NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Institute of Medicine (US) Board on Population Health and Public Health Practice. Sex-Specific Reporting of Scientific Research: A Workshop Summary. Washington (DC): National Academies Press (US); 2012.

Cover of Sex-Specific Reporting of Scientific Research

Sex-Specific Reporting of Scientific Research: A Workshop Summary.

Show details

CLOSING REMARKS

Clayton offered closing comments on behalf of the workshop sponsor. The purpose of research is to inform, she said, and, for those involved in health research, to increase knowledge about human biology and to foster development of evidence-based health policy and clinical care.

Journal editors, Clayton pointed out, are uniquely positioned as gatekeepers for much of the scientific knowledge that reaches the public domain. They have the power to advance appropriate consideration of sex differences, she said, acknowledging that the term appropriate is subject to interpretation and that “one size does not fit all.” Journal editors and editorial bodies, such as the ICMJE, can set standards for the inclusion of sex-related information in manuscripts submitted to their publications, including the sex of origin of tissues and cells and the sex of animals and humans in preclinical and clinical studies. They are also in a position to set guidelines to encourage authors to think about analysis and reporting of sex differences.

Clayton reiterated that NIH requires the inclusion of women and minorities, as scientifically appropriate, in all clinical research that is supported by NIH. For a phase 3 clinical trial, if an evidence review reveals a likelihood of a sex-based difference, the study must be designed to allow comparisons between males and females, and the results must be provided to NIH in the final progress report. However, NIH does not have any control over what is published in the scientific literature. Together, the scientific community needs to find ways to ensure that this information gets out so that it can be helpful to researchers, clinicians, and policy-makers, she said. Funding is more limited than at other times, so scientists should also be efficient in collecting as many data as possible from studies. She concluded by noting that patients who participate in trials are relying on researchers to get the maximum information from clinical research.

Copyright © 2012, National Academy of Sciences.
Bookshelf ID: NBK84185
PubReader format: click here to try

Views

Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...