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Dive into the research topics where John Antoniou is active.

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Featured researches published by John Antoniou.


American Journal of Pathology | 2008

Cleavage of type II collagen by cathepsin K in human osteoarthritic cartilage.

Valeria M. Dejica; John S. Mort; Sheila Laverty; M. David Percival; John Antoniou; David J. Zukor; A. Robin Poole

Cathepsin K is a cysteine protease of the papain family that cleaves triple-helical type II collagen, the major structural component of the extracellular matrix of articular cartilage. In osteoarthritis (OA), the anabolic/catabolic balance of articular cartilage is disrupted with the excessive cleavage of collagen II by collagenases or matrix metalloproteinases. A polyclonal antibody against a C-terminal neoepitope (C2K) generated in triple-helical type II collagen by the proteolytic action of cathepsin K was prepared and used to develop an enzyme-linked immunosorbent assay to study the generation of this epitope and the effects of its presence in normal adult and osteoarthritic femoral condylar articular cartilage. The generation of the C2K epitope in explant culture and the effect of a specific cathepsin K inhibitor were studied. The neoepitope, which is not generated by the collagenase matrix metalloproteinase-13, increased with age in articular cartilage and was significantly elevated in osteoarthritic cartilage compared with adult nonarthritic cartilage. Moreover, in explants from three of eight OA patients, the generation of the neoepitope in culture was significantly reduced by a specific, nontoxic inhibitor of cathepsin K. These data suggest that cathepsin K is involved in the cleavage of type II collagen in human articular cartilage in certain OA patients and that it may play a role in both OA pathophysiology and the aging process.


Advances in Orthopedic Surgery | 2014

Clinical and Radiological Outcome of the Newest Generation of Ceramic-on-Ceramic Hip Arthroplasty in Young Patients

Avishai Reuven; Grigorios N. Manoudis; Ahmed A. Aoude; Olga L. Huk; John Antoniou

Ceramic-on-ceramic articulations have become an attractive option for total hip arthroplasty in young patients. In this study, we retrospectively evaluated the short- to midterm clinical and radiographic results in 51 consecutive patients (61 hips) using the newest generation of ceramic implants. Results obtained in our study showed positive clinical and radiological outcomes. Both HHS and UCLA activity scores doubled after surgery and tended to increase over time. There was one infection requiring a two-stage revision and a case of squeaking that began 2 years postoperatively after a mechanical fall. The overall survival rate of the implants was 98.4% at six years with revision for any reason as the end point. Based on these results, fourth generation ceramics offer a viable option for young and active patients.


Global Spine Journal | 2012

Effect of In-Utero Exposure to High Dose Diethylstilbestrol on Intervertebral Disk in Adult Male and Female Progeny

S. Al Rowas; Rahul Gawri; Rami Haddad; Abdulaziz Almaawi; Lorraine E. Chalifour; John Antoniou; Fackson Mwale

Introduction In utero exposure to Diethylstilbestrol (DES) has been shown to adversely affect a number of estrogen sensitive tissues, including bone. Effects of in utero DES exposure have also been shown to affect the third generation. Environmental exposure to estrogens was shown to be higher than anticipated. The aim of this study is to determine the effect of in utero exposure to DES on the intervertebral disk (IVD) of adult mice. Materials and Methods Animal Manipulation - Pregnant C57/bl mice were injected with either vehicle (peanut oil) or one of the three doses of DES (0.1, 1.0, and 10.0 µg/kg/day) at 11 to 14 days of gestation. A minimum of three dames were set for each group. Pups were then allowed to grow to adulthood without further intervention until 3 months of age. At this point, mice were randomized into two groups; one group with a once daily swimming regimen which started as 5 minutes and was escalated to a maximum of 1 hour. The second group was left to their normal activity level and considered sedentary. All animals were sacrificed at exactly 4 months of age. Histology, the lumbar segment of the spines was dissected from three animals per group for histologic evaluation, sections were stained with 0.1% Safranin O and counter stained with 0.02% Fast Green. All slides were scanned and measurements of intervertebral disk height were taken using the NDPview software. Three measurements of disk height were taken per disk and the means compared for control versus DES exposed mice. Proteoglycan content-proteoglycans in the supernatant were measured using the DMMB assay. Statistical analysis-all statistical analyses were done using ANOVA and Fischer Least Significant Difference Post Hoc test, except for histological quantitative analysis where the Mann-Whitney test was used. Results Parameters associated with IVD degeneration were found to have higher scores in DES exposed mice versus controls (Fig. 1). Clefts in the NP were only significantly increased in the female swim group at 0.1 µg/kg/day (p = 0.007) whereas the female sedentary group showed significant increases at all three doses of DES (p < 0.0001 for all three). NP clefting was less evident in males, where the male swim group showed a significant increase at 0.1 and 1.0 µg/kg/day (p = 0.002 and p = 0.02) and the male sedentary group showed a significant increase at 10.0 µg/kg/day (p = 0.002). Tears in the AF showed a similar pattern as NP clefting, where the female swim group was only affected at 0.1 µg/kg/day (p = 0.001) and the female sedentary group showed significant increases at all three doses (p < 0.001 for all three). The male swims showed increased AF tearing at 0.1 and 10.0 µg/kg/day (p = 0.02 and p = 0.0004) while the male sedentary group showed a significant increase at 10.0 µg/kg/day (p = 0.007). Granular changes were significantly increased at all three doses in the female swim group (p = 0.0003, p = 0.002 and p = 0.0003). The female sedentary group showed significant increases at 1.0 and 10.0 µg/kg/day (p = 0.0001 and p = 0.03). Male swims showed significant increases at 0.1 and 10.0 µg/kg/day (p < 0.0001 for both). Sedentary males showed no significant granular changes compared to control. Mucous degeneration was only increased in the female swim group at all three doses of DES (p = 0.004, p = 0.03 and p = 0.03). The female sedentary group showed nonsignificant increases at 0.1 and 1.0 µg/kg/day. No significant changes in mucous degeneration were seen in the males. Cell clustering was significantly increased in the female swim group at 10.0 µg/kg/day (p = 0.002). The female sedentary group showed significant increases at 0.1 and 1.0 µg/kg/day (p = 0.002 and p = 0.03). The male sedentary group showed significant increases at 1.0 and 10.0 µg/kg/day (p < 0.0001 and p = 0.0007). No significant changes were seen in the male swim group compared to control. DES had little effect on male IVDs than those of females. Swimming caused an overall worsening of scores in females. Males were less affected by swimming than females. Proteoglycan content in the intervertebral disk was significantly decreased at 0.1 µg/kg/day and 1.0 µg/kg/day. A significant increase was noted at 10.0 µg/kg/day as compared to control. Conclusion The intervertebral disk was recently shown to be an estrogen-sensitive tissue. This had a clinical effect in obese postmenopausal women undergoing hormone replacement therapy. Our study shows that DES in utero exposure can cause nuclear extrusion and affect the intervertebral disk. The mechanisms of the effects of DES are however not well understood and further studies are necessary. This study might shed light on the possible increased risk of disk degeneration in the sons and daughters of mothers exposed during gestation, as well as their children. Furthermore, this new found environmental exposure to estrogen agonists makes it important to understand the full effects that such estrogen agonists may have. I confirm having declared any potential conflict of interest for all authors listed on this abstract Yes Disclosure of Interest None declared


Orthopaedic Proceedings | 2011

SEMEN METAL ION LEVELS AND SPERM QUALITY IN PATIENTS WITH METAL ON METAL TOTAL HIP REPLACEMENT

Vasileios Nikolaou; Alain Petit; Olga L. Huk; Stephane G. Bergeron; John Antoniou


Orthopaedic Proceedings | 2011

THE EFFECT OF OPERATIVE FACTORS ON OUTLIER ION LEVELS IN PATIENTS WITH METAL ON METAL HIP IMPLANTS

Mitchell Bernstein; Stephane G. Bergeron; Alain Petit; Olga L. Huk; John Antoniou


Orthopaedic Proceedings | 2012

TYPE X COLLAGEN EXPRESSION IN MESENCHYMAL STEM CELLS FROM OSTEOARTHRITIC PATIENTS: SUPPRESSION IN PELLET CULTURE AFTER PRE-CULTURE ON NITROGEN RICH PLASMA POLYMERS

Sonia Rampersad; Alain Petit; Juan Carlos Ruiz; M. R. Wertheimer; John Antoniou; Fackson Mwale


Orthopaedic Proceedings | 2012

A SURVEY OF THE CANADIAN RESURFACING WORKING GROUP EXPERIENCE: RATES OF CONVERSION FROM RSA TO THR

James N Powell; Paul E. Beaulé; John Antoniou; Robert B. Bourne; Emil H. Schemitsch; P.-A. Vendittoli; Frank Smith; Jason Werle; Guy Lavoie; Colin Burnell; Étienne Belzile; Paul Y. Kim; Martin Lavigne; Olga L. Huk; Greg O'connor; Arno Smit


Orthopaedic Proceedings | 2012

ARE LEVELS OF ANTIOXIDANT ENZYMES AND CYCLOXYGENASE-1 IN MESENCHYMAL STEM CELLS FROM OSTEOARTHRITIC PATIENTS RELATED TO STEM CELL HYPERTROPHY?

Fackson Mwale; Alain Petit; Guoying Yao; John Antoniou


Orthopaedic Proceedings | 2012

HIGH DOSE NEONATAL EXPOSURE TO DIETHYSTILBESTEROL AFFECTS THE MUSCULOSKELETAL SYSTEM OF MICE PROGENY AT ADULTHOOD

Abdulaziz Almaawi; Sora Al Rowas; Lorraine E. Chalifour; Alain Petit; Rami Haddad; John Antoniou; Fackson Mwale


Orthopaedic Proceedings | 2012

LONG TERM HUMAN INTERVERTEBRAL DISC ORGAN CULTURE: FROM IMPOSSIBLE TO I'M POSSIBLE

Rahul Gawri; Fackson Mwale; Jean Ouellet; Thomas Steffen; Peter J. Roughley; John Antoniou; Lisbet Haglund

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Alain Petit

Jewish General Hospital

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Olga L. Huk

McGill University Health Centre

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Peter J. Roughley

Shriners Hospitals for Children

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Rami Haddad

Jewish General Hospital

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