The Effect of Isotretinoin on Biotinidase Activity

Background: Among the reaction and effects of isotretinoin, mucocutaneous reactions, xerosis and erythema of the skin as well as elevation of liver enzymes and lipids except high density lipoprotein have been reported. Objective: Since biotinidase is mainly produced in the liver and partial biotinidase deficiency causes dermatological manifestations, seborrheic dermatitis, alopecia etc., isotretinoin side effects in relation to biotinidase activity were studied. Methods: Forty-two (n = 42) patients with severe cystic acne had liver function tests, lipid estimations, serum biotin as well as biotinidase activity evaluations before (value 1) and on the 30th day (value 2) of treatment with isotretinoin monotherapy (Roaccutane 0.5 mg/kg/24 h). The same laboratory tests were evaluated in 50 controls only once. Moreover, the effect of isotretinoin on a known plasma biotinidase activity was evaluated after incubation in vitro with various concentrations of the drug. Results: A statistically significant elevation of liver enzymes and lipids, except high density lipoprotein, was observed at the end of this study. On the contrary, biotinidase activity was found to be significantly decreased as compared to the initial values (value 1 = 4.70 ± 0.89 nmol/min/l, value 2 = 2.50 ± 0.8 nmol/min/l, p < 0.001) and to controls (5.2 ± 0.9 nmol/min/l vs. value 2 = 2.50 ± 0.8 nmol/min/l, p < 0.001). Additionally, biotin levels showed no significant alterations and the in vitro incubation of the enzyme with various concentrations of the drug exhibited no effect on its activity. Conclusion: It is suggested that isotretinoin isomers-metabolites act in the liver, resulting in low biotinidase activity.

[1]  J. Saurat Systemic retinoids. What's new? , 1998, Dermatologic clinics.

[2]  R. Marks,et al.  Retinoids: A Clinician's Guide , 1997 .

[3]  E. Papakonstantinou,et al.  Plasma biotinidase levels in patients with cystic acne under isotretinoin treatment , 1997 .

[4]  D. Kochhar,et al.  Tretinoin: a review of the nonclinical developmental toxicology experience. , 1997, Journal of the American Academy of Dermatology.

[5]  H J Clewell,et al.  A physiologically based pharmacokinetic model for retinoic acid and its metabolites. , 1997, Journal of the American Academy of Dermatology.

[6]  L. Leondiadis,et al.  Indirect enzyme-linked method for determining biotin in human serum. , 1997, Journal of immunoassay.

[7]  W. Meigel How safe is oral isotretinoin? , 1997, Dermatology.

[8]  M. James Isotretinoin for severe acne , 1996, The Lancet.

[9]  S. Holmes,et al.  Isotretinoin and skin fragility , 1995, The British journal of dermatology.

[10]  R. Marks,et al.  Adverse Reactions to Oral Retinoids , 1993, Drug safety.

[11]  Aileen E M Taylor,et al.  Fatty liver following isotretinoin therapy , 1991, The British journal of dermatology.

[12]  B. Wolf,et al.  Biotinidase Deficiency a , 1985, Advances in pediatrics.

[13]  B. Wolf,et al.  Low biotinidase activities in the sera of patients with impaired liver function: evidence that the liver is the source of serum biotinidase. , 1990, Clinica chimica acta; international journal of clinical chemistry.

[14]  M. Blitzer,et al.  Partial biotinidase deficiency: clinical and biochemical features. , 1990, The Journal of pediatrics.

[15]  B. Wolf,et al.  Biotinidase—A Possible Mechanism for the Recycling of Biotin , 1985 .

[16]  S. Wallace Biotinidase deficiency: presymptomatic treatment. , 1985, Archives of disease in childhood.