Context Knee osteoarthritis (OA) is a leading cause of disability in older persons.
Few risk factors for disease progression or functional decline have been identified.
Hip-knee-ankle alignment influences load distribution at the knee; varus and
valgus alignment increase medial and lateral load, respectively.
Objective To test the hypotheses that (1) varus alignment increases risk of medial
knee OA progression during the subsequent 18 months, (2) valgus alignment
increases risk of subsequent lateral knee OA progression, (3) greater severity
of malalignment is associated with greater subsequent loss of joint space,
and (4) greater burden of malalignment is associated with greater subsequent
decline in physical function.
Design and Setting Prospective longitudinal cohort study conducted March 1997 to March
2000 at an academic medical center in Chicago, Ill.
Participants A total of 237 persons recruited from the community with primary knee
OA, defined by presence of definite tibiofemoral osteophytes and at least
some difficulty with knee-requiring activity; 230 (97%) completed the study.
Main Outcome Measures Progression of OA, defined as a 1-grade increase in severity of joint
space narrowing on semiflexed, fluoroscopically confirmed knee radiographs;
change in narrowest joint space width; and change in physical function between
baseline and 18 months, compared by knee alignment at baseline.
Results Varus alignment at baseline was associated with a 4-fold increase in
the odds of medial progression, adjusting for age, sex, and body mass index
(adjusted odds ratio [OR], 4.09; 95% confidence interval [CI], 2.20-7.62).
Valgus alignment at baseline was associated with a nearly 5-fold increase
in the odds of lateral progression (adjusted OR, 4.89; 95% CI, 2.13-11.20).
Severity of varus correlated with greater medial joint space loss during the
subsequent 18 months (R = 0.52; 95% CI, 0.40-0.62
in dominant knees), and severity of valgus correlated with greater subsequent
lateral joint space loss (R = 0.35; 95% CI, 0.21-0.47
in dominant knees). Having alignment of more than 5° (in either direction)
in both knees at baseline was associated with significantly greater functional
deterioration during the 18 months than having alignment of 5° or less
in both knees, after adjusting for age, sex, body mass index, and pain.
Conclusion This is, to our knowledge, the first demonstration that in primary knee
OA varus alignment increases risk of medial OA progression, that valgus alignment
increases risk of lateral OA progression, that burden of malalignment predicts
decline in physical function, and that these effects can be detected after
as little as 18 months of observation.
Twelve percent of the US population aged 25 to 75 years has symptoms
and signs of osteoarthritis (OA).1 Disability
due to OA is largely a result of knee or hip involvement. The risk of disability
attributable to knee OA alone is as great as that due to cardiac disease and
greater than that due to any other medical condition in elderly persons.2 Knee OA also substantially increases risk of disability
due to other medical conditions.3 Increased
awareness of the impact of knee OA has provided impetus to accelerate development
of disease-modifying agents (ie, treatments that delay OA progression).4 At present, there are no disease-modifying drugs for
OA.
Poor understanding of the natural history of OA contributes to the slow
development of interventions that modify the course of the disease. This deficiency
of knowledge hinders development of novel interventions to target factors
responsible for disease progression and functional decline; it also clouds
the ability to identify patients who are unlikely to benefit from investigational
treatments.
In the investigation of a candidate risk factor in OA studies, 3 key
questions arise. Does the factor contribute to (1) incidence (ie, new occurrence)
of osteoarthritic disease? (2) disease progression in those who already have
OA? and (3) disability in those with OA? The literature on knee OA is weighted
toward the first question. However, the second and third questions are crucial
to the goal of reducing the burden of knee OA. In a subset of individuals,
knee OA remains in the mild state that characterizes newly developed OA; Dieppe5 has stated that in this subset, OA should not even
be considered a disease—OA that progresses beyond mild stages is responsible
for the bulk of both individual and societal costs of OA. Knowledge of the
factors that lead to progression and functional decline will aid development
of interventions to modify disease course and patient-centered outcomes.
In the investigation of knee OA progression, the recommended primary
outcome is joint space change, measured via radiographic images acquired using
special protocols that maximize accuracy and reliability.6-13
The sparse literature regarding progression is limited by its reliance on
conventional, extended-knee radiography (ie, without the protocols now considered
essential).
Osteoarthritis is widely believed to be the result of local mechanical
factors acting within the context of systemic susceptibility.14-16
Certain site-specific factors in the local joint environment govern how load
is distributed across the articular cartilage of a given joint. However, the
effect of such factors on OA progression or patient-centered outcomes is largely
unexamined.
At the knee, alignment (ie, the hip-knee-ankle angle) is a key determinant
of load distribution. In theory, any shift from a neutral or collinear alignment
of the hip, knee, and ankle affects load distribution at the knee.17 The load-bearing axis is represented by a line drawn
from mid femoral head to mid ankle. In a varus knee, this line passes medial
to the knee and a moment arm is created, which increases force across the
medial compartment. In a valgus knee, the load-bearing axis passes lateral
to the knee, and the resulting moment arm increases force across the lateral
compartment.17 Disproportionate medial transmission
of load results from a stance-phase adduction moment.18
This adduction moment reflects the magnitude of intrinsic compressive load
on the medial compartment during gait.19 Varus-valgus
alignment is a key determinant of this moment.
These mechanical effects of alignment on load distribution make it biologically
plausible that both varus and valgus alignment contribute to OA progression.
Further support comes from animal studies17
as well as surgical studies, which identify knee alignment as a predictor
of knee procedure outcomes. The question that has not been answered is, does
knee alignment influence risk of structural progression and functional decline
in knee OA?
In this study, we tested whether (1) varus alignment at baseline increases
risk of subsequent medial tibiofemoral compartment OA progression, (2) valgus
alignment at baseline increases risk of subsequent lateral compartment OA
progression, (3) severity of varus or valgus malalignment at baseline is correlated
with subsequent change in medial or lateral joint space width, respectively,
and (4) greater burden of malalignment at baseline is associated with greater
subsequent deterioration in physical function.
The Mechanical Factors in Arthritis of the Knee (MAK) study is a longitudinal
study of the contribution of mechanical factors to disease progression and
functional decline in knee OA. Participants were recruited from the community
through advertising in periodicals targeting elderly persons, 67 neighborhood
organizations, letters to members of the registry of the Buehler Center on
Aging at Northwestern University, Chicago, Ill, and local referrals.
Inclusion and exclusion criteria were based on National Institute of
Arthritis and Musculoskeletal and Skin Diseases/National Institute on Aging–sponsored
multidisciplinary workshop recommendations for knee OA progression studies.6 Inclusion criteria were definite tibiofemoral osteophyte
presence (Kellgren/Lawrence [K/L] radiographic grade ≥2) of 1 or both knees
and at least some difficulty with knee-requiring activity. Exclusion criteria
were corticosteroid injection within the previous 3 months or history of avascular
necrosis, rheumatoid or other inflammatory arthritis, periarticular fracture,
Paget disease, villonodular synovitis, joint infection, ochronosis, neuropathic
arthropathy, acromegaly, hemochromatosis, Wilson disease, osteochondromatosis,
gout, pseudogout, or osteopetrosis. Approval was obtained from the Office
for the Protection of Research Subjects–Institutional Review Board of
Northwestern University. Written informed consent was obtained from all participants.
To assess alignment, a single anteroposterior radiograph of the lower
extremity was obtained. A 130 × 36-cm graduated grid cassette was used
to include the full limb of tall participants.20
By filtering the x-ray beam in a graduated fashion, this cassette accounts
for the unique soft tissue characteristics of the hip and ankle. Participants
stood without footwear, with tibial tubercles facing forward. The tibial tubercle,
a knee-adjacent site not distorted by OA, was used as positioning landmark.21 The patella is often used to position normal knees,20 but the possibility of patellofemoral OA precluded
this approach. The x-ray beam was centered at the knee at a distance of 2.4
m. A setting of 100 to 300 mA/s and 80-90 kV was used, depending on limb size
and tissue characteristics.
Alignment was measured as the angle formed by the intersection of the
mechanical axes of the femur (the line from femoral head center to femoral
intercondylar notch center) and the tibia (the line from ankle talus center
to the center of the tibial spine tips).17,21,22
A knee was defined as varus when alignment was more than 0° in the varus
direction, valgus when it was more than 0° in the valgus direction, and
neutral when alignment was 0°.20,22-24
The angle made by the femur and tibia on a knee x-ray was not used because
it does not consider the proximal femur, femoral or tibial shafts, or ankle25; is highly variable as opposed to full-limb measurements22; and is not typically used in orthopedic clinical
or biomechanical studies.
One experienced reader made all measurements. Reliability was high for
measurements of varus (intraclass correlation coefficient [ICC], 0.99) and
valgus (ICC, 0.98) alignment.
Because physical examination laxity tests are unreliable,26,27
a device to measure varus-valgus laxity was designed by Thomas Buchanan, PhD.28,29 This device and the measurement protocol
address sources of variation in knee laxity tests, ie, inadequate thigh and
ankle immobilization, incomplete muscle relaxation, variation of the knee
flexion angle, variation of load applied, and imprecise measurement of rotation.26,27,30
The system consists of a bench with an arc-shaped, low-friction track
running medially and laterally. The distal shank is attached to a sled, which
travels within the track. A handheld dynamometer fits into the sled and is
used to apply load. Participants assumed a seated position, with the thigh
and ankle immobilized and the study knee at 20° flexion.31
An auditory signal indicates when a load of 40 newtons (12 newtons/m) has
been applied.32
Laxity was measured as the angular deviation at the sled after varus
and valgus load. Total rotation, the sum of varus and valgus rotation for
each knee, was examined as previously described.32-34
All laxity measurements were performed by the same examiner and assistant.
Our reliability with this device was very good (within-session ICC, 0.85-0.96;
between-session ICC, 0.84-0.90).
For knee radiographs at baseline and 18 months, the Buckland-Wright
protocol35 was followed. This protocol meets
recommendations for knee OA studies provided by multidisciplinary workshops6 and the Task Force of the Osteoarthritis Research
Society International.9 Per this protocol,
knee position, criteria for beam alignment relative to knee center, radiopaque
markers to account for magnification, and measurement landmarks were specified.
All radiographs were obtained in the same unit by 2 trained technicians.
The standing semiflexed view of the knee in this protocol is optimal
for joint space assessment because it achieves superimposition of the anterior
and posterior joint margins.12,36,37
The knee was flexed until the tibial plateau was horizontal, parallel to the
beam and perpendicular to the film. To control for rotation, the heel was
fixed and the foot rotated until the tibial spines were central within the
femoral notch. Knee position was confirmed by fluoroscopy before films were
taken. Foot maps made at baseline were used to standardize repositioning at
18 months. These protocol elements enhance accuracy and precision of joint
space assessment.12,37 Even without
fluoroscopic confirmation, the semiflexed view was superior to the extended
or schuss views38; the fluoroscopic approach,
by confirming the same position in all radiographs, further reduces variability.
Joint space assessment is the widely recommended primary outcome for
knee OA progression studies9,11,39
and provides a compartment-specific measure, which was required in this study.
Medial and lateral progression were defined as a 1-grade or greater
increase in severity of joint space narrowing in the medial and lateral compartments,
respectively. We used the 4-grade scale (ie, 0 = none; 1 = possible; 2 = definite;
and 3 = severe) with atlas representations from Altman et al.8
Joint space was also measured at the narrowest point in each compartment.
The femoral boundary was the distal convex margin of the condyles. The tibial
boundary was the line extending from tibial spine to outer margin, across
the center of the articular fossa, defined by the superior margin of the bright
radiodense band of the subchondral cortex.35,40
The narrowest interbone distance of each compartment was measured using calipers
with electronic readout.6,40,41
Joint space area and midcompartment width are less sensitive to change than
narrowest joint space width.35
Other approaches (ie, osteophyte grade, K/L grade) had limitations.
Although osteophytes can be graded per compartment, they are often more prominent
in the uninvolved compartment. The K/L grade provides a global score without
separate information for the medial and lateral compartments (ie, 0 = normal;
1 = possible osteophytes; 2 = definite osteophytes and possible joint space
narrowing; 3 = moderate/multiple osteophytes, definite narrowing, some sclerosis,
and possible attrition; and 4 = large osteophytes, marked narrowing, severe
sclerosis, and definite attrition).
One experienced reader assessed radiographs using an atlas.8 Reliability for joint space grading (κ coefficient,
0.80-0.86) and measurement (ICC, 0.95-0.98) was very good. Reading of knee
and full-limb radiographs occurred in separate sessions. The reader was blinded
to knee data when assessing alignment and to alignment data when assessing
knee radiographs.
Physical Function and Pain
Physical function was assessed using an observed measure, chair-stand
performance (rate of chair stands per minute, based on the time required to
complete 5 repetitions of rising from a chair and sitting down), using the
protocol of Guralnik et al42 and Seeman et
al.43 The sit-stand transfer is closely linked
to knee status.44 Of the lower-extremity joints,
the knee often exhibits the greatest peak torques during this task.45-47 Average pain during
the past week was recorded on separate 0- to 100-mm visual analog scales (VASs)
for each knee.
For analyses of OA progression, knees not at risk of progressing (ie,
those with the highest grade of joint space narrowing at baseline) were excluded.
Descriptive data (proportions) and correlations were provided separately for
dominant and nondominant knees, with dominance ascertained using the question,
"In order to kick a ball, which leg would you use?" All statistical tests
were conducted using a nominal α level of .05. The risk of progression
was analyzed from logistic regression, using generalized estimating equations
(GEEs) to include data from 1 or both knees of each participant. Odds ratios
(ORs) were calculated for medial and lateral progression, first entering alignment
(unadjusted OR), then adding age, sex, and body mass index (BMI) (adjusted
OR). Odds ratios were recalculated after additional adjustment for laxity.
The associated 95% confidence intervals (CIs) were calculated; a 95% CI of
more than 1.00 indicates that alignment is significantly associated with progression.
The same approach was taken to explore the relationship between alignment
and progression assessed using K/L grade.
Next, the relationship between baseline varus alignment (in degrees;
varus as a positive value, neutral as 0, and valgus as a negative value) and
change in medial joint space width from baseline to 18 months, each as a continuous
variable, was examined in dominant knees using linear regression analysis.
A decrease in joint space was analyzed as a positive value. Similarly, the
relationship between baseline valgus alignment (valgus as a positive value,
neutral as 0, and varus as a negative value) and change in lateral joint space
width from baseline to 18 months was examined.
For analyses of physical function, participants whose chair-stand performance
could not further decline (ie, those who could not perform the test at baseline)
were excluded. Participants were divided into 3 alignment groups based on
having 0, 1, or 2 knees with baseline alignment of more than 5° from neutral
(in either direction). Change from baseline to 18 months in chair-stand rate
was regressed on alignment group status to evaluate unadjusted and age-, sex-,
and BMI-adjusted differences between groups. To explore the mediating role
of pain, further analyses additionally adjusted for pain.
We also explored the relationship between baseline alignment group and
functional decline, designated as at least 20% worsening in chair-stand rate.
Logistic regression analysis was used to evaluate the unadjusted and adjusted
odds of performance decline related to alignment group status.
Of 237 participants at risk for progression in at least 1 knee, 7 (3%)
did not return at 18 months; 5 died and 2 could not be reached. Selected characteristics
of these participants are presented in Table 1. No participant received therapy that might have affected
the progression rate.
In dominant knees, medial OA progression occurred in 28 (31%) of 89
varus vs 9 (9%) of 102 nonvarus knees. Of the 37 dominant knees with medial
progression, 28 (76%) were varus at baseline. Mean varus alignment was 3.34°
at baseline and 3.82° at 18 months. Results were similar in nondominant
knees.
Lateral OA progression occurred in 19 (22%) of 88 valgus vs 5 (5%) of
103 nonvalgus knees. Of 24 dominant knees with lateral progression, 19 (79%)
were valgus. Mean valgus alignment was 3.21° at baseline and 3.24°
at 18 months. Results were similar in nondominant knees.
The average change in the compartment that was narrower at baseline
was a loss of 0.45 mm over 18 months. Definite joint space narrowing (grade ≥2)
was present in either the medial or the lateral compartment but never in both.
In no knee did both medial and lateral progression occur; tibiofemoral progression
was a unicompartmental event.
In GEE logistic regression analyses, varus vs nonvarus (referent) alignment
at baseline was associated with a 5-fold increase in the odds of medial progression
during the subsequent 18 months (Table 2). After adjustment for age, sex, and BMI, varus alignment was still
associated with a 4-fold increase in the odds of medial progression.
In calculating risk in varus vs nonvarus knees, we recognized that medial
OA may be associated with varus, valgus, or neutral alignment. Therefore,
the risk associated with varus alignment was compared with the risk conferred
by any other possible alignment for a given knee. To determine the progression
risk associated with varus alignment when the comparison group was neutral
or nearly neutral knees, we repeated the analysis with a referent group consisting
of neutral (0°) or mildly valgus (≤2°) knees. Varus alignment was
still associated with a 3-fold increase in risk of medial progression in adjusted
analyses (Table 2).
In GEE logistic regression analyses, valgus vs nonvalgus (referent)
alignment at baseline was associated with an almost 4-fold increase in the
odds of lateral progression during the subsequent 18 months (Table 2). This relationship persisted after adjustment for age,
sex, and BMI.
When the referent group was neutral or nearly neutral (≤2° varus)
knees, valgus alignment was associated with a more than 3-fold increase in
the odds of subsequent lateral OA progression in both unadjusted and adjusted
analyses (Table 2).
These logistic regression analyses were repeated after additionally
controlling for varus-valgus laxity, with little effect on results. The OR
for the relationship between varus alignment and medial progression, adjusting
for age, sex, BMI, and laxity, was 4.01 (95% CI, 2.19-7.62). The OR for the
relationship between valgus alignment and lateral progression, adjusting for
age, sex, BMI, and laxity, was 4.78 (95% CI, 2.08-11.02).
Results of analyses of medial progression were not affected by excluding
lateral progressors from the nonprogressor group. Results of analyses of lateral
progression also were not affected by excluding medial progressors from the
nonprogressor group.
Malalignment Severity at Baseline and Change in Joint Space
The relationship between baseline severity of varus alignment and change
in medial joint space width from baseline to 18 months, each as a continuous
variable, was examined in dominant knees. Greater varus alignment correlated
with greater subsequent loss of joint space (R =
0.52; 95% CI, 0.40-0.62).
Similarly, the relationship between baseline severity of valgus and
change in lateral joint space width from baseline to 18 months was examined
in dominant knees. Severity of valgus correlated with the magnitude of loss
of lateral joint space width (R = 0.35; 95% CI, 0.21-0.47).
These relationships persisted after adjustment for age, sex, BMI, and laxity.
Alignment at Baseline and Progression of K/L Grade
Given the historical role of the K/L grading system in knee OA studies,
we also examined the relationship between baseline alignment and K/L grade
progression (≥1-grade increase). However, knees that progress by K/L grade
include some knees with medial progression and other knees with lateral progression.
Therefore, this analysis tests a different hypothesis—does varus alignment
increase risk of progression in either the medial (mechanically stressed by
varus alignment) or the lateral (not stressed) compartment, and does valgus
alignment increase risk of progression in either the medial (not stressed)
or the lateral (stressed by valgus alignment) compartment? Notably, there
is no rationale to support a link between varus alignment and lateral progression
or between valgus alignment and medial progression.
Even with this limitation of the K/L grading system, valgus alignment
was associated with an increase in risk of K/L grade progression (OR, 2.51;
95% CI, 0.91-6.89), and varus alignment was associated with a significant
increase in risk of K/L grade progression (OR, 3.61; 95% CI, 1.33-9.85), further
attesting to the strength of their effects. Finally, absolute severity of
malalignment as a continuous variable was significantly associated with K/L
grade progression.
Burden of Knee Malalignment at Baseline and Change in Physical Function
Burden of malalignment at baseline predicted deterioration in physical
function between baseline and 18 months. Participants were classified into
1 of 3 groups at baseline: those who had alignment of 5° or less in both
knees (n = 126), 1 knee with alignment of more than 5° (n = 52), or both
knees with alignment of more than 5° (n = 37). Physical functional outcome
was analyzed as a continuous variable, ie, change in chair-stand rate from
baseline to 18 months. Change did not differ between the first 2 groups, but
significantly greater deterioration in chair-stand performance was found in
participants who had alignment of more than 5° in both knees vs participants
who had alignment of 5° or less in both knees (Table 3). The difference between these groups persisted after adjusting
for age, sex, and BMI.
We also explored the relationship between burden of malalignment and
functional decline, designating decline as at least 20% worsening in chair-stand
rate. Thirty-four (16%) of the 215 participants able to perform the test at
baseline had functional decline by this definition, including 10% of the 126
with alignment in both knees of 5° or less, 21% of the 52 with alignment
of more than 5° in 1 knee, and 27% of the 37 with alignment of more than
5° in both knees. The odds of functional decline were doubled (OR, 2.33;
95% CI, 0.97-5.62) by having 1 knee with alignment of more than 5° vs
both knees with alignment of 5° or less and were tripled by having alignment
of more than 5° in both knees vs alignment of 5° or less in both knees
(OR, 3.22; 95% CI, 1.28-8.12). This association persisted after adjusting
for age, sex, and BMI.
Burden of Malalignment, Functional Deterioration, and Pain
To explore whether pain is an intervening variable in the relationship
between knee alignment and functional deterioration, first we examined the
relationship between alignment and pain at baseline, then we examined whether
the relationship between alignment and functional deterioration was lost after
accounting for pain. Average pain increased as malalignment increased (alignment
<4° = pain score of 25.2 mm on the VAS; alignment >4° but <8°
= pain score of 37.7 mm; and alignment ≥8° = pain score of 41.2 mm).
Pain severity was significantly associated with malalignment severity. Specifically,
the GEE logistic regression analysis of alignment and pain showed an average
VAS increase of 10 mm in knee pain with each 5° of malalignment. This
relationship persisted after adjustment for age, sex, and BMI. Next, we repeated
the analysis of the relationship between alignment group and change in chair-stand
rate after additionally accounting for pain. As shown in Table 3, the burden of malalignment at baseline (ie, 2 vs 0 knees)
continued to be significantly associated with subsequent functional deterioration.
Varus alignment at baseline increased risk of medial knee OA progression
over the 18 months of our study, and valgus alignment increased risk of subsequent
lateral knee OA progression. The severity of varus malalignment at baseline
correlated with the magnitude of medial joint space loss, and the baseline
severity of valgus malalignment correlated with the magnitude of lateral joint
space loss. A greater burden of malalignment at baseline was linked to greater
decline in an observed measure of physical function. To our knowledge, this
is the first demonstration that alignment influences risk of subsequent primary
OA disease progression and decline in functional status and that these effects
can be detected after as little as 18 months of observation.
In theory, varus and valgus alignment may each be a cause or result
of progressive knee OA; therefore, it was essential to examine alignment at
the beginning of the period during which progression was evaluated. Varus
or valgus alignment that predates knee OA may be due to genetic, developmental,
or posttraumatic factors. Animal model data support a link between preexisting
varus or valgus alignment and OA development.17
Knee alignment that results from knee OA may be due to loss of cartilage and
bone height. However, even as a consequence of osteoarthritic disease, varus
or valgus alignment may contribute to subsequent progression. The results
of the current study, especially given the influence of alignment on load
distribution, support this concept.
The presence of a relationship between alignment and progression by
18 months underscores the importance of alignment as a risk factor. In knee
OA progression studies, 18 months is a relatively early follow-up point, at
which an effect may not as yet be detectable. The importance of alignment
was further demonstrated by the finding of a strong relationship with progression
even when the referent group included only neutral or nearly neutral knees.
The alignment-associated odds of progression may be even greater at longer
follow-up. The odds may be substantially greater if malalignment and knee
OA are in a vicious cycle.
Varus or valgus alignment may stretch the capsule and collateral ligaments,
increasing varus-valgus laxity, a potential mechanism of the alignment effect.
If laxity were playing this role, then controlling for laxity should lead
to a reduction in the alignment-progression relationship. In our study, this
did not occur, suggesting that an increase in laxity is not a major mechanism
for the alignment effect. Our study had more women than men; this sex distribution
matches that of knee OA in the general population. The effects of alignment
were independent of sex.
Burden of malalignment influenced patient-centered outcome, physical
function assessed by chair-stand performance. In knee OA, risk factor profiles
for structural disease progression and for disability overlap but are not
identical. It was necessary to specifically examine the relationship between
alignment and functional status. Longitudinal studies of patient-centered
outcomes in knee OA have been rare; knowledge about risk factors has been
derived chiefly from cross-sectional studies. We explored whether pain was
an intervening factor in the alignment effect on function. While the strength
of the alignment-function relationship was reduced slightly after accounting
for pain, a significant relationship persisted, suggesting that at least some
portion of the alignment effect is independent of pain.
The results of this study are consistent with biomechanical studies
that have revealed that varus and valgus alignment increase medial and lateral
load, respectively.17,48,49
During gait, the impact of valgus on load distribution may not be comparable
with that of varus alignment. In the normally aligned ambulating knee, load
is disproportionately transmitted to the medial compartment.50
Varus alignment further increases medial load during gait.22
Valgus alignment is associated with an increase in lateral compartment peak
pressures49; however, more load is still borne
medially until more severe valgus is present.51,52
Therefore, we expected to find that varus alignment had a stronger effect
on medial progression risk than valgus on lateral progression risk, but the
effects of varus and valgus were similar in magnitude. The severity of varus
was similar to that of valgus; the lack of difference in potency could not
be attributed to more severe valgus malalignment. Certainly, alignment in
either direction increases compartmental load, giving credence to the concept
that varus and valgus alignment each may contribute to subsequent progression.
Differences between the magnitude of the effects of varus and valgus alignment
may emerge with further follow-up.
A relationship between varus or valgus alignment and the natural progression
of primary knee OA has not previously been demonstrated. Beliefs regarding
this relationship have rested on biomechanical models and studies that are
cross-sectional or of short duration and surgical outcome studies. Testing
the immediate or short-term mechanical impact of a factor is not equivalent
to testing its impact on a long-term structural outcome in a patient. The
stage of investigation represented by the current study was necessary, both
to demonstrate and to quantify the long-term effects of knee alignment on
patient outcomes. Several orthopedic studies have demonstrated that knee alignment
is associated with surgical outcome (eg, arthroplasty,53
osteotomy,54 meniscectomy,55-57
and meniscal debridement58). While extremely
important, these data do not address the role played by knee alignment in
the nonsurgical, natural evolution of knee OA. In the operated knee, the development
or progression of OA is linked to several factors not at play in natural progression
(eg, nature of surgery and stage of OA at time of surgery).
Investigation of the influence of alignment on natural structural or
patient-centered outcomes in unselected populations has been rare. Schouten
et al59 found that patient recollection of
"bow-legs or knock-knees in childhood" was associated with a 5-fold increase
in risk of OA progression. Others found that presence of "varus/valgus deformity,"
not further defined, did not differ between those who progressed and those
who did not.60 In another study involving patients
who were selected from a hospital practice on the basis of not having undergone
surgery, and in whom alignment was considered only at the end of follow-up,
50% of 35 varus knees had progressive joint space narrowing.61
The proportion of participants whose OA progressed in the current study
is comparable with studies using similar recruitment methods.11,62
Also, an average joint space loss of 0.45 mm was detected over 18 months,
or 0.30 mm over 12 months. This rate falls within the range of annual joint
space loss in the literature (0.12 to 0.62 mm/y). Comparison with population-based
studies, which have tended to use conventional, extended-knee radiography,
is not possible. In previous progression studies, medial and lateral knee
OA have been treated as a single condition, despite a belief that they differ
in rate of progression and risk factor profile. Our results provide evidence
that tibiofemoral OA progresses asymmetrically and illustrate that local risk
factors are not only specific to joint but also to compartment.
The goal of this study was to examine the influence of alignment on
structural and functional outcomes in patients with established OA. There
is growing awareness that risk factors for incident OA differ from risk factors
for OA progression. It is likely that knee alignment has a different effect
on risk of incident OA from that shown here on risk of progression. The former
effect may be smaller, given the less vulnerable state of the healthy knee.
However, the effect on risk of incident OA cannot be inferred from these results
and should be specifically examined.
These results suggest the need to develop and test, in patients with
knee OA, the effect of interventions that reduce the stresses imposed by a
given alignment. Interventions that reduce load in the stressed compartment
on an ongoing basis may have a disease-modifying effect. Interventions that
may hold promise (eg, "unloading" orthoses) have been examined in short-term
studies; their long-term tolerability and effect on symptoms have been minimally
evaluated, and their effect on progression and long-term functional outcomes
is unknown.
In summary, varus alignment at baseline increased risk of subsequent
medial OA progression and valgus alignment at baseline increased risk of subsequent
lateral OA progression. Baseline severity of malalignment was correlated with
the magnitude of subsequent joint space loss. Burden of malalignment at baseline
was linked to greater decline in physical function.
1.Lawrence RC, Helmick CG, Arnett FC.
et al. Estimates of the prevalence of arthritis and selected musculoskeletal
disorders in the United States.
Arthritis Rheum.1998;41:778-799.Google Scholar 2.Guccione AA, Felson DT, Anderson JJ.
et al. The effects of specific medical conditions on the functional limitations
of elders in the Framingham Study.
Am J Public Health.1994;84:351-358.Google Scholar 3.Ettinger WH, Davis MA, Neuhaus JM, Mallon KP. Long-term physical functioning in persons with knee osteoarthritis
from NHANES I: effects of comorbid medical conditions.
J Clin Epidemiol.1994;47:809-815.Google Scholar 5.Dieppe P. Theories on the pathogenesis of OA.
Presented at: Stepping Away From OA: A Scientific Conference on the
Prevention of Onset, Progression, and Disability of Osteoarthritis; July 23-24,
1999; Bethesda, Md. Summary available at: http://www.nih.gov/niams/reports/oa/oaconfsumsc.htm. Accessed February 6, 2001. 6.Dieppe P, Altman RD, Buckwalter JA.
et al. Standardization of methods used to assess the progression of osteoarthritis
of the hip or knee joints. In: Kuettner KE, Goldberg VM, eds. Osteoarthritic
Disorders. Rosemont, Ill: American Academy of Orthopaedic Surgeons;
1995:481-496.
7.Mazzuca SA, Brandt KD. Plain radiography as an outcome measure in clinical trials involving
patients with knee osteoarthritis.
Rheum Dis Clin North Am.1999;25:467-480.Google Scholar 8.Altman RD, Hochberg M, Murphy WA, Wolfe F, Lequesne M. Atlas of individual radiographic features in osteoarthritis.
Osteoarthritis Cartilage.1995;3:3-70.Google Scholar 9.Task Force of the Osteoarthritis Research Society. Design and conduct of clinical trials in patients with osteoarthritis.
Osteoarthritis Cartilage.1996;4:217-244.Google Scholar 10.Mazzuca SA, Brandt KD, Katz BP. Is conventional radiography suitable for evaluation of a disease-modifying
drug in patients with knee osteoarthritis?
Osteoarthritis Cartilage.1997;5:217-226.Google Scholar 11.Ravaud P, Giraudeau B, Auleley GR.
et al. Radiographic assessment of knee OA: reproducibility and sensitivity
to change.
J Rheumatol.1996;23:1756-1764.Google Scholar 12.Buckland-Wright JC, Macfarlane DG, Lynch JA, Jasani MK, Bradshaw CR. Joint space width measures cartilage thickness in osteoarthritis of
the knee.
Ann Rheum Dis.1995;54:263-268.Google Scholar 13.Buckland-Wright JC. Quantitative radiography of osteoarthritis.
Ann Rheum Dis.1994;53:268-275.Google Scholar 14.Dieppe P. The classification and diagnosis of osteoarthritis. In: Kuettner KE, Goldberg VM, eds. Osteoarthritic
Disorders. Rosemont, Ill: American Academy of Orthopaedic Surgeons;
1995:7.
15.Kuettner KE, Goldberg VM. Introduction. In: Kuettner KE, Goldberg VM, eds. Osteoarthritic
Disorders. Rosemont, Ill: American Academy of Orthopaedic Surgeons;
1995:xxi-xxv.
16.Pelletier JP, Martel-Pelletier J, Howell DS. Etiopathogenesis of osteoarthritis. In: Koopman WJ, ed. Arthritis and Allied Conditions:
A Textbook of Rheumatology. Baltimore, Md: Williams & Wilkins;
1997:1969-1984.
17.Tetsworth K, Paley D. Malalignment and degenerative arthropathy.
Orthop Clin North Am.1994;25:367-377.Google Scholar 18.Andriacchi TP. Dynamics of knee malalignment.
Orthop Clin North Am.1994;25:395-403.Google Scholar 19.Schipplein OD, Andriacchi TP. Interaction between active and passive knee stabilizers during level
walking.
J Orthop Res.1991;9:113-119.Google Scholar 20.Moreland JR, Bassett LW, Hanker GJ. Radiographic analysis of the axial alignment of the lower extremity.
J Bone Joint Surg Am.1987;69:745-749.Google Scholar 21.Chao EY, Neluheni EV, Hsu RW, Paley D. Biomechanics of malalignment.
Orthop Clin North Am.1994;25:379-386.Google Scholar 22.Hsu RW, Himeno S, Conventry MB, Chao EY. Normal axial alignment of the lower extremity and load-bearing distribution
at the knee.
Clin Orthop.1990;255:215-227.Google Scholar 23.Cooke TD, Li J, Scudamore RA. Radiographic assessment of bony contributions to knee deformity.
Orthop Clin North Am.1994;25:387-393.Google Scholar 24.Hilding MB, Lanshammar H, Ryd L. A relationship between dynamic and static assessments of knee joint
load.
Acta Orthop Scand.1995;66:317-320.Google Scholar 25.Goldberg VM, Kettelkamp DB, Coyler RA. Osteoarthritis of the knee. In: Moskowitz RW, Howell DS, Goldberg VM, Mankin HJ, eds. Osteoarthritis: Diagnosis and Medical/Surgical Management. Philadelphia,
Pa: WB Saunders Co; 1992:599-620.
26.Cushnaghan J, Cooper C, Dieppe P.
et al. Clinical assessment of osteoarthritis of the knee.
Ann Rheum Dis.1990;49:768-770.Google Scholar 27.Noyes FR, Cummings JF, Grood ES.
et al. The diagnosis of knee motion limits, subluxations, and ligament injury.
Am J Sports Med.1991;19:163-171.Google Scholar 28.Sharma L, Lou C, Felson DT.
et al. Laxity in healthy and osteoarthritic knees.
Arthritis Rheum.1999;42:861-870.Google Scholar 29.Sharma L, Hayes KW, Felson DT.
et al. Does laxity alter the relationship between strength and physical function
in knee osteoarthritis?
Arthritis Rheum.1999;42:25-32.Google Scholar 30.Markolf KL, Graff-Radford A, Amstutz HC. In vivo knee stability.
J Bone Joint Surg Am.1978;60:664-674.Google Scholar 31.Markolf KL, Bargar WL, Shoemaker SC, Amstutz HC. The role of joint load in knee stability.
J Bone Joint Surg Am.1981;63:570-585.Google Scholar 32.Brage ME, Draganich LF, Pottenger LA, Curran JJ. Knee laxity in symptomatic osteoarthritis.
Clin Orthop.1994;304:184-189.Google Scholar 33.Pottenger LA, Phillips FM, Draganich LF. The effect of marginal osteophytes on reduction of varus-valgus instability
in osteoarthritic knees.
Arthritis Rheum.1990;33:853-858.Google Scholar 34.Wada M, Imura S, Baba H, Shimada S. Knee laxity in patients with osteoarthritis and rheumatoid arthritis.
Br J Rheumatol.1996;35:560-563.Google Scholar 35.Buckland-Wright CB. Protocols for precise radio-anatomical positioning of the tibiofemoral
and patellofemoral compartments of the knee.
Osteoarthritis Cartilage.1995;3(suppl A):71-80.Google Scholar 36.Messieh SS, Fowler PJ, Munro T. Anteroposterior radiographs of the osteoarthritic knee.
J Bone Joint Surg Br.1990;72:639-640.Google Scholar 37.Buckland-Wright JC, Macfarlane DG, Williams SA, Ward RJ. Accuracy and precision of joint space width measurements in standard
and macroradiographs of osteoarthritic knees.
Ann Rheum Dis.1995;54:872-880.Google Scholar 38.Buckland-Wright JC, Wolfe F, Ward RJ, Flowers N, Hayne C. Substantial superiority of semiflexed (MTP) views in knee osteoarthritis.
J Rheumatol.1999;26:2664-2674.Google Scholar 39.Altman RD, Fries JF, Bloch DA, Carstens J.
et al. Radiographic assessment of progression in osteoarthritis.
Arthritis Rheum.1987;30:1214-1225.Google Scholar 40.Lequesne M. Quantitative measurements of joint space during progression of osteoarthritis:
chondrometry. In: Kuettner KE, Goldberg VM, eds. Osteoarthritic
Disorders. Rosemont, Ill: American Academy of Orthopaedic Surgeons;
1995:427-444.
41.Buckland-Wright JC, Macfarlane DG. Radioanatomic assessment of therapeutic outcome in osteoarthritis. In: Kuettner KE, Goldberg VM, eds. Osteoarthritic
Disorders. Rosemont, Ill: American Academy of Orthopaedic Surgeons;
1995:51-65.
42.Guralnik JM, Ferrucci L, Simonsick EM, Salive ME, Wallace RB. Lower-extremity function in persons over the age of 70 as a predictor
of subsequent disability.
N Engl J Med.1995;332:556-561.Google Scholar 43.Seeman TE, Charpentier PA, Berkman LF.
et al. Predicting changes in physical performance in a high-functioning elderly
cohort: MacArthur studies of successful aging.
J Gerontol.1994;49:M97-M108.Google Scholar 44.Pai YC, Chang HJ, Chang RW, Sinacore JM, Lewis JL. Alteration in multijoint dynamics in patients with bilateral knee osteoarthritis.
Arthritis Rheum.1994;37:1297-1304.Google Scholar 45.Fleckenstein SJ, Kirby RL, MacLeod DA. Effect of limited knee-flexion range on peak hip moments of force while
transferring from sitting to standing.
J Biomech.1988;21:915-918.Google Scholar 46.Pai YC, Rogers MW. Speed variation and resultant joint torques during sit-to-stand.
Arch Phys Med Rehabil.1991;72:881-885.Google Scholar 47.Schultz AB, Alexander NB, Ashton-Miller JA. Biomechanics analysis of rising from a chair.
J Biomech.1992;25:1383-1391.Google Scholar 48.McKellop HA, Llinas A, Sarmiento A. Effects of tibial malalignment on the knee and ankle.
Orthop Clin North Am.1994;25:415-423.Google Scholar 49.Bruns J, Volkmer M, Luessenhop S. Pressure distribution at the knee joint.
Arch Orthop Trauma Surg.1993;113:12-19.Google Scholar 50.Morrison JB. The mechanics of the knee joint in relation to normal walking.
J Biomech.1970;3:51-61.Google Scholar 51.Johnson F, Leitl S, Waugh W. The distribution of load across the knee.
J Bone Joint Surg Br.1980;62:346-349.Google Scholar 52.Harrington IJ. Static and dynamic loading patterns in knee joints with deformities.
J Bone Joint Surg Am.1983;65:247-259.Google Scholar 53.Ritter MA, Faris PM, Keating EM, Meding JB. Postoperative alignment of total knee replacement.
Clin Orthop.1994;299:153-156.Google Scholar 54.Yasuda K, Majima T, Tsuchida T, Kaneda K. A ten- to 15-year follow-up observation of high tibial osteotomy in
medial compartment osteoarthritis.
Clin Orthop.1992;282:186-195.Google Scholar 55.Allen PR, Denham RA, Swan AV. Late degenerative changes after meniscectomy.
J Bone Joint Surg Br.1984;66:666-671.Google Scholar 56.Neyret P, Donell ST, Dejour H. Results of partial meniscectomy related to the state of the anterior
cruciate ligament.
J Bone Joint Surg Br.1993;75:36-40.Google Scholar 57.Boe S, Hansen H. Arthroscopic partial meniscectomy in patients aged over 50.
J Bone Joint Surg Br.1986;68:707.Google Scholar 58.Ogilvie-Harris DJ, Fitsialos DP. Arthroscopic management of the degenerative knee.
Arthroscopy.1991;7:151-157.Google Scholar 59.Schouten JS, van den Ouweland FA, Valkenburg HA. A 12-year follow up study in the general population on prognostic factors
of cartilage loss in osteoarthritis of the knee.
Ann Rheum Dis.1992;51:932-937.Google Scholar 60.Dougados M, Gueguen A, Nguyen M.
et al. Longitudinal radiologic evaluation of osteoarthritis of the knee.
J Rheumatol.1992;19:378-384.Google Scholar 61.Miller R, Kettelkamp DB, Laubenthal KN.
et al. Quantitative correlations in degenerative arthritis of the knee.
J Bone Joint Surg Am.1973;55:956-962.Google Scholar 62.Ledingham J, Regan M, Jones A, Doherty M. Factors affecting radiographic progression of knee osteoarthritis.
Ann Rheum Dis.1995;54:53-58.Google Scholar