Fraudulent Research Floods Nutrition Field, Corroding Credibility

By Erik Goldman, Editor

The proliferation of fraudulent clinical research has reached epidemic proportions, creating a major headache for practitioners. There were roughly 10,000 fraudulent papers retracted by medical journals last year, the highest number on record. While the problem affects all areas of medicine, the field of nutrition is especially vulnerable (Image: PeopleImages–Yuri A/Shutterstock)

Good medical practice is based on trust.

Patients trust that practitioners are knowledgeable, and that they use their knowledge intheir patients’ best interests. In turn, practitioners trust that researchers run their studies honestly, and that editors and peer-reviewers of the medical journals carefully scrutinize the papers they receive, sift out the garbage, and only publish studies that pass clinical, statistical, and ethical muster. 

Research itself is also a trust proposition. From the lead investigators who design trials, and the Institutional Review Boards (IRBs) that approve them, to the research assistants and post-doctoral fellows who crunch the data, and the authors who write and submit the papers, there’s a thread of trust that depends on the right people doing the right things at each point along the path.

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Featured Articles

Hibiscus & Lemon Verbena: Herbal Allies for BP Regulation

Written by Jonathan Jones, PhD, Contributing Writer

Hibiscus sabdariffa (hibiscus) and Lippia citriodora (lemon verbena) are two polyphenol-rich botanicals that, when combined, can act synergistically to regulate blood pressure. Oxidative stress, a key factor in the development and progression of hypertension, can lead to vascular damage and atherosclerosis. Mitigating oxidative stress is, therefore, an important aspect of managing hypertension. Natural polyphenols, like […]

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FDA Increases Oversight of Diagnostic Tests

Written by Erik Goldman, Editor

The Food and Drug Administration has issued new rules aimed at bolstering the agency’s oversight and regulation of the diagnostic testing field. Specifically, the FDA is taking aim at Laboratory-Developed Tests (LDTs), which are defined as in vitro medical tests designed, manufactured, and processed by a single clinical laboratory. Historically, LDTs were unique, highly targeted […]

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HPC Video

The Latest Applications of Predictive Genomics in Longevity Medicine

Written by Erik Goldman

Risk assessment is a foundation of good clinical practice. Accurate and individualized risk prediction allows for informed decision-making, enhanced disease screening and personalized risk-reduction strategies for your patients.

We’re all aware of the use of penetrant genes like BRCA1/2 as genomic markers for cancer susceptibility. But there is a lesser-known disease susceptibility indicator known as polygenic risk score (PRS), that can be highly valuable in clinical practice.

In this FREE webinar, Dr. Joel Evans will explore the role of PRS in clinical decision-making. He’ll highlight the value of PRS when integrated with other clinical risk factors in assessing a patient’s risk of developing disease, and describe how to implement this type of clinically-integrated genetic technology in longevity-focused precision medicine practice.

As a women’s healthcare practitioner with a passion for hormone replacement therapy, Dr. Evans will focus specifically on the benefits of PRS for breast cancer risk assessment. He’ll also touch on application of the same technology for other cancers including ovarian, colorectal, pancreatic, prostate and melanoma, and other common disorders like type 2 diabetes and heart disease.


With PRS assessment, you can now offer your patients the latest in disease risk prediction to create personalized treatment plans to increase health span, wellness, and longevity.

You’ll learn:

  • The basics of predictive genomics in the context of polygenic risk
  • How assessment of polygenic risk, in combination with other clinical risk factors, can positively impact your implementation of longevity medicine
  • Practical approaches for utilizing the latest in genomic-integrated clinical risk prediction into your clinical practice
SPONSORED BY

Joel Evans, MD, is Chief Medical Officer at geneType, and is a board-certified OB/GYN and international lecturer. He is the Director of The Center for Functional Medicine in Ridgefield, CT, and Chief of Medical Affairs for the Institute for Functional Medicine. Dr. Evans is renowned for his passion for mind-body medicine. His special interest in breast cancer led him to serve as the Medical Director of the Keep A Breast Foundation. Dr. Evans brings decades of applied research about cancer risk and prevention to his patients, and to the functional medicine community.

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