht UMC, Maastricht, The Netherlands. drpgeusens@gmail.com. ReumaClinic, Bretheistraat 149, Genk, 3600, Belgium. drpgeusens@gmail.com.
245    12
$a A 12-week randomized, double-blind, placebo-controlled multicenter study of choline-stabilized orthosilicic acid in patients with symptomatic knee osteoarthritis / $c P. Geusens, K. Pavelka, J. Rovensky, J. Vanhoof, N. Demeester, M. Calomme, D. Vanden Berghe,
520    9_
$a BACKGROUND: The aim of this study was to assess the efficacy of choline-stabilized orthosilicic acid (ch-OSA) in patients with symptomatic knee osteoarthritis (OA). METHODS: In a multicenter, double-blind, placebo-controlled study, 211 patients with knee OA (Kellgren and Lawrence grade II or III) and moderate to moderately severe pain were randomly allocated to ch-OSA or placebo for 12 weeks. The primary outcome was the change in the WOMAC pain subscale from baseline to week 12. Secondary outcomes were changes from baseline to week 12 in WOMAC total, WOMAC stiffness, WOMAC physical function, Subject Global Assessment and levels of cartilage degradation biomarkers C-terminal telopeptide of collagen type II (CTX-II) and cartilage oligomeric matrix protein (COMP). Pre-specified subgroup analyses included the effect of gender. RESULTS: A total of 166 (120 women, 46 men) patients were included in the analysis (87 and 79 in the ch-OSA and placebo group, respectively). In the total study population, no differences were observed between the two treatment groups for the different outcomes but significant treatment x gender interactions were found. In men taking ch-OSA, a significant improvement in WOMAC total, WOMAC stiffness and WOMAC physical function as well as a lower increase in biomarker levels of cartilage degradation was observed, but not in women. The change in WOMAC pain showed a similar positive trend in men taking ch-OSA. CONCLUSION: After 12 weeks of treatment, no effect was found of ch-OSA in the total study population on clinical parameters and biomarkers, but a gender interaction was observed. In men, ch-OSA was found effective in reducing symptoms of knee OA, which was associated with a slight but significant reduction of biomarkers that are related to cartilage degradation. TRIAL REGISTRATION: The study was registered retrospectively: ISRCTN88583133 . Registration date: 2015-10-07.
650    _2
$a aplikace orální $7 D000284
650    _2
$a senioři $7 D000368
650    _2
$a biologické markery $x analýza $7 D015415
650    _2
$a chrupavka $x patologie $7 D002356
650    _2
$a chrupavkový oligomerní matrixový protein $x analýza $7 D064236
650    _2
$a cholin $x aplikace a dávkování $x terapeutické užití $7 D002794
650    _2
$a kolagen typ II $x analýza $7 D024043
650    _2
$a dvojitá slepá metoda $7 D004311
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a lidé $7 D006801
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a lidé středního věku $7 D008875
650    _2
$a artróza kolenních kloubů $x farmakoterapie $7 D020370
650    _2
$a management bolesti $x metody $7 D059408
650    _2
$a měření bolesti $7 D010147
650    _2
$a sexuální faktory $7 D012737
650    _2
$a kyselina křemičitá $x aplikace a dávkování $x terapeutické užití $7 D012824
650    _2
$a výsledek terapie $7 D016896
655    _2
$a časopisecké články $7 D016428
655    _2
$a multicentrická studie $7 D016448
655    _2
$a randomizované kontrolované studie $7 D016449
700    1_
$a Pavelka, Karel $u Institute of Rheumatology, Prague, Czech Republic.
700    1_
$a Rovensky, Jozef $u , Nábrežie I. Krasku 4782/4, Piešťany, Slovakia.
700    1_
$a Vanhoof, Johan $u ReumaClinic, Bretheistraat 149, Genk, 3600, Belgium.
700    1_
$a Demeester, Nathalie $u Research & Development, Bio Minerals NV, Destelbergen, Belgium.
700    1_
$a Calomme, Mario $u Research & Development, Bio Minerals NV, Destelbergen, Belgium.
700    1_
$a Vanden Berghe, Dirk $u Department of Pharmaceutical Sciences, University of Antwerp, Antwerp-Wilrijk, Belgium.
773    0_
$w MED00008193 $t BMC musculoskeletal disorders $x 1471-2474 $g Roč. 18, č. 1 (2017), s. 2
856    41
$u https://pubmed.ncbi.nlm.nih.gov/28056936 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20171025 $b ABA008
991    __
$a 20171030124316 $b ABA008
999    __
$a ok $b bmc $g 1254754 $s 992188
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 18 $c 1 $d 2 $e 20170105 $i 1471-2474 $m BMC musculoskeletal disorders $n BMC Musculoskelet Disord $x MED00008193
LZP    __
$a Pubmed-20171025

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...