Joined March 2010
The Human Heart of Clinical Innovation: Connection, Community, and Co-Production, Celebrate the Wins at CNS Summit! linkedin.com/pulse/human-hea… via @LinkedIn
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Patients are science and medicine's most underused resource; linkedin.com/pulse/patients-… via @LinkedIn
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Dr. Amy Price retweeted
Dartmouth President is a cognitive psychologist and this is a brilliant peice. I've pulled some quotes... “Jobs that require advanced AI skills are growing eight times faster than the job market overall” “Colleges must start by being clear about what a degree is actually worth in the AI age.” AI should be experienced “Our ambition at Dartmouth is for every undergraduate to experience a team-based AI project that relates to their coursework by the time they graduate.” Practice beats prohibition “if higher education opts for prohibition, we will squander the chance to help shape how this technology gets used in the world” “There will not be a one-size-fits-all solution to the challenges of supplying this education.” “Universities that fail to produce graduates who can use it productively will consign themselves to irrelevance.”
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Dr. Amy Price retweeted
Hi all, The Lp(a) HORIZON trial has released topline data and, quite shockingly, missed its primary endpoint. In other words, lowering Lp(a) in patients with prior MI, stroke or peripheral arterial disease, who were otherwise very well treated for LDL-C, blood pressure, diabetes and other risk factors, did not reduce the primary cardiovascular endpoint. We obviously need to see the full data before making firm conclusions, and I don’t want to speculate too much without the details. But this is a big enough result that it is worth summarizing what we know, what we don’t know, and what this may mean for our patients after 20+ years of trying to test the “Lp(a) hypothesis.” What we know: 1-There are hundreds if not thousands of genetic, epidemiologic and Mendelian-randomization studies showing that elevated Lp(a) is associated with MI, stroke, peripheral arterial disease and aortic stenosis. That body of evidence is very strong. 2-However, much of those data come from community-based populations, often before the era of intensive LDL-C lowering and modern secondary prevention. 3-There has been much less information about how much residual risk Lp(a) carries in someone who has already had an event and is then treated very aggressively. 4-HORIZON may have had some of the best-treated patients of any recent cardiovascular outcomes trial. Baseline LDL-C was about 65 mg/dL, a measured LDL-C contains the cholesterol carried on Lp(a), so in reality, 15-20 points lower. 5-In patients with very high Lp(a), if you correct LDL-C for Lp(a)-cholesterol, the actual LDL-C carried by LDL particles may have been closer to 45–50 mg/dL, perhaps even lower in some patients. 6-This raises a very basic question: Can you still demonstrate a major incremental benefit from lowering another apoB-containing particle when the underlying LDL burden has already been driven this low? What we don’t know: 1-What was the actual corrected LDL-C in these patients? I think it would be extremely informative to directly measure Lp(a)-C and calculate corrected LDL-C. This may tell us a lot about the biological setting in which pelacarsen was being tested. 2- What was the OxPL status? Our prior work has suggested that much of the pro-inflammatory biology associated with Lp(a) is related to its enrichment in oxidized phospholipids. Did OxPL fall? Did patients with higher OxPL derive more benefit? Was Lp(a) concentration actually identifying the patients with the most pathogenic particles? 3- Did we measure the right component of Lp(a) for trial inclusion? We generally measure molar particle concentration. But is molar concentration itself the main driver of risk, or is it partly a surrogate for what the particle carries? Cholesterol? Triglycerides? Oxidized phospholipids? Other proteins? Could two patients with the same Lp(a) concentration have very different Lp(a)-mediated risk? I think this question deserves much more attention. 3- Were the genetic data telling us exactly what we thought they were telling us? The genetic data are extremely compelling, but genetics reflect lifelong exposure. A clinical trial treats patients late in life, often after decades of arterial injury and after an event has already occurred. Those are not necessarily the same experiment. Could there also be some unrecognized biology linked to the LPA locus that we have not completely accounted for? That possibility should at least be considered. 3- Does very low LDL-C modify the Lp(a) risk relationship? Maybe Lp(a) is particularly important when LDL-C is higher, but its contribution becomes smaller once LDL-C is driven to very low levels. Again, we need the data. 4- Does aspirin or other antiplatelet therapy reduce part of the risk associated with Lp(a)? Lp(a) has potentially important prothrombotic effects. Almost everyone in a trial like HORIZON is receiving contemporary antiplatelet therapy. Could that blunt one component of the risk associated with Lp(a)? 5- Why are these patients still having events? This may be one of the most interesting questions of all. These are patients with LDL-C around 65 mg/dL, and perhaps corrected LDL-C substantially lower, yet cardiovascular events continue to occur. What is driving that residual risk? Inflammation? Thrombosis? Plaque burden that is already too advanced? Other lipoprotein characteristics? Something we are not measuring? 6- Do we need to re-examine some basic assumptions about atherosclerosis? We have spent decades focusing heavily on the quantity of circulating lipoproteins. But perhaps lipoproteins are relatively benign until they undergo biological modification in the artery wall. Oxidation may be one of those key modifications. For some patients, the answer may be to remove more particles from the circulation. For others, perhaps the better approach is to prevent their oxidation or block the downstream biological effects of oxidized lipids. The recent difficulties with anti-inflammatory approaches, including IL-6 inhibition, make these mechanistic questions even more interesting. 7- Was there something specific about pelacarsen, the degree or timing of Lp(a) lowering, advanced disease, trial duration, background therapy or patient selection that mitigated a potential benefit? We simply don’t know yet. That is why the detailed results will be so important. What does this mean for patients today? If you have already had an MI, stroke or PAD, the immediate lesson is very clear: 1- Get all of your established risk factors treated aggressively. 2- Get LDL-C/apoB very low. 3- Control blood pressure. 4- Control diabetes. 5- Don’t smoke. 6- Use appropriate antiplatelet and other guideline-directed therapies. HORIZON shows us what modern secondary prevention should look like. If you have elevated Lp(a) but have never had an event, the genetic and epidemiologic data still suggest increased lifetime risk. Until the other 4 outcome trials read out, I would continue to treat every modifiable risk factor aggressively. We should wait for those trials before drawing broad conclusions about the entire field. I think the story of Lp(a) therapy is beginning, not ending. We also need to show tremendous respect and gratitude to the patients who participated in HORIZON and to the investigators and companies that invested enormous resources to actually test the Lp(a) hypothesis, to the ultimate benefit to peole with elevated Lp(a) to best guide how to manage risk. More to come as we go forward.
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Dr. Amy Price retweeted
When clinical data disappoint, financial headlines arrive quickly. This Labor Day weekend, I am thinking about the people at @Novartis who worked on #Pelacarsen. They deserve recognition from their employer and from the entire biopharma scientific community. They carried the responsibility of patients who enrolled in the trial with hope. They believed in the science and in the possibility of changing the course of cardiovascular disease. Their disappointment is real and deserves acknowledgment. Their work mattered, their commitment mattered and what they learned will inform future discovery! My thoughts on why disappointing data should never diminish the people behind the pursuit, published in @BeingWellpub: medium.com/beingwell/when-th…
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Replying to @AmyPricePhD
Well, we don't know much yet because we don't have much information other than what's in the press release and what we know about the design of the trial. It could be that the effect of the drug was just too small for a trial that size to be able to show a
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statistically significant benefit. It will be interesting to see if patients with higher lp(a) levels showed any benefit. Also, the patients were not just on LDL-lowering drugs, they are also on other risk-lowering drugs such as aspirin or other antiplatelets, antihypertensives,
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and so on. My understanding is that some of the other lp(a) drugs will have larger lp(a) reductions and will be tested in patients with higher lp(a) levels.
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Dr. Amy Price retweeted
Defending the Mechanistic Plausibility of Protracted and Delayed Antidepressant Withdrawalm via @DanielCohrsMD psychiatrymargins.com/p/defe…
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Dr. Amy Price retweeted
Artificial intelligence (AI) tools widely used by @rcgp GPs could miss key information shared by patients in consultations and lead to 'deskilling' of doctors, @KathrinCressw et al researchers have warned via @nickbostock gponline.com/ai-scribes-desk… @CoryRohlfsen @raj_mehta
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Dr. Amy Price retweeted
Cancer immunotherapy pyramid: scaling up potency and promise
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Warm congratulations to *you* Dr Amy Price and your co-author Christine Von Raesfeld on the publication of your work. Gratitude for sharing it with me. It is ALWAYS important to speak of the harms and benefits of medicines AND new health technologies like AI. YES, it is not ethical to build a *super highway* without guide-rails or an *offramp* Love the synergies this work builds with Pope Leo’s encyclical on the same topic.🌻
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So excited to co-author this very real paper with Christine Von Raesfeld Real-World Data Needs Real-World Doctors @pash22 @PGee51 @yuriquintana jopm.jmir.org/2026/1/e97972 @breastlessAfrik
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We are honored to announce that FDA's Cynthia (Cyndi) Grossman, Ph.D. Director, Division of Patient-Centered Development, will join the DCI Network’s Patient-Powered Digital Health 2026 conference as a keynote speaker. lnkd.in/evTNrmGQ Dr. Grossman serves as Director of the Division of Patient-Centered Development within the Center for Devices and Radiological Health at the U.S. Food and Drug Administration, where she leads efforts to advance patient-centered approaches across medical product development and digital health innovation. Her keynote presentation, “Patient Input and Digital Health Technologies: A Regulatory Perspective Across the Product Lifecycle,” comes at a critically important moment for healthcare, AI, and patient engagement. Dr. Grossman has spent her career advancing methods to integrate the voices of patients, caregivers, and communities into biomedical research, healthcare delivery, and regulatory science. Her work spans government, industry, nonprofits, and academic research, with leadership roles involving real-world evidence, patient-centered outcomes research, behavioral science, and digital health innovation. Her background includes prior service at NIH, leadership of research programs focused on HIV prevention and care, and major collaborations supported through NIH and PCORI funding. Her participation strongly aligns with the mission of Patient-Powered Digital Health 2026, which focuses on: • Patient co-design and authentic partnership • Trust, transparency, ethics, and equity in AI • Real-world evidence and measurable patient outcomes • Scalable digital health solutions that patients actually adopt and trust • AI-powered patient engagement The timing of this keynote is especially significant given recent FDA activity emphasizing patient engagement and Patient Preference Information (PPI) in medical product development and digital health evaluation. As discussed in a recent LinkedIn article "FDA Elevates the Patient Voice: New Guidance Signals the Future of Patient Preference Information (PPI) and Digital Health Innovation" lnkd.in/eazyEzWc , regulators are increasingly emphasizing measurable patient-centered evidence throughout the product lifecycle. At DCI Network 2026, we aim to move beyond theoretical discussions and focus on practical, evidence-based strategies for building trustworthy, scalable, and patient-centered AI systems. The conference brings together healthcare systems, life sciences organizations, patient advocates, researchers, innovators, regulators, and technology leaders at Harvard Medical School and BIDMC to co-design the future of patient-centered digital health. Dr. Grossman’s expertise makes her perspective invaluable to our community. Register Before June 1st and you can use coupon 15OFFDCIJ26  to get 15% off lnkd.in/eZzMawU9
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Amber Lockridge, PhD NIH Post Doc, Personal Capacity youtu.be/-duDkthVMPk?si=SUSC… via @YouTube
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