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dc.contributor.authorSadighi, A
dc.contributor.authorSafa, J
dc.contributor.authorVatankhah, AM
dc.contributor.authorGhorashi, S
dc.contributor.authorAharilahagh, A
dc.contributor.authorDavari-Farid, S
dc.contributor.authorNezami-Nargabad, O
dc.contributor.authorNaghavi-Behzad, M
dc.contributor.authorPiri, R
dc.contributor.authorPishahang, P
dc.contributor.authorBabapoor-Farrokhran, S
dc.contributor.authorFakour, S
dc.contributor.authorGhodratnezhad-Azar, N
dc.date.accessioned2018-08-26T05:36:21Z
dc.date.available2018-08-26T05:36:21Z
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/39478
dc.description.abstractDiabetic nephropathy (DN) is characterized by albuminuria, hypertension, and a progressive decline in glomerular filtration rate. The 3-hydroxy-3-methylglutaryl coenzyme A is a well-known agent that is active in lowering total plasma and low-density lipoprotein cholesterol (LDL-C) levels in cases with hypercholesterolemia. Hence, in this study, proteinuria changes at the beginning and after the withdrawal of lovastatin in patients with type 2 DN (T2DN) were studied.Lovastatin was administered for thirty male patients with T2DN and then was withdrawn. Twenty-four hours, urine creatinine and protein levels were determined.The mean levels of total cholesterol and LDL-C were reduced without any change in the triglyceride (TG) level while the high-density lipoprotein cholesterol (HDL-C) level was increased. There was a reverse linear correlation between the changes in the level of HDL-C and the changes in the level of 24 h urine protein after 90 days of lovastatin therapy (P = 0.007, r = -0.484).Short-term 3-month lovastatin therapy has no effect on proteinuria levels in patients with T2DN despite the antihyperlipidemic effects and reverse correlation of proteinuria with HDL-C.
dc.language.isoEnglish
dc.relation.ispartofNigerian medical journal : journal of the Nigeria Medical Association
dc.titleShort-term effects of lovastatin therapy on proteinuria of type 2 diabetic nephropathy: A clinical trial study.
dc.typearticle
dc.citation.volume57
dc.citation.issue5
dc.citation.spage253
dc.citation.epage259
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.4103/0300-1652.190600


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