Differences in nephrotoxicity risk and renal effects among anti‐viral therapies against hepatitis B. Issue 3 (4th December 2014)
- Record Type:
- Journal Article
- Title:
- Differences in nephrotoxicity risk and renal effects among anti‐viral therapies against hepatitis B. Issue 3 (4th December 2014)
- Main Title:
- Differences in nephrotoxicity risk and renal effects among anti‐viral therapies against hepatitis B
- Authors:
- Koklu, S.
Gulsen, M. T.
Tuna, Y.
Koklu, H.
Yuksel, O.
Demir, M.
Guner, R.
Dogan, Z.
Kucukazman, M.
Poyrazoglu, O. K.
Biyik, M.
Ozturk, N. A.
Aydogan, T.
Coban, S.
Kocaman, O.
Sapmaz, F.
Gokturk, S. H.
Karaca, C.
Demirezer, A.
Tanoglu, A.
Yildirim, B.
Altinbas, A.
Atak, B. M.
Cosar, A. M.
Alkan, E.
Other collaborators
Koklu, Seyfettin
Gulsen, Murat Taner
Tuna, Yasar
Koklu, Hayretdin
Yuksel, Osman
Demir, Mehmet
Guner, Rahmet
Dogan, Zeynal
Kucukazman, Metin
Poyrazoglu, Orhan Kursat
Biyik, Murat
Ozturk, Nevin A.
Aydogan, Timucin
Coban, Sahin
Kocaman, Orhan
Sapmaz, Ferda
Gokturk, Savas H.
Karaca, Cetin
Demirezer, Aylin
Tanoglu, Alpaslan
Yildirim, Beytullah
Altinbas, Akif
Atak, Burcu M.
Cosar, Arif M.
Alkan, Erhan
Tufan, Zeliha K.
Kekilli, Murat
Ataseven, Huseyin
Purnak, Tugrul
Basar, Omer
Koklu, Nimet
Ozturk, Omer
Bakkaloglu, Kagan
Besisik, Fatih
Kockar, Cem
Arslan, Serab
Unverdi, Selman
… (more) - Abstract:
- <abstract abstract-type="main" id="apt13036-abs-0001"> <title>Summary</title> <sec id="apt13036-sec-0001" sec-type="section"> <title>Background</title> <p>Results are conflicting with respect to the renal effects of anti‐viral agents used for hepatitis B virus infection.</p> </sec> <sec id="apt13036-sec-0002" sec-type="section"> <title>Aim</title> <p>To compare short and long‐term renal effects in real‐life settings and to determine risk factors for renal impairment during treatment.</p> </sec> <sec id="apt13036-sec-0003" sec-type="section"> <title>Methods</title> <p>2221 treatment‐naïve patients were enrolled. Among these, 895 (302 lamivudine, 27 telbivudine, 282 entecavir, 273 tenofovir and 11 adefovir initiated patients) had 'repeated measures' of creatinine (baseline, 1st, 6th, 12th and 24th month of treatment). Telbivudine and adefovir groups were excluded from further analysis because of the low number of patients. We calculated the glomerular filtration rate (GFR) using the Modification of Diet in Renal Disease (MDRD) formula at each time point. Hypophosphataemia was also recorded. Risk factors for renal impairment were analysed.</p> </sec> <sec id="apt13036-sec-0004" sec-type="section"> <title>Results</title> <p>Tenofovir caused a decline in GFR at each time point when compared to baseline levels. However, lamivudine and entecavir did not change GFR. GFR‐shifting from ≥90 to 60–89 mL/min/1.73 m<sup>2</sup> was comparable among groups. The proportion of patients whose<abstract abstract-type="main" id="apt13036-abs-0001"> <title>Summary</title> <sec id="apt13036-sec-0001" sec-type="section"> <title>Background</title> <p>Results are conflicting with respect to the renal effects of anti‐viral agents used for hepatitis B virus infection.</p> </sec> <sec id="apt13036-sec-0002" sec-type="section"> <title>Aim</title> <p>To compare short and long‐term renal effects in real‐life settings and to determine risk factors for renal impairment during treatment.</p> </sec> <sec id="apt13036-sec-0003" sec-type="section"> <title>Methods</title> <p>2221 treatment‐naïve patients were enrolled. Among these, 895 (302 lamivudine, 27 telbivudine, 282 entecavir, 273 tenofovir and 11 adefovir initiated patients) had 'repeated measures' of creatinine (baseline, 1st, 6th, 12th and 24th month of treatment). Telbivudine and adefovir groups were excluded from further analysis because of the low number of patients. We calculated the glomerular filtration rate (GFR) using the Modification of Diet in Renal Disease (MDRD) formula at each time point. Hypophosphataemia was also recorded. Risk factors for renal impairment were analysed.</p> </sec> <sec id="apt13036-sec-0004" sec-type="section"> <title>Results</title> <p>Tenofovir caused a decline in GFR at each time point when compared to baseline levels. However, lamivudine and entecavir did not change GFR. GFR‐shifting from ≥90 to 60–89 mL/min/1.73 m<sup>2</sup> was comparable among groups. The proportion of patients whose baseline creatinine increased more than 25% was comparable among all anti‐virals. GFR showed a decline in patients who switched from entecavir to tenofovir. One patient with compensated cirrhosis needed to change from tenofovir because of renal safety. Seven and three patients developed transient hypophosphataemia in the tenofovir and lamivudine groups, respectively.</p> </sec> <sec id="apt13036-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Although tenofovir caused a decline in GFR, differences between the anti‐viral agents do not appear to be so impressive. In patients with and without renal risk factors at baseline, there is no impact of anti‐virals, including tenofovir.</p> </sec> </abstract> … (more)
- Is Part Of:
- Alimentary pharmacology & therapeutics. Volume 41:Issue 3(2015)
- Journal:
- Alimentary pharmacology & therapeutics
- Issue:
- Volume 41:Issue 3(2015)
- Issue Display:
- Volume 41, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 41
- Issue:
- 3
- Issue Sort Value:
- 2015-0041-0003-0000
- Page Start:
- 310
- Page End:
- 319
- Publication Date:
- 2014-12-04
- Subjects:
- Digestive organs -- Diseases -- Treatment -- Periodicals
Digestive organs -- Effect of drugs on -- Periodicals
Gastrointestinal system -- Diseases -- Treatment -- Periodicals
Gastrointestinal system -- Effect of drugs on -- Periodicals
615.73 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2036 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/apt.13036 ↗
- Languages:
- English
- ISSNs:
- 0269-2813
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0787.886000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3441.xml