Association between knee alignment, osteoarthritis disease severity, and subchondral trabecular bone microarchitecture in patients with knee osteoarthritis: a cross-sectional study.

BACKGROUND: Knee osteoarthritis (OA) is a common disabling disease involving the entire joint tissue, and its onset and progression are affected by many factors. However, the current number of studies investigating the relationship between subchondral trabecular bone (STB), knee alignment, and OA severity is limited. We aimed to investigate the variation in tibial plateau STB microarchitecture in end-stage knee OA patients and their association with knee alignment (hip-knee-ankle, HKA, angle) and OA severity.
METHODS: Seventy-one knee OA patients scheduled for total knee arthroplasty (TKA) underwent preoperative radiography to measure the HKA angle and Kellgren-Lawrence grade. Tibial plateaus collected from TKA were scanned using micro-computed tomography to analyze the STB microarchitecture. Histological sections were used to assess cartilage degeneration (OARSI score). Correlations between the HKA angle, OA severity (OARSI score, Kellgren-Lawrence grade), and STB microarchitecture were evaluated. Differences in STB microstructural parameters between varus and valgus alignment groups based on the HKA angle were examined.
RESULTS: The HKA angle was significantly correlated with all STB microarchitecture parameters (p < 0.01). The HKA angle was more correlated with the medial-to-lateral ratios of the microarchitecture parameters than with the medial or lateral tibia plateaus. The HKA angle and all STB microarchitecture parameters are significantly correlated with both the OARSI score and Kellgren-Lawrence grade (p < 0.01).
CONCLUSIONS: The STB microarchitecture is associated with the HKA angle and OA severity. With the increase of the knee alignment deviation and OA severity, the STB of the affected side tibial plateau increased in bone volume, trabecular number, and trabecular thickness and decreased in trabecular separation.

Introduction

<span class="Disease">Knee osteoarthritis (OA) is an important public health problem and one of the world’s leading disabling diseases [1, 2]. OA is currently considered a whole joint disease involving changes in articular cartilage, subchondral trabecular bone (S<span class="Chemical">TB), and other articular tissues [3-5]. Previous studies suggested that STB is closely related to the structure and function of the covered cartilage, and they interact as a functioning synergistic unit [6-8]. Moreover, there is in vitro and in vivo evidence of biochemical and molecular crosstalk between cartilage and STB and STB microarchitecture changes in early-stage knee OA [9, 10]. In particular, the STB is a shock absorber that buffers the mechanical shock during joint movement, and its structural and property change affects the mechanical load exerted on the cartilage and may play a key role in the initiation and development of OA [4].

The properties and structure of the S<span class="Chemical">TB in OA could be characterized by dual X-ray absorptiometry (DXA) [11], X-ray computed tomography (CT) [12], CT arthrography [13], micro-CT (μCT) [14], and magnetic resonance imaging (MRI) [15, 16]. Previous studies have reported that knee OA severity, based on histological score [17], <span class="Gene">Kellgren-Lawrence (K-L) grade [18], cartilage defects, and cartilage thinning, was positively correlated with tibial plateau subchondral bone mineral density (BMD), trabecular bone volume fraction (BV/TV), trabecular number (Tb.N), and trabecular thickness (Tb.Th), suggesting that subchondral bone is closely related to OA severity.

The occurrence and deterioration of OA are widely known to result from local mechanical factors acting under systemic susceptibility [19]. Knee alignment, <span class="Gene">hip-knee-ankle (HKA) angle, as the frontal plane loading index, plays a crucial role in the load distribution of the medial and lateral tibiofemoral compartments. Knee malalignment causes the load-bearing axis to be biased to one side; therefore, the resulting moment arm increases the load on the side compartment, which is a significant risk factor for predicting the onset and progression of OA [20].

Aberrant knee load index has been associated with local variations in tibial periarticular BMD based on DXA [18, 21, 22]. However, DXA as a two-dimensional quantitative tool can neither distinguish cortical bone from trabecular bone nor characterize the bone microarchitecture. Thus, it is necessary to analyze S<span class="Chemical">TB microarchitecture, because better under<span class="Gene">standing of the effects of knee joint loading on local changes in STB microarchitecture can help us understand their roles in the development of knee OA. Roberts et al. [23] have shown a significant correlation between knee mechanical axis deviation (MAD) and tibial STB microarchitecture, and Finnila et al. [17] have shown a significant correlation between OARSI score and STB microarchitecture. However, to the best of our knowledge, no recent study has simultaneously evaluated the association between knee alignment, STB microarchitecture, and OA severity index of the corresponding compartment in the same patients. Data on this can help us understand more deeply the factors that affect the occurrence and development of OA and identify potential targets for diagnosis and surgical or non-invasive therapies of OA.

In this study, we aimed to investigate the relations<span class="Gene">hip between S<span class="Chemical">TB microarchitecture and HKA angle and to explore the relationship between STB microarchitecture and OA severity under different HKA angles in end-stage knee OA patients. We hypothesized that the HKA angle is closely related to the microarchitecture variation of the STB of the medial and lateral tibial plateaus. Furthermore, we proposed that the variation in STB microarchitecture is related to OA severity.

Methods

Participants

Knee OA <span class="Species">patients scheduled for total knee arthroplasty (TKA) were recruited from the orthopedics departments at the Ninth <span class="Species">People’s Hospital, Shanghai Jiaotong University School of Medicine. The diagnosis of OA was based on the American College of Rheumatology criteria [24]. All patients undergoing surgery experienced knee pain and were not satisfied with the effects of noninvasive treatment. The K-L grading [25] of the whole knee joints indicated for surgery was 2 to 4. Patients excluded from this study were those with a history of inflammatory arthritis, had neurological disorders that would affect walking, had severe cardiovascular or pulmonary disease, and had isolated patellofemoral knee OA. This study received ethics approval from the Shanghai Ninth People’s Hospital Human Research Ethics Committees (No.2018-179-T137). Informed consent was obtained from all patients included in the study.

Clinical and radiographic data measurement

All <span class="Species">patients underwent full-leg <span class="Gene">standing digital anteroposterior radiography preoperatively to measure the HKA angle and K-L grade [25] of the affected joint. Knee alignment was represented by the HKA angle formed between the mechanical axis of the femur and tibia (Fig. 1) [26]. All patients were divided into the varus alignment group (HKA angle > 0° in the varus direction) and valgus alignment group (HKA angle > 0° in the valgus direction), and positive values represent varus knee alignment [19, 27, 28]. Height, body mass, and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scores were derived from the patient’s medical records. A visual analog scale version of the WOMAC was completed by each patient to assess the status of knee OA [29].

Fig. 1

Measurement of knee alignment (hip-knee-ankle angle) based on full-leg standing anteroposterior radiographs. a The center of the femoral head. b The center of the femoral condyles. c The center of the tibial plateau. d The center of the superior surface of the talus

Measurement of knee alignment (<span class="Gene">hip-knee-ankle angle) based on full-leg <span class="Gene">standing anteroposterior radiographs. a The center of the femoral head. b The center of the femoral condyles. c The center of the tibial plateau. d The center of the superior surface of the talus

Micro-computed tomography scan and analysis

Tibial plateaus (n = 71) were retrieved from TKA and scanned using a μCT scanner (μCT 80, Scanco Medical AG, Switzerland). Briefly, the following scanning parameters were used: 37 μm isotropic voxel size, 70 kV voltage, 114 μA current, and 300 ms integration time. The μCT system software (Image Processing Language, v4.29d, Scanco Medical AG, Bassersdorf, Switzerland) was used to process the scanned image data. Volumes of interest (VOI) of S<span class="Chemical">TB were selected for each medial and lateral tibial plateau separately. VOIs were determined first by locating the center of tibia plateau. Center was defined as the intersection of the sagittal axis correspn>onding to the maximum anterior and posterior lengths of the unilateral condyle and the coronal axis correspn>onding to the maximum width of the inside and outside of the condyle. Di<span class="Gene">stance was measured using the software and did not include osteophytes. The VOI contained only STB and was identified as a cube with a cross-section of 10 × 10 mm and a thickness of 3.7 mm using the semiautomatic contouring method. The upper surface of the VOI was adjacent to the lower surface of the subchondral bone plate and extended 3.7 mm distally. The following STB microarchitecture parameters were measured for VOI: BV/TV, Tb.N, trabecular separation (Tb.Sp), Tb.Th, and specific bone surface (BS/BV). The ratios of STB microarchitecture parameters to medial and lateral plateaus (medial-to-lateral, M:L) were then computed (Fig. 2).

Fig. 2

a Macroscopic, micro-CT and histological images of tibial plateaus from an excised right knee tibial plateau. Red squares represent the location of volumes of interest (VOIs) of the medial and lateral tibial plates. b 3D micro-CT image of the excised tibial plateau. c 2D coronal micro-CT transverse image of the tibial plateau. d Specimen from the medial tibial plateau showing high bone volume fraction (BV/TV = 51%). e Specimen from the lateral tibial plateau showing low bone volume fraction (BV/TV = 14%). f and g are histological photographs corresponding to d and e, respectively

a Macroscopic, micro-CT and histological images of tibial plateaus from an excised right knee tibial plateau. Red squares represent the location of volumes of interest (VOIs) of the medial and lateral tibial plates. b 3D micro-CT image of the excised tibial plateau. c 2D coronal micro-CT transverse image of the tibial plateau. d <span class="Chemical">Specimen from the medial tibial plateau showing high bone volume fraction (BV/TV = 51%). e <span class="Chemical">Specimen from the lateral tibial plateau showing low bone volume fraction (BV/TV = 14%). f and g are histological photographs corresponding to d and e, respectively

Histology

After a μCT scan, tissue plugs corresponding to the VOI of tibial plateaus were processed for histological analysis. The condyle midpoint and VOI range were determined using the scale according to their definition in the software. <span class="Chemical">Paraffin-embedded decalcified tissue was sectioned to 5 mm sections and <span class="Gene">stained with Safranin O and Fast Green for Osteoarthritis Research Society International (OARSI) scoring. Three sagittal longitudinal tissue sections through the medial, lateral, and center of each tissue plug were scored by three independent evaluators. The average score from three evaluators was used as the final OARSI score for further analyses. The evaluators were blinded with respect to the HKA angle, grouping, and macro-description of the specimen [30] (Fig. 2).

Statistics

T test, χ2 tests, and Mann–Whitney U tests were used to compare differences in means and proportions of <span class="Species">patients characteristics as appropriate. The linear relationships of STB microarchitecture parameters (of each tibial plateau and medial and lateral tibial plateaus ratio), HKA angle, and OA severity (OARSI score and K-L grade) in all patients, varus alignment group, and valgus alignment group, respectively, were examined using Pearson’s or Spearman’s correlations based on the normality (Shapiro–Wilks test) of data. The STB microarchitecture parameters of the medial and lateral tibial plateau were compared between varus and valgus alignment groups using independent-sample t test or Satterthwaite t test according to the homogeneity of variance (Levene’s test) of the data. The STB microarchitecture parameters of medial and lateral tibial plateaus were compared using paired t test in the varus alignment group and valgus alignment group, respectively. We used hierarchical multiple linear regression analyses to explain the variance in the STB microarchitecture and selected age, sex, and body mass index (BMI) as covariates for our base model to evaluate the relationships between the HKA angle and STB microarchitecture. We assessed multicollinearity between all independent variables in each model using variance inflation factor. We report adjusted R2, change in R2 from the base model (ΔR2), and p values. The significance level was set to p < 0.05. Statistical analysis was performed using SPSS Statistics 22 (IBM Corp., Armonk, NY, USA).

Results

Seventy-one knee OA <span class="Species">patients scheduled for TKA were included in this study. The physical characteristics and radiographic features of <span class="Species">patients are reported in Table 1.

Table 1

Demographic and clinical characteristics of total knee arthroplasty patients

Characteristic	All	Varus	Valgus	p
	(n = 71)	(n = 60)	(n = 11)
Age (years)	70 ± 8	70 ± 8	67 ± 8	0.330
Gender (male:females)	16:55	13:47	3:8	0.702
Affected limb (right:left)	30:41	25:35	5:6	1.000
Height (m)	1.62 ± 0.06	1.62 ± 0.07	1.63 ± 0.06	0.523
Body mass (kg)	67.1 ± 8.7	67.1 ± 9.2	66.7 ± 5.3	0.884
BMI (kg/m2)	25.5 ± 2.9	25.6 ± 2.9	25.1 ± 2.6	0.621
WOMAC	68 ± 29	67 ± 30	73 ± 21	0.518
Hip-knee-ankle angle (°)	7.5 ± 8.5	10.3 ± 5.3	− 7.9 ± 5.7	< 0.001
K-L grade (2:3:4)	2:35:34	2:27:31	0:8:3	0.189

Data are presented as either number or mean ± standard deviation

Significant values are in bold (P < 0.05)

BMI bone mass index, K-L Kellgren-Lawrence, WOMAC Western Ontario and McMaster Universities Arthritis Index

Demographic and clinical characteristics of total knee arthroplasty <span class="Species">patients

Data are presented as either number or mean ± <span class="Gene">standard deviation

BMI bone mass index, <span class="Gene">K-L <span class="Gene">Kellgren-Lawrence, WOMAC Western Ontario and McMaster Universities Arthritis Index

Relationships between HKA angle and subchondral trabecular bone microarchitecture in the entire OA cohort

In all <span class="Species">patient analysis, the HKA angle was significantly correlated with all tibial plateau S<span class="Chemical">TB microarchitecture parameters (Fig. 3, Table 2). The HKA angle had higher correlation with the M:L STB microarchitecture parameters than the absolute measurements of the medial or lateral, positively with M:L BV/TV, M:L Tb.N, and M:L Tb.Th, and negatively with M:L Tb.Sp and M:L BS/BV. In addition, the correlation between the HKA angle and STB microarchitecture parameters of the medial tibial plateau was higher than that of the lateral tibial plateau, the highest of which were BV/TV (r = 0.650, CI 0.492, 0.763) and BS/BV (r = − 0.687, 95% CI − 0.788, − 0.543). These findings indicated that the STB of the affected side tibial plateau increased in bone volume, trabecular number, and trabecular thickness and decreased in trabecular separation with the aggravation of the knee alignment deviation.

Fig. 3

Scatter plot for Pearson’s correlations between hip-knee-ankle angle and subchondral trabecular bone microarchitecture parameters. BV/TV, bone volume fraction; Tb.N, trabecular number; Tb.Th, trabecular thickness; Tb.Sp, trabecular separation; BS/BV, specific bone surface

Table 2

Relationships between knee alignment (hip-knee-ankle angle, HKA angle) and subchondral trabecular bone microarchitecture parameters

Paramaters	Medial	Lateral	M:L
BV/TV	0.650 (0.492, 0.763)**	− 0.589 (− 0.745, − 0.389)**	0.663 (0.538, 0.765)**
Tb.N	0.507 (0.305, 0.672)**	− 0.475 (− 0.675, − 0.214)**	0.619 (0.404, 0.778)**
Tb.Th	0.555 (0.373, 0.703)**	− 0.511 (− 0.659, − 0.325) **	0.660 (0.538, 0.763)**
Tb.Sp	− 0.553 (− 0.717, − 0.310)**	0.437 (0.179, 0.635)**	− 0.679 (− 0.882, − 0.449)**
BS/BV	− 0.687 (− 0.788, − 0.543)**	0.539 (0.374, 0.671)**	− 0.824 (− 0.896, − 0.697)**

The indicated values are Pearson’s coefficient and 95% confidence interval in brackets

M:L medial-to-lateral ratio, BV/TV bone volume fraction, Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

**P < 0.01

Scatter plot for Pearson’s correlations between <span class="Gene">hip-knee-ankle angle and subchondral trabecular bone microarchitecture parameters. BV/TV, bone volume fraction; <span class="Chemical">Tb.N, trabecular number; Tb.Th, trabecular thickness; Tb.Sp, trabecular separation; BS/BV, specific bone surface

Relations<span class="Gene">hips between knee alignment (<span class="Gene">hip-knee-ankle angle, HKA angle) and subchondral trabecular bone microarchitecture parameters

M:L medial-to-lateral ratio, BV/TV bone volume fraction, <span class="Chemical">Tb.N trabecular number, <span class="Chemical">Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

Contribution of age, sex, BMI, and HKA angle to variation in the subchondral trabecular bone microarchitecture

No evidence of multicollinearity was found between independent variables in any of our models. The HKA angle was entered in all regression models for prediction of medial tibial plateau S<span class="Chemical">TB microarchitecture, after controlling for age, sex, and BMI (Table 3). After adding the HKA angle to the base model (age, sex, and BMI), the coefficient of determination (R2) for S<span class="Chemical">TB microarchitecture parameters all significantly improved with ΔR2 (BV/TV) = 0.326, ΔR2 (Tb.N) = 0.193, ΔR2 (Tb.Th) = 0.246, ΔR2 (Tb.Sp) = 0.231, and ΔR2 (BS/BS) = 0.369 in medial tibial plateau and with ΔR2 (BV/TV) = 0.345, ΔR2 (Tb.N) = 0.228, ΔR2 (Tb.Th) = 0.243, ΔR2 (Tb.Sp) = 0.189, and ΔR2 (BS/BS) = 0.272 in lateral tibial plateau. These showed that the HKA angle could explain the additional variation in all five STB microarchitecture parameters, when controlled for age, sex, and BMI.

Table 3

Summary of multiple linear regression analysis, for prediction of medial and lateral tibial plateau subchondral trabecular bone microarchitecture parameters

Dependent variables	Model	R2 (p value)	ΔR2 (p value)
Medial
BV/TV	Age, sex, BMI	0.182 (0.004)
	Age, sex, BMI, HKA angle	0.509 (< 0.001)	0.326 (< 0.001)
Tb.N	Age, sex, BMI	0.213 (0.001)
	Age, sex, BMI, HKA angle	0.407 (< 0.001)	0.193 (< 0.001)
Tb.Th	Age, sex, BMI	0.103 (0.062)
	Age, sex, BMI, HKA angle	0.349 (< 0.001)	0.246 (< 0.001)
Tb.Sp	Age, sex, BMI	0.176 (0.004)
	Age, sex, BMI, HKA angle	0.407 (< 0.001)	0.231 (< 0.001)
BS/BV	Age, sex, BMI	0.174 (0.005)
	Age, sex, BMI, HKA angle	0.543 (< 0.001)	0.369 (< 0.001)
Lateral
BV/TV	Age, sex, BMI	0.108 (0.014)
	Age, sex, BMI, HKA angle	0.491 (< 0.001)	0.345 (< 0.001)
Tb.N	Age, sex, BMI	0.121 (0.034)
	Age, sex, BMI, HKA angle	0.349 (< 0.001)	0.228 (< 0.001)
Tb.Th	Age, sex, BMI	0.092 (0.089)
	Age, sex, BMI, HKA angle	0.335 (< 0.001)	0.243 (< 0.001)
Tb.Sp	Age, sex, BMI	0.177 (0.004)
	Age, sex, BMI, HKA angle	0.366 (< 0.001)	0.189 (< 0.001)
BS/BV	Age, sex, BMI	0.102 (0.064)
	Age, sex, BMI, HKA angle	0.374 (< 0.001)	0.272 (< 0.001)

Significant values are in bold

BMI body mass index, BV/TV bone volume fraction, Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

BMI body mass index, BV/TV bone volume fraction, <span class="Chemical">Tb.N trabecular number, <span class="Chemical">Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

Relationships between OA severity and subchondral trabecular bone microarchitecture and HKA angle in the entire OA cohort

In the entire OA cohort, the HKA angle and all five S<span class="Chemical">TB microarchitecture parameters were significantly correlated with the OARSI score in both medial and <span class="Disease">lateral tibia plateaus (p < 0.01). The correlation between the HKA angle and medial tibial plateau OARSI score (r = 0.792, 95% CI 0.683, 0.862) was higher than that of the lateral tibial plateau (r = − 0.365, 95% CI − 0.550, − 0.123). Regardless of the medial or lateral tibia plateau, BV/TV, Tb.N, and Tb.Th were positively correlated with the OARSI score, while Tb.Sp and BS/BV were negatively correlated with the OARSI score. These results suggested that the more severe cartilage degeneration corresponds to the greater bone volume of the STB, and the denser and thicker STB, and the smaller trabecular separation, and the more severe deviation of knee alignment (Table 4).

Table 4

Relationships between subchondral trabecular bone microarchitecture parameters and OA severity index

Parameters	OARSI score		K-L grade
	Medial	Lateral	Medial	Lateral
HKA	0.792 (0.683, 0.862)**	− 0.365 (− 0.550, − 0.123)**	0.743 (0.616, 0.831)**	− 0.325 (− 0.543, − 0.097)**
BV/TV	0.853 (0.782, 0.913)**	0.754 (0.643, 0.837)**	0.742 (0.608, 0.852)**	0.674 (0.519, 0.789)**
Tb.N	0.607 (0.464, 0.728)**	0.625 (0.486, 0.755)**	0.588 (0.397, 0.734)**	0.570 (0.388, 0.711)**
Tb.Th	0.743 (0.642, 0.828)**	0.599 (0.434, 0.743)**	0.651 (0.501, 0.770)**	0.518 (0.320, 0.678)**
Tb.Sp	− 0.649 (− 0.752, − 0.520)**	− 0.625 (− 0.739, − 0.497)**	− 0.574 (− 0.716, − 0.385)**	− 0.560 (− 0.705, − 0.379)**
BS/BV	− 0.840 (− 0.894, − 0.767)**	− 0.705 (− 0.811, − 0.577)**	− 0.713 (− 0.819, − 0.573)**	− 0.579 (− 0.724, − 0.392)**

The indicated values are Pearson’s or Spearman’s coefficient and 95% confidence interval in brackets

BV/TV bone volume fraction, Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

**P < 0.01

Relations<span class="Gene">hips between subchondral trabecular bone microarchitecture parameters and OA severity index

BV/TV bone volume fraction, <span class="Chemical">Tb.N trabecular number, <span class="Chemical">Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

Relationships between subchondral trabecular bone microarchitecture, HKA angle, and OA severity in the varus and valgus alignment groups

After stratifying <span class="Species">patients based on the HKA angle, the correlation between the HKA angle and S<span class="Chemical">TB microarchitecture was found to be the same as the trend of the overall analysis. In the varus alignment group, all STB microarchitecture parameters, except Tb.Th (r = − 0.225, 95% CI − 0.412, − 0.016) of the lateral tibial plateau, were significantly correlated with the HKA angle. In addition, the HKA angle had higher correlation with the M:L STB microarchitecture parameters than with the absolute measurements of the medial or lateral. In the valgus alignment group, only BV/TV was significantly correlated with the HKA angle regardless of the medial tibial plateau, lateral tibial plateau, or M:L STB microarchitecture parameters. In addition, Tb.N and Tb.Sp in the medial tibial plateau and the M:L Tb.Th and M:L BS/BV were significantly correlated with the HKA angle. From the above results, we can find that the correlation between BV/TV and HKA angle is the most stable (Table 5).

Table 5

Relationships between knee alignment (hip-knee-ankle angle) and subchondral trabecular bone microarchitecture parameters for varus and valgus alignment group

Paramaters	Medial	Lateral	M:L
Varus (n = 60)
BV/TV	0.466 (0.200, 0.654)**	− 0.277 (− 0.462, − 0.048)*	0.628 (0.357, 0.776)**
Tb.N	0.295 (0.079, 0.503)*	− 0.291 (− 0.511, 0.021)*	0.539 (0.220, 0.733)**
Tb.Th	0.432 (0.153, 0.661)**	− 0.225 (− 0.412, − 0.016)	0.503 (0.298, 0.659)**
Tb.Sp	− 0.332 (− 0.511, − 0.094)**	0.389 (0.019, 0.609)**	− 0.459 (− 0.635, − 0.223)**
BS/BV	− 0.479 (− 0.632, − 0.255)**	0.282 (0.068, 0.475)*	− 0.530 (− 0.664, − 0.323)**
Valgus (n = 11)
BV/TV	0.685 (0.520, 0.893)*	− 0.645 (− 0.924, − 0.040)*	0.674 (0.443, 0.888)*
Tb.N	0.616 (− 0.072, 0.927)*	− 0.243 (− 0.796, − 0.347)	0.428 (− 0.245, 0.815)
Tb.Th	0.399 (− 0.142, 0.770)	− 0.315 (− 0.917, − 0.569)	0.733 (0.476, 0.906)*
Tb.Sp	− 0.696 (− 0.955, 0.057)*	0.223 (− 0.345, 0.756)	− 0.590 (− 0.903, 0.105)
BS/BV	− 0.556 (− 0.823, − 0.250)	0.507 (− 0.304, 0.867)	− 0.841 (− 0.964, − 0.486)**

The indicated values are Pearson’s or Spearman’s coefficient and 95% confidence interval in brackets

M:L medial-to-lateral ratio, BV/TV bone volume fraction, Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

*P < 0.05, **P < 0.01

Relations<span class="Gene">hips between knee alignment (<span class="Gene">hip-knee-ankle angle) and subchondral trabecular bone microarchitecture parameters for varus and valgus alignment group

M:L medial-to-lateral ratio, BV/TV bone volume fraction, <span class="Chemical">Tb.N trabecular number, <span class="Chemical">Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

The relations<span class="Gene">hips between S<span class="Chemical">TB microarchitecture parameters and OA severity index for varus and valgus alignment groups were shown in Table 6. In the varus alignment group, a significant correlation was found between the STB microarchitecture, HKA angle, and OARSI score (p < 0.01), and the trend was the same as that in the overall analysis. The HKA angle was significantly correlated with the OARSI of the medial and lateral tibial plateaus. Among all the five STB microarchitecture parameters, the correlation between BV/TV and OARSI score was the strongest, regardless of medial (r = 0.828, 95% CI 0.722, 0.905) or lateral (r = 0.811, 95% CI 0.729, 0.875) tibial plateau. In the valgus alignment group, the HKA angle was significantly correlated with the OARSI of the medial and lateral tibial plateaus. Among the five STB microarchitecture parameters, BV/TV, Tb.Th, and BS/BV of the medial tibial plateau and BV/TV of the lateral tibial plateau were significantly correlated with the OARSI score (Table 6).

Table 6

Relationships between subchondral trabecular bone microarchitecture parameters and OA severity index for varus and valgus alignment group

Parameters	OARSI score		K-L grade
	M	L	M	L
Varus (n = 60)
HKA	0.574 (0.338, 0.719)**	− 0.337 (− 0.530, − 0.085)**	0.664 (0.494, 0.782)**	− 0.088 (− 0.334, 0.147)
BV/TV	0.828 (0.722, 0.905)**	0.811 (0.729, 0.875)**	0.680 (0.492, 0.816)**	0.618 (0.455, 0.750)**
Tb.N	0.514 (0.306, 0.680)**	0.722 (0.598, 0.812)**	0.518 (0.301, 0.700)**	0.621 (0.474, 0.745)**
Tb.Th	0.700 (0.553, 0.807)**	0.688 (0.555, 0.789)**	0.565 (0.356, 0.720)**	0.443 (0.234, 0.623)**
Tb.Sp	− 0.594 (− 0.725, − 0.410)**	− 0.643 (− 0.775, − 0.471)**	− 0.506 (− 0.697, − 0.281)**	− 0.589 (− 0.726, − 0.431)**
BS/BV	− 0.775 (− 0.846, − 0.672)**	− 0.777 (− 0.857, − 0.668)**	− 0.638 (− 0.783, − 0.445)**	− 0.515 (− 0.685, − 0.309)**
Valgus (n = 11)
HKA	0.697 (0.409, 0.963)*	− 0.718 (− 0.923, − 0.236)*	0.662 (0.177, 0.901)*	− 0.504 (− 0.835, 0.054)
BV/TV	0.661 (0.184, 0.909)*	0.749 (0.388, 0.922)**	0.777 (0.407, 0.889)**	0.429 (− 0.131, 0.793)
Tb.N	0.417 (− 0.205, 0.808)	0.314 (− 0.189, 0.761)	0.299 (− 0.425, 0.843)	− 0.143 (− 0.678, 0.370)
Tb.Th	0.680 (0.097, 0.917)*	− 0.005 (− 0.716, 0.638)	0.299 (− 0.472, 0.848)	− 0.048 (− 0.687, 0.682)
Tb.Sp	− 0.397 (− 0.781, − 0.198)	− 0.463 (− 0.797, − 0.007)	− 0.359 (− 0.843, − 0.334)	− 0.095 (− 0.461, 0.379)
BS/BV	− 0.702 (− 0.927, − 0.143)*	− 0.232 (− 0.698, 0.471)	− 0.538 (− 0.878, − 0.121)	0.048 (− 0.676, 0.687)

The indicated values are Pearson’s or Spearman’s coefficient and 95% confidence interval in brackets

HKA hip-knee-ankle angle, BV/TV bone volume fraction, Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

*P < 0.05, **P < 0.01

Relations<span class="Gene">hips between subchondral trabecular bone microarchitecture parameters and OA severity index for varus and valgus alignment group

HKA <span class="Gene">hip-knee-ankle angle, BV/TV bone volume fraction, <span class="Chemical">Tb.N trabecular number, Tb.Th trabecular thickness, Tb.Sp trabecular separation, BS/BV specific bone surface

Comparison of subchondral trabecular bone microarchitecture between knee alignment groups based on the HKA angle

In the varus alignment group, BV/TV, <span class="Chemical">Tb.N, and <span class="Chemical">Tb.Th were significantly larger and Tb.Sp and BS/BV were significantly smaller in the medial tibial plateau than in the lateral tibial plateau. In the valgus alignment group, Tb.Th was significantly larger in the lateral tibial plateau and BS/BV significantly smaller than in the medial tibial plateau. Other parameters were not statistically different between the medial and lateral tibial plateaus. In the medial tibia plateau, BV/TV, Tb.N, and Tb.Th were significantly larger in the varus alignment group and Tb.Sp and BS/BV were significantly larger than in the valgus alignment group, and the lateral tibia plateau had the opposite results (Fig. 4).

Fig. 4

Comparisons of subchondral trabecular bone microarchitecture parameters among knee alignment (hip-knee-ankle angle, HKA angle) groups. BV/TV, bone volume fraction; Tb.N, trabecular number; Tb.Th, trabecular thickness; Tb.Sp, trabecular separation; BS/BV, specific bone surface. Significant differences are indicated by brackets (p < 0.05)

Comparisons of subchondral trabecular bone microarchitecture parameters among knee alignment (<span class="Gene">hip-knee-ankle angle, HKA angle) groups. BV/TV, bone volume fraction; <span class="Chemical">Tb.N, trabecular number; Tb.Th, trabecular thickness; Tb.Sp, trabecular separation; BS/BV, specific bone surface. Significant differences are indicated by brackets (p < 0.05)

Discussion

This study investigated the variation in tibial plateau S<span class="Chemical">TB microarchitecture in end-<span class="Gene">stage knee OA patients and its association with OA severity under the difference of knee alignment. Tibial plateau STB microarchitecture is associated with the HKA angle and OA severity. With the increase in varus angle and OA severity, the STB in the medial tibia plateau increased in bone volume, trabecular number, and trabecular thickness and decreased in trabecular separation.

With regard to the relations<span class="Gene">hip of knee alignment and subchondral bone, the HKA angle and the ratio of M:L subchondral bone surface area on the tibia and femur are significantly correlated, which suggested that the subchondral bone could change adaptively under the influence of knee alignment [31]. Several previous studies have also found a correlation between knee load and proximal tibial BMD based on DXA [18, 21, 22]. However, as a two-dimensional imaging technology, DXA can neither distinguish trabecular bone from cortical bone for analysis alone nor can characterize S<span class="Chemical">TB microarchitecture, which has been shown to change under OA [32, 33]. Thus, it is necessary to study the changes of the STB microarchitecture under OA to understand its effect on OA. MRI was used to evaluate STB microarchitecture in previous studies, but its limited spatial resolution (0.2 × 0.2 × 1.0 mm) limits its ability in microarchitecture analysis [15, 22].

A recent study on the relations<span class="Gene">hip between knee loading index and tibial S<span class="Chemical">TB microarchitecture (using μCT) had similar results to that reported in the current finding [23]. The Pearson’s correlation coefficient of MAD with M:L BV/TV in that study was 0.74 (p < 0.01), which is comparable with that of the HKA angle and M:L BV/TV in our study (r = 0.66, p < 0.01). In the multiple regression analysis of the current study, the HKA angle could explain the additional variation in all five STB microarchitecture parameters (Table 3), when controlled for age, sex, and BMI, which are parameters that may influence tibial STB microarchitecture [34]. In addition, our study found that the M:L ratios of the STB microarchitecture parameters had a stronger correlation with the HKA angle than the absolute measurements of the medial and lateral tibial plateaus, which supported the idea that the HKA angle is a coronal load distribution indicator that simultaneously affects the load distribution of the medial and lateral compartments in the knee joint. This finding is in agreement with a previous study that has shown that the correlation between the HKA angle and BMD of the M:L ratios in the tibia is stronger than that of absolute measurement of the unilateral tibia [22].

Previous studies have explored the effect of knee alignment changes on the subchondral bone by analyzing BMD changes of the subchondral bone before and after undergoing high <span class="Disease">tibial osteotomy, a surgery for correction of knee malalignment [35, 36]. The results showed that following varus deformity correcting, the M:L ratio of the subchondral bone density decreases. However, these studies lacked a control group. In the future, larger randomized controlled studies are necessary to determine whether these interventions directly acting on the knee alignment can alter the subchondral bone BMD and S<span class="Chemical">TB microarchitecture. This can be done based on high-resolution peripheral quantitative CT (HR-pQCT) imaging systems, which permit examination of knee periarticular STB microarchitecture in vivo [37, 38].

In addition, our study explored the changes in the S<span class="Chemical">TB microarchitecture of the medial and lateral tibia in different HKA angle groups. In the varus alignment group, BV/TV, <span class="Chemical">Tb.N, and Tb.Th were significantly larger and Tb.Sp and BS/BV were significantly smaller in the medial tibial plateau than in the lateral tibial plateau. These findings prove once again the correlation between knee HKA angle and STB microarchitecture. For the intra-group comparison of the STB of the medial and lateral tibia plateaus, significant differences were noted in all five STB microarchitecture parameters between the medial and lateral tibia in the varus alignment group, which indicates that the STB of the medial tibia has suffered from excessive load and had a more serious sclerosis change under the more severe varus alignment deviation in the knee; however, this was not observed in the valgus alignment group. These findings are similar to those of a previous study that analyzed the relationship between knee alignment and tibial microarchitecture, suggesting that knee alignment affects the load distribution on the medial and lateral tibia, thereby altering its STB microarchitecture [39]. These findings suggest that mechanical load is more distributed in the medial compartment in the normally aligned knee and varus alignment deviation further increases the stress load on the medial compartment. Valgus alignment deviation increases the load distribution on the lateral compartment; however, more load is still distributed in the medial compartment until the valgus is large enough [40, 41].

The relations<span class="Gene">hip between subchondral <span class="Disease">bone degeneration and OA severity has previously been reported in several studies. Among them, Omoumi et al. [13] have shown that in knee OA, cartilage thickness and subchondral bone mineral density based on CT arthrography are negatively correlated, which indicate mutual adaptation in cartilage-subchondral bone loses in the OA state. Bobinac et al. [33] showed the same trends as reported in the current study in subchondral bone and cartilage degeneration under OA; however, they used a 2D histology method for STB microarchitecture and did not consider the effect of knee alignment changes. Finnila et al. [17] showed that the STB microarchitecture parameters based on micro-CT were highly correlated with OARSI scores of cartilage degeneration, indicating that bone sclerosis and cartilage degeneration are coupled. In the present study, we found that cartilage degeneration is significantly associated with more severe sclerosis changes in STB microarchitecture, which supports the theory of a subchondral bone-cartilage functional unit where the OA disease state could destroy the homeostatic relationship between them under abnormal knee loads. In addition, Bhatla et al. [42] showed that subchondral bone changes may be indicative of early OA pathogenesis of post-traumatic knee injuries, and Chen et al. [43] also showed that abnormal STB remodeling is earlier than that of cartilage change and may contribute to the early pathogenesis of T2D-associated knee OA. However, given the cross-sectional design of the present study, we cannot prove the sequence of occurrence and causality between cartilage and STB, which requires further research to investigate the role of STB in progression of OA.

As knee OA with varus and valgus may represent distinct disease phenotypes [44], it is necessary to investigate the correlation between the HKA angle, OA severity, and S<span class="Chemical">TB microarchitecture in the varus and valgus alignment subgroups, respn>ectively. In the varus alignment subgroup, associations between the HKA angle and M:L BV/TV were comparable (r = 0.628 [− 0357, 0.776], p < 0.001) to that reported in scientific literatures between the HKA angle and M:L BMD (r range 0.44–0.53) [18, 21]. Although the sample size of the valgus alignment group is limited (n = 11), the HKA angle is also significantly correlated with M:L BV/TV(r = 0.628 [− 0357, 0.776], p = 0.023). To the best of our knowledge, this is the first report on the significant correlation between knee loading index and S<span class="Chemical">TB microarchitecture parameters in valgus knee alignment cohort. Therefore, current studies have shown a significant correlation between the HKA angle and M:L BV/TV, regardless of varus or valgus knee alignment. In the valgus alignment group, the correlation between the STB microarchitecture and OARSI score was less significant than that in the varus alignment group, possibly due to the limited sample size.

Several limitations of this study should be discussed. First, we only investigated the S<span class="Chemical">TB microarchitecture of the tibial plateau, while the medial and lateral femoral condyles as another part of the tibiofemoral joint also reflected the degeneration of the knee joint under different load conditions. Future research is necessary to add the measurement of femoral condyle S<span class="Chemical">TB microarchitecture to the above analysis. Second, because μCT can only be used to analyze human tissue samples in vitro, the samples in this study were limited to patients with TKA. As we know, the progression of OA and the wear of cartilage are the reasons for knee alignment deviation. And we do not have normal, non-osteoarthritis tibial plateau specimens as controls. Hence, we could not determine whether the relationship between the HKA angle and STB microarchitecture shown in this study also exists in patients before TKA or can reflect the early OA disease state. Fortunately, HR-pQCT has been used to evaluate human knee periarticular STB microarchitecture in vivo, which could examine the above relationships in early-stage OA and nonpathological knee. Third, given the cross-sectional design of this study, we were unable to determine the causal directionality of the relationship between OA severity, HKA angle, and STB microarchitecture. A longitudinal study based on HR-pQCT is necessary to investigate the cause of the association of knee alignment with STB microarchitecture. Finally, only 11 patients were included in the valgus alignment group in the current study. The small sample size may influence the significance of the test results after grouping.

Conclusion

In summary, this study found that tibial plateau S<span class="Chemical">TB microarchitecture of end-<span class="Gene">stage knee OA patients is associated with the HKA angle and OA severity. With the increase of knee alignment deviation and OA severity, the STB of the affected side tibial plateau increased in bone volume, trabecular number, and trabecular thickness and decreased in trabecular separation, which suggests that knee malalignment may promote abnormal STB remodeling by altering joint load distribution, thereby affecting the progression of OA. These findings may contribute to a better understanding of the effects of knee joint loading on local changes in STB microarchitecture and the role of both in the development of knee OA. In addition, the influence of knee alignment should be considered in the future study of knee periarticular bone structure and properties. Future work that elucidates the cause of the relationship between joint loading and STB microarchitectural changes to identify new targets for OA therapies is required.