Czy proces zapalny odgrywa rolę w patogenezie obumierania tłuszczowatego?

Introduction

Necrobiosis lipoidica (NL) is a granulomatous skin disease of still unknown pathogenesis which usually appears in middle-aged women [1]. The NL more frequently is observed in diabetic patients, but it also may be accompanied by sarcoidosis, connective tissue diseases or inflammatory bowel diseases [2–4]. The NL association with diabetes mellitus is still controversial. Although up to 75% of patients with NL suffer from diabetes mellitus (DM), only 0.3–1% of diabetic patients present skin lesions of NL [5]. In the literature there are scarce data on the pathogenesis of necrobiosis lipoidica. Microangiopathy is considered as one of the most important phenomena in NL. Vascular endothelial growth factor (VEGF) is one of the most important factors involved in the initial process of angiogenesis [6, 7]. Effector cells for VEGF are endothelial cells. The VEGF is a mitogenic factor for these cells and promotes their proliferation. Their excessive proliferation is one of the phenomena involved in microangiopathy. Endothelial dysfunction is also due to increased production of the vasoconstrictor and pro-inflammatory peptide, i.e. endothelin-1. Some authors also suggest immunological disturbances leading to deposits of immunoglobulins in skin vessels and disturbances in platelet aggregation [8–12]. Recent literature data show that tumor necrosis factor α (TNF-α) inhibitors such as adalimumab, infliximab or etanercept are beneficial in treatment of recalcitrant cases of necrobiosis lipoidica, which probably results from the fact that TNF-α plays an important role in development of inflammation and granulomas in the course of NL [13–16].

Objective

The observations and suggestions of disturbed angiogenesis leading to microangiopathy in the course of NL were the reason why we decided to assess serum level of VEGF, endothelin and TNF-α in NL patients.

Material and methods

The study group consisted of 17 patients with NL (13 women, 4 men, mean age 48.22 ±15.99 years), 37 patients with diabetes mellitus (10 women, 27 men, mean age 52.11 ±17.41) and 23 healthy volunteers (10 women, 13 men, mean age 44.13 ±9.33 years) who served as the control group. Four patients with NL suffered additionally from DM type II.
Serum samples obtained from all subjects were stored at a temperature of –25°C until further analysis.
Serum concentrations of TNF-α, VEGF and endothelin-1 were examined with the ELISA test according to the manufacturer’s procedure. For TNF-α and VEGF we used assays obtained from R&D Systems Quantikine (Minneapolis, USA), and for endothelin-1 assay from IBL International GmbH (Hamburg, Germany).

Statistical analysis

For statistical analysis the Mann-Whitney test, 2 test with Yates’ correlation and Spearman correlation were used. Statistical significance was found when p < 0.05.

Results

In the NL group mean serum concentration of TNF-α was 1.421 pg/ml (min. 0.001, max. 3.060 pg/ml) and of VEGF 286.533 pg/ml (min. 98.875 pg/ml, max. 555.524 pg/ml). Maximal concentration of endothelin-1 in these patients was 0.804 fmol/ml, although in most patients (16/17) its concentration was under the examined values.
In diabetic patients mean serum concentration of TNF-α was 1.998 pg/ml (min. 0.001, max. 9.570 pg/ml) and of VEGF 294.697 pg/ml (min. 13.841 pg/ml, max. 794.584 pg/ml). Maximal serum concentration of endothelin-1 was 10.201 fmol/ml, and in most examined patients (31/38) its values were under the diagnostic level.
In the control group mean serum concentration of TNF-α was 0.580 pg/ml (min. 0.000, max. 2.490 pg/ml) and of VEGF 241.451 pg/ml (min. 50.360 pg/ml, max. 463.830 pg/ml). Maximal serum concentration of endothelin-1 was 0.964 fmol/ml, and in 11 out of examined patients its values were not diagnostic. Detailed values of serum concentrations of TNF-α and VEGF are shown in Table I.
Analyzing VEGF serum concentration we found no differences between the examined groups, i.e. either between NL patients and controls, or between diabetic patients and controls, or between NL patients and diabetic ones (p > 0.05 for all comparisons).
Significant differences were found in mean serum concentration of TNF-α between the controls and other examined groups. The TNF-α concentration in the controls was statistically lower when compared to the NL patients and diabetic patients (p < 0.05 for all comparisons). There were no significant differences in TNF-α serum values between NL and diabetic groups (p > 0.05) (Table II).
As endothelin-1 serum values were undetectable in most cases it was impossible to perform statistical analysis. However, we found significant differences in frequency of detectable endothelin 1 values between the NL group and controls. Statistically more frequently these values were found in the controls than in the NL group (p < 0.05) (Fig. 1.).

Discussion

Necrobiosis lipoidica is a rare granulomatous skin disease of unknown etiology. In some cases it coexists with diabetes mellitus. In the available literature there are only scarce data on its pathogenesis. According to our knowledge there are no data on the serum levels of proinflammatory cytokines and factors involved in angiogenesis in patients with NL. Thus, observations made in our study are original. The TNF-α increases both proliferation and apoptosis in multiple cells and in this way it regulates their number [17]. This protein plays many important roles in our organism and is involved in the development of various diseases, including psoriasis, psoriatic arthritis, rheumatoid arthritis, Crohn’s disease and diabetes mellitus type II [18]. Beneficial effects of TNF-α inhibitors were observed in most of these diseases, which confirms its crucial role in their pathogenesis [19].
We decided to assess TNF-α serum concentration in NL patients due to recent literature data indicating high effectiveness of TNF-α inhibitors (adalimumab, etanercept or infliximab) in NL patients. The authors of these publications suggest that it may result from an important role of TNF-α in generation of granulomas and pathogenesis of NL [13–16].
Literature data unequivocally prove the role of increased serum levels of TNF-α and inflammation in the development of diabetes mellitus [20]. In our study we revealed that concentration of this protein was significantly higher in NL and diabetic patients when compared to the controls, but we found no differences between the two examined patient groups. We should highlight that in the available literature there are no papers on TNF-α concentrations in NL, so our observation is the first one; however, because of the relatively small group of patients it requires further investigations.
As microangiopathy and disturbances in angiogenesis are considered as processes involved in NL [21], we also decided to examine serum concentrations of VEGF and endothelin-1 in the patients with this disease. In NL patients the VEGF serum level did not significantly differ when compared to the controls and diabetic patients. These results may indicate that an imbalance in angiogenesis in the course of NL takes place only locally and it has no systemic effect which is observed in the patients with malignancies or rheumatoid arthritis. In the literature there are many papers reporting increased levels of VEGF in diabetic patients, especially with retinopathy [22]. Our negative observations may result from the fact that all our diabetic patients were under close diabetic control, and the retinopathy that occurred in 12 of them was in very early stages. Endothelin-1 serum level was not investigated in NL patients. The results of the studies in the group of diabetic patients with controlled disease revealed that its level was comparable to the control group and our results are in line with this observation. According to Ugurlu et al. [23] endothelin serum concentration cannot be used to assess local imbalance of angiogenesis.

Conclusions

Based on the obtained results we may assume that inflammation with enhanced synthesis of TNF-α in NL patients is the primary event in pathogenesis of the disease, with subsequent impairment of angiogenesis.

Acknowledgments

The study was supported by Medical University Research Project number 503/1-152-01/503-01.

References

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Otrzymano: 4 IV 2014 r.
Zaakceptowano: 12 V 2014 r.