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Revista Española de Enfermedades Digestivas

versión impresa ISSN 1130-0108

Rev. esp. enferm. dig. vol.107 no.9 Madrid sep. 2015

 

LETTERS TO THE EDITOR

 

Pitavastatin: other statin to be used and monitored

Pitavastatina: otra estatina a emplear y vigilar

 

 


Key words: Pitavastatin. Adverse drug events. Liver toxicity, Statin.

Palabras clave: Pitavastatina. Reacción adversa. Hepatotoxicidad. Estatina.


 

Dear Editor,

After having read the interesting original document recently published in The Spanish Journal of Gastroenterology "Hepatotoxicity associated with statin use: Analysis of the cases included in the Spanish Hepatotoxicity Registry" (1) we would like to communicate the following clinical case:

A 48-years-old male came to the hospital last April 2013 due to intense asthenia, weight loss and diarrhea. In his medical history, special note was made to his obesity, smoking, moderate alcohol intake, high blood pressure, endogenous depression, dyslipidemia and acute myocardial infarction. His daily treatment consisted of escitalopram 10 mg, alprazolam 0.5 mg three times a day, and since four months ago pitavastatin 2 mg, atenolol 50mg and aspirin 100 mg once daily. Neither herbal products nor hepatotoxic substances were taken. At the hospital admission, his vital signs and physical examination were normal. The complete blood count, blood clotting and CPK tests were normal. Liver biochemistry showed a cholestatic pattern. A former liver biochemistry made four months earlier was also normal. Autoimmunity tests (autoantibodies and immunoglobulin values) and serology tests for HBV, HCV, EBV and CMV were negative. Stool test, ileocolonoscopy, abdominal ultrasonography and magnetic resonance cholangiography were also normal. Symptoms and liver biochemistry normalized progressively over 6days after hospital admission. Twenty four hours after discharge, a control blood test showed an increase in ALT, AST and alkaline phosphatase (AF) once he restarted home intake of pitavastatin, which had been interrupted during his hospital admission (Fig.1). Pitavastatin was finally replaced by simvastatin 20 mg once daily. Since then, the liver biochemistry has shown and maintained normal values.

 

 

Pitavastatin was marketed in Spain in 2011, and it is the 8th available statin in tablets of 1, 2 and 4 mg. By August 2012, there was no cases reported to the Spanish Hepatotoxicity Registry probably due to its recently marketing and safety profile (1). In a post-marketing surveillance performed in 20,000 Japanese patients taking 1 or 2 mg of pitavastatin for more than 100 weeks, 10.4% of them had some adverse drug event, only 1% was considered severe and 7% of them discontinued the treatment. The most common biochemistry abnormalities were CPK increase in 7.2% of patients, AST increase in 1.8%, ALT increasein 1.5% and GGT increase in 1% of patients (2). The pitavastatin metabolism, independently of the cytochrome P450, is one of the pitavastatin advantages versus other statins, making pitavastatin safer in terms of drug-drug interaction, but this is not unique to pitavastatin (3,4).

Statins are safe and probably more beneficial for patients with liver diseases (5) but a reasonable risk management plan seems to be needed, mainly in the post-marketing period as for any drug. Registries of Adverse Drug or other substances Reactions as far as a regular publication of data are needed for a safe medical practice (1,6).

 

Natalia Mora-Cuadrado, Román Santana-Lora, Luis Fernández-Salazar
and José Manuel González-Hernández

Gastroenterology Department. Universitary Clinic Hospital. Valladolid.
Primary Health Care Area, Valladolid. Valladolid, Spain

 

References

1. Perdices EV, Medina-Caliz I, Hernando S, et al. Hepatotoxicity associated with statin use: Analysis of the cases included in the Spanish Hepatotoxicity Registry. Rev Esp Enferm Dig 2014;106: 246-54.         [ Links ]

2. Teramoto T. Pitavastatin: Clinical effects from the LIVES Study. Atheroscler Suppl 2011;12:285-8. DOI: 10.1016/S1567-5688(11)70888-1.         [ Links ]

3. Wensel TM, Waldrop BA, Wensel B. Pitavastatin: A new HMG-CoA reductase inhibitor. Ann Pharmacother 2010;44:507-14. DOI: 10.1345/aph.1M624.         [ Links ]

4. Corsini A, Ceska R. Drug-drug interactions with statins: will pitavastatin overcome the statins' Achilles' heel? Curr Res Med Opin 2011;27:1551-62.         [ Links ]

5. Kalaitzakis E, Bjornsson ES. Use of statins in patients with liver disease. Minerva Gastroenterol Dietol 2014;60:15-24.         [ Links ]

6. Garcia-Cortes M, Borraz Y, Lucena MI, et al. Liver injury induced by "natural remedies": An analysis of cases submitted to the Spanish Liver Toxicity Registry. Rev Esp Enferm Dig 2008;100:688-95.         [ Links ]

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