International Journal of Vascular Medicine

International Journal of Vascular Medicine / 2021 / Article

Research Article | Open Access

Volume 2021 |Article ID 6699029 | https://doi.org/10.1155/2021/6699029

Shigeko Inokuma, Yasuo Kijima, "Thermal Disparity among Fingers and Its Amelioration by CO2-Water Bathing in Connective Tissue Disease Patients", International Journal of Vascular Medicine, vol. 2021, Article ID 6699029, 5 pages, 2021. https://doi.org/10.1155/2021/6699029

Thermal Disparity among Fingers and Its Amelioration by CO2-Water Bathing in Connective Tissue Disease Patients

Academic Editor: Alberto Caggiati
Received18 Oct 2020
Revised09 Mar 2021
Accepted14 Mar 2021
Published07 Apr 2021

Abstract

Objective. Correlation between a low finger temperature and thermal disparity among fingers was studied in connective tissue disease (CTD) patients. Whether the thermal disparity may be ameliorated by hand immersion in a warm carbon dioxide- (CO2-) water bath was analyzed. Methods. CTD patients with suspected peripheral circulation disorder underwent a thermography test. From before to 30 min after hand immersion in CO2-water (CO2 bathing; 1000 ppm CO2, 42°C, 10 min), the nailfold temperatures were measured. The mean temperature (m-Temp) and the coefficient of variation of the temperature ( of one hand; the mean of CVs of both hands was adopted as the indicator of thermal disparity) were monitored. The correlation between m-Temp and CV was also analyzed. Results. Forty-seven (45 females and 2 males) patients were included, 32 of whom had Raynaud’s phenomenon. The m-Temp was at the baseline, increased to immediately after CO2 bathing, and remained significantly higher than that at the baseline until 30 min after (). The CV was at the baseline, decreased to immediately after CO2 bathing, and remained significantly lower than the baseline until 30 min after (). Between m-Temp and CV, a negative correlation was observed throughout the measurements. Conclusion. Thermal disparity was observed at baseline measurement in CTD patients. Warm CO2 bathing markedly ameliorated the disparity, and this amelioration remained until after 30 min. Throughout the observation, the lower the m-Temp, the more severe the thermal disparity among fingers.

1. Introduction

Peripheral vascular involvement is one of the major features associated with connective tissue diseases (CTDs). We previously reported that thermal disparity among fingers is a characteristic feature of conditions with disturbed peripheral circulation including Raynaud’s phenomenon [1]. CO2 has long been known to improve peripheral circulation, with its effect usually observed after exposure of the whole body for a certain number of days [2]. In this study, we evaluated whether exposure to warm water containing CO2 may ameliorate the thermal disparity among fingers and whether this amelioration can be achieved after only a short period of exposure. These are intriguing issues, and their clarification might in turn elucidate the pathophysiology of some peripheral vasculature diseases.

2. Patients and Methods

Patients who visited the Japanese Red Cross Medical Center, were diagnosed as having a CTD, and were suspected of having peripheral circulation disorder as determined by their doctors in charge were included. They underwent a thermography test before and after immersing their hands in CO2-water. The test was performed within the routine clinical setting under the public health insurance system, and the results were retrospectively analyzed.

After acclimatization to room temperature (25°C) for 15 min, both hands were immersed into a 42°C CO2-water bath for 10 min (CO2 bathing). The water contained 1,000 ppm CO2 (Carbothera Onpar™, Mitsubishi Rayon Cleansui Co., Ltd., Japan). Before (-10 min) and 0, 3, 5, 10, 15, 20, and 30 min after CO2 bathing, nailfold temperature (Temp) of the ten fingers was measured by thermography (INFRAEYE3000™, Nihonkoden, Japan). CO2 bathing and Temp measurement were carried out in a sitting position with the hands placed at a level below the heart throughout the test.

As an indicator of thermal disparity among fingers, the coefficient of variation (CV) was adopted. CV was calculated as SD/mean temperature (m-Temp). In this study, the mean of right and left hand CVs was used throughout. The correlation between m-Temp and CV was also examined. Results were statistically analyzed by the paired -test.

This work was supported by Research Award, Japanese Society of Balneology, Climatology and Physical Medicine, 2016. This study was approved by the Ethics Committee, Chiba Central Medical Center: H30-R19.

3. Results

Forty-seven (45 females and two males) patients aged were included. Thirty-two had Raynaud’s phenomenon. The underlying CTDs were primary Sjögren disease in nine, pernio in nine, primary Raynaud disease in eight, systemic lupus erythematosus in five, systemic sclerosis in two, mixed connective tissue disease, calcinosis–Raynaud phenomenon–esophageal dysmotility–sclerodactyly–telangiectasia syndrome, polyarteritis nodosa, and Hashimoto disease in one each, and undifferentiated connective tissue disease in 10. Five were taking prednisolone ( mg/day), and 34 a PGI2 derivative (beraprost Na, 60 µg/day).

The time-course changes in Temp of each finger of one hand of a patient are shown in Figure 1 as a representative case. In this patient, the baseline Temp varied from finger to finger, resulting in a high CV at baseline. Then, after CO2 bathing, the thermal disparity disappeared, and CV diminished.

In Figure 2(a), the m-Temp at each measurement of each patient is plotted in a single line. In Figure 2(b), the changes in the mean and SD of the m-Temps of the 47 patients enrolled are shown. The means and SDs of the m-Temps were at the baseline, at 0 min, at 3 min, at 5 min, at 10 min, at 15 min, at 20 min, and at 30 min after CO2 bathing (, baseline vs. each measurement after CO2 bathing; , immediately after vs. 5 to 30 min after; ns, 3 min vs. 5 to 20 min after; and , 3 min after vs. 30 min after).

The time-course changes in the CV in each patient are plotted in a single line in Figure 3(a). Figure 3(b) shows that the means and SDs of CVs were at the baseline, at 0 min, at 3 min, at 5 min, at 10 min, at 15 min, at 20 min, and at 30 min after CO2 bathing (, baseline vs. each measurement after CO2 bathing; ns, 3 min vs. 5 to 30 min after).

When dividing the patients into two groups with a baseline CV lower and higher than the mean, 30 patients showed a lower CV. In these 30 patients, their mean CVs were similar in all the measurements and no significant difference was observed between the baseline CV and each CV after CO2 bathing (data not shown). On the other hand, in all of the 17 patients with a CV higher than the mean at the baseline, CV decreased significantly after CO2 bathing, and a statistically significant decrease from that at the baseline was observed in all the measurements. In this latter group, after the initial CV decrease, CV reincreased gradually, and from 15 min after CO2 bathing until the last measurement, CV became significantly higher than that immediately after CO2 bathing (data not shown).

The correlation between m-Temp and CV is shown in Figure 4 for each measurement. At the baseline, both m-Temp and CV differed from patient to patient; CV showed a tenfold difference. Patients with a higher CV showed a wide range of m-Temps. In patients with a lower CV, mostly a higher Temp was observed. Immediately after CO2 bathing, data points appeared clustered; the patients with a lower Temp and/or a higher CV at the baseline showed a higher Temp and a lower CV. Then afterward, the data points gradually returned to their original positions prior to CO2 bathing. However, Temp increase and CV decrease were still preserved 30 min after. Between m-Temp and CV, a significant correlation was observed in all the measurements (, at any measurement).

4. Discussion

Disturbed peripheral circulation is one of the major features of CTDs. Not only the extremities but also internal organs including the lungs and intestines may also be involved in it, sometimes resulting in severe diseases such as pulmonary hypertension and pseudoileus. Recurrent vasoconstriction, narrowing, or obstruction may develop in small-caliber peripheral vasculatures; the possible pathogenetic mechanisms of which include autonomic nerve system dysfunction, vasculitides, and remodeling of the vascular structure. They are thought to develop usually unevenly from vessel to vessel. A notable case is Raynaud’s phenomenon, in which the skin surface color and temperature differ markedly among fingers, not only at an attack but also even at the time without an attack (Figure 1). We have observed a thermal disparity in patients with Raynaud’s phenomenon [1]. As an indicator of this thermal disparity, CV would be appropriate to be adopted.

In this study, we focused on thermal disparity. Here, we basically determined whether a low m-Temp, which is due to poor peripheral perfusion, is associated with a high CV. This association is clearly shown in Figure 4; at each measurement, a statistically significant negative correlation was observed between m-Temp and CV. An additional noteworthy observation is that at the baseline, three patients with a substantially low m-Temp did not show a very high CV (Figure 4, -10 min); it is considered that long-standing invasion might have led to diffuse vascular remodeling, resulting in a markedly low temperature in all fingers and consequently in a rather low CV. As far as we know, no study focusing on thermal disparity as an indicator of disturbed perfusion has been reported except for our previous report [1].

When adopting CV change to evaluate an effect of CO2 bathing, only a 10 min exposure clearly decreased CV. Immediately after CO2 bathing, simultaneously with an m-Temp increase, CV markedly decreased, as shown by the clustered data points in Figure 4. This likely reflected a greater increase in blood flow in fingers with disturbed perfusion. Another possible explanation is that cooling to the baseline Temp level after warm CO2 bathing easily occurs in fingers with well-maintained perfusion. However, this is not likely because that as is shown in Figure 1, fingers with a primarily low Temp did not show a higher temperature than others with a primarily high Temp after CO2 bathing. If flowmetry was also carried out in addition to thermometry, it might be helpful in analyzing the flow [36], although flowmetry has not been widely used in a routine clinical setting. The CV decrease was sustained until 30 min after CO2 bathing (Figures 1 and 3). This sustained CV decrease was in contrast to the Temp increase; m-Temp finally decreased significantly 30 min after CO2 bathing not only from m-Temp immediately after but also from m-Temp 3 min after bathing (Figure 2). Amelioration of thermal disparity by CO2 bathing was outstanding.

Therapies that can ameliorate the disparity would be beneficial and should be applied. Natural spring of CO2-water has long been known to have a warming effect and to cure vascular disorders ever since the Middle Ages [5]. In recent investigations, not only long-term but also short-term exposure to CO2-water has been examined. Ogoh et al. showed that lower-leg immersion in 38°C water containing 1000 ppm CO2 for 20 min enhanced skin blood flow, possibly through endothelial-cell-mediated vasodilatation [7]. Finzgar et al. reported that 35 min gaseous CO2 exposure of a lower limb increased laser Doppler flux [8]. Nishimura et al. showed cutaneous blood flow increase with repeated CO2-water bathing [9]. Some of the studies compared the effect of CO2-water to tap water. Regarding the pathological aspect, Akahane et al. showed that a significantly larger number of capillaries were formed four weeks after muscle injury in rats with transcutaneous CO2 therapy than in rats without it [10].

To the best of our knowledge, this is the first report of an effect of CO2 bathing focusing on thermal disparity. Although infrared thermography has long been used in various studies, it has never been applied to study from this point of view [1115]. As a limitation of this study, only a single exposure to CO2 was carried out. Repeated bathing for a substantial duration might potentially reverse remodeling, resulting in recovery from vascular involvement that frequently develops in CTDs. Comparison to the effect with tap water will show a difference, as studies adopting both CO2 and tap water have shown a better effect with the former.

5. Conclusion

In conclusion, this study showed that thermal disparity among fingers is a characteristically important finding of disturbed peripheral perfusion in CTD, that the lower the finger temperatures, the higher the thermal disparity, and that CO2 bathing ameliorated the thermal disparity until after 30 min.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors have no conflict of interest related to this study and no related exclusive license.

Authors’ Contributions

Both authors contributed to conception and design. Yasuo Kijima mainly collected the data. Analysis and interpretation of data were mainly by Shigeko Inokuma.

Acknowledgments

This work was supported by Research Award, Japanese Society of Balneology, Climatology and Physical Medicine, 2016.

References

  1. M. Horikoshi, S. Inokuma, Y. Kijima et al., “Thermal disparity between fingers after cold-water immersion of hands: a useful indicator of disturbed peripheral circulation in Raynaud phenomenon patients,” Internal Medicine, vol. 55, no. 5, pp. 461–466, 2016. View at: Publisher Site | Google Scholar
  2. R. Fabry, P. Monnet, and J. Schmidt, “Clinical and microcirculatory effects of transcutaneous CO2 therapy in intermittent claudication. Randomized double-blind clinical trial with a parallel design,” Vasa, vol. 38, pp. 213–224, 2009. View at: Publisher Site | Google Scholar
  3. Z. B. Stoyneva, S. M. Dermendjiev, D. G. Medjidieva, and V. E. Vodenicharov, “Microvascular reactivity during sympathetic stimulations in Raynaud’s phenomenon,” International Angiology, vol. 35, no. 6, pp. 593–598, 2016. View at: Google Scholar
  4. S. N. Lambova, “The place of nailfold capillaroscopy among instrumental methods for assessment of some peripheral ischaemic syndromes in rheumatology,” Folia Med (Plovdiv), vol. 58, no. 2, pp. 77–88, 2016. View at: Publisher Site | Google Scholar
  5. E. D. Pagourelias, P. G. Zorou, M. Tsaligopoulos, V. G. Athyros, A. Karagiannis, and G. K. Efthimiadis, “Carbon dioxide balneotherapy and cardiovascular disease,” International Journal of Biometeorology, vol. 55, no. 5, pp. 657–663, 2011. View at: Publisher Site | Google Scholar
  6. K. Melsens, S. Van Impe, S. Paolino, A. Vanhaecke, M. Cutolo, and V. Smith, “The preliminary validation of laser Doppler flowmetry in systemic sclerosis in accordance with the OMERACT filter: a systematic review,” Seminars in Arthritis and Rheumatism, vol. 50, no. 2, pp. 321–328, 2020. View at: Publisher Site | Google Scholar
  7. S. Ogoh, R. Nagaoka, T. Mizuno et al., “Acute vascular effects of carbonated warm water lower leg immersion in healthy young adults,” Physiological Reports, vol. 4, no. 23, article e13046, 2016. View at: Publisher Site | Google Scholar
  8. M. Finzgar, Z. Melik, and K. Cankar, “Effect of transcutaneous application of gaseous carbon dioxide on cutaneous microcirculation,” Clinical Hemorheology and Microcirculation, vol. 60, no. 4, pp. 423–435, 2015. View at: Publisher Site | Google Scholar
  9. N. Nishimura, J. Sugenoya, T. Matsumoto et al., “Effects of repeated carbon dioxide-rich water bathing on core temperature, cutaneous blood flow and thermal sensation,” European Journal of Applied Physiology, vol. 87, no. 4-5, pp. 337–342, 2002. View at: Publisher Site | Google Scholar
  10. S. Akahane, Y. Sakai, T. Ueha et al., “Transcutaneous carbon dioxide application accelerates muscle injury repair in rat models,” International Orthopaedics, vol. 41, no. 5, pp. 1007–1015, 2017. View at: Publisher Site | Google Scholar
  11. J. D. Pauling, J. A. Shipley, N. D. Harris, and N. McHugh, “Use of infrared thermography as an endpoint in therapeutic trials of Raynaud’s phenomenon and systemic sclerosis,” Clinical and Experimental Rheumatology, vol. 30, 2 Suppl 71, pp. S103–S115, 2012. View at: Google Scholar
  12. S. Youakim, “Infrared thermometry in the diagnosis of hand-arm vibration syndrome,” Occupational Medicine, vol. 60, no. 3, pp. 225–230, 2010. View at: Publisher Site | Google Scholar
  13. M. Chojnowski, “Infrared thermal imaging in connective tissue diseases,” Reumatologia, vol. 55, no. 1, pp. 38–43, 2017. View at: Publisher Site | Google Scholar
  14. M. A. C. van der Weijden, L. M. van Vugt, D. Valk et al., “Exploring thermography: a promising tool in differentiation between infection and ischemia of the acra in systemic sclerosis,” International Journal of Rheumatic Diseases, vol. 20, no. 12, pp. 2190–2193, 2017. View at: Publisher Site | Google Scholar
  15. O. Schlager, M. E. Gschwandtner, K. Herberg et al., “Correlation of infrared thermography and skin perfusion in Raynaud patients and in healthy controls,” Microvascular Research, vol. 80, no. 1, pp. 54–57, 2010. View at: Publisher Site | Google Scholar

Copyright © 2021 Shigeko Inokuma and Yasuo Kijima. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


More related articles

 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder
Views439
Downloads593
Citations

Related articles

Article of the Year Award: Outstanding research contributions of 2020, as selected by our Chief Editors. Read the winning articles.