Research Article | Open Access
Pedro Contreiras Pinto, Luís Monteiro Rodrigues, "An Experimental In Vivo Model to Characterize “Heavy Legs” Symptom in Topical Formulations", Dermatology Research and Practice, vol. 2009, Article ID 547039, 5 pages, 2009. https://doi.org/10.1155/2009/547039
An Experimental In Vivo Model to Characterize “Heavy Legs” Symptom in Topical Formulations
The “Heavy legs” symptom is regarded as an early expression of chronic venous failure, estimated to affect 40% of the population in developing countries. A new methodology is proposed to approach the “tired or heavy legs” symptom. Seven females with this complaint applied a standard topical formulation during 28 days in one leg randomly chosen. Local blood flow records were obtained instantaneously and during postural change with a laser doppler flowmeter (LDF). High-frequency sonography and local morphometry were also obtained at Days 0, 14, and 28. When compared with D0, LDF values present a significant decrease of both basal and dynamical values after Day 14 and Day 28 suggesting that this effect may result from the formulation application, also involving the related massage. Centimetric measurements and sonographic analysis also supported those inferences. The proposed methodology can evaluate the dynamical changes of “heavy legs” symptom and eventually be very useful to assess the related claim support.
The “tired” or “heavy” legs sensation is one of the most frequently referred symptoms in early stages of vascular peripheral disease. This general designation includes a wide variety of pathologies, such as chronic venous insufficiency (CVI), which seems to affect up to 40% of the developed countries population [1, 2]. This helps to justify the relevant variety of medicinal (OTC) and health care products (cosmetics included), mostly topical cutaneous formulations, emerging in the last years to mitigate that condition. Depending on the regulatory space (EU, USA, or Japan) these formulations may even be considered as borderline products [3, 4]. In any case its efficacy and claim substantiation is far from being demonstrated, not only because the mechanisms explaining the symptom are still partially unknown but also because there is no directly related golden standard.
A competent venous system comprehends a superficial and a deep circulation beds connected by perforating veins. The two circuits work together to store and return blood to the heart . A series of valves and muscle pumps helps to keep the blood flowing, preventing the backflow. CVI appears when blood flow in the venous system is jeopardized, in most cases by valvular reflux, thrombotic obstruction of the valves, or both [5, 6]. In the progress of the pathology, there is an increase of the microvascular blood flow that causes the capillaries to become dilated and tortuous [5, 7]. This increases the hydrostatic forces that lead to edema, decreases oxygenation of the surrounding tissues, and evokes skin changes, often stasis dermatitis . In the early stages of this evolution, subtle symptoms such as leg achiness, heavy legs, and leg tension sensations are often present [5–7]. Pathophysiology suggests that “tired” or “heavy” complaints should be related with the progressive dysfunction of peripheral vascular beds, involving structural, haemodynamical, and/or functional (local related autoregulation) capacities, although only a few papers addressed these issues [1, 2] in most cases by Laser Doppler Flowmetry (LDF), a widely known noninvasive technique. Apart from its recognized usefulness, LDF is known to suffer from several methodological limitations [8, 9] motivating other approaches. It is often associated to the topical application of vasoactive drugs [10, 11], to local heating [12–15], and to reactive hyperemia  by postural changes [17, 18] or by suprasystolic pressure cuff (or even other postural maneuvers), specially focusing the lower limb. These strategies help to reduce part of the methodological constrains and provide a dynamical-functional view over the vascular function [8, 16, 19, 20].
Concerning the referred topical formulations claiming to reduce the involved discomfort, one should note that “application” commonly involves a mechanical (massage) effect that should obviously be associated to any eventual reduction of the symptom expression, independently from any other therapeutical activity. But again, it would be necessary to properly design the experimental approach to quantitatively describe these eventual effects.
This was the challenge reflected in the present paper, for example, to develop a sensitive methodology contributing to characterize the condition, eventually useful to substantiate the so-called “tired or heavy legs” improvement claims, for topical formulations.
2. Material and Methods
Seven female volunteers (mean age: y.o.) with healthy skin were selected from the database of the Experimental Dermatology Unit and included in the study. All the volunteers presented the “tired legs” complaint, confirmed by clinical evaluation, specially the presence of oedema, and a questionnaire. Inclusion criteria involved nonsmoking, no vasoactive medication or product, and restriction to drink coffee, tea, or any substance affecting microcirculation one day before lab evaluations. The presence of any pathology or symptom beside the “tired legs” was the main non-inclusion criteria. Volunteers were fully informed about the study objectives and gave their written consent. All procedures adopted were in full compliance with the Helsinki Declaration and its subsequent amendments. The project protocol was previously submitted and approved by the institution’s Ethical Commission.
An alkyl-acrylate crosspolymer gel formulation with no vasoactive substances was used. This polymer is one of the most popular component of “heavy (or tired) legs” market formulations being allegedly able to improve the sensation of discomfort implicit in the complaint, by a local massage effect .
2.3. Experimental Protocol
Volunteers were treated twice a day for 28 days, with 2 g of the formulation, applied in one randomly chosen lower limb (foot and leg), by gentle massage. The contralateral limb was used as a (negative) control. The study was therefore open to the volunteers and to the investigator. All observations and measurements were performed at day 0 (D0), at day 14 (D14), and at the end of the study (D28). All measurements were performed in a controlled room (Relative Humidity 50%; Temperature ) following a 20-minutes stabilization.
The microcirculation blood flow, expressed in Blood Perfusion Units (BPUs) was assessed by the LDF system Periflux 5010 (Perimed, Stocholm, Sweden). Measurements were obtained after a steady local recording at rest, and dynamically, following a postural change like the sustained elevation of the limb from the seated position, by the same observer. This provocation induced a local (vascular) adaptative response eventually modifiable by the test product.
High-frequency (16 MHz) sonography (Dermascan C—Cortex Technology, Denmark) was also used to complement the analysis.
Foot and ankle (centimetric) perimeters were also registered.
2.4. Data Analysis
Statistically, the number of volunteers chosen is supported by adequate nonparametric approach. Descriptive statistics (MS Excel) and Wilcoxon Signed Ranks Test (SPSS 16.0) were applied, and a confidence level of 95% adopted.
Results presented in Table 1 show a significant increase in the control leg blood flow, when compared with basal, after 14 and 28 days. In the treated leg, no statistical differences were found no matter the obvious increase in the mean values. It should be noted however that, during this period, climatic conditions did changed, with an increase in the ambient temperature after day 17th during the protocol execution. Results from the absolute variation during dynamical provocations are presented in Table 2. These show that in the treated leg there are no differences regarding D0, while in the control leg there is a variation increase, specially noted on Day 14.
In order to minimize the influence of intrinsic and extrinsic complicants (including the mentioned temperature changes), data were normalized by the quotient between the basal application value and the corresponding control in each evaluation day (Figure 1).
Morfometric data were obtained by measuring the leg and ankle perimeters at D0, D14, and D28. Variations related to Day 0 and the corresponding statistics are summarized in Table 3. Although not significant, suggestive differences are seen in the nontreated limb (leg and ankle) at D14 and D28.
Sonographic analysis of selected oedemacious areas was performed in a few volunteers () to further explore and eventually illustrate the studied effects. Analysis took place at both internal and external faces of the ankle and included the total (cutaneous) thickness calculation. Results from D28 were very expressive (Figures 2 and 3) confirming a clear reduction of the oedema, when compared with D0, already detectable in D14. Additionally, in D28, volunteer’s control leg presented an increase in the cutaneous thickness ( mm) while the treated leg has shown a reduction of mm at the same evaluation period.
LDF is commonly used to assess local vascular conditions in a wide variety of pathologies from peripheral vascular disease  to diabetes [14, 15] or the Raynaud’s syndrome [17, 18, 22]. LDF’s dynamical assessment during limb postural changes proved to be very useful [8, 22], providing an interesting amount of information related with the local vascular function, especially regarding the veno-arterial reflex, although with different experimental approaches [8, 18, 22, 23]. In healthy subjects, a modification of posture from lying to standing involved an increase in the precapillary resistance of the foot’s skin microcirculation, leading to an increase in local blood flow . When the leg is lowered from supine, a decrease on the red cell flux was described . Changing from supine to seated reportedly evoked a reduction in the lower limb blood volume . More recently, an increase of the foot’s blood flow by elevation of the leg ( regarding the thigh) from seating was described . Thus, these views provided a practical noninvasive, functional approach to study the impact of vasoactive substances or products on the peripheral perfusion conditions, offering new insights for comparative purposes.
When compared with D0, a significant reduction of basal LDF, in the treated area, 19% and 36% in D14 and D28, respectively, was noted, while provocation values decreased 33% and 18% in D14 and D28. Although significant differences in the provocation values could not be found, this clear tendency should be considered. This potential effect of minimizing the huge (microcirculatory) variations evoked by the ambient temperature rising was only present in the treated limb. As shown in Table 1, LDF values in the treated leg at D14 or D28, at rest, were similar to basal. A totally different condition was seen in the nontreated limb. Dynamical experiences corroborated those findings (Table 2) suggesting that the intervention, involving the formulation and the massage effect, determined some protective action that was maintained during the 28 days.
Morfometric results confirmed the minimizing effect of the intervention since, in the treated limb, the differences were clearly less evident.
Results from sonographic measurements at the selected oedemacious areas demonstrated the oedema and skin thickness reduction that can only be related with the formulation application, probably involving a local blood flow improvement. In the control leg the blood flow increase was pronounced, suggesting some involvement of the veno-arterial reflex which could induce or maintain the oedema and the high skin thickness .
No matter the present pilot-study approach and the apparent reduced number of volunteers, this methodology did prove to be able to characterize the vascular condition of each individual, allowing to discriminate the effects from a topical intervention on the peripheral vascular status of the lower limb. The proposed model may also help to look further to the vascular failure pathophysiology.
- R. Chiesa, E. M. Marone, C. Limoni, M. Volonté, E. Schaefer, and O. Petrini, “Effect of chronic venous insufficiency on activities of daily living and quality of life: correlation of demographic factors with duplex ultrasonography findings,” Angiology, vol. 58, no. 4, pp. 440–449, 2007.
- J. M. Callejas, J. Manasanch, R. Abad et al., “Epidemiology of chronic venous insufficiency of the lower limbs in the primary care setting,” International Angiology, vol. 23, no. 2, pp. 154–163, 2004.
- S. Young, “Regulatory assessment of cosmetic product,” in Skin Moisturization, Cosmetic Science and Technologies Series, J. Leyden and A. Rawlings, Eds., pp. 635–650, Marcel Dekker, New York, NY, USA, 2002.
- V. Rogiers, “Efficacy claims of cosmetics in Europe must be scientifically substantiated from 1997,” Skin Research and Technology, vol. 1, no. 1, pp. 44–46, 1995.
- C. Bahr, “CVI and PAD: a review of venous and arterial disease,” JAAPA, vol. 20, no. 8, pp. 20–25, 2007.
- T. J. Kelechi and P. A. Bonham, “Measuring venous insufficiency objectively in the clinical setting,” Journal of Vascular Nursing, vol. 26, no. 3, pp. 67–73, 2008.
- J. D. Raffetto, “Dermal pathology, cellular biology, and inflammation in chronic venous disease,” Thrombosis Research, vol. 123, supplement 4, pp. S66–S71, 2009.
- C. I. Wright, C. I. Kroner, and R. Draijer, “Non-invasive methods and stimuli for evaluating the skin's microcirculation,” Journal of Pharmacological and Toxicological Methods, vol. 54, no. 1, pp. 1–25, 2006.
- E. Berardesca, J. L. Lévêque, P. Masson et al., “EEMCO guidance for the measurement of skin microcirculation,” Skin Pharmacology and Applied Skin Physiology, vol. 15, no. 6, pp. 442–456, 2002.
- M. Berghoff, M. Kathpal, S. Kilo, M. J. Hilz, and R. Freeman, “Vascular and neural mechanisms of ACh-mediated vasodilation in the forearm cutaneous microcirculation,” Journal of Applied Physiology, vol. 92, no. 2, pp. 780–788, 2002.
- P. Kvandal, A. Stefanovska, M. Veber, H. D. Kvermmo, and K. A. Kirkebøen, “Regulation of human cutaneous circulation evaluated by laser Doppler flowmetry, iontophoresis, and spectral analysis: importance of nitric oxide and prostaglandines,” Microvascular Research, vol. 65, no. 3, pp. 160–171, 2003.
- D. L. Kellogg Jr., “In vivo mechanisms of cutaneous vasodilation and vasoconstriction in humans during thermoregulatory challenges,” Journal of Applied Physiology, vol. 100, no. 5, pp. 1709–1718, 2006.
- N. Charkoudian, “Skin blood flow in adult human thermoregulation: how it works, when it does not, and why,” Mayo Clinic Proceedings, vol. 78, no. 5, pp. 603–612, 2003.
- S. Golay, C. Haeberli, A. Delachaux et al., “Local heating of human skin causes hyperemia without mediation by muscarinic cholinergic receptors or prostanoids,” Journal of Applied Physiology, vol. 97, no. 5, pp. 1781–1786, 2004.
- P. Contreiras Pinto, S. Moniz, and L. M. Rodrigues, “Assessment of the effect of temperature on the dynamics of cutaneous microcirculatory response,” Revista Lusófona de Ciência e Tecnologias da Saúde, vol. 5, no. 1, pp. 61–67, 2008.
- L. M. Rodrigues, P. Contreiras Pinto, and A. Leal, “Transcutaneous flow related variables measured in vivo: the effects of gender,” BMC Dermatology, vol. 1, article 4, 2001.
- A. Abu-Own, J. H. Scurr, and P. D. C. Smith, “Effect of leg elevation on the skin microcirculation in chronic venous insufficiency,” Journal of Vascular Surgery, vol. 20, no. 5, pp. 705–710, 1994.
- J. C. de Graaff, D. T . Ubbink, J. A. van der Spruit, S. M. Lagarde, and M. J. H. M. Jacobs, “Influence of peripheral arterial disease on capillary pressure in the foot,” Journal of Vascular Surgery, vol. 38, no. 5, pp. 1067–1074, 2003.
- P. Contreiras Pinto, F. Rei, M. Fernandes, and L. M. Rodrigues, “Characterization of the peripheral vascular function by a hemodynamical response to a passive postural change in the lower limb,” Revista Lusófona de Ciência e Tecnologias da Saúde, vol. 3, no. 2, pp. 145–153, 2006.
- A. C. Shore, K. J. Price, D. D. Sandeman, J. H. Tripp, and J. E. Tooke, “Posturally induced vasoconstriction in diabetes mellitus,” Archives of Disease in Childhood, vol. 70, no. 1, pp. 22–26, 1994.
- C. L. Felty and T. W. Rooke, “Compression therapy for chronic venous insufficiency,” Seminars in Vascular Surgery, vol. 18, no. 1, pp. 36–40, 2005.
- I. O. W. Man, K. Glover, P. Nixon, R. Poyton, R. Terre, and M. C. Morrissey, “Effect of body position on foot and ankle volume in healthy subjects,” Clinical Physiology and Functional Imaging, vol. 24, no. 6, pp. 323–326, 2004.
- J. C. de Graaff, D. T. Ubbink, S. M. Lagarde, and M. J. H. M. Jacobs, “Postural changes in capillary pressure in the hallux of healthy volunteers,” Journal of Applied Physiology, vol. 95, no. 6, pp. 2223–2228, 2003.
Copyright © 2009 Pedro Contreiras Pinto and Luís Monteiro Rodrigues. 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.