Pioglitazone versus Rosiglitazone: Effects on Lipids, Lipoproteins, and Apolipoproteins in Head-to-Head Randomized Clinical Studies

المؤلفون المشاركون

Tan, Meng H.
Deeg, Mark A.

المصدر

PPAR Research

العدد

المجلد 2008، العدد 2008 (31 ديسمبر/كانون الأول 2008)، ص ص. 1-6، 6ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2008-07-16

دولة النشر

مصر

عدد الصفحات

6

التخصصات الرئيسية

الأحياء

الملخص EN

Peroxisome proliferator-activated receptors (PPARs) play an important role in regulating both glucose and lipid metabolism.

Agonists for both PPARγ and PPARγ have been used to treat dyslipidemia and hyperglycemia, respectively.

In addition to affecting glucose metabolism, PPARγ agonists also regulate lipid metabolism.

In this review, we will focus on the randomized clinical trials that directly compared the lipid effects of the thiazolidinedione class of PPARγ agonists, pioglitazone and rosiglitazone, head-to-head either as monotherapy or in combination with other lipid-altering or glucose-lowering agents

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Deeg, Mark A.& Tan, Meng H.. 2008. Pioglitazone versus Rosiglitazone: Effects on Lipids, Lipoproteins, and Apolipoproteins in Head-to-Head Randomized Clinical Studies. PPAR Research،Vol. 2008, no. 2008, pp.1-6.
https://search.emarefa.net/detail/BIM-988211

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Deeg, Mark A.& Tan, Meng H.. Pioglitazone versus Rosiglitazone: Effects on Lipids, Lipoproteins, and Apolipoproteins in Head-to-Head Randomized Clinical Studies. PPAR Research No. 2008 (2008), pp.1-6.
https://search.emarefa.net/detail/BIM-988211

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Deeg, Mark A.& Tan, Meng H.. Pioglitazone versus Rosiglitazone: Effects on Lipids, Lipoproteins, and Apolipoproteins in Head-to-Head Randomized Clinical Studies. PPAR Research. 2008. Vol. 2008, no. 2008, pp.1-6.
https://search.emarefa.net/detail/BIM-988211

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-988211