VOL. 90-B, No. 4, APRIL 2008 411
ASPECTS OF CURRENT MANAGEMENT
The assessment of early osteoarthritis
T. C. B. Pollard,
S. E. Gwilym,
A. J. Carr
From the Nuffield
Orthopaedic Centre,
Oxford, England
T. C. B. Pollard, BSc(Hons),
MRCS, Specialist Registrar &
Botnar Surgical Research
Fellow
S. E. Gwilym, MRCS,
Specialist Registrar &
Girdlestone Research Fellow
A. J. Carr, ChM, FRCS,
Nuffield Professor of
Orthopaedic Surgery
Nuffield Department of
Orthopaedic Surgery
University of Oxford, Nuffield
Orthopaedic Centre, Windmill
Road, Headington, Oxford OX3
7LD, UK.
Correspondence should be sent
to Mr T. C. B. Pollard; e-mail:
Tom.Pollard@ndos.ox.ac.uk
©2008 British Editorial Society
of Bone and Joint Surgery
doi:10.1302/0301-620X.90B4.
20284 $2.00
J Bone Joint Surg [Br]
2008;90-B:411-21.
Treatment strategies for osteoarthritis most commonly involve the removal or replacement
of damaged joint tissue. Relatively few treatments attempt to arrest, slow down or reverse
the disease process. Such options include peri-articular osteotomy around the hip or knee,
and treatment of femoro-acetabular impingement, where early intervention may
potentially alter the natural history of the disease. A relatively small proportion of patients
with osteoarthritis have a clear predisposing factor that is both suitable for modification
and who present early enough for intervention to be deemed worthwhile. This paper
reviews recent advances in our understanding of the pathology, imaging and progression of
early osteoarthritis.
As the burden of osteoarthritis (OA) rises with
increased life expectancy, the need to address
diseases of the elderly becomes more pressing.
Between 1991 and 2000, the number of pri-
mary total hip replacements being undertaken
in England increased by 18%, and the number
of primary knee replacements more than
doubled.
1
Revision hip and knee arthroplasty
increased by 154% and 300%, respectively,
1
over this period, and projections to 2010 for
primary hip and knee arthroplasty estimate
increases of 22% and 63%, respectively.
1
Longer term projections of primary hip and
knee arthroplasty in the United States from
2005 to 2030 predict an increased demand of
174% and 673%, respectively.
2
Whereas
arthroplasty is usually successful in relieving
pain and improving function, it has inherent
disadvantages compared with treatment that
preserves the joint. Investigation of the cost-
effectiveness of early treatment to preserve the
natural joint is both worthwhile and necessary.
Unfortunately, progress has been hampered by
a number of major obstacles that make it diffi-
cult to design new treatments and assess their
outcome. Our understanding of the early
pathology of OA is poor, particularly in terms
of reliable assays or biomarkers. Human tissue
suitable for study is difficult to obtain. The
tissue commonly studied is often obtained as
macroscopically less-involved cartilage from
patients undergoing arthroplasty. Such tissue
may have been altered by previous medical
treatment.
3
There are no good animal models
of chronic disease, and the validity of animal
models that use a single injury to initiate OA is
questionable. From a clinical perspective, dis-
ease progression is traditionally monitored
with radiography,
4
but its correlation with
symptoms in early disease is poor. Longitudinal
studies that rely on plain radiographs to evalu-
ate treatments are difficult, as measurable pro-
gression is slow and not universal. Moreover,
they require trial periods of at least two years in
large cohorts of patients.
Little treatment is available for early OA.
Surgical options to reduce or prevent disease
progression may aim to restore normal anat-
omy, eliminate biomechanical factors, or resur-
face isolated cartilage defects by grafting. The
development of disease-modifying drugs has
been disappointing, failing to replicate their
success in rheumatoid arthritis and with none
meeting food and drug administration (FDA)
approval for clinical practice.
5
Clinical trials of
drugs in advanced OA aimed at matrix regen-
eration or preservation have not been success-
ful, at least not using a single agent. This may
well be because the mechanical environment
remains abnormal and hostile to cartilage
regeneration.
5
Sensitive techniques that could detect early
OA and reliably monitor its progression would
identify patients who may benefit from joint
preserving intervention for entry into clinical
trials, thereby aiming to reduce the number of
patients needing arthroplasty. The identifica-
tion of those subjects who are likely to progress
rapidly would be particularly useful when
designing trials. This review outlines recent
Aspects of current management