Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Efficacy of wIRA in the treatment of sacroiliitis in male patients with ankylosing spondylitis and its effect on serum VEGF levels

Journal of Orthopaedic Surgery and Research volume 14, Article number: 313 (2019) Cite this article

Abstract

Background

This study aimed to assess the efficacy of water-filtered infrared A (wIRA) in sacroiliitis in male patients with ankylosing spondylitis (AS) and the effect of wIRA therapy on serum vascular endothelial growth factor (VEGF).

Methods

One hundred twenty male AS patients with active sacroiliitis were randomly divided into wIRA group and control group. wIRA treatment was performed twice daily for 5 consecutive days with 24-h interval before switching the treatment (crossover design). Bath ankylosing spondylitis disease activity index (BASDAI) scores, pain visual analogue scale (VAS), and morning stiffness VAS were recorded prior to and after each treatment period. Additionally, C-reactive protein (CRP), serum VEGF, and resistance index (RI) of sacroiliac joints detected by ultrasonography were recorded at baseline and after the first and second treatment period, respectively. The efficacy was examined by using repeated measures analysis of variance (ANOVA).

Results

BASDAI, pain VAS, and morning stiffness VAS scores decreased significantly (P < 0.001) after wIRA treatment and no-wIRA treatment (control group), and the difference between the two groups was significant (P < 0.001). CRP declined and RI increased during the wIRA treatment as compared with the no-wIRA treatment (P < 0.001). The increase in RI was associated with improvement of pain VAS scores (P = 0.018), while serum VEGF was unaffected by the treatment.

Conclusions

wIRA treatment achieved symptom and pain relief for AS patients with active sacroiliitis. wIRA treatment also improved RI revealed by ultrasonography, and this effect was associated with improved pain VAS scores.

Introduction

Ankylosing spondylitis (AS), associated with human leukocyte antigen B27, is a chronic immune disorder mainly affecting the axial skeleton, which predominantly affects the young and middle-aged males. Its pathogenesis is largely unknown. AS first invades the synovial membrane of the sacroiliac joint (SIJ). As the disease progresses, articular cartilage and bone are destroyed, and osseous ankylosis and deformity of the spine or peripheral joints, or even disability are finally developed [1]. Early diagnosis and treatment of sacroiliitis are important for improving clinical outcomes. In 1992, Maugars et al. [2] began to treat sacroiliitis by hormone injection into the SIJ, after which some domestic reports have been published in this field. But due to limited conditions, such treatment for sacroiliitis is not extensively utilized. Water-filtered infrared-A (wIRA) treatment represents the latest achievement in medical immunology science. This treatment targets the deep subcutaneous tissues, alleviating local inflammation and benefiting skin trauma, ulcers, burns, and bedsores [3]. However, wIRA treatment has been rarely applied to sacroiliitis in AS. The present study aimed to evaluate the efficacy of wIRA in AS treatment.

Materials and methods

Diagnostic and exclusion criteria

Male patients treated at the Department of Rheumatology from December 2015 to February 2018 who met the following inclusion criteria were recruited: aged > 16, conforming to the 1984 Modified New York Criteria for AS [4], and currently in the active stage. The qualifying features of AS were as follows: (1) morning stiffness visual analogue scale (VAS) scores ≥ 3 and (2) VAS scores ≥ 3 in at least two of the items below: ① patient overall scores, ② back pain in the nighttime and overall back pain, and ③ bath ankylosing spondylitis disease activity index (BASDAI). The patients were combined with at least one active inflammatory lesion in the SIJ confirmed by magnetic resonance imaging (MRI) [5]. A total of 120 cases were recruited, with a course of 6.83 ± 3.2 years. They were aged 17–61 years old (average, 32.1 ± 10.5 years). All patients received methotrexate (MTX, 7.5–20 mg/week) and celecoxib (200 mg/day). Exclusion criteria were as follows: (1) fever; (2) uncontrolled hypertension; (3) diabetes; (4) skin bursts at the affected site; (5) severe liver, kidney, and cardiac insufficiency; (6) active gastrointestinal ulcers in the past 3 months and gastrointestinal bleeding in the past 6 months; (7) biologic therapy in the past 3 months; (8) interstitial pulmonary fibrosis; and (9) other conditions deemed unsuitable for the research.

The informed consent was signed by all subjects. The protocol was approved by the Ethics Committee of Shengli Oilfield Central Hospital (No. Q/ZXYY-ZY-YWB-LL201515).

Study design

The randomized controlled cross-over design was adopted in this study. Using a random number table and remainder method, the subjects were divided into group A (wIRA treatment) and group B (no-wIRA treatment), with 60 subjects in each group. Patients in group A first received wIRA treatment twice daily, 20 min each time for 5 consecutive days. Each treatment cycle lasted for 5 days, and the first stage was finished after the first cycle, followed by 24-h washout period before the next cycle. The second stage was no-wIRA treatment, which was finished 5 days later. Group B received no-wIRA treatment for 5 days, followed by 24-h washout period before the next cycle. The second stage was wIRA treatment twice daily, for 20 min each time for 5 consecutive days.

C-reactive protein (CRP), serum vascular endothelial growth factor (VEGF), and resistance index (RI) of sacroiliac joints detected by ultrasonography were recorded at baseline and after the first and the second treatment period, respectively.

Ultrasonography of SIJ

Siemens S2000 Ultrasound System with 14L5 transducer (probe frequency 7–14 MHz, total gain 50 dB, color Doppler gain 80–90 dB, dynamic range 50–60 dB, and wall filter 30–40 Hz) was used. The subjects took a prone position, and an appropriate frequency was chosen for the transducer, which was placed at the level of posterior superior iliac spine. First, the iliac bone, sacrum, and first sacral foramina were located on one side by two-dimensional ultrasonography. The upper part of SIJ was scanned slightly laterally and obliquely at the level of the first sacral foramina, and then transversely and obliquely towards caudal. The position of the SIJ was determined along with the manifestations upon two-dimensional ultrasonography. Next, following a reverse path, color Doppler ultrasonography was applied to the blood flow inside and on the periphery of the SIJ. The cross section with the most abundant blood flow signals was chosen for the measurements of RI, and the mean value of the three measurements was taken.

Disease and clinical symptom evaluation

BASDAI was composed of six items concerning AS-related symptoms, such as fatigue, spinal pain, joint swelling, local tenderness, and morning stiffness, which were measured using a 0–10 scale. The higher the score, the higher the disease activity [6]. Pain VAS scores and morning stiffness VAS scores were also measured on a 0–10 scale, and the higher the score, the higher the activity.

Serum collection and measurements

From each subject, about 3 ml of the fasting venous blood was collected, and the serum was isolated and cryopreserved at − 80 °C. ELISA kit (Wuhan Boster Bioengineering Limited Company) was used to determine the serum level of VEGF in strict accordance with the instructions. CRP levels were determined by immunoturbidimetric assay.

wIRA treatment device

Hydrosun™ 750H treatment device (product No. 15700081; power 230 V-50/60Hz, 775 W), imported from Germany by Beijing Haite Technology Co., Ltd., was used. The wIRA light source was placed at about 20–30 cm from the SIJ, and the temperature was adjusted according to the patients’ sensation to avoid burn.

Statistical analysis

SPSS 19.0 software was used for statistical analysis. Continuous variables were expressed as x ± s, and categorical variables as percentages. Measurements obeying to a normal distribution and homogeneity of variance were analyzed by t test. Otherwise, the measurements were analyzed by Mann-Whitney U test. The influence factors between and within the groups and their interactions were analyzed by repeated ANOVA measures. The efficacy before and after different treatment regimens was compared by paired t test (Bonferroni correction, P value × 2). Ordered multi-class data were compared by Kruskal-Wallis H test, and correlation between two categorical variables was examined by χ2 test. P < 0.05 indicated a significant difference.

Results

Baseline information

A total of 120 cases were finally recruited. At the baseline, there was no significant difference in age, course of disease, BASDAI, CRP, VEGF, pain VAS, morning stiffness VAS, and positive rates of HLA-B27 between the two groups (P > 0.05). See Table 1.

Table 1 Baseline information of the patients
Full size table

Changes of BASDAI, pain VAS scores, and morning stiffness VAS scores

All patients receiving wIRA treatment had a reduction in BASDAI, pain VAS scores, and morning stiffness VAS scores than before (P < 0.001), which were also significantly different from those of the control group (no-wIRA treatment) (P < 0.001). Different treatment regimens had no impact on BASDAI, pain VAS scores, and morning stiffness VAS scores. At the end of treatment regimen A, these three scores (7.82 ± 0.67; 7.39 ± 0.57; 7.38 ± 0.51, respectively) were not significantly different from those at the end of treatment regimen B (7.83 ± 0.50; 7.19 ± 0.57; 7.14 ± 0.51, respectively), except that they were much lower than the baseline (P < 0.001). See Table 2.

Table 2 Changes of BASDAI, pain VAS scores, and Morning stiffness-VAS scores
Full size table

Changes of CRP, VEGF, and RI

CRP levels decreased after the end of the first stage of treatment regimen A (receiving wIRA treatment) (P < 0.001), and it began to increase after the second stage (P = 0.032). The VEGF level slightly decreased after wIRA treatment in either regimen, but there was no significant difference than before treatment (P = 0.230 and P = 0.120). RI showed an apparent increase at the end of the first stage of treatment regimen A (P < 0.001), and it declined further after the end of the second stage (P < 0.001), but remained higher than the baseline (P < 0.001). See Table 3. Among all patients receiving wIRA treatment, the improvement of pain VAS scores was greater in those with ≥ 40% increase in RI than in those with < 40% increase in RI, and the difference was of statistical significance (P = 0.018). However, there was no significant difference in BASDAI and morning stiffness VAS scores (P = 0.319, P = 0.651, respectively). See Fig. 1.

Table 3 Changes of CRP, VEGF and RI
Full size table
Fig. 1
figure 1

Influence of RI changes on BASDAI, pain VAS scores, and morning stiffness VAS scores. Among all patients receiving wIRA treatment, the improvement of pain VAS scores was greater in those with ≥ 40% increase in RI than in those with < 40% increase in RI. However, there was no significant difference in BASDAI and morning stiffness VAS scores

Full size image

Discussion

AS is featured by axial skeleton invasion and progressive spine rigidity as well as early involvement of the SIJ. The pathology of sacroiliitis is associated with extensive infiltration of inflammatory cells, such as CD4+ and CD8+ T cells and macrophages. Tumor necrosis factor-α (TNF-α), secreted by the activated T-lymphocytes, can promote the secretion of VEGF by peripheral blood monocytes and synovial cells. VEGF, acting on the osteoblasts, activates the osteoblasts and promotes the osteogenic effect. Several physical and chemical factors at the inflammatory sites are conducive to the expression and secretion of VEGF [7]. Liu et al. [8] found an upregulation of VEGF mRNA in the synovial tissues of AS patients, which was associated with increased BASDAI scores. This indicated that VEGF may directly participate in the differentiation of fibroblasts at the inflammatory sites into osteoclasts. Qian et al. [9] reported a positive expression of VEGF in the synovial tissues of the SIJ in AS patients at the active stage. Moreover, the count of positive cells and mean gray value differed significantly as compared with the control group. This offered evidence that VEGF is closely related to cartilage and bone destruction and bone sclerosis at the SIJ. In addition, hypoxia within the inflammatory joint is very likely to induce an upregulation of hypoxia-inducible factor-1α (HIF-1α), which further leads to the expressions of VEGF and its receptor [10]. Multiple mechanisms may be implicated in the hypoxia within the SIJ. For example, following the bone destruction of SIJ, a large amount of granulation tissues will be formed as a compensatory mechanism, thus affecting local circulation. Inflammatory stimulation causes significant intraarticular synovial hyperplasia, finally resulting in hypoxia of the articular joint and synovium due to hypermetabolism of the newly formed synovium and granulation tissues. In the meantime, the balance of angiogenetic regulation is disrupted by long-term inflammatory stimulation, with local appearance of abnormal pannus. The isolation effect provided by the pannus between the synovium and joint cartilage will also lead to local hypoxia. VEGF is upregulated directly as a result of hypoxia, or through activation of osteoblasts near the sites of bone damage. Before formation of new cartilage, vascular invasion first occurs, and osteoblasts are transported to the sites of ossification and activated. The activated osteoblasts further cause an upregulation of VEGF. Hypoxia and VEGF interact with each other, leading to formation of new bones and finally progressive SIJ fusion and ossification of the ligament [11].

VEGF has been found as an important proangiogenic factor participating in the occurrence and development of arthritis [12]. In the inflammatory SIJ at an active stage, a large amount of VEGF is expressed, which further leads to excessive angiogenesis [13], with local release of inflammatory factors. As a result, there will be a vasodilatation and an increase in blood perfusion at the lesions. An enhancement is usually observed at the lesions revealed by MRI, and there are more abundant blood flow signals revealed by color Doppler ultrasonography, with a reduction in arterial RI. Zhu et al. [14] reported that the angiogenesis of SIJ coincided with the low resistance signals and activity of AS. There was no healthy control group in our study, and we observed an increase of baseline VEGF [(181.54 ± 20.82) pg/ml] and reduction of RI (0.53 ± 0.03) in AS patients, with a detection rate of 90%. This agreed with the previous studies [15,16,17]. After the wIRA treatment, the RI value of SIJ was significantly increased in AS patients, indicating the weakening of local blood flow signals and attenuation of inflammation. The pain VAS score was also improved significantly, especially in those achieving an increase in RI by over 40%. The above findings on efficacy of wIRA treatment guide the individualized wIRA treatment, but more controlled trials with a large sample size are needed to optimize the intensity and course of treatment.

Sacroiliitis is an early clinical manifestation of AS, and most patients report lower back pain in the nighttime and (or) progressive spine rigidity and deformity. It has been reported [18] that active inflammation of AS is closely related to patients’ life quality and that an effective treatment modality of sacroiliitis is important for improving the outcome. Back in 1992, some scholars [2, 19,20,21] began to perform CT- or MRI-guided SIJ intra-articular injection of glucocorticoids to treat serum-negative spondyloarthropathy, which were effective in attenuating SIJ inflammation. However, this treatment modality is invasive and places a higher requirement on physician’s skills, contributing to a low acceptance among the patients [22]. Alternatively, wIRA provides a feasible and non-invasive treatment for sacroiliitis. To our knowledge, wIRA has been rarely applied to sacroiliitis, though it has extensive application in skin trauma, burn, thrombosis-related skin ulcer, chronic venous stasis ulcer, bedsores, and other acute and chronic wounds [3]. The benefits of infrared illumination have been widely recognized, but the absorption of radiation at specific wavelength in the infrared region will lead to excessive heating of the skin surface [23]. In contrast, wIRA increases local skin temperature without overheating the skin tissues, which is conducive to tissue perfusion, oxidative metabolism, and disease improvement [24, 25]. wIRA utilizes water-filtering layer to remove the ultraviolet radiation and most radiation in the far-infrared region, while preserving the visible band and infrared A radiation. By making full use of the radiation at a wavelength of 560–1400 nm, which is of the highest therapeutic value and absorbed most by the human tissues, wIRA can reach about 7 cm under the skin. At this depth, wIRA activates the immune system of the lesions and enhances mitochondrial oxygen utilization. Moreover, there will be an increase in oxygen partial pressure of the tissues and enhancement of enzymatic reactions implicating the catalase and superoxide dismutase. In the meantime, the activation of the immune system will facilitate clearing of immunocomplexes and reduce the metabolic products. The pain will be relieved by reducing tonus of the sympathetic nerve and stimulation from the dolorific inflammatory factors and by regulating the pain receptors. Furthermore, oxygen partial pressure of the local inflammatory tissues can significantly affect the VEGF concentration and the density of its receptor, thus improving local blood flow and reducing synovial inflammation and pannus formation [26,27,28]. In the present study, RI of sacroiliitis increased significantly from 0.53 ± 0.05 to 0.85 ± 0.04 (P < 0.001) after the wIRA treatment. But once the treatment stopped, RI decreased from 0.85 ± 0.04 to 0.63 ± 0.04 (P < 0.001), indicating that the development of local joint inflammation is driven by systemic and local factors. wIRA treatment alone probably fails to improve the prognosis, as evidenced by the CRP level. Besides, there was a downward trend of serum VEGF levels after wIRA treatment than before, but not significantly. From this, we could infer that local physical therapy was unable to change the systemic inflammatory status. Nevertheless, pain VAS and morning stiffness VAS scores improved significantly in AS patients after wIRA treatment, with a reduction in BASDAI. The treatment efficacy was much more pronounced than the simple use of NSAIDs (P < 0.001). wIRA treatment improved the patients’ life quality and compliance in this study.

The present study was limited in the following aspects. Synovial angiogenesis in sacroiliitis in AS patients leads to an increase in venous blood flow. Anatomically, the arteries and veins in the SIJ are very close to each other, which may cause interference to the measurement of blood flow spectrum, resulting in misjudgment. The use of antirheumatic drugs [29] and MTX [30] may inhibit vascular endothelial cell proliferation or angiogenesis, thus affecting the serum VEGF level.

Conclusions

Finally, wIRA treatment can effectively relieve local inflammation of sacroiliitis in AS, reducing pain and clinical symptoms. Theoretically, there may be less need for NSAIDs, and wIRA treatment may be more appropriate for patients contraindicated for NSAIDs, as an important adjuvant therapy for sacroiliitis.

Availability of data and materials

The datasets used and analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

ANOVA:

Analysis of variance

AS:

Ankylosing spondylitis

BASDAI:

Bath ankylosing spondylitis disease activity index

CRP:

C-reactive protein

HIF-1α:

Hypoxia-inducible factor-1α

MRI:

Magnetic resonance imaging

MTX:

Methotrexate

RI:

Resistance index

SIJ:

Sacroiliac joint

TNF-α:

Tumor necrosis factor-α

VAS:

Visual analogue scale

VEGF:

Vascular endothelial growth factor

wIRA:

Water-filtered infrared A

References

  1. Dejaco C, Duftner C, Schirmer M. Imaging techniques for early diagnosis of ankylosing spondylitis. Wien Med Wochenschr. 2008;158:191–4.

    Article  Google Scholar 

  2. Maugars Y, Mathis C, Vilon P, et al. Corticosteroid injection of the sacroiliac joint in patients with seronegative spondylarthropathy. Arthritis Rheum. 1992;35:564–8.

    Article  CAS  Google Scholar 

  3. Hoffmann G. Water-filtered infrared-A (wIRA) in acute and chronic wounds. GMS Krankenhhyg Interdiszip. 2009;4:Doc12.

    PubMed  PubMed Central  Google Scholar 

  4. Van Der Linden S, Valkenburg HA, Cats A. Evaluation of diagnostic criteria for ankylosing spondylitis. A proposal for modification of the New York criteria. Arthritis Rheum. 1984;27:361–8.

    Article  Google Scholar 

  5. Aydingoz U, Yildiz AE, Ozdemir ZM, et al. A critical overview of the imaging arm of the ASAS criteria for diagnosing axial spondyloarthritis: what the radiologist should know. Diagn Interv Radiol. 2012;18:555–65.

    PubMed  Google Scholar 

  6. Garrett S, Jenkinson T, Kennedy LG, et al. A new approach to defining disease status in ankylosing spondylitis: the Bath Ankylosing Spondylitis Disease Activity Index. J Rheumatol. 1994;21:2286–91.

    CAS  Google Scholar 

  7. Clarkin CE, Emery RJ, Pitsillides AA, et al. Evaluation of VEGF-mediated signaling in primary human cells reveals a paracrine action for VEGF in osteoblast-mediated crosstalk to endothelial cells. J Cell Physiol. 2008;214:537–44.

    Article  CAS  Google Scholar 

  8. Liu KG, He QH, Tan JW, Liao GJ. Expression of TNF-α, VEGF, and MMP-3 mRNAs in synovial tissues and their roles in fibroblast-mediated osteogenesis in ankylosing spondylitis. Genet Mol Res. 2015;14:6852–8.

    Article  CAS  Google Scholar 

  9. Qian YM, Chu TW, Li JM, et al. Controlled clinical trials on the pathological expressions of VEGF in patients with active ankylosing spondylitis. Zhongguo Gu Shang. 2008;21:649–51.

    CAS  PubMed  Google Scholar 

  10. Gaber T, Dziurla R, Tripmacher R, et al. Hypoxia inducible factor (HIF) in rheumatology: low O2! See what HIF can do! Ann Rheum Dis. 2005;64:971–80.

    Article  CAS  Google Scholar 

  11. Lin L, Shen Q, Xue T, et al. Heterotopic ossification induced by Achilles tenotomy via endochondral bone formation: expression of bone and cartilage related genes. Bone. 2010;46:425–31.

    Article  CAS  Google Scholar 

  12. Lee SS, Joo YS, Kim WU, et al. Vascular endothelial growth factor levels in the serum and synovial fluid of patients with rheumatoid arthritis. Clin Exp Rheumatol. 2001;19:321–4.

    CAS  PubMed  Google Scholar 

  13. Francois RJ, Gardner DL, Degrave EJ, et al. Histopathologic evidence that sacroiliitis in ankylosing spondylitis is not merely enthesitis. Arthritis Rheum. 2000;43:2011–24.

    Article  CAS  Google Scholar 

  14. Zhu J, Xing C, Jiang Y, et al. Evaluation of complex appearance in vascularity of sacroiliac joint in ankylosing spondylitis by color Doppler ultrasonography. Rheumatol Int. 2012;32:69–72.

    Article  Google Scholar 

  15. Drouart M, Saas P, Billot M, et al. High serum vascular endothelial growth factor correlates with disease activity of spondylarthropathies. Clin Exp Immunol. 2003;132:158–62.

    Article  CAS  Google Scholar 

  16. Klauser A, Halpern EJ, Frauscher F, et al. Inflammatory low back pain: high negative predictive value of contrast-enhanced color Doppler ultrasound in the detection of inflamed sacroiliac joints. Arthritis Rheum. 2005;53:440–4.

    Article  Google Scholar 

  17. Unlü E, Pamuk ON, Cakir N. Color and duplex Doppler sonography to detect sacroiliitis and spinal inflammation in ankylosing spondylitis. Can this method reveal response to anti-tumor necrosis factor therapy? J Rheumatol. 2007;34:110–6.

    PubMed  Google Scholar 

  18. Dagfinrud H, Mengshoel AM, Hagen KB, et al. Health status of patients with ankylosing spondylitis: a comparison with the general population. Ann Rheum Dis. 2004;63:1605–10.

    Article  CAS  Google Scholar 

  19. Hanly JG, Mitchell M, MacMillan L, et al. Efficacy of sacroiliac corticosteroid injections in patients with inflammatory spondyloarthropathy: results of a 6 month controlled study. J Rheumatol. 2000;27:719–22.

    CAS  PubMed  Google Scholar 

  20. Günaydin I, Pereira PL, Daikeler T, et al. Magnetic resonance imaging guided corticosteroid injection of the sacroiliac joints in patients with therapy resistant spondyloarthropathy: a pilot study. J Rheumatol. 2000;27:424–8.

    PubMed  Google Scholar 

  21. Althoff CE, Bollow M, Feist E, et al. CT-guided corticosteroid injection of the sacroiliac joints: quality assurance and standardized prospective evaluation of long-term effectiveness over six months. Clin Rheumatol. 2015;34:1079–84.

    Article  Google Scholar 

  22. Chang MC, Ahn SH. The effect of intra-articular stimulation by pulsed radiofrequency on chronic sacroiliac joint pain refractory to intra-articular corticosteroid injection: a retrospective study. Medicine. 2017;96(26):1–5.

    Article  Google Scholar 

  23. Cho S, Shin MH, Kim YK, et al. Effects of infrared radiation and heat on human skin aging in vivo. J Investig Dermatol Symp Proc. 2009;14(1):15–9.

    Article  CAS  Google Scholar 

  24. Mercer JB, Nielsen SP, Hoffmann G. Improvement of wound healing by water-filtered infrared-A (wIRA) in patients with chronic venous stasis ulcers of the lower legs including evaluation using infrared thermography. Ger Med Sci. 2008;6:Doc11.

    PubMed  PubMed Central  Google Scholar 

  25. Niinikoski J. Current concepts of the role of oxygen in wound healing. Ann Chir Gynaecol Suppl. 2001;215:9–11.

    Google Scholar 

  26. Hoffmann G. Principles and working mechanisms of water-filtered infrared-A (wIRA) in relation to wound healing. GMS Krankenhhyg Interdiszip. 2007;2:Doc54.

    PubMed  PubMed Central  Google Scholar 

  27. Hartel M, Hoffmann G, Wente MN, et al. Randomized clinical trial of the influence of local water-filtered infrared A irradiation on wound healing after abdominal surgery. Br J Surg. 2006;93:952–60.

    Article  CAS  Google Scholar 

  28. Hartel M, Illing P, Mercer JB, et al. Therapy of acute wounds with water-filtered infrared-A (wIRA). GMS Krankenhhyg Interdiszip. 2007;2:Doc53.

    PubMed  PubMed Central  Google Scholar 

  29. Syngle V, Syngle A, Garg N, et al. Predictors of autonomic neuropathy in rheumatoid arthritis. Auton Neurosci. 2016;201:54–9.

    Article  CAS  Google Scholar 

  30. Ballara SC, Miotla JM, Paleolog EM. New vessels, new approaches: angiogenesis as a therapeutic target in musculoskeletal disorders. Int J Exp Pathol. 1999;80:235–50.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

Not applicable.

Author information

Author notes

  1. Jian Xu and Yao Deng contributed equally to this work.

Authors and Affiliations

  1. Department of Rheumatology and Immunology, Shengli Oilfield Central Hospital, No. 31 of Jinan Road, Dongying, 257034, Shandong, China

    Jian Xu, Yao Deng, Chun-Yan Yu, Zhao-Meng Gao, Xi-Rui Yang, Qi Zhang & Lei Zhang

Authors
  1. Jian Xu
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Yao Deng
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Chun-Yan Yu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Zhao-Meng Gao
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Xi-Rui Yang
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Qi Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Lei Zhang
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

JX and LZ contributed to the conception and design. JX, YD, CYY, ZMG, XRY, and QZ contributed to the provision of study materials or patients and collection and assembly of data. JX, YD, CYY, ZMG, XRY, and QZ carried out the data analysis and interpretation. All authors participated in the writing of the manuscript. All authors gave approved the final manuscript.

Corresponding author

Correspondence to Lei Zhang.

Ethics declarations

Ethics approval and consent to participate

The informed consent was signed by all subjects. The protocol was approved by the Ethics Committee of Shengli Oilfield Central Hospital (No. Q/ZXYY-ZY-YWB-LL201515). Written informed consent was obtained from all patients enrolled in the investigation.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Xu, J., Deng, Y., Yu, CY. et al. Efficacy of wIRA in the treatment of sacroiliitis in male patients with ankylosing spondylitis and its effect on serum VEGF levels. J Orthop Surg Res 14, 313 (2019). https://doi.org/10.1186/s13018-019-1322-7

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13018-019-1322-7

Keywords

Journal of Orthopaedic Surgery and Research

ISSN: 1749-799X