- Short paper
- Open Access
Positive pleiotropic effects of HMG-CoA reductase inhibitor on vitiligo
© Noël et al; licensee BioMed Central Ltd. 2004
- Received: 09 February 2004
- Accepted: 10 May 2004
- Published: 10 May 2004
HMG-CoA reductase inhibitors (statins) are commonly used in medicine to control blood lipid disorder. Large clinical trials have demonstrated that statins greatly reduces cardiovascular-related morbidity and mortality in patients with and without coronary artery disease. Also, the use of HMG-CoA reductase inhibitors has been reported to have immunosuppressive effects.
We describe an unusual case of regression of vitiligo in a patient treated with high dose simvastatin. The relation between simvastatin and regression of vitiligo in this case report may be related to the autoimmune pathophysiology of the disease.
This unexpected beneficial impact provides another scientific credence to the hypothesis that immune mechanisms play a role in the development of vitiligo and that the use of statins as immuno-modulator could be of use not only for treatment relative to organ transplant but in other pathologies such as vitiligo.
- Atrophic Gastritis
- Vitiligo Patient
A 55 year-old man was recruited in a clinical trial where medications have to be weaned. He had suffered from previous myocardial infarcts in 1988, 1992 and 1999. The subject is an ex smoker and is intolerant to aspirin and non-steroidal anti-inflammatory medication since the age of 28 years. He has also been diagnosed with vitiligo since he was 31 year old. Skin depigmentation has been mostly present on the face, chest and hands areas. Numerous treatment have been tried to alleviate the vitiligo without success. Strangely, the patient mentioned that signs of vitiligo was somewhat alleviated after he was given an HMG-CoA reductase (simvastatin) to control high blood cholesterol levels.
The subject had been treated with metoprolol (Lopressor®; Novartis Pharmaceutical, New York, USA) 50 mg per os BID and clopidogrel (Plavix®; Bristol-Myers Squibb, New-York, USA) 75 mg per os OD since October 1999 as well as simvastatin (Zocor®; Merck Frosst, New Jersey, USA) 80 mg at bedtime since September 2000.
Except for mild skin signs of vitiligo, mainly in the face and hands, physical examination upon entry in the study was normal with blood pressure at 120/80 mmHg and elevated low-density lipoprotein (LDL) cholesterol of 4.37 mmol/L, high-density lipoprotein (HDL) of 1.2 mmol/L and triglycerides (TG) concentrations at 1.9 mmol/L.
Vitiligo is an acquired skin depigmenting disorder characterized by the loss of melanocytes, exocrine cells, from basal layer of the epidermal and the matrix portion of the hair bulb. It results in well-defined white patches, often symmetrically distributed. Vitiligo occurs worldwide in about 1% of the population, mostly man between the age of 10–30 years regardless of race, but more troublesome in dark skin individuals. So far, the cause of vitiligo has remained unknown but might involve genetic factors, autoimmunity (lopecia areata, thyroid disorders, Addison's adrenal disease, atrophic gastritis, pernicious anaemia, and diabetes), toxic metabolites and/or a higher vulnerability of melanocytes .
HMG-CoA reductase inhibitors (statins) are commonly used in medicine to control blood lipid disorder. Large clinical trials have demonstrated that statins greatly reduces cardiovascular-related morbidity and mortality in patients with and without coronary artery disease [2–4]. After its ingestion, the inactive lactone is hydrolysed in β-hydroxyl acid and inhibits the hydroxy-3 methyl-3 glutaryl coenzyme A (HMG-CoA) reductase . The role of the regulatory enzyme HMG-CoA essentially limits the mevalonate pathway through which cells synthesize cholesterol. Although the pharmacokinetics and the metabolic pathway of simvastatin are complex, it basically reduces the synthesis of LDL cholesterol by the liver and other cells and increases its catabolism .
The relation between simvastatin and regression of vitiligo in this case report may be related to the autoimmune pathophysiology of the disease. This hypothesis is supported by the frequent association of vitiligo with autoimmune diseases  and studies demonstrated that most vitiligo patients have antibodies against melanocytes . Although the application of the following animal model to the human disorder remains to be better establish, the Smyth line chicken model who depicts spontaneous postnatal expression of vitiligo showed an increase in T cells in the feather pulp and circulating inflammatory leukocytes . In human, circulating antibodies and T lymphocytes which react against melanocyte antigens are present in the sera of patient with vitiligo  and higher proportion of activated peripheral T cells, as determined by the expression of HLA-DR, has also been found in patients with vitiligo compared to healthy individual . In a study of 49 biopsies from the margin of depigmented cutaneous lesions, the expression of Major Histocompatibility Complex class II (MHC-II) antigens demonstrates activation of the infiltrating T cells . Lesional T cells rather than circulatory anti-melanocytic antibody may also be responsible for the autoimmune patchy destruction on cutaneous melanocytes in vitiligo . When compared to healthy individuals, a significant proportion of patients with vitiligo had circulating antibodies and T lymphocytes, which react against melanocytes antigen present in the sera . Indeed, it has been reported that normal melanocytes are capable of presenting antigenic peptide fragment to well-defined proliferative cytotoxic T cells in a MHC class II-restricted manner . Therefore, since these molecules have important roles in normal antigen presentation and the activation of helper T lymphocytes, their expression by the melanocytes may contribute to the abnormal cellular immune response seen in vitiligo. Kawakami et al.  further confirmed that T cells specific response for melanoma cells and melanocytes appear to be involved in the rejection of melanoma tumour as well as in the development of autoimmune reaction of patient with vitiligo. Since a number of reasonably effective therapies for vitiligo (psoralen with ultraviolet A radiation, topical corticosteroids and topical cytotoxic drugs) are immunosuppressive in their mode of action, animal models of the disease and the association of vitiligo with MHC antigens, we reasonably speculate that immune mechanisms may play a major role in the development of vitiligo.
Interestingly, the use of lipid lowering agent, specifically HMG-CoA reductase inhibitors, has been reported to have immunosuppressive effects in a study of heart transplant recipients . The drug-induced reduction of LDL cholesterol may lead to more free cyclosporin in the blood where its immunosuppressive effect is due to blockade of interleukin-2 synthesis in activated T lymphocytes . Kwak et al.  showed that statins act as direct inhibitors of the induction of MHC-II expression by interferon-gamma (IFN-γ) and thus as repressor of MHC-II mediated T-lymphocytes activation in human endothelial cells. Using RNAse protection assay and flow cytometry, it was observed that simvastatin, in a dose dependent fashion, reduced IFN-γ induced MHC-II expression (mRNA and protein) through actions on the CIITA promoter I . It is important to note that the subject of this case report was on a high dose of simvastatin (80 mg OD). Regulation of the expression of MHC-II genes is highly complex, and this tight control directly affects the T-lymphocyte activation and thus the modulation of the immune response. Consequently, by repressing the induction of MHC-II, and subsequent T lymphocytes activation, the action of HMG-CoA reductase inhibitor, mostly used as lowering blood cholesterol agent, may provide new type of immuno modulation as suggested by our case report and literature on organ transplant recipients.
We describe an unusual case of regression of vitiligo in a patient treated with high dose simvastatin. This unexpected beneficial impact provides another scientific credence to the hypothesis that immune mechanisms play a role in the development of vitiligo and that the use of statins as immuno-modulator could be of use not only for treatment relative to organ transplant but in other pathologies such as vitiligo. However, even though reduced chronic rejection and decreased graft arteriosclerosis was seen in rats recipients of heterotopic heart transplant [18, 19] and a reduction of acute rejection reactions was documented in pravastatin-treated human subjects compared with controls receiving only prednisone, azathioprine and cyclosporine , caution should be use when associating statins in purely immune-related pathologies. Other clinical trials have failed to demonstrate clinical benefits of statins as immuno-modulators in transplant patients . Therefore, a prospective study should be initiated to try to answer the hypothesis associating the use of statins as an immuno-modulator for the treatment of vitiligo.
The authors want to express their gratitude to Dr Jean Davignon for his scientific input. Written consent was obtained from the patient for publication of the study.
- Kemp EH, Waterman EA, Weetman AP: Autoimmune aspects of vitiligo. Autoimmunity. 2001, 34: 65-77.View ArticlePubMedGoogle Scholar
- MRC/BHF Heart Protection Study of cholesterol lowering with simvastatin in 20, 536 high-risk individuals: a randomised placebo-controlled trial. Lancet. 2002, 360: 7-22.Google Scholar
- LaRosa JC, He J, Vupputuri S: Effect of statins on risk of coronary disease: a meta-analysis of randomized controlled trials. JAMA. 1999, 282: 2340-6. 10.1001/jama.282.24.2340View ArticlePubMedGoogle Scholar
- Maron DJ, Fazio S, Linton MF: Current perspectives on statins. Circulation. 2000, 101: 207-13.View ArticlePubMedGoogle Scholar
- Palinski W, Tsimikas S: Immunomodulatory effects of statins: mechanisms and potential impact on arteriosclerosis. J Am Soc Nephrol. 2002, 13: 1673-81.View ArticlePubMedGoogle Scholar
- Macaron C, Winter RJ, Traisman HS, Kahan BD, Lasser AE, Green OC: Vitiligo and juvenile diabetes mellitus. Arch Dermatol. 1977, 113: 1515-7. 10.1001/archderm.113.11.1515View ArticlePubMedGoogle Scholar
- Naughton GK, Eisinger M, Bystryn JC: Antibodies to normal human melanocytes in vitiligo. J Exp Med. 1983, 158: 246-51.View ArticlePubMedGoogle Scholar
- Smyth JR, McNeil M: Alopecia areata and universalis in the Smyth chicken model for spontaneous autoimmune vitiligo. J Investig Dermatol Symp Proc. 1999, 4: 211-5.View ArticlePubMedGoogle Scholar
- al-Fouzan A, al-Arbash M, Fouad F, Kaaba SA, Mousa MA, al-Harbi SA: Study of HLA class I/IL and T lymphocyte subsets in Kuwaiti vitiligo patients. Eur J Immunogenet. 1995, 22: 209-13.View ArticlePubMedGoogle Scholar
- Abdel-Naser MB, Ludwig WD, Gollnick H, Orfanos CE: Nonsegmental vitiligo: decrease of the CD45RA+ T-cell subset and evidence for peripheral T-cell activation. Int J Dermatol. 1992, 31: 321-6.View ArticlePubMedGoogle Scholar
- Badri AM, Todd PM, Garioch JJ, Gudgeon JE, Stewart DG, Goudie RB: An immunohistological study of cutaneous lymphocytes in vitiligo. J Pathol. 1993, 170: 149-55.View ArticlePubMedGoogle Scholar
- Le Poole IC, Mutis T, van den Wijngaard RM, Westerhof W, Ottenhoff T, de Vries RR, Das PK: A novel, antigen-presenting function of melanocytes and its possible relationship to hypopigmentary disorders. J Immunol. 1993, 151: 7284-92.PubMedGoogle Scholar
- Kawakami Y, Suzuki Y, Shofuda T, Kiniwa Y, Inozume T, Dan K, Sakurai T, Fujita T: T cell immune responses against melanoma and melanocytes in cancer and autoimmunity. Pigment Cell Res. 2000, 13 Suppl 8: 163-9.View ArticlePubMedGoogle Scholar
- Kobashigawa JA: Statins as immunosuppressive agents. Liver Transpl. 2001, 7: 559-61. 10.1053/jlts.2001.0070559View ArticlePubMedGoogle Scholar
- Wenke K, Meiser B, Thiery J, Nagel D, von Scheidt W, Steinbeck G, Seidel D, Reichart B: Simvastatin reduces graft vessel disease and mortality after heart transplantation: a four-year randomized trial. Circulation. 1997, 96: 1398-402.View ArticlePubMedGoogle Scholar
- Kwak B, Mulhaupt F, Myit S, Mach F: Statins as a newly recognized type of immunomodulator. Nat Med. 2000, 6: 1399-402. 10.1038/82219View ArticlePubMedGoogle Scholar
- Kwak B, Mulhaupt F, Veillard N, Pelli G, Mach F: The HMG-CoA reductase inhibitor simvastatin inhibits IFN-gamma induced MHC class II expression in human vascular endothelial cells. Swiss Med Wkly. 2001, 131: 41-6.PubMedGoogle Scholar
- Maggard MA, Ke B, Wang T, Kaldas F, Seu P, Busuttil RW, Imagawa DK: Effects of pravastatin on chronic rejection of rat cardiac allografts. Transplantation. 1998, 65: 149-55.View ArticlePubMedGoogle Scholar
- Meiser BM, Wenke K, Thiery J, Wolf S, Devens C, Seidel D, Hammer C, Billingham ME, Reichart B: Simvastatin decreases accelerated graft vessel disease after heart transplantation in an animal model. Transplant Proc. 1993, 25: 2077-9.PubMedGoogle Scholar
- Kobashigawa JA, Katznelson S, Laks H, Johnson JA, Yeatman L, Wang XM, Chia D, Terasaki PI, Sabad A, Cogert GA, et a.l.: Effect of pravastatin on outcomes after cardiac transplantation. N Engl J Med. 1995, 333: 621-7. 10.1056/NEJM199509073331003View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.