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CORRESPONDENCES |
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| Year : 2018 | Volume
: 63
| Issue : 3 | Page : 268-270 |
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| ANCA-associated vasculitis in a case of congenital leptin deficiency |
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Atiya Yaseen, Shagufta Rather, Faizan Yunus, Iffat Hassan
Department of Dermatology, Venereology and Leprosy, Government Medical College, University of Kashmir, Srinagar, Jammu and Kashmir, India
| Date of Web Publication | 21-May-2018 |
Correspondence Address:
Dr. Atiya Yaseen
Department of Dermatology, Venereology and Leprosy, Government Medical College, University of Kashmir, Srinagar, Jammu and Kashmir
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/ijd.IJD_52_18
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How to cite this article:
Yaseen A, Rather S, Yunus F, Hassan I. ANCA-associated vasculitis in a case of congenital leptin deficiency. Indian J Dermatol 2018;63:268-70 |
How to cite this URL:
Yaseen A, Rather S, Yunus F, Hassan I. ANCA-associated vasculitis in a case of congenital leptin deficiency. Indian J Dermatol [serial online] 2018 [cited 2022 Jun 29];63:268-70. Available from: https://www.e-ijd.org/text.asp?2018/63/3/268/232726 |
Sir,
Leptin (Greek “leptos” = “thin”) is a hormone that helps to regulate metabolism by inhibiting food intake and promoting energy expenditure. In addition to being a key factor in regulating body weight, leptin plays an important role in the regulation of immune system and various other physiological responses.[1] Congenital leptin deficiency, caused by LEP gene mutation and inherited as an autosomal recessive disorder, presents with severe obesity early in life, following a normal birth weight. Affected individuals suffer from hypogonadotropic-hypogonadism, which if untreated leads to delayed puberty and infertility. This form of leptin deficiency is extremely rare with less than 30 patients reported in the literature so far.[2] Leptin deficiency is also suspected to be involved in the pathophysiology of ANCA-associated vasculitis (AAV). Kümpers et al . found that leptin levels are negatively correlated with the disease activity.[3] Further studies are needed to gauge the role of leptin as a potential therapeutic target in the treatment of autoimmune disorders.
A 10-year-old girl, a product of second degree consanguineous marriage, first in birth order, presented with multiple painful, red, raised lesions on the trunk and extremities since 5 days. Examination revealed palpable purpura and ulcerations of variable sizes and shapes over the legs, arms, forearms, dorsa of hands and feet, chest, and abdomen [Figure 1] and [Figure 2]. There was predominant extensor distribution with koebnerization appreciated at places. Mucosae were not involved. General physical examination revealed moon facies [Figure 3], morbid obesity with a weight of 90 kg, height 137 cm, and a BMI of 47.95. She had difficulty in walking due to excessive weight. Acanthosis nigricans was also noted in the axilla and neck [Figure 4]. Rest of the systemic examination was within normal limits. Investigations revealed neutrophilic leukocytosis (white blood cell count –19,950/cumm; N = 80.5, L = 17, M = 5.9, E = 01). Liver and renal parameters, routine and 24 h urinary examination were unremarkable. Rheumatoid factor, hepatitis B surface antigen, anti-HCV antibodies, HIV ELISA, antinuclear antibody, lupus anticoagulant, and cryoglobulins were also negative. Fasting plasma glucose and insulin levels were normal. Triglycerides were marginally raised. cANCA was positive, and skin biopsy was suggestive of leukocytoclastic vasculitis with neutrophilic infiltrate and nuclear debris around vessel walls [Figure 5]. | Figure 5: Leukocytoclastic vasculitis with neutrophilic infiltrate and nuclear debris (arrows) (H and E, ×00)
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According to her parents, the patient had uneventful antenatal and perinatal period and was apparently normal till the age of 6 months when they suspected excessive eating and weight gain by the child. The consultation was sought for the same, and the child was evaluated for leptin deficiency in view of the early onset obesity. Her anthropometric measurements at that time were: weight 10.75 kg (>95th percentile), height 64.4 cm (between 25th and 50th percentile), and BMI 25.84 kg/m2. Baseline investigations, echocardiography, serum cortisol level, and thyroid function test did not reveal any abnormality. Serum leptin levels were inappropriately low 0.8 ng/ml (1.7–10.9 ng/ml). The patient was diagnosed as a case of leptin deficiency but was subsequently lost to follow-up till date when the patient reported to us with the purpuric rash. During the intervening period, the patient had normal developmental milestones with no mental retardation or language deficit.
There was also history of excessive weight gain in her younger 9-month-old male sibling [Figure 6]. He likewise was of normal weight at birth but was presently obese. His weight was 9 kg (>90th centile), length was 64 cm (10th centile), and BMI was 21.97 kg/m2. On evaluation, he too was diagnosed as having leptin deficiency (Serum leptin levels: 1.1 ng/ml). Due to unavailability at our center, genetic analysis could not be performed in either of the two cases.
The index case was treated with tapering doses of steroids and showed remarkable improvement of skin lesions. Endocrinology consultation was sought. She was advised leptin replacement therapy which could not be administered, as the patient could not afford the same.
Congenital leptin deficiency is one of the rare causes of early-onset obesity. It was first described in two cousins from an inbred Pakistani kindred by Montague et al .[4] Subsequent cases were reported by Farooqi et al ., Gibson et al ., Strobel et al . and Wabitsch et al .[5],[6],[7],[8] A homozygous frameshift or missense mutation in the LEP gene (7q31.3) results in the characteristic phenotype of severe hyperphagia and extreme obesity early in infancy. Administration of recombinant human leptin [recombinant methionyl human leptin (r-metHuLeptin)] has resulted in sustained positive results in this non-syndromic disorder of excessive weight gain. Active ANCA-associated vasculitis is associated with functionally defective regulatory T cells and consequently decreased levels of leptin. Kümpers et al . suggested that low levels of leptin may enhance the inflammatory process in disorders that involve innate immunity. Invasion and destruction of activated endothelium by primed neutrophils is a salient feature of vasculitis. Notably, leptin may partake in this process because microvascular endothelial cells and neutrophils both express the leptin receptor. It is thus conceivable that leptin attenuates the neutrophil chemotaxis in vasculitis. Further effects of leptin on microvascular endothelial cells include increased proliferation and inhibition of apoptosis. However, on the contrary, Yilmaz et al . have shown that Leptin level was higher in Takayasu arteritis patients than in healthy controls albeit the difference was not statistically significant.[9] Similarly, studies performed in other forms of systemic vasculitis (Henoch-Schönlein purpura and Behcet's disease) have shown increased levels of leptin during active disease periods.[10],[11] Whether leptin has a role in vasculitis or its altered levels in this disorder is a mere coincidental finding needs to be probed. Larger studies are required to consolidate this finding. Our case emphasizes the need for early detection of congenital leptin deficiency, which if misdiagnosed runs the risk of severe obesity-associated complications (especially type II diabetes).
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.
 References | |  |
| 1. | Zhang F, Basinski MB, Beals JM, Briggs SL, Churgay LM, Clawson DK, et al. Crystal structure of the obese protein leptin-E100. Nature 1997;387:206-9.  [ PUBMED] |
| 2. | Fatima W, Shahid A, Imran M, Manzoor J, Hasnain S, Rana S, et al. Leptin deficiency and leptin gene mutations in obese children from Pakistan. Int J Pediatr Obes 2011;6:419-27. [ PUBMED] |
| 3. | Kümpers P, Horn R, Brabant G, Woywodt A, Schiffer M, Haller H, et al. Serum leptin and ghrelin correlate with disease activity in ANCA-associated vasculitis. Rheumatology (Oxford) 2008;47:484-7. |
| 4. | Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, Wareham NJ, et al. Congenital leptin deficiency is associated with severe early-onset obesity in humans. Nature 1997;387:903-8. [ PUBMED] |
| 5. | Farooqi IS, Jebb SA, Langmack G, Lawrence E, Cheetham CH, Prentice AM, et al. Effects of recombinant leptin therapy in a child with congenital leptin deficiency. N Engl J Med 1999;341:879-84. [ PUBMED] |
| 6. | Gibson WT, Farooqi IS, Moreau M, DePaoli AM, Lawrence E, O'Rahilly S, et al. Congenital leptin deficiency due to homozygosity for the delta133G mutation: Report of another case and evaluation of response to four years of leptin therapy. J Clin Endocrinol Metab 2004;89:4821-6. |
| 7. | Strobel A, Issad T, Camoin L, Ozata M, Strosberg AD. A leptin missense mutation associated with hypogonadism and morbid obesity. Nat Genet 1998;18:213-5. [ PUBMED] |
| 8. | Wabitsch M, Funcke JB, Lennerz B, Kuhnle-Krahl U, Lahr G, Debatin KM, et al. Biologically inactive leptin and early-onset extreme obesity. N Engl J Med 2015;372:48-54. [ PUBMED] |
| 9. | Yilmaz H, Gerdan V, Kozaci D, Solmaz D, Akar S, Can G, et al. Ghrelin and adipokines as circulating markers of disease activity in patients with Takayasu arteritis. Arthritis Res Ther 2012;14:R272. [ PUBMED] |
| 10. | Aliyazicioglu Y, Ozkaya O, Yakut H, Islek I, Alvur M. Leptin levels in Henoch-Schönlein purpura. Clin Rheumatol 2007;26:371-5. [ PUBMED] |
| 11. | Evereklioglu C, Inalöz HS, Kirtak N, Doganay S, Bülbül M, Ozerol E, et al. Serum leptin concentration is increased in patients with Behçet's syndrome and is correlated with disease activity. Br J Dermatol 2002;147:331-6. |
[Figure 1], [Figure 2], [Figure 3], [Figure 4], [Figure 5], [Figure 6] |
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