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in-cites - an editorial component of ISI Essential Science Indicators
Citing URL: http://www.in-cites.com/research/2003/november_10_2003-3.html

SCI-BYTES What's New in Research:
November 10, 2003
             

  Previous | Main SCI-BYTES Menu (current year) | 2003 Menu

Hot Paper in Medicine

"Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy
due to type 2 diabetes,"
by Edmund J. Lewis and 9 others, New England Journal of Medicine, 345(12):
851-60, 20 September 2001.


Abstract: "Background It is unknown whether either the angiotensin-II-receptor blocker irbesartan or the
calcium-channel blocker amlodipine slows the progression of nephropathy in patients with type 2 diabetes independently of its capacity to lower the systemic blood pressure. Methods We randomly assigned 1715 hypertensive patients with nephropathy due to type 2 diabetes to treatment with irbesartan (300 mg daily), amlodipine (10 mg daily), or placebo. The target blood pressure was 135/85 mm Hg or less in all groups. We compared the groups with regard to the time to the primary composite end point of a doubling of the base-line serum creatinine concentration, the development of end-stage renal disease, or death from any cause. We also compared them with regard to the time to a secondary cardiovascular composite end point. Results The mean duration of follow-up was 2.6 years. Treatment with irbesartan was associated with a risk of the primary composite end point that was 20 percent lower than that in the placebo group (P=0.02) and 23 percent lower than that in the amlodipine group (P=0.006). The risk of a doubling of the serum concentration was 33 percent lower in the irbesartan group than in the placebo group (P=0.003) and 37 percent lower in the irbesartan group than in the amlodipine group (P<0.001). Treatment with irbesartan was associated with a relative risk of end-stage renal disease that was 23 percent lower than that in both other groups (P=0.07 for both comparisons). These differences were not explained by differences in the blood pressures that were achieved. The serum creatinine concentration increased 24 percent more slowly in the irbesartan group than in the placebo group (P=0.008) and 21 percent more slowly than in the amlodipine group (P=0.02). There were no significant differences in the rates of death from any cause or in the cardiovascular composite end point. Conclusions The angiotensin-II receptor blocker irbesartan is effective in protecting against the progression of nephropathy due to type 2 diabetes. This protection is independent of the reduction in blood pressure it causes."

This 2001 report from the New England Journal of Medicine was cited 62 times in current journal articles
indexed in the Thomson ISI database during July-August 2003. During that two-month period, this was the
third-most-cited paper in medicine, aside from reviews, published in the last two years. Prior to the most recent
bimonthly count, citations to the paper have accrued as follows:

May-June 2003: 41 citations
March-April 2003: 53
January-February 2003: 47
November-December 2002: 57
September-October 2002: 38
July-August 2002: 29
May-June 2002: 27
March-April 2002: 20
January-February 2002: 16
November-December 2001: 8
September-October 2001: 4

Total citations to date: 402

SOURCE: Hot Papers Database (Included with a subscription to the ISI print newsletter Science Watch®, available from the ISI Research Services Group. Packaged on a CD-ROM that is mailed with each Science Watch issue, the Hot Papers Database contains data on hundreds of highly cited papers published during the last two years. User interface permits searching by author, organization, journal, field, and more. Total citations, as well as citations accrued during successive bimonthly periods, can be assessed and graphed. An updated CD containing the most recent bimonthly data is mailed with every new issue of Science Watch, six times a year. The CD also includes an electronic version of the Science Watch issue in HTML format, for personal desktop access.)


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