Int J Clin Pract. 2018;e13208. wileyonlinelibrary.com/journal/ijcp
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1 of 7
https://doi.org/10.1111/ijcp.13208
© 2018 John Wiley & Sons Ltd
Received: 18 January 2018
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Accepted: 22 April 2018
DOI: 10.1111/ijcp.13208
ORIGINAL PAPER
The effect of 12-week garlic supplementation on symptom
relief in overweight or obese women with knee osteoarthritis
Ahmad Salimzadeh
1
| Elham Alipoor
2
| Sahar Dehghani
3
| Mehdi Yaseri
4
|
Mostafa Hosseini
4
| Christine Feinle-Bisset
5,6
| Mohammad Javad Hosseinzadeh-Attar
2,3,5,6
1
Rheumatology Research Center, Sina
Hospital, Tehran University of Medical
Sciences, Tehran, Iran
2
Department of Clinical Nutrition, School of
Nutritional Sciences and Dietetics, Tehran
University of Medical Sciences, Tehran, Iran
3
Department of Nutrition and
Biochemistry, School of Public
Health, International Campus, Tehran
University of Medical Sciences, Tehran, Iran
4
Department of Epidemiology and
Biostatistics, School of Public Health, Tehran
University of Medical Sciences, Tehran, Iran
5
Centre of Research Excellence in
Translating Nutritional Science to Good
Health, University of Adelaide, Adelaide,
Australia
6
Adelaide Medical School, University of
Adelaide, Adelaide, Australia
Correspondence
Mohammad Javad Hosseinzadeh-Attar,
School of Nutritional Sciences and Dietetics,
Tehran University of Medical Sciences,
Tehran, Iran.
Email: hosseinzadeh.md.phd@gmail.com;
mhosseinzadeh@tums.ac.ir
Funding information
Tehran University of Medical Sciences and
Health Services, Grant/Award Number:
18329
Summary
Aims: Chronic joint pain and stiffness, and functional disability, are the major debili-
tating features of osteoarthritis (OA). The aim of this study was to assess the effect
of 12-week supplementation with a garlic supplement on knee osteoarthritis out-
comes in overweight or obese women.
Methods: Seventy-six postmenopausal overweight or obese women (25≤BMI≤40
kg/m
2
) with medically diagnosed knee OA participated in this randomised double-
blind, placebo-controlled, parallel-design trial. After randomisation into 2 groups,
patients received a daily dose of either 1000 mg odourless garlic tablet, or placebo,
for 12 weeks. The total Western Ontario and McMaster Universities Osteoarthritis
Index (WOMAC), as well as pain, stiffness and physical function subscales, were eval-
uated pre- and poststudy. Anthropometric parameters and body composition (using
bioelectrical impedance analysis) were also assessed.
Results: Following 12-week supplementation in overweight or obese women with
OA, stiffness (but not pain, function or WOMAC total score) was significantly lower
in the garlic group compared with the placebo group (1.4 ± 1.6 vs 2.5 ± 1.9, P = .023).
The changes in WOMAC parameters showed no statistically significant differences
between the 2 groups. WOMAC total score (38.4 ± 15.9-30.6 ± 15.7, P = .004) and
all the subscales, including pain (8.3 ± 3.7-7 ± 4.4, P = .026), stiffness (2.3 ± 1.6-
1.4 ± 1.6, P = .013) and physical function (27.7 ± 11.9-22.2 ± 12.4, P = .001) improved
significantly in the garlic group postintervention compared with pre-intervention;
although pain subscale also decreased in the placebo group (9.6 ± 3.1-6.9 ± 3.7,
P < .001).
Conclusions: Although pre- to postintervention knee OA symptoms were improved
in overweight or obese women receiving 12 weeks garlic supplement, there was no
significant difference in WOMAC changes compared with the placebo group. Further
clinical trials are required to investigate the therapeutic value of garlic ingredients,
and the potential role of placebo effect, in the management of OA symptoms.
1 | INTRODUCTION
Osteoarthritis (OA) is the most prevalent joint disease worldwide.
This debilitating disease results in impaired quality of life and
considerable financial burden.
1
Chronic and disabling pain is the
main symptom of OA. This pain originates from complex cellular
interactions between spinal neurons (central mechanisms) and
joints (peripheral level).
2
Unlike the acute pain associated with a
trauma or surgery that subsides over time. OA-induced pain per-
sists despite treatment, exacerbating the functional incapacity
of patients.
1
Pain aetiology in OA is multifactorial. Inflammation