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J G Peyron

Publications and source records attributed to J G Peyron.

At least 19 recordsLinked to original sources

A risk-benefit assessment of injections of hyaluronan and its derivatives in the treatment of osteoarthritis of the knee.

Hyaluronan is critical for the homeostasis of the joint as an organ, in part, because it provides the rheological properties (viscosity and elasticity) of the synovial fluid. These properties depend upon both the concentration and the molecular weight of the hyaluronan in the synovial fluid. In osteoarthritis, the hyaluronan is both smaller in size and lower in concentration. Thus, it is rational and physiologically meaningful to treat osteoarthritis with viscosupplementation, i.e. injection of material designed to increase the rheological properties of the synovial fluid. It is important, though, to assess the risks and benefits of such a physiological treatment. There are various products on the market for viscosupplementation. These include hyaluronan preparations of relatively low molecular weight (Hyalgan and ARTZ), a hyaluronan preparation of intermediate molecular weight, but still lower molecular weight than that of the hyaluronan in normal healthy synovial fluid (Orthovisc), and a cross-linked hyaluronan (a hylan) of high molecular weight (Synvisc). The evidence from in vitro and in vivo models of osteoarthritis and from clinical trials to date suggests that efficacy, as would be expected by mechanistic reasoning, depends strongly upon molecular weight. The available evidence indicates that these products differ little in the incidence and severity of adverse events (about 2 to 4%, almost always local swelling, and with no adverse sequelae). All are very well tolerated in comparison to nonsteroidal anti-inflammatory drug therapy, although direct comparisons are few. The only potentially serious adverse event is joint infection, which is rare and directly dependent upon the number of injections, among other factors. No infection has been related to contamination of any of the products. In summary, treatment with low molecular weight preparations of hyaluronan seems to be effective. However, viscosupplementation with hyaluronan preparations may have slightly higher risk and less benefit than viscosupplementation with hylans, because the relatively lower molecular weight hyaluronan preparations require more injections which may incur higher costs and theoretically an increased chance of infection. Viscosupplementation with hylans is clearly effective, and the available evidence suggests that the benefits almost certainly outweigh the risks.

Animals↗

Intraarticular hyaluronan injections in the treatment of osteoarthritis: state-of-the-art review.

Viscosupplementation (restoring the rheological properties of a tissue matrix) by injection of hyaluronan into the joints has been in use for 2 decades, mostly for osteoarthritis (OA) of the knee, using doses of 20-25 mg of hyaluronan of 500,000 to 2,500,000 M(r), in sequences of 2 to 10 weekly injections. Pain relief appears in a few days, progresses over a few weeks, and often lasts several months. Some data suggest the benefit can last 6 months to one year. Tolerance is universally reported as very good. Those responding to hyaluronan are 65-80%, compared to 30-35% responding to control. Compared to local steroid injections, the effect of hyaluronan appears significantly more lasting. More highly viscoelastic preparations of hyaluronan can be expected to make this therapy even more attractive.

Animals↗

Clinical features of osteoarthritis, diffuse idiopathic skeletal hyperostosis, and hypermobility syndromes.

In 1990, there were signs of a renewed interest in clinical studies about several aspects of osteoarthritis. The work-up of classic data and the use of new information from epidemiologic surveys as well as careful radiographic monitoring of selected groups of patients have brought us broader views on the general course of the condition. In addition, the biochemical disturbances underlying certain types of early degenerative arthritis that could help us to understand some of the mechanisms that may be operative in osteoarthritis have been disclosed. Finally, a few pieces of new information have been incorporated into the knowledge of diffuse idiopathic skeletal hyperostosis and the hypermobility syndrome.

Animals↗

Is osteoarthritis a preventable disease?

Since most of the pathophysiological steps of the initiation of osteoarthritis are not understood, its prevention can only mean decreasing or abolishing its risk factors. Excess mechanical stresses certainly can be minimized by correcting developmental or acquired anatomical or functional defects, probably by decreasing occupational or sports hazards and perhaps by avoiding overweight. Effective control of chondrolytic/inflammatory episodes is a promising prospect. Opposing the effects of age remains a remote expectation.

Humans↗

Epidemiological aspects of osteoarthritis.

An epidemiological approach can shed some light on several aspects of osteoarthritis (OA). OA is an ubiquitous condition, with an age-linked prevalence, rising slowly until the age of 50 and rapidly thereafter, especially in women. Its etiology is clearly multifactorial, the main factors being ageing, mechanical stress hereditary and/or constitutional factors, and inflammation. Structural and physical features of cartilage alter with age. These alterations are underlaid by biochemical changes. Mechanical stress is sometimes acute but most often long-standing. Familial or constitutional factors, or the possible triggering role of inflammation, are particularly well documented in certain subsets of OA. Finally, the possibility of an underlying metabolic disturbance remains a stimulating, though yet unproven, prospect.

Aging↗

Risk factors in osteoarthritis--how do they work?

Extrinsic risk factors of osteoarthritis (OA) comprise anatomical defects and mechanical insults. They alter the strength and/or the direction of forces inflicted on the matrix. This leads to damage of the fibrous network by as yet conjectural pathways. The main intrinsic risk factor is aging. Some pieces of evidence seem to point to quantitative or qualitative defects in the stabilizing factors of proteoglycan aggregates of old persons.

Aging↗

Osteoarthritis. The epidemiologic viewpoint.

Large epidemiologic studies of osteoarthritis (OA) performed over the past 30 years have confirmed that OA is a ubiquitous condition, that it is linked to age, that it is more frequent and more widespread in women older than 45 years of age, and that mechanical overuse of the joints is probably instrumental in the occurrence or the location of certain cases of OA. Epidemiologic evidence points to the existence of an entity of "generalized OA" composed of three or more locations with involvement of the interphalangeals. Heredity in cases associated with distal interphalangeal OA and inflammation in cases with proximal interphalangeal OA are the factors found to be most closely correlated to generalized OA. Surveys of several series of OA of the hip have pointed to the existence of several clinicoradiologic subsets that could have different clinical correlates and various pathophysiologic mechanisms. Because several conditions, such as crystal arthropathy, diffuse skeletal hyperostosis, and subsets of OA, have been described in recent years, a reappraisal of an epidemiologic approach of OA is advisable.

Adult↗

Noncollagenous proteins in cartilage of normal subjects and patients with degenerative joint disease. A gel electrophoretic study.

Normal articular cartilage from subjects of various ages and cartilage from patients with degenerative joint disease were extracted with 4M guanidinium chloride. After dialysis against 8M urea pH 6.8, a 0.2M NaCl fraction was obtained by ion exchange chromatography on DE-52 in 8M urea. This fraction was concentrated, reduced, and analyzed by sodium dodecyl sulfate--polyacrylamide gel electrophoresis (7% gels). Six major noncollagenous protein bands (P1-P6) were found; 2 were identified as the link proteins. The approximate molecular weights of P1-P6 were: 87,000, 64,000, 56,000, 46,000, 41,000, and 27,000. A similar sodium dodecyl sulfate-polyacrylamide gel electrophoresis pattern of P1-P6 was found in young baboons, in normal young and aged humans, and in patients with degenerative joint disease. Peaks corresponding to extracted collagen were decreased in older patients and increased in patients with degenerative joint disease, even those of advanced age.

Adolescent↗

[Biochemistry of collagen and the locomoter apparatus (Hereditary connective tissue diseases and rheumatic diseases. Part I].

The elementary collagen molecule consists of three chains rolled into a spiral and ending in nonhelical telopeptides. In cutaneous collagen, there are two types of chains, in cartilaginous collagen there is only one. In the synthesis, several enzymes play successive parts: proline hydroxylase, lysine hydroxylase, then pro-collagen peptidase and finally, lysine oxidase and hydroxylysine oxidase; their coordinated actions ultimately allow the chains to establish the transverse intra and intermolecular links which give the collagen fiber its cohesion. The type and number of these transverse links vary from one tissue to another. Specific collagenases make collagen degradation possible.

Animals↗

[Biochemistry of collagen and locomotor apparatus. Hereditary diseases of the connective tissue and rheumatic diseases (3)].

In inflammatory granuloma, synovial sclerosis or inflammation and in Dupuytren's contracture, the neocollagen contains chains and/or transverse links that are characteristic of rapidly growing immature tissues. In arthrosis, a conversion of collagen synthesis towards a cutaneous type may occur. The destruction of cartilage in rheumatoid arthritis is brought about by a specific collagenase that originates from the inflamed synovial membrane. Finally, certain forms of osteoporosis may be due to alterations of the osseous collagen which impair the mechanism of calcification.

Animals↗

[The biochemistry of collagen and the locomotor apparatus. Hereditary diseases of connective tissue and rheumatologic diseases (part 2)].

In lathyrism, the toxic agent directly blocks the development of the transverse links in the collagen fibre, while in bovine dermatosparaxis there is a deficiency of procollagen peptidase. Of the many clinical forms of the Ehlers-Danlos syndrome, some are due to a deficiency of lysine oxidase, others to deficiency of lysine hydroxylase and still others to procollagen peptidase deficiency. The essential deficiency in Marfan's disease is still unknown, but that in homocystinuria causes blocking of the groups necessary to form the transverse links. In osteogenesis imperfecta, which is probably a heterogeneous group, there is deficient consolidation of the collagen fibrils, the cause of which is still unknown. One possibility is a quantitative imbalance between chains of different types. In scleroderma there is excessive synthesis of an apparently normal connective tissue; the cause of this is also still unknown.

Aminopropionitrile↗