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Anais Brasileiros de Dermatologia

On-line version ISSN 1806-4841

An. Bras. Dermatol. vol.81 no.6 Rio de Janeiro Nov./Dec. 2006

http://dx.doi.org/10.1590/S0365-05962006000600003 

CLINICAL, EPIDEMIOLOGICAL, LABORATORY AND THERAPEUTIC INVESTIGATION

 

Capillaroscopy findings in lupus erythematosus*

 

 

Anamaria da Silva FacinaI; Mario Luiz Cardoso PucinelliII; Mônica Ribeiro Azevedo VasconcellosIII; Luci Biaggi FerrazIV; Fernando Augusto de AlmeidaV

IFacina AS. Master's degree in Dermatology from the Universidade Federal de São Paulo (UNIFESP) . Voluntary physician of the Dermatology Service at the (UNIFESP) - São Paulo (SP), Brazil
IIPucinelli MLC. PhD in Rheumatology from the Universidade Federal de São Paulo (UNIFESP). Physician of the Rheumatology Service at the (UNIFESP) - São Paulo (SP), Brazil
IIIVasconcellos MRA. Master's degree in Dermatology from the (UNIFESP) Physician of the Dermatology Service at the Universidade Federal de São Paulo - São Paulo (SP), Brazil
IVFerraz LB. Master's degree in Dermatology from the (UNIFESP) Voluntary physician of the Dermatology Service at the Universidade Federal de São Paulo - São Paulo (SP), Brazil
VAlmeida FA. PhD. Adjunct professor of the Dermatology Service at the Universidade Federal de São Paulo (UNIFESP) - São Paulo (SP), Brazil

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ABSTRACT

BACKGROUND: Capillaroscopy is an useful diagnostic tool that is non-invasive, reproducible, able to assess the capillaries in the periungal region and that assists in the differential diagnosis of connective tissue diseases.
OBJETIVES: The aim of the study was to distinguish chronic cutaneous lupus erythematosus and systemic lupus erythematosus from controls assessed by nailfold capillaroscopy.
METHODS: Seventy patients with lupus erythematosus (37 with chronic cutaneous lupus erythematosus and 33 with systemic lupus erythematosus) were studied by the technique of capillary microscopy and compared to 32 controls.
RESULTS: The presence of ectatic (p=0.027; p=0.001), meandering (p=0.001; p=0.007), corkscrew capillaries (p=0.011; p=0.005) and nailfold bleeding (p=0.004; p=0.001) distinguished between the two groups of patients (chronic cutaneous lupus erythematosus and systemic lupus erythematosus) from controls. The variable meandering loops could be predictive for systemic lupus erythematosus (OR=8.308). The independent variables ectatic loops (OR=12.164) end nailfold bleedings (OR=5.652) were predictive for chronic cutaneous lupus erythematosus.
CONCLUSIONS: Capillaroscopy can help in the management of patients, since the presence of typical capillaroscopic abnormalities seems to be related to the development of lupus erythematosus. The independent predictive variables for systemic lupus erythematosus were meandering loops, and, for chronic cutaneous lupus erythematosus, ectasic loops and nailfold bleedings.

Keywords: Capillaries; Lupus erythematosus, discoid; Lupus erythematosus, systemic; Microscopic angioscopy


 

 

INTRODUCTION

Lupus erythematous is a chronic multifactorial inflammatory disorder caused by changes in the immune system with genetic, environmental and hormonal interactions. Its diagnosis is made by means of clinical history, physical examination and complemented by tests, such as histopathology, direct and indirect immunofluorescence and routine laboratory tests (complete blood count - CBC, erythrocyte sedimentation rate - ERS, type I urine analysis).1

Nailfold capillaroscopy (NFC) is a method enabling direct assessment of capillaries of the periungal region by means of stereoscopic microscopy.2, 3 This method combines several advantages: it is noninvasive; it is reproducible; it allows early distinction of primary Raynaud phenomenon (RP) from that secondary to connective tissue disorders.4,5 The microvascular changes found through capillaroscopy seen in lupus, dermatomyositis, Sjögren syndrome and scleroderma have been widely studied.4-7

The typical capillaroscopic pattern in systemic lupus erythematous (SLE pattern) consists basically of increased capillary tortuosity, which may affect the three branches of the capillary loop, with changes like meandering, corkscrew or circumvolutions and lengthening of loops, which at times resemble glomeruloid structures.3,7 Andrade et al.3 performed quantitative analytical assessment in 40 patients with SLE and concluded that very long and abundant meandering capillaries may suggest the diagnosis of systemic lupus. Jaramillo et al.8 studied 15 SLE patients and observed capillary tortuosity in all of them. Tortuosity is a relevant morphological criterion, which, nonetheless, may be considered a normal finding when found in less than 5% of capillaries. Reduction in the number of capillaries may also be part of this pattern.4,6,8 Studer et al.9 reported that SLE patients had a statistically significant higher number of bleedings, greater rate of plexus depiction, larger diameter in the three parts of the capillary loop (arterial, transitional and venous) than controls. It is worth emphasizing that a normal examination does not rule out the possibility of connective tissue disease, and it is unlikely in the case of progressive systemic sclerosis, for which the negative predictive value is 99.4%.10

With the aim of improving the characterization of SLE and chronic cutaneous lupus erythematous (CCLE), the present study attempts to correlate the capillaroscopic findings in both conditions and to compare them to those of controls.

 

PATIENTS AND METHODS

Patients

Patients seen at the Collagen Disease Outpatient's Clinic of the Department of Dermatology and of the Rheumatology Course of the Universidade Federal de São Paulo - Escola Paulista de Medicina - Hospital São Paulo, from February 1997 to September 1999, took part in this study. The study had been previously approved by the Ethics Committee of Hospital São Paulo and all patients signed informed consent forms.

Patients were randomly selected, and the exclusion criterion was presence of other systemic diseases, such as hypertension, diabetes mellitus and lung diseases. Patients suspected of other associated collagen diseases were also excluded. People with systemic diseases and with suspected Raynaud phenomenon were excluded from the control group.

One hundred and two subjects were studied and assigned to three different groups: SLE (33), CCLE (37) and control (32).

The CCLE and the SLE groups were identified according to the ARA criteria11 by means of history (photosensitivity) and laboratory tests (CBC, urine I, 24-hour proteinuria, indirect immunofluorescence, histopathology).

Capillaroscopy

a - Microscope

A stereomicroscope Olympus SZ 40, with six to 40 times magnification was used. To count the capillaries in the fourth and fifth fingers, 10 times magnification was employed and to assess the morphology of capillary loops, a 15-times magnification was performed in 10 fingers.

A precision reticulum with 10 divisions corresponding to one millimeter of the field observed, for 10mm was set in the right eye piece. This allowed immediate counting of the number of capillaries in each millimeter of the distal row.

b - Lighting

A low voltage tungsten incandescent lamp (6 volts and 15 watts) that releases small amount of heat on the skin at study, not causing dilatation of the vessels, was used. Its light is collimated by means of a convergent lens and the light beam shines on the skin surface at a 45 degree angle, and uncomfortable glare is prevented.

Dry oil is rubbed on the skin surface to reduce refraction and to add transparency, thus improving the visualization of vessels.

A plastic green filter was used to enhance contrast between the capillaries and surrounding tissues.

Capillaroscopy was performed in all 10 fingers with the hand at the heart level. The readings were double-blind and done by two independent examiners. The agreement rate of the two capillaroscopic readings was greater than 80% for each parameter, showing good reproducibility. The parameters analyzed were: number of loops per millimeter, presence of ectatic capillaries, presence of corkscrew capillaries, presence of meandering capillaries and nailfold bleeding.3,7,12

Statistical Analysis

Qualitative variables are depicted in tables displaying absolute (n) and relative (%) frequencies. The association between these variables was assessed by the chi-square test or by the likelihood ratio, or the Fisher exact test. Quantitative variables were assessed by analysis of variance with one classification factor. The statistically significant variables in the univariate analysis were used to adjust the logistic regression model. Results of logistic regression were expressed as the odds ratio and their 95% confidence intervals. The level of significance adopted was p<0.05.13

 

RESULTS

Mean age among the three groups was not statistically different (Table 1). The groups were homogeneous regarding sex and skin color (Tables 2 and 3, respectively).

The distribution of the mean number of loops in the two types of lupus erythematosus and in the control group was not different (Table 4).

The discriminatory power of the presence of ectatic capillaries was, on the contrary, demonstrated. No difference was found between the SLE and the CCLE groups. Between the SLE and control groups and between the CCLE and control groups, differences were found with p=0.005, that is, they were statistically significant (Table 5).

 

 

Regarding the presence of meandering capillaries, no difference was found between SLE and CCLE patients. However, the difference between SLE and control groups and between CCLE and control groups was at p=0.001 (Table 6).

 

 

As to corkscrew capillaries, the two lupus groups were not different, opposed to what was found when both, the CCLE and the SLE groups were compared with control groups, p=0.003 (Table 7).

 

 

The presence of nailfold bleeding was not statistically different between the SLE and the CCLE groups. Comparing the SLE with controls and CCLE with controls, p=0.001 (Table 8).

 

 

By using logistic regression for the CCLE group relative to the control group, nailfold bleeding and ectatic capillaries were predicted variables for CCLE, and this model was adjusted for age (Table 9). On the other hand, meandering capillaries were a predictive variable for SLE (Table 10).

 

 

 

 

The presence of nailfold bleeding increased the risk for CCLE five fold and that of ectatic capillaries, by 12 fold. The finding of meandering capillaries increased the risk for SLE by eight fold.

 

DISCUSSION

Panoramic periungal capillaroscopy has become a relevant diagnostic tool in connective tissue diseases. Many investigators have analyzed pictures of the periungal bed, seeking patterns in the capillaries that could distinguish different connective tissue diseases.7,15,14-16 Others have nailfold capillaroscopy using more powerful lenses in order to measure the diameters of loops and their curvature.4,9,16-23 Some authors have attempted the use of the dermatoscope, such as Dermalite® with the same purpose.24,25 After the method was established by Maricq2, using panoramic PUC with variable magnification from 10 to 20 times, several studies have followed these standardization.3,26

Some investigators have found a reduction in the total number of capillary loops in lupus patients.7,12,27 In the present study the number of capillaries per millimeter was not different among patients with SLE, CCLE and controls, the mean number of capillaries per millimeter being 9.08 in SLE, 9.50 in CCLE and 9.53 in controls, in accordance to the findings of Andrade et al.3

Kabasakal et al.19 observed difference in the number of ectatic loops in 22 SLE patients and 38 healthy individuals (p<0.005). Studer et al.,9 assessed 12 patients with CCLE, 10 with SLE and 15 controls and found that loop diameter was greater in SLE than in CCLE and controls, but no difference was found between the CCLE and control groups. Dancour et al.28 found statistical difference in capillary diameter between 21 SLE patients and 21 controls.

In this study, the presence of ectatic capillary discriminated SLE and CCLE patients from controls (p=0.027) and (p=0.001) respectively, but did not differentiate the CCLE and the SLE groups from each other (p=0.321), and was a predictive parameter (odds ratio = 12.164) for the CCLE group (Table 9).

Caspary et al.17 reported less than 10% incidence of tortuous capillaries in 29 controls, of 15% in 29 SLE patients with associated Raynaud phenomenon and 18% in 29 lupus patients with no associated Raynaud phenomenon. Riccierri et al.29 found that in 44 SLE patients, meandering capillaries were present in 16%. Jaramillo et al.8 reported 12/15 (80%) capillaries in SLE and Maricq et al.12, in 25 of 60 patients (42%). Opposing this, Bongard et al.,18 described a reduction in meandering capillaries in 16% of SLE patients. Ercole27 also found an increase in the mean number of meandering capillaries in SLE patients (p<0.01) compared to controls.

In the present study, the parameter meandering capillaries did not discriminate between the CCLE and the SLE groups (p=0.220), but it discriminated either group from the control group (p=0.011 and p=0.005, respectively) (Table 6) and was predictive of SLE (odds ratio of 8.308).

Corkscrew capillaries were found in 7/33 (21.2%) patients with SLE, 8/37 (21.6%) with CCLE and in no control subject, in the present study. The method separated the CCLE and the SLE from the control groups, but not between each other. No reference was found in the literature on such association of the presence of corkscrew capillaries and lupus.

In the present study, the parameter nailfold bleeding besides separating the SLE and the CCLE from the control group (p=0.004 and p=0.001, respectively) (Table 8), was also predictive of CCLE (odds ratio of 5.6520) (Table 9). Previous studies also reported higher frequency of nailfold bleeding in SLE patients than in normal subjects.22,29

Andrade et al.3 inferred that the occurrence of micropetechiae of focal distribution was related to everyday microtrauma that may occur in healthy individuals. They also stated that because it is a dynamic phenomenon, agreement may be low in two consecutive readings (72%) with variable intervals from weeks to months. They also observed that of 112 healthy subjects with more than three micropetechiae at capillaroscopy, 106 had clustered lesions, and only six had disseminated distribution.3

The findings of the present study regarding the CCLE group may perhaps be explained by the fact that many patients of this group had often times, in addition to localized cutaneous LE lesions, disseminated skin lesions aside from presenting arthralgia or arthritis, although not fulfilling the ARA criteria for SLE

 

CONCLUSION

Capillaroscopy proved to be useful when applied in clinical practice, and that patients with specific capillaroscopic changes have higher probability of having lupus erythematosus, and the independent predictive variables were meandering capillaries for SLE, and ectatic capillaries and nailfold bleeding for CCLE. It was also concluded that the capillaroscopic variables were not useful for discriminating the groups with CCLE from SLE between each other.

 

ACKNOWLEDGEMENT

To Capes for financial support.

 

REFERENCES

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9. Studer A, Hunziker T, Lutolf O, Schmidli J, Chen D, Mahler F. Quantitative nailfold capillary microscopy in cutaneous and systemic lupus erythematous and localized and systemic scleroderma. J Am Acad Dermatol. 1991;24:941-5.        [ Links ]

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16. Cutolo M, Pizzorni C, Tuccio M, Burroni A, Craviotto C, Basso M, et al. Nailfold videocapillaroscopic patterns and serum autoantibodies in systemic sclerosis. Rheumatology. 2004;43:719-26.        [ Links ]

17. Caspary L, Schmees C, Schoetensack I, Hartung K, Stannat S, Deicher H, et al. Alterations of the nail fold capillary morphology associated with Raynaud phenomenon in patients with systemic lupus erythem atosus. J Rheumatol. 1991;18:559-66.        [ Links ]

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19. Kabasakal Y, Elvins DM, Ring EFJ, MCHugh NJ. Quantitative nailfold capillaroscopy findings in a population with connective tissue disease and in normal healthy controls. Ann Rheum Dis.1996;55:507-12.        [ Links ]

20. Ohtsuka T. Nailfold capillary abnormalities in patients with Sjögren's syndrome and systemic lupus erythematosus. Br J Dermatol. 1997;136:94-6.        [ Links ]

21. Ohtsuka T. The relation between nailfold bleeding and capillary microscopic abnormality in patients with con nective tissue diseases. Intern J Dermatol.1998;37:23-6.        [ Links ]

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23. Furtado RNV, Pucinelli MLC, Cristo VV, Andrade LEC, Sato EI. Scleroderma-like nailfold capillaroscopic abnor malities are associated with anti-U1-RNP antibodies and Raynaud’s phenomenon in SLE patients. Lupus. 2002;11:35-41.        [ Links ]

24. Sontheimer RD. A portable digital microphotography unit for rapid documentation of periungual nailfold capillary changes in autoimmune connective tissue dis eases. `J Rheumatol. 2004;31:539-44.        [ Links ]

25. Bergman R, Sharony L, Schapira D, Nahir MA, Balbir- Gurman A. The handheld dermatoscope as a nail-fold capillaroscopic instrument. Arch Dermatol. 2003; 139:1027-30.        [ Links ]

26. Andrade LEC. Capilaroscopia periungueal. Estudo da metodologia e tentativa de padronização da normalidade para a população brasileira [tese]. São Paulo: Escola Paulista de Medicina; 1987.        [ Links ]

27. Ercole LP. Capilaroscopia periungueal. Valor prático no diagnóstico das doenças do tecido conjuntivo: artrite reumatóide, lúpus eritematoso sistêmico, esclerodermia e dermatomiosite. Rev Bras Reumatol. 1994;34:289-97.        [ Links ]

28. Dancour MA, Vaz JL, Bottino DA, Bouskela E. Nailfold videocapillaroscopy in patients with systemic lupus erythematosus. Rheumatol Int. 2006;26:633–7.        [ Links ]

29. Riccieri V, Spadaro A, Ceccarelli F, Scrivo R, Germano V, Valesini G. Nailfold capillaroscopy changes in systemic lupus erythematosus: correlations with disease activity and autoantibody profile. Lupus. 2005;14:521-5.        [ Links ]

 

 

Mailing address:
Anamaria da Silva Facina
R. Estado de Israel, 465, Apt 111 - Vila Clementino
04022-001 São Paulo - SP
Tel.: (11) 5084-2246 / (11) 9463-3040
Fax: (11) 5575-7200
E-mail: dermatologista@hotmail.com

The authors declare no conflict of interts

Received on Dec. 02 of 2005.
Approved by the Consultive Council and accepted for publication on Nov. 19 of 2006.

 

 

* Study carried out at the Universidade Federal de São Paulo, Department of Dermatology.