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DOI: 10.1055/s-0040-1713757
Functional Evaluation and Pain Symptomatology of the Foot and Ankle in Individuals with Severe Obesity - Controlled Transversal Study[*]
Article in several languages: português | EnglishAbstract
Objective The present study aims to evaluate the prevalence of foot and ankle pain complaints, radiographic parameters, and functional performance in subjects with severe obesity (body mass index [BMI] > 40) who are candidates to bariatric surgery.
Methods Forty severely obese patients were evaluated at a bariatric surgery outpatient facility. These severely obese subjects (BMI > 40) were divided into two subgroups: those with BMI < 50 (n = 24) and BMI > 50 (n = 16). These patients were compared with a control group of 42 volunteers with a mean BMI value of 24. The following parameters were assessed: foot pain (according to the visual analog scale [VAS]), functional performance (according to the American Orthopeadic Foot and Ankle Society [AOFAS] scale, including forefoot, midfoot and hindfoot domains), age, gender, hallux metatarsal-phalangeal angle, hallux intermetatarsal angle, talocalcaneal angle, calcanean pitch angle and Meary angle.
Results Incidence of foot pain was higher in the severely obese group compared with the control group (p < 0.0001; odds ratio [OR]: 4.2). Functional performance according to the AOFAS scale was lower in obese subjects compared with the control group (p < 0.0001; OR for hindfoot, 4.81; OR for midfoot, 3.33).
Conclusion The incidence of foot pain was higher in the group of severely obese patients compared with the control group. According to the AOFAS scale, functional forefoot, midfoot and hindfoot performance was worse in severely obese individuals.
#
Introduction
Today, obesity is one of the most challenging public health problems in modern society. It is estimated that there are currently over one billion overweight people in the world, with 300 million obese people.[1] This condition affects not only developed countries, but also developing countries, where carbohydrates ingestion is widespread due to their low cost.[2]
Population studies have shown that obesity is an independent risk factor for knee pain and arthrosis.[3] [4] [5]
In obese patients, feet pain incidence has been less studied in the literature than obesity-related knee pain.[3] [4] [5]
Obesity results in feet pain and biomechanical changes secondary to flat foot deformity, plantar fat alterations, decreased muscle strength and gait pattern abnormalities.[6] This process leads to loss of balance and risk of falling, interfering with the mobility of these individuals.[6] [7]
Currently, there is a new strand of studies due to the discovery of visceral fat-generate proteins, the so-called adipokines. The best known adipokine is leptin, which plays a role in insulin action and inflammatory cytokines production by chondrocytes.[8] Recent studies have shown a higher incidence of knee pain and osteoarthritis related to high levels of serum adipokines and metabolic syndrome.[9]
The literature on pain incidence, functional performance level and foot and ankle radiographic alignment parameters in severely obese individuals, with a body mass index (BMI) > 40, is scarce. A compilation of these data is required to properly ascertain the importance of this problem. Clinical and imaging parameters that may indicate the need for early intervention are essential to formulate therapeutic and preventive strategies for this growing group of economically active people.
The main objective of the present study is to evaluate the prevalence of pain, determined by a visual analog scale (VAS), in a sample of severely obese individuals (BMI > 40) and compare it to a control group consisting of people with a mean BMI of 24. The secondary objectives are the determination of functional differences according to the American Orthopaedic Foot and Ankle Society (AOFAS) scale[10] and radiographic parameters for morphological evaluation of the foot in both groups. Our initial hypothesis is that a higher prevalence of pain and a lower functional performance are expected in people with severe obesity compared with the control group.
#
Methodology
The present study complies with the Declaration of Helsinki rules and it was approved by the hospital's Research Ethics Committee (CAAE 69073215.2.0000.5646, opinion 2.127.775). All participants (both from the obese and control groups) signed an informed consent form.
This was an observational, cross-sectional study. Data for the present research were collected by orthopedics residents from our service from June 2017 to April 2018.
Forty patients ([Table 1]) from the bariatric surgery outpatient facility at our hospital were included. The sample consisted of 10 men and 30 women, with an average age of 45.45 years old (range, 25 to 63 years old).
GENDER |
AGE (years) |
WEIGHT (kg) |
CLASSIFICATION |
HEIGHT (m) |
BMI |
VAS |
SIDE |
H |
M |
F |
AMF |
AIM° |
APC° |
ATC |
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 |
Female |
61 |
92 |
PATIENT |
1.5 |
40.9 |
9 |
LEFT |
47 |
79 |
93 |
normal |
normal |
NORMAL |
FLAT |
2 |
Female |
42 |
110 |
PATIENT |
1.64 |
40.9 |
9 |
RIGHT |
49 |
60 |
95 |
mild |
normal |
NORMAL |
NORMAL |
3 |
Female |
64 |
105 |
PATIENT |
1.6 |
41 |
8 |
RIGHT |
28 |
52 |
100 |
normal |
normal |
NORMAL |
FLAT |
4 |
Female |
45 |
108 |
PATIENT |
1.62 |
41.2 |
10 |
LEFT |
65 |
53 |
74 |
normal |
mild |
NORMAL |
NORMAL |
5 |
Female |
32 |
99 |
PATIENT |
1.55 |
41.6 |
8 |
RIGHT |
50 |
65 |
93 |
normal |
moderate |
FLAT |
NORMAL |
6 |
Male |
27 |
158 |
PATIENT |
1.95 |
41.6 |
8 |
LEFT |
85 |
82 |
85 |
normal |
normal |
NORMAL |
NORMAL |
7 |
Female |
47 |
97.5 |
PATIENT |
1.52 |
42.2 |
7 |
RIGHT |
67 |
64 |
95 |
normal |
normal |
NORMAL |
NORMAL |
8 |
Male |
47 |
123 |
PATIENT |
1.7 |
42.6 |
0 |
LEFT |
80 |
85 |
85 |
normal |
normal |
NORMAL |
NORMAL |
9 |
Male |
62 |
108 |
PATIENT |
1.59 |
42.7 |
8 |
RIGHT |
72 |
76 |
93 |
normal |
moderate |
NORMAL |
NORMAL |
10 |
Male |
25 |
143 |
PATIENT |
1.83 |
42.7 |
10 |
RIGHT |
67 |
100 |
100 |
moderate |
moderate |
NORMAL |
NORMAL |
11 |
Male |
30 |
128 |
PATIENT |
1.73 |
42.77 |
7 |
RIGHT |
82 |
100 |
73 |
normal |
mild |
NORMAL |
NORMAL |
12 |
Male |
40 |
150 |
PATIENT |
1.87 |
42.9 |
6 |
RIGHT |
79 |
85 |
82 |
normal |
normal |
NORMAL |
FLAT |
13 |
Female |
58 |
136 |
PATIENT |
1.77 |
43.4 |
9 |
RIGHT |
30 |
32 |
83 |
moderate |
severe |
NORMAL |
NORMAL |
14 |
Female |
53 |
102 |
PATIENT |
1.52 |
44.15 |
5 |
RIGHT |
67 |
100 |
100 |
moderate |
moderate |
NORMAL |
NORMAL |
15 |
Female |
19 |
109 |
PATIENT |
1.57 |
44.2 |
8 |
RIGHT |
67 |
49 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
16 |
Female |
38 |
122 |
PATIENT |
1.66 |
44.3 |
9 |
LEFT |
80 |
82 |
93 |
normal |
mild |
FLAT |
NORMAL |
17 |
Female |
49 |
103 |
PATIENT |
1.52 |
44.58 |
8 |
RIGHT |
71 |
56 |
100 |
normal |
normal |
NORMAL |
NORMAL |
18 |
Female |
47 |
124 |
PATIENT |
1.65 |
45.5 |
7 |
RIGHT |
72 |
60 |
77 |
normal |
moderate |
NORMAL |
CAVUS |
19 |
Female |
53 |
97 |
PATIENT |
152 |
45.8 |
0 |
RIGHT |
88 |
89 |
90 |
normal |
mild |
NORMAL |
NORMAL |
20 |
Female |
43 |
126 |
PATIENT |
1.65 |
46.3 |
8 |
RIGHT |
68 |
45 |
90 |
normal |
normal |
NORMAL |
CAVUS |
21 |
Female |
63 |
116 |
PATIENT |
1.58 |
46.5 |
7 |
RIGHT |
52 |
87 |
100 |
normal |
mild |
CAVUS |
NORMAL |
22 |
Male |
50 |
142 |
PATIENT |
1.72 |
48 |
6 |
RIGHT |
60 |
100 |
78 |
moderate |
moderate |
NORMAL |
NORMAL |
23 |
Female |
63 |
115 |
PATIENT |
1.55 |
48.87 |
8 |
LEFT |
82 |
100 |
73 |
moderate |
mild |
FLAT |
NORMAL |
24 |
Female |
33 |
140 |
PATIENT |
1.68 |
49.6 |
5 |
RIGHT |
67 |
89 |
70 |
mild |
moderate |
NORMAL |
NORMAL |
25 |
Female |
52 |
130 |
PATIENT |
1.61 |
50.2 |
3 |
LEFT |
78 |
75 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
26 |
Male |
61 |
146 |
PATIENT |
1.69 |
51.12 |
10 |
LEFT |
57 |
100 |
57 |
mild |
mild |
NORMAL |
FLAT |
27 |
Female |
45 |
120 |
PATIENT |
1.53 |
51.26 |
3 |
RIGHT |
73 |
62 |
100 |
moderate |
moderate |
NORMAL |
NORMAL |
28 |
Female |
41 |
140 |
PATIENT |
1.65 |
51.42 |
8 |
RIGHT |
93 |
53 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
29 |
Female |
44 |
120 |
PATIENT |
1.52 |
51.94 |
5 |
LEFT |
84 |
82 |
100 |
mild |
mild |
FLAT |
NORMAL |
30 |
Female |
55 |
116 |
PATIENT |
1.48 |
52.16 |
8 |
LEFT |
51 |
100 |
100 |
mild |
moderate |
NORMAL |
NORMAL |
31 |
Female |
42 |
113 |
PATIENT |
1.47 |
52.29 |
6 |
RIGHT |
50 |
45 |
72 |
normal |
normal |
NORMAL |
CAVUS |
32 |
Female |
36 |
123 |
PATIENT |
1.53 |
52.59 |
5 |
LEFT |
58 |
100 |
100 |
moderate |
moderate |
NORMAL |
NORMAL |
33 |
Female |
27 |
135 |
PATIENT |
1.58 |
54.08 |
7 |
RIGHT |
41 |
61 |
100 |
normal |
normal |
NORMAL |
NORMAL |
34 |
Female |
37 |
145 |
PATIENT |
1.62 |
55.25 |
7 |
LEFT |
64 |
100 |
100 |
mild |
mild |
NORMAL |
NORMAL |
35 |
Female |
51 |
133 |
PATIENT |
1.55 |
55.4 |
10 |
LEFT |
29 |
39 |
90 |
normal |
normal |
NORMAL |
NORMAL |
36 |
Female |
40 |
132 |
PATIENT |
1.54 |
55.66 |
8 |
RIGHT |
81 |
100 |
83 |
moderate |
moderate |
NORMAL |
NORMAL |
37 |
Male |
40 |
165 |
PATIENT |
1.72 |
55.77 |
5 |
LEFT |
69 |
100 |
70 |
moderate |
mild |
NORMAL |
NORMAL |
38 |
Female |
36 |
162 |
PATIENT |
1.65 |
59.5 |
7 |
LEFT |
88 |
73 |
95 |
normal |
mild |
NORMAL |
NORMAL |
39 |
Female |
37 |
153 |
PATIENT |
1.58 |
61.29 |
5 |
RIGHT |
55 |
64 |
100 |
normal |
normal |
NORMAL |
NORMAL |
40 |
Male |
59 |
181 |
PATIENT |
1.79 |
71.6 |
7 |
RIGHT |
89 |
100 |
100 |
normal |
severe |
NORMAL |
NORMAL |
The control group ([Table 2]) consisted of volunteers (employees, resident physicians, and patients from the general, non-bariatric surgery outpatient facility) from matched gender and age for comparison with the obese group. The control group consisted of 42 people, including 12 men and 30 women, with an average age of 43.9 years old (range, 24 to 61 years old).
GENDER |
AGE |
WEIGHT (kg) |
CLASSIFICATION |
HEIGHT (m) |
BMI |
VAS |
SIDE |
H |
M |
F |
AMF |
AIM |
APC |
ATC |
AM |
|
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 |
Female |
61 |
80 |
CONTROL |
1.62 |
30.48 |
3 |
LEFT |
49 |
66 |
100 |
normal |
normal |
CAVUS |
NORMAL |
CAVUS |
2 |
Female |
58 |
61 |
CONTROL |
1.54 |
25.72 |
3 |
LEFT |
41 |
58 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
NORMAL |
3 |
Female |
45 |
62 |
CONTROL |
1.54 |
26.14 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
4 |
Female |
44 |
65 |
CONTROL |
1.68 |
23.03 |
0 |
RIGHT |
58 |
58 |
100 |
normal |
moderate |
FLAT |
NORMAL |
FLAT |
5 |
Female |
38 |
74 |
CONTROL |
1.74 |
22.4 |
0 |
LEFT |
60 |
90 |
90 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
6 |
Female |
54 |
89 |
CONTROL |
1.7 |
30.45 |
3 |
RIGHT |
41 |
56 |
100 |
normal |
moderate |
FLAT |
NORMAL |
FLAT |
7 |
Female |
27 |
57 |
CONTROL |
1.71 |
19.15 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
8 |
Female |
38 |
59 |
CONTROL |
1.63 |
22.21 |
5 |
LEFT |
100 |
100 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
NORMAL |
9 |
Female |
60 |
62 |
CONTROL |
1.59 |
24.52 |
0 |
RIGHT |
57 |
53 |
100 |
mild |
mild |
NORMAL |
NORMAL |
NORMAL |
10 |
Female |
35 |
69 |
CONTROL |
1.71 |
23.6 |
0 |
RIGHT |
100 |
100 |
100 |
mild |
mild |
NORMAL |
NORMAL |
NORMAL |
11 |
Female |
37 |
72 |
CONTROL |
1.73 |
24.06 |
6 |
LEFT |
100 |
100 |
100 |
mild |
mild |
FLAT |
NORMAL |
FLAT |
12 |
Female |
53 |
69 |
CONTROL |
1.62 |
26.29 |
7 |
RIGHT |
58 |
66 |
100 |
moderate |
moderate |
FLAT |
NORMAL |
FLAT |
13 |
Female |
41 |
72 |
CONTROL |
1.7 |
24.91 |
4 |
LEFT |
100 |
100 |
100 |
mild |
mild |
NORMAL |
NORMAL |
NORMAL |
14 |
Female |
20 |
54 |
CONTROL |
1.59 |
21.36 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
15 |
Male |
42 |
87 |
CONTROL |
1.81 |
26.56 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
16 |
Male |
30 |
70 |
CONTROL |
1.71 |
23.66 |
0 |
RIGHT |
100 |
100 |
100 |
moderate |
moderate |
NORMAL |
NORMAL |
NORMAL |
17 |
Male |
47 |
74 |
CONTROL |
1.73 |
25.01 |
4 |
LEFT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
18 |
Male |
24 |
76 |
CONTROL |
1.74 |
25.1 |
0 |
RIGHT |
100 |
100 |
100 |
moderate |
normal |
NORMAL |
NORMAL |
NORMAL |
19 |
Male |
27 |
78 |
CONTROL |
1.7 |
26.99 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
20 |
Male |
35 |
76 |
CONTROL |
1.69 |
26.61 |
6 |
LEFT |
100 |
100 |
100 |
moderate |
mild |
NORMAL |
NORMAL |
NORMAL |
21 |
Male |
61 |
76 |
CONTROL |
1.72 |
25.69 |
0 |
RIGHT |
53 |
49 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
22 |
Male |
56 |
92 |
CONTROL |
1.79 |
28.71 |
3 |
RIGHT |
100 |
100 |
100 |
mild |
mild |
NORMAL |
NORMAL |
NORMAL |
23 |
Female |
25 |
50 |
CONTROL |
1.65 |
18.4 |
0 |
LEFT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
24 |
Female |
56 |
52 |
CONTROL |
1.6 |
20.3 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
CAVUS |
25 |
Female |
35 |
55 |
CONTROL |
1.53 |
23.5 |
0 |
RIGHT |
100 |
100 |
75 |
moderate |
normal |
NORMAL |
NORMAL |
NORMAL |
26 |
Female |
50 |
57 |
CONTROL |
1.6 |
22.3 |
3 |
RIGHT |
100 |
90 |
100 |
normal |
normal |
NORMAL |
NORMAL |
CAVUS |
27 |
Female |
33 |
65 |
CONTROL |
1.68 |
23 |
1 |
RIGHT |
100 |
100 |
92 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
28 |
Male |
34 |
79 |
CONTROL |
1.81 |
24 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
CAVUS |
29 |
Female |
60 |
60 |
CONTROL |
1.54 |
25.3 |
2 |
LEFT |
88 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
30 |
Female |
47 |
575 |
CONTROL |
1.67 |
20.4 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
31 |
Female |
61 |
57 |
CONTROL |
1.53 |
24.3 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
32 |
Female |
51 |
54 |
CONTROL |
1.55 |
22.5 |
0 |
LEFT |
100 |
100 |
100 |
normal |
normal |
CAVUS |
NORMAL |
CAVUS |
33 |
Male |
58 |
73 |
CONTROL |
1.7 |
25.3 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
34 |
Male |
52 |
83 |
CONTROL |
1.8 |
25 |
0 |
LEFT |
100 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
CAVUS |
35 |
Female |
40 |
62 |
CONTROL |
1.71 |
21.2 |
0 |
LEFT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
36 |
Female |
42 |
58 |
CONTROL |
1.55 |
24.1 |
5 |
LEFT |
90 |
100 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
37 |
Female |
53 |
60 |
CONTROL |
1.57 |
24.3 |
2 |
RIGHT |
87 |
92 |
92 |
moderate |
moderate |
NORMAL |
FLAT |
NORMAL |
38 |
Female |
60 |
49 |
CONTROL |
1.55 |
20.4 |
6 |
LEFT |
64 |
95 |
100 |
normal |
normal |
NORMAL |
NORMAL |
NORMAL |
39 |
Male |
27 |
82 |
CONTROL |
1.79 |
25.2 |
0 |
RIGHT |
100 |
100 |
100 |
normal |
moderate |
NORMAL |
NORMAL |
NORMAL |
40 |
Female |
43 |
54 |
CONTROL |
1.53 |
23.1 |
0 |
LEFT |
85 |
85 |
75 |
normal |
moderate |
NORMAL |
NORMAL |
NORMAL |
41 |
Female |
48 |
63 |
CONTROL |
1.59 |
24.9 |
0 |
LEFT |
75 |
72 |
75 |
moderate |
severe |
NORMAL |
NORMAL |
NORMAL |
42 |
Female |
35 |
75 |
CONTROL |
1.75 |
24.5 |
0 |
LEFT |
100 |
100 |
100 |
normal |
mild |
NORMAL |
NORMAL |
NORMAL |
The inclusion criteria for the obese group were adult patients with BMI > 40 who were candidates for bariatric surgery and consented to participate in the study. The exclusion criteria were previous performance of surgical procedures (orthopedic, vascular, dermatological, or plastic surgery) in any segment of the lower limbs (hip, knee, ankle, and foot). Individuals with sequelae from lower limb fractures or conditions with surgical indication, whether orthopedic (hip or knee arthrosis, ankle or foot arthrosis) or vascular (arterial or venous insufficiency, ulcers, digital or skin necrosis) were excluded from the research.
Weight and height were measured at the Bariatric Surgery Outpatient Facility. The BMI was calculated by dividing the weight in kilograms (kg) by the square of the height in meters. For classification purposes, a BMI < 20 is considered underweight, whereas values from 20 to 24.9 are normal, and between 25 and 29.9 indicate overweight; BMIs > 30, 40 and 50, respectively, represent obesity, morbid obesity, and superobesity.[7]
Anteroposterior (AP) and lateral radiographs from both feet from obese and control subjects were taken under load.
The following radiological parameters were measured:
-
1) hallux metatarsal-phalangeal angle (AMF) measured in AP radiographs: normal, < 15°; mild, 15 to 19°; moderate, 20 to 39°; severe, > 40°;
-
2) intermetatarsal angle (AIM) measured in AP radiographs: normal, < 9; mild, 9-11; moderate, 12-15; severe, > 16;
-
3) talocalcaneal angle (ATC) measured in AP radiographs: cavus foot, < 20°; normal, 20 to 30°; flat foot, > 40°;
-
4) Calcaneal pitch angle (APC) measured in lateral radiographs: flat foot, < 10; normal, 10-30; cavus foot, > 30;
-
5) Meary angle (AM) or talus-first metatarsal bone angle measured in lateral radiographs. A normal value would be zero. A plantar deviation > 10° indicates a cavus foot, whereas a dorsal deviation > 10° indicates a flat foot.
The AMF and the AIM assess and grade hallux valgus deformity. The ATC, APC and AM assess whether feet are normal or present deformities such as flat or cavus feet.
Pain in daily living activities (walking, going up and down stairs, rest) was assessed in a simple way by the VAS, with values ranging from 0 (no pain) to 10 (most severe pain possible). For a more objective assessment, a score from 1 to 3 was classified as mild pain, from 4 to 6, moderate pain, and from 7 to 10, severe pain. Values > 3 were noted as significant for odds ratio (OR).
The AOFAS scale[10] was used for functional evaluation of the feet. This classification addresses pain, function, use of shoes, distance covered, poor foot alignment and gait pattern. It analyzes the forefoot (hallux and small toes), midfoot and hindfoot/ankle as separate domains. The scale has decreasing values from 100 to zero for each domain (values < 70 are deemed unsatisfactory).
The following parameters from the study and control groups were statistically correlated: VAS, AOFAS scale (forefoot [F], midfoot [M] and hindfoot [H]), AMF, AM, ATC, APC and AIM. The relationship between the VAS and age and the VAS and gender was also assessed.
Visual analogue scale and BMI values were correlated.
Obese subjects were divided in two subgroups: patients with morbid obesity, with a BMI between 40 and 50, and those with superobesity, with a BMI > 50. These subgroups consisted of 24 and 16 subjects, respectively. Visual analogue scale and AOFAS scale parameters were evaluated comparatively between these two subgroups.
Data analysis was performed focusing on the most symptomatic limb (most responsible for VAS score). This methodology aims to avoid compromising the statistical analysis if both limbs (feet) are evaluated as separate statistical units, as previously described by Menz.[11]
#
Statistical Analysis
The G2 Wilks test was used to assess pain (VAS) in control and obese groups and between obese subgroups; in addition, it was used to determine the relationship between VAS score and gender and VAS score and age. This test was also used to analyze radiographic angles (AMF, AIM, APC, AM and ATC). The Mann-Whitney test was used to analyze AOFAS scale scores. A Pearson correlation matrix was used to ascertain the correlation between VAS and BMI scores. Significance was determined at p < 0.05.
#
Results
Foot pain was reported by 38 out of 40 (95%) obese patients and by 16 out of 42 (38%) control subjects ([Figure 1]). Among obese patients, there were 19 (47.5%) cases of severe pain, 17 (42.5%) cases of moderate pain, 2 (5%) cases of mild pain, and 2 (5%) subjects referred no pain. In the control group, there were 8 (19.05%) cases of moderate pain, 8 (19.05%) cases of mild pain and 26 (61.90%) subjects referred no pain.
There was no difference between the obese and control groups regarding age and gender, as shown by t-student tests (p = 0.3554) and difference in proportion test (p = 0.539), respectively ([Table 3]).
PARAMETER |
OBESE GROUP |
CONTROL GROUP |
STATISTICAL ANALYSIS |
---|---|---|---|
Gender |
Male. 25%; Female. 75% |
Male. 28.5%; Female. 71.5% |
p = 0.539 |
Age |
44.85 |
43.8 (Mean value) |
p = 0.3554 |
VAS |
95% with pain |
40% with pain |
p = 0.0001 |
AOFAS H (mean value) |
65.87 |
88.23 |
p < 0.0001 |
AOFAS M (mean value) |
76.1 |
91.19 |
p < 0.0001 |
AOFAS F (mean value) |
89.59 |
97.59 |
p < 0.0001 |
APC |
N = 87.5% |
N = 85.71% |
p = 0.8585 |
C = 2.5% |
C = 4.70% |
||
F = 10% |
F = 9.52% |
||
ATC |
N = 82.5% |
N = 97.6% |
p = 0.031 |
C = 7.5% |
C = 0% |
||
F = 10% |
F = 2.6% |
||
AM |
N = 67.5% |
N = 76.2% |
p = 0.743 |
C = 12.5% |
C = 14.3% |
||
F = 17.5% |
F = 9.5% |
||
AMF |
N = 45% |
N = 66.6% |
p = 0.743 |
AIM |
N = 30% |
N = 42.85% |
p = 0.54 |
Gender x VAS |
---------------------------- |
-------------------------- |
p = 0.33 for obese subjects |
p = 0.6417 for control subjects |
|||
BMI X VAS |
---------------------------- |
-------------------------- |
p = 0.1407 for obese subjects |
p = 0.2343 for control subjects |
The referred pain scale (VAS) showed a higher prevalence of feet pain in the obese group compared with the control group according to the G2-Wilks test (p = 0.0001), with an OR value of 4.2.
The AOFAS scale in its three domains, that is, forefoot, midfoot and hindfoot, showed a lower functional performance in the obese group compared with control subjects according to the Mann-Whitney test (p < 0.0001) ([Figure 2]). Odds ratios for hindfoot and midfoot were 4.810 and 3.33, respectively. The OR value for the forefoot could not be determined because no control subject presented a value < 70.
Pain, as assessed by the VAS, was not related to BMI in the obese or control groups, as shown by Pearson tests (p = - 0.1407 and p = 0.2343, respectively.)
The ATC values were higher in the obese group, configuring a higher prevalence of flat feet, as shown by the G2 Wilks test (p = 0.0317).
There were no statistical differences between the obese and control groups regarding the remaining evaluated parameters ([Table 3]).
Comparison between morbidly obese and supermorbidly obese subjects did not show statistical differences regarding the evaluated parameters ([Table 4]).
PARAMETER |
OBESE BMI < 50 |
OBESE BMI > 50 |
STATISTICAL ANALYSIS |
---|---|---|---|
VAS |
91.6 |
100% |
p = 0.075 |
Severe pain = 58% |
Severe pain = 31.2% |
||
AOFAS Hindfoot domain |
65.62 |
66.25 |
p = 0.428 |
AOFAS Midfoot domain |
74.58 |
78.37 |
p = 0.264 |
#
Discussion
The present case series agrees with other studies from the literature[2] [11] that show an increased prevalence of foot pain in obese individuals in relation to the general population. In this study, there was 95% pain in the obese group and 40% in the control group. Melo et al.[12] described similar data, with 85% pain in lower limbs from morbidly obese patients undergoing reduction gastroplasty. In the general population, these rates range from 14% in adolescents to 42% in people > 65 years old.[11] Our study revealed that a severely obese patient (BMI > 40) presents an OR of 4.2 for significant foot pain compared to a control group of people with a mean BMI of 24. In a meta-analysis, Butterworh et al.[2] described an OR of 3.1 for feet pain in obese patients compared with people with a BMI < 25.
All three domains from the AOFAS functional scale[10] were more altered in obese patients than in control subjects. This finding agrees with the higher report of calcaneal posterior pain by obese people,[2] as well as with the greater mechanical overload in the midfoot that result in local pain.[6] [13] Compared to the control group, OR values corresponding to the hindfoot and midfoot from severely obese individuals (BMI > 40) of 4.81 and 3.33, respectively, ratify the higher incidence of poor functional performance for daily activities, quality of life and movement.
Even though the interplay between increased body weight and BMI and lower limb pain initially seems to result from biomechanical factors determined by increased load alone, new evidence relates joint pain to systemic metabolic syndrome.[2] [14] [15] [16]
Visceral adipose tissue, as well as the truncal light fatty tissue, constitute true endocrine organs that secrete cytokines, interleukins, adipokines and leptins.[17] Leptin is reportedly related to pro-inflammatory effects and the destruction of chondrocytes.[14]
Our study showed no statistical relationship between referred pain (VAS) and BMI when comparing obese subjects. Other authors[2] [11] reported that BMI would not be independently associated with foot pain. Butterworth et al.[2] emphasized that a high fat mass would be especially related to foot pain. Body mass alone would not be an independent factor for pain.[2] [12] These observations suggest the presence of systemic, not just biomechanical, factors determining the onset of foot pain in obese individuals.
Case series[18] [19] from the literature described a higher prevalence of flat feet in obese subjects. Our study showed a higher prevalence of increased ATC, consistent with flat feet, in obese individuals. There were no statistical differences between obese and control subjects regarding other studied angles. Some authors[20] reported that there is little relationship between joint pain and radiographic changes. Another factor to consider is that morbidly obese subjects are usually younger.[21] As a result, there was no time to develop radiological arthrosis or secondary deformities, and radiological changes would not be identified despite the pain.[21]
Our research showed no statistical difference regarding angular measurements in radiographs to assess the prevalence of conditions such as hallux valgus. A hallux valgus deformity would not be necessarily associated with pain. However, data on its prevalence in obese people are conflicting. For Frey et al.,[22] hallux valgus would be related to normal BMI, and not to obesity. However, Cho et al.[23] correlated hallux valgus to increased BMI values. Nguyen et al.[24] reported that obesity and female gender would be protective factors for hallux valgus. This would be due to the fact that women with BMI < 25 tend to wear high heels, pointed toes shoes, whereas obese females, for having wider feet, wear flat shoes that do not compress the forefoot area.[24]
Menz et al.[25] described a higher prevalence of foot pain in women compared to men (25% versus 19%) in a general population from Framinghan, MA, USA. However, our study revealed no differences between severely obese men and women regarding both the prevalence and severity of feet pain.
Our case series showed no differences in feet functional parameters using the AOFAS scale and in the level of pain (VAS) when comparing morbidly and supermorbidly obese subjects. Our data disagrees from other authors who showed greater functional impairment in superobese individuals.[7] Further studies, including a larger number of individuals, may evidence such differences.
Our study is limited by its cross-sectional design; although the studied parameters may present correlations, it is not possible to determine a cause-effect relationship. Therefore, our statistical analysis cannot affirm that excessive obesity results in pain and low functional level or if these factors would have a reverse causal effect, that is, determining the occurrence of obesity due to the sedentary lifestyle. Another factor worth mentioning is the nondiscrimination of clinical comorbidities such as hypertension, diabetes, and other systemic diseases in obese and control subjects, which may have generated bias in data analysis. In addition, the sample studied was relatively small, which limits the scope of conclusions. However, it should be noted that the study group constitutes a very specific universe of people with extremely severe (morbid) obesity (BMI > 40) and indication for bariatric surgery, while most data from the researched literature[2] [12] refer to overweight or mildly obese individuals.
A higher prevalence of foot pain and functional impairment was demonstrated in the studied obese population. The indirect relationship between increased BMI in severely obese patients and pain according to the VAS corroborates the suspicions that systemic mechanisms, not only biomechanical factors, determine pain and functional impairment. These findings reinforce the importance of further studying the involvement of the musculoskeletal system in people with severe obesity.
Our data will help to understand musculoskeletal conditions resulting from obese-related metabolic syndrome and to formulate preventive and therapeutic strategies in this special subgroup of individuals.
#
Conclusions
Severe obesity (BMI > 40) is related to a higher prevalence of foot pain. Severely obese people have a worse AOFAS functional score in the forefoot, midfoot and hindfoot regions.
#
#
Conflito de Interesses
Os autores declaram não haver conflito de interesses.
* Study developed at the Hospital Federal de Ipanema, Rio de Janeiro, RJ, Brazil.
-
Referências
- 1 Thomas D, Elliott EJ. Low glycaemic index, or low glycaemic load, diets for diabetes mellitus. Cochrane Database Syst Rev 2009; (01) CD006296
- 2 Butterworth PA, Landorf KB, Smith SE, Menz HB. The association between body mass index and musculoskeletal foot disorders: a systematic review. Obes Rev 2012; 13 (07) 630-642
- 3 Harms S, Larson R, Sahmoun AE, Beal JR. Obesity increases the likelihood of total joint replacement surgery among younger adults. Int Orthop 2007; 31 (01) 23-26
- 4 Jinks C, Jordan K, Croft P. Disabling knee pain--another consequence of obesity: results from a prospective cohort study. BMC Public Health 2006; 6: 258
- 5 Martins GC, Martins Filho LF, Raposo AH, Gamallo RB, Menegazzi Z, Abreu AV. Radiographic evaluation and pain symptomatology of the knee in severely obese individuals - controlled transversal study. Rev Bras Ortop 2018; 53 (06) 740-746
- 6 Mickle KJ, Steele JR. Obese older adults suffer foot pain and foot-related functional limitation. Gait Posture 2015; 42 (04) 442-447
- 7 Fabris SM, Faintuch J, Brienze SL. et al. Are knee and foot orthopedic problems more disabling in the superobese?. Obes Surg 2013; 23 (02) 201-204
- 8 Sowers M, Karvonen-Gutierrez CA, Palmieri-Smith R, Jacobson JA, Jiang Y, Ashton-Miller JA. Knee osteoarthritis in obese women with cardiometabolic clustering. Arthritis Rheum 2009; 61 (10) 1328-1336
- 9 Li H, George DM, Jaarsma RL, Mao X. Metabolic syndrome and components exacerbate osteoarthritis symptoms of pain, depression and reduced knee function. Ann Transl Med 2016; 4 (07) 133
- 10 Kitaoka HB, Alexander IJ, Adelaar RS, Nunley JA, Myerson MS, Sanders M. Clinical rating systems for the ankle-hindfoot, midfoot, hallux, and lesser toes. Foot Ankle Int 1994; 15 (07) 349-353
- 11 Menz H. Two feet, or one person? Problems associated with statistical analysis of paired data on foot and ankle medicine. Foot 2004; 14 (01) 2-5
- 12 Melo IT, São-Pedro M. Musculoskeletal pain in lower limbs in obese patients before and after bariatric surgery. Arq Bras Cir Dig 2012; 25 (01) 29-32
- 13 Walsh TP, Butterworth PA, Urquhart DM. et al. Increase in body weight over a two-year period is associated with an increase in midfoot pressure and foot pain. J Foot Ankle Res 2017; 10: 31
- 14 Gandhi R, Takahashi M, Smith H, Rizek R, Mahomed NN. The synovial fluid adiponectin-leptin ratio predicts pain with knee osteoarthritis. Clin Rheumatol 2010; 29 (11) 1223-1228
- 15 Kalichman L, Li L, Kobyliansky E. Prevalence, pattern and determinants of radiographic hand osteoarthritis in Turkmen community-based sample. Rheumatol Int 2009; 29 (10) 1143-1149
- 16 de Mello AP, Martins GCDS, Heringer AR. et al. Back pain and sagittal spine alignment in obese patients eligible for bariatric surgery. Eur Spine J 2019; 28 (05) 967-975
- 17 Dumond H, Presle N, Terlain B. et al. Evidence for a key role of leptin in osteoarthritis. Arthritis Rheum 2003; 48 (11) 3118-3129
- 18 Abdel-Fattah MM, Hassanin MM, Felembane FA, Nassaane MT. Flat foot among Saudi Arabian army recruits: prevalence and risk factors. East Mediterr Health J 2006; 12 (1-2): 211-217
- 19 Otsuka R, Yatsuya H, Miura Y. et al. [Association of flatfoot with pain, fatigue and obesity in Japanese over sixties]. Nippon Koshu Eisei Zasshi 2003; 50 (10) 988-998
- 20 Kinds MB, Welsing PM, Vignon EP. et al. A systematic review of the association between radiographic and clinical osteoarthritis of hip and knee. Osteoarthritis Cartilage 2011; 19 (07) 768-778
- 21 Frilander H, Viikari-Juntura E, Heliövaara M, Mutanen P, Mattila VM, Solovieva S. Obesity in early adulthood predicts knee pain and walking difficulties among men: A life course study. Eur J Pain 2016; 20 (08) 1278-1287
- 22 Frey C, Zamora J. The effects of obesity on orthopaedic foot and ankle pathology. Foot Ankle Int 2007; 28 (09) 996-999
- 23 Cho NH, Kim S, Kwon DJ, Kim HA. The prevalence of hallux valgus and its association with foot pain and function in a rural Korean community. J Bone Joint Surg Br 2009; 91 (04) 494-498
- 24 Nguyen US, Hillstrom HJ, Li W. et al. Factors associated with hallux valgus in a population-based study of older women and men: the MOBILIZE Boston Study. Osteoarthritis Cartilage 2010; 18 (01) 41-46
- 25 Menz HB, Dufour AB, Casey VA. et al. Foot pain and mobility limitations in older adults: the Framingham Foot Study. J Gerontol A Biol Sci Med Sci 2013; 68 (10) 1281-1285
Endereço para correspondência
Publication History
Received: 08 August 2019
Accepted: 15 April 2020
Article published online:
29 October 2020
© 2020. Sociedade Brasileira de Ortopedia e Traumatologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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-
Referências
- 1 Thomas D, Elliott EJ. Low glycaemic index, or low glycaemic load, diets for diabetes mellitus. Cochrane Database Syst Rev 2009; (01) CD006296
- 2 Butterworth PA, Landorf KB, Smith SE, Menz HB. The association between body mass index and musculoskeletal foot disorders: a systematic review. Obes Rev 2012; 13 (07) 630-642
- 3 Harms S, Larson R, Sahmoun AE, Beal JR. Obesity increases the likelihood of total joint replacement surgery among younger adults. Int Orthop 2007; 31 (01) 23-26
- 4 Jinks C, Jordan K, Croft P. Disabling knee pain--another consequence of obesity: results from a prospective cohort study. BMC Public Health 2006; 6: 258
- 5 Martins GC, Martins Filho LF, Raposo AH, Gamallo RB, Menegazzi Z, Abreu AV. Radiographic evaluation and pain symptomatology of the knee in severely obese individuals - controlled transversal study. Rev Bras Ortop 2018; 53 (06) 740-746
- 6 Mickle KJ, Steele JR. Obese older adults suffer foot pain and foot-related functional limitation. Gait Posture 2015; 42 (04) 442-447
- 7 Fabris SM, Faintuch J, Brienze SL. et al. Are knee and foot orthopedic problems more disabling in the superobese?. Obes Surg 2013; 23 (02) 201-204
- 8 Sowers M, Karvonen-Gutierrez CA, Palmieri-Smith R, Jacobson JA, Jiang Y, Ashton-Miller JA. Knee osteoarthritis in obese women with cardiometabolic clustering. Arthritis Rheum 2009; 61 (10) 1328-1336
- 9 Li H, George DM, Jaarsma RL, Mao X. Metabolic syndrome and components exacerbate osteoarthritis symptoms of pain, depression and reduced knee function. Ann Transl Med 2016; 4 (07) 133
- 10 Kitaoka HB, Alexander IJ, Adelaar RS, Nunley JA, Myerson MS, Sanders M. Clinical rating systems for the ankle-hindfoot, midfoot, hallux, and lesser toes. Foot Ankle Int 1994; 15 (07) 349-353
- 11 Menz H. Two feet, or one person? Problems associated with statistical analysis of paired data on foot and ankle medicine. Foot 2004; 14 (01) 2-5
- 12 Melo IT, São-Pedro M. Musculoskeletal pain in lower limbs in obese patients before and after bariatric surgery. Arq Bras Cir Dig 2012; 25 (01) 29-32
- 13 Walsh TP, Butterworth PA, Urquhart DM. et al. Increase in body weight over a two-year period is associated with an increase in midfoot pressure and foot pain. J Foot Ankle Res 2017; 10: 31
- 14 Gandhi R, Takahashi M, Smith H, Rizek R, Mahomed NN. The synovial fluid adiponectin-leptin ratio predicts pain with knee osteoarthritis. Clin Rheumatol 2010; 29 (11) 1223-1228
- 15 Kalichman L, Li L, Kobyliansky E. Prevalence, pattern and determinants of radiographic hand osteoarthritis in Turkmen community-based sample. Rheumatol Int 2009; 29 (10) 1143-1149
- 16 de Mello AP, Martins GCDS, Heringer AR. et al. Back pain and sagittal spine alignment in obese patients eligible for bariatric surgery. Eur Spine J 2019; 28 (05) 967-975
- 17 Dumond H, Presle N, Terlain B. et al. Evidence for a key role of leptin in osteoarthritis. Arthritis Rheum 2003; 48 (11) 3118-3129
- 18 Abdel-Fattah MM, Hassanin MM, Felembane FA, Nassaane MT. Flat foot among Saudi Arabian army recruits: prevalence and risk factors. East Mediterr Health J 2006; 12 (1-2): 211-217
- 19 Otsuka R, Yatsuya H, Miura Y. et al. [Association of flatfoot with pain, fatigue and obesity in Japanese over sixties]. Nippon Koshu Eisei Zasshi 2003; 50 (10) 988-998
- 20 Kinds MB, Welsing PM, Vignon EP. et al. A systematic review of the association between radiographic and clinical osteoarthritis of hip and knee. Osteoarthritis Cartilage 2011; 19 (07) 768-778
- 21 Frilander H, Viikari-Juntura E, Heliövaara M, Mutanen P, Mattila VM, Solovieva S. Obesity in early adulthood predicts knee pain and walking difficulties among men: A life course study. Eur J Pain 2016; 20 (08) 1278-1287
- 22 Frey C, Zamora J. The effects of obesity on orthopaedic foot and ankle pathology. Foot Ankle Int 2007; 28 (09) 996-999
- 23 Cho NH, Kim S, Kwon DJ, Kim HA. The prevalence of hallux valgus and its association with foot pain and function in a rural Korean community. J Bone Joint Surg Br 2009; 91 (04) 494-498
- 24 Nguyen US, Hillstrom HJ, Li W. et al. Factors associated with hallux valgus in a population-based study of older women and men: the MOBILIZE Boston Study. Osteoarthritis Cartilage 2010; 18 (01) 41-46
- 25 Menz HB, Dufour AB, Casey VA. et al. Foot pain and mobility limitations in older adults: the Framingham Foot Study. J Gerontol A Biol Sci Med Sci 2013; 68 (10) 1281-1285