Third, given the purpose of the AIFA Registry, there was no comparator-treated group. Conversely, the main strength is the very large and heterogeneous
diabetes cohort, including the complete dataset from an entire European nation, where drugs were used under strict regulatory access, requiring online registration for reimbursement. In conclusion, data on the compliance, safety, and effectiveness of incretin-based therapies derived from the AIFA Registry, while not capturing any new safety signal, provide a comprehensive framework for health-care providers to regulate the use of these drugs in the community. These data might be useful to address several important points, including the independent Sorafenib concentration effect of baseline HbA1c on its decline, the safety and effectiveness in subjects with diabetes over 75, and the effectiveness of incretins – also including liraglutide and saxagliptin from August 2010 – in the large cohort of obese subjects with BMI >35. These analyses will be carried out when the monitoring data will be available in the new and updated in-house web platform currently
being developed. Whenever effective strategies of lifestyle changes selleck compound preliminary to any further step in treatment intensification fail, the implementation of new treatments, including incretin-based therapies, should be dictated by solid data on long-term safety and effectiveness in the context of available drugs for type 2 diabetes, favoring a patient-centered approach. [4]. S.M., G.M., D.M., and L.P. conceived the study and interpreted
the results from the AIFA Registry. S.M., G.M., D.M., A.S., P.D.S., and M.P.T. wrote the first draft of the manuscript. Data analysis was performed by CINECA. All the named authors critically reviewed and commented on multiple drafts of the report, approved the final version of the manuscript, and read and met the ICMJE criteria for authorship. The implementation of AIFA Anti-diabetics Monitoring Registry is supported by a contribution from the manufactures of the monitored drugs. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the Cediranib (AZD2171) manuscript. S.M. takes the responsibility for the contents of the article. S.M., A.S., P.D.S., C.T. and D.M. declare that no competing interests exist. G.M. has been involved in studies on anti-diabetic drugs sponsored by Boehringer Ingelheim, Eli Lilly, NovoNordisk, and Sanofi; and has received honoraria for lectures from pharmaceutical companies producing anti-diabetics: Merck Sharp & Dome, Eli Lilly, Sanofi, and Novartis. These potential conflicts did not affect the given contributions to this article. M.P.T.