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Is the Truth Out There? Space Offers Hematology Insights

Is the Truth Out There? Space Offers Hematology Insights

Medscape6 days ago

MILAN — An unexpected highlight here at this year's European Hematology Association (EHA) Congress came from beyond planet Earth. In a packed session titled Space Hematology , researchers and clinicians explored how frontier science intersects with practical medicine. Although the International Space Station and spaceflight might seem distant from the clinic, space offers a uniquely revealing experimental environment for hematology and for medicine more broadly.
Microgravity, radiation exposure, circadian disruption, isolation, and other extreme conditions challenge human physiology in ways that are both scientifically illuminating and clinically relevant. Insights from experiments under these conditions can offer new perspectives for both treating and understanding the underlying mechanisms of hemoglobinopathies, coagulation disorders, or white blood cell dysfunction.
Joseph Borg, PhD
Perhaps most compelling, however, is this: Research conducted in space is no longer an expensive, distant aspiration — it is becoming a practical extension of the terrestrial laboratory. 'The technical and economic accessibility of space research has dramatically improved, and it will likely continue to do so, just as we saw with whole genome sequencing (WGS),' said Joseph Borg, PhD, professor and principal investigator at the University of Malta and investigator at NASA GeneLab, in an interview with Medscape Medical News . 'Regarding WGS, what once cost millions is now affordable for a large number of laboratories.'
Space as a Lab: New Data From Far Away
During the session, Borg presented findings showing that adult astronauts exhibit elevated levels of fetal hemoglobin (HbF), a molecule typically absent after infancy. His team, which has conducted annual experiments in space since 2021, analyzed peripheral blood using advanced omics technologies. Samples were collected pre-flight, during missions, and post-return. One study, published in Nature Communications , reported significant overexpression of gamma-globin genes ( HBG1 , HBG2 ), suggesting reactivation of fetal erythropoiesis during spaceflight. This pattern was consistent across different missions, including a polar orbit flight.
Borg highlighted that the clinical relevance of these findings is that — in disorders like sickle cell disease or beta-thalassemia — increased HbF can reduce symptoms and improve quality of life. While gene-editing approaches like CRISPR-Cas9 aim to achieve this, they remain complex and costly. Inducing HbF through environmental triggers akin to those in space might offer a simpler alternative.
Roopen Arya, MD
Thrombosis risk in space has also transitioned from theoretical concern to real issue. 'Until 2019, there were no reported cases of venous thromboembolism (VTE) in astronauts,' noted Roopen Arya, MD, professor of thrombosis and hemostasis and clinical director for hematological medicine at King's College Hospital, UK. That changed with a case of jugular vein thrombosis described in JAMA Network Open . NASA's VTE working group subsequently developed in-flight diagnostic and treatment protocols.
Another study on the secretome of civilians participating in a short-duration mission showed transient changes in coagulation and inflammatory markers. 'Very interesting data, even if we currently don't know what they mean,' Arya commented.
Finally, white blood cell function is also altered in space. Judith-Irina Buchheim, MD, anesthesiologist at Ludwig-Maximilians-Universität (LMU) München, Germany, presented evidence that spaceflight can reduce NK cell cytotoxicity, affect T-cell activation, and trigger a state resembling inflammaging.
'If you're interested in aging research, space is probably the right choice for your experiments,' she said. 'You can see the effects prospectively very quickly, as early as 6 months.' Buchheim is also a member of the European Space Agency Medical Board and is leading its expert group for studying the effects of isolation, confinement, and extreme environments on the human body.
Down to Earth: Why Space Medicine Matters
Are these findings clinically applicable to Earth-based medicine or are they just curiosities from an elite group of astronauts and space agencies? According to the speakers, the implications are far-reaching.
Astronauts offer ideal study subjects; they are healthy, highly monitored, and highly motivated individuals.
Space acts as a physiological accelerator, revealing stress-response patterns and disease models that could take years to emerge on Earth.
Insights into HbF reactivation could inspire pharmacologic mimicry.
Coagulation changes may refine risk stratification for hospitalized or immobilized patients.
And immune dysregulation observed in space could help clarify mechanisms of aging, vaccine response, and infection susceptibility.
Space-based research also drives technological innovation. Devices miniaturized for orbit — blood analyzers, sequencing platforms — can be reengineered for bedside diagnostics in rural or low-resource settings, improving access to care.
Why Space Hematology and Why Now?
The inclusion of space hematology in the EHA Congress was deliberate. 'Most hematologists are not experts in space medicine, but this is already in the news and may become part of our clinical routine in 10-15 years,' Martin Dreyling, MD, professor of medicine and head of the lymphoma program at the Department of Medicine III, LMU Hospital Munich, told Medscape Medical News . He is the chair of the of the Scientific Program Committee for the EHA 2025 Congress, the group of experts in charge of selecting the topics to be presented at the event. Young investigators are especially drawn to the field, he added, attracted by its novelty, data richness, and interdisciplinary collaborations. Attendance by many early-career hematologists at the Milan session confirmed this growing interest.
Martin Dreyling, MD
With private companies offering logistical support, space is also now an optional arm in experimental design. 'It's about adding a new layer to your research and going deeper into biological mechanisms,' Borg explained to Medscape Medical News . He also emphasized the need for ethical oversight. Astronauts provide informed consent for biological sampling, and some opt to receive personal results. Nowadays, great attention to these issues is also needed for the 'new astronauts': that is, people who will be able to access commercial spaceflight and who are not as trained and risk-aware as traditional astronauts.
It's tempting to ask whether data obtained from such a small and selected group of individuals are really significant for the population on Earth. Yet, despite small sample sizes, insights are accumulating. As more samples and subjects are sent into space and as repositories like the Space Omics and Medical Atlas grow, the potential for clinical translation increases. The long-term vision is a broader pool of space travelers, including commercial passengers, undergoing real-time health monitoring to yield diverse datasets.
'This is not a diversion from medicine's mission; it's an extension,' Borg told Medscape Medical News . 'Every doctor seeks better tools, new therapeutics, and deeper understanding. Space provides an extraordinary testbed that may reveal what Earth conceals.'
From hemoglobin switching and thrombotic risk to immunosenescence and real-time drug testing, space hematology is no longer just a scientific curiosity. It's a fast-evolving frontier of translational research, he concluded.

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Novo Nordisk A/S: CagriSema 2.4 mg / 2.4 mg demonstrated 22.7% mean weight reduction in adults with overweight or obesity in REDEFINE 1, published in New England Journal of Medicine
Novo Nordisk A/S: CagriSema 2.4 mg / 2.4 mg demonstrated 22.7% mean weight reduction in adults with overweight or obesity in REDEFINE 1, published in New England Journal of Medicine

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Novo Nordisk A/S: CagriSema 2.4 mg / 2.4 mg demonstrated 22.7% mean weight reduction in adults with overweight or obesity in REDEFINE 1, published in New England Journal of Medicine

Data presented simultaneously at the American Diabetes Association's® 85th Scientific Sessions, showed mean weight reduction in the highest range of efficacy observed with existing weight loss interventions1 When adhering to treatment, weight loss of ≥5%, ≥20%, ≥25%, and ≥30% was observed in 97.6%, 60.2%, 40.4% and 23.1% of patients respectively at 68 weeks1* The REDEFINE clinical programme is ongoing to further investigate efficacy and safety of CagriSema, including recently initiated REDEFINE 112 Bagsværd, Denmark, 22 June – Today, The New England Journal of Medicine (NEJM) published results from Novo Nordisk's phase 3 REDEFINE 1 trial evaluating the efficacy and safety of investigational CagriSema plus lifestyle interventions for weight loss in adults with obesity or overweight who have a weight-related medical complication and without diabetes.1 REDEFINE 1 met its co-primary endpoints and achieved statistically significant and clinically meaningful weight loss at 68 weeks in patients taking CagriSema versus placebo.1 These data, along with the related phase 3 REDEFINE 2 study conducted in adults with overweight or obesity and type 2 diabetes, were presented today during a scientific symposium at the American Diabetes Association's (ADA) 85th Scientific Sessions and published in NEJM. 'In REDEFINE 1, participants saw significant and clinically meaningful weight loss under a protocol that allowed investigators to maintain patients on a submaximal dose if deemed best for the patient. We also witnessed low, single-digit discontinuation rates due to adverse events in both REDEFINE 1 and 2,' said Martin Holst Lange, executive vice president and head of Development at Novo Nordisk. 'These results reinforce our confidence in CagriSema, and we continue to study the potential of this combination through the REDEFINE trials.' CagriSema is an investigational product that combines the GLP-1 RA, semaglutide, with an amylin analogue, cagrilintide. The REDEFINE 1 trial found that treatment with CagriSema resulted in greater weight loss of 22.7% at 68 weeks versus 2.3% in the placebo group if all patients adhered to treatment.1* When evaluating the treatment effect regardless of adherence, those treated with CagriSema achieved statistically significant weight loss of 20.4% at 68 weeks versus 3.0% for the placebo group.1** In addition, a supportive secondary analysis showed that half (50.7%) of trial participants with obesity treated with CagriSema reached the threshold for non-obesity (BMI < 30 kg/m2) at the end of treatment, from a mean BMI of 38 kg/m2 at the start of treatment. In the placebo group,10.2% reached that threshold at 68 weeks.1 Select confirmatory secondary endpoints showed that if all participants adhered to treatment 40.4% of those receiving CagriSema achieved a body weight reduction of ≥25%.* Additionally, 23.1% lost ≥30% of their body weight.1* When applying the treatment policy estimand, 34.7% of participants treated with CagriSema achieved ≥25% body-weight reduction and 19.3% achieved ≥30% body-weight reduction.1** In a prespecified analysis of 252 participants, the relative reduction in fat and lean soft-tissue mass from baseline to week 68 was -35.7% (fat mass) and -14.4% (lean soft-tissue mass) for those treated with CagriSema versus –5.7% and –4.3% for the placebo group, respectively.1 "In REDEFINE 1, CagriSema provided weight loss in the highest range of efficacy observed with existing weight loss interventions,' said lead investigator Timothy Garvey, MD, professor of medicine and director of the Diabetes Research Center at the University of Alabama at Birmingham. 'Investigators were allowed some flexibility in dose adjustments to balance efficacy and safety, but regardless of dose adjustments participants lost significant weight. These findings are relatable to clinical practice, where dosing is often adjusted based on individual needs and clinical judgement.' Safety data generated in the REDEFINE 1 and 2 trials were comparable with the GLP-1 RA class. Overall, discontinuation rates due to adverse events were low, with 6% for CagriSema versus 3.7% for placebo in REDEFINE 1 and 8.4% with CagriSema versus 3% with placebo in REDEFINE 2.1,3 In REDEFINE 1, adverse events were mainly gastrointestinal (79.6% in the CagriSema group vs. 39.9% with placebo), including nausea (55% vs. 12.6 %), constipation (30.7% vs. 11.6%), vomiting (26.1% vs. 4.1%) and were mostly transient and mild-to-moderate in severity.1 Results from REDEFINE 2, a phase 3 study that evaluated the efficacy and safety of CagriSema plus lifestyle interventions in adults with obesity and type 2 diabetes (T2D), were also simultaneously presented during a scientific symposium at the ADA's Scientific Sessions and published in NEJM.3 In REDEFINE 2, if all participants adhered to treatment, the estimated mean change in body weight from baseline to week 68 was –15.7% with CagriSema versus –3.1% with placebo.3* When applying the treatment policy estimand, the estimated mean change in body weight from baseline to week 68 was –13.7% with CagriSema versus –3.4% with placebo.3** A greater proportion of participants receiving CagriSema, compared with placebo, reduced their body weight by >5% (83.6% vs. 30.8% of participants), ≥10% (65.6% vs. 10.3%), ≥15% (43.9% vs. 2.4%), and ≥20% (22.9% vs. 0.5%;).3 The safety results from CagriSema in REDEFINE 2 were similar to those reported in REDEFINE 1.3 The REDEFINE clinical programme will continue to assess the efficacy and safety of CagriSema. Most recently, Novo Nordisk initiated the REDEFINE 11 trial with the first patient visit occurring in early June 2025. REDEFINE 11 will explore further weight loss potential and safety of CagriSema 2.4 mg / 2.4 mg through a longer trial duration and other protocol changes compared to REDEFINE 1 and 2. * Based on the trial product estimand; this estimand estimates what the effect would be if all participants adhered to treatment ** Based on the treatment policy estimand: treatment effect regardless of treatment adherence About CagriSemaCagriSema is being investigated by Novo Nordisk as a once-weekly subcutaneous injectable treatment for adults with overweight or obesity (REDEFINE programme) and as a treatment for adults with type 2 diabetes (REIMAGINE programme). CagriSema is a fixed-dose combination of a long-acting amylin analogue, cagrilintide 2.4 mg and semaglutide 2.4 mg. About the REDEFINE clinical trial programmeREDEFINE is a phase 3 clinical development programme with once-weekly subcutaneous CagriSema in obesity. REDEFINE 1 and REDEFINE 2 have enrolled approximately 4,600 adults with overweight or obesity. REDEFINE 1 was a double-blind, placebo-and active-controlled 68-week efficacy and safety phase 3 trial of once-weekly CagriSema, cagrilintide 2.4 mg and semaglutide 2.4 mg versus placebo in 3,417 adults with obesity or overweight with one or more comorbidities and without type 2 diabetes. REDEFINE 2 was a double-blind, randomized, placebo- and controlled 68-week efficacy and safety phase 3 trial of once-weekly CagriSema versus placebo in 1,206 adults with type 2 diabetes and either obesity or overweight. Multiple REDEFINE clinical trials are currently underway including: REDEFINE 3, an event-driven cardiovascular outcomes phase 3 trial; REDEFINE 4 an 84-week head-to-head efficacy and safety phase 3 trial of once-weekly CagriSema versus once-weekly tirzepatide; and REDEFINE 11, a phase 3 trial with longer duration and other protocol changes compared to REDEFINE 1 and 2. About obesity Obesity is a serious chronic, progressive, and complex disease that requires long-term management.4-6 One key misunderstanding is that this is a disease of just lack of willpower, when in fact there is underlying biology that may impede people with obesity from losing weight and keeping it off.4,6 Obesity is influenced by a variety of factors, including genetics, social determinants of health, and the environment.7,8 Novo Nordisk is a leading global healthcare company founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat serious chronic diseases built upon our heritage in diabetes. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 77,400 people in 80 countries and markets its products in around 170 countries. For more information, visit Facebook, Instagram, X, LinkedIn and YouTube. Contacts for further information Media: Ambre James-Brown +45 3079 9289 abmo@ Liz Skrbkova (US) +1 609 917 0632 lzsk@ Investors: Jacob Martin Wiborg Rode +45 3075 5956 jrde@ Ida Schaap Melvold +45 3077 5649 idmg@ Sina Meyer +45 3079 6656 azey@ Max Ung +45 3077 6414 mxun@ Frederik Taylor Pitter +1 609 613 0568 fptr@ References: Garvey WT, Blüher MD, Contreras CKO, et al. CagriSema in Adults with Overweight or Obesity. New England Journal of Medicine 2025. doi: 10.1056/NEJMoa2502081 A Research Study to Look at How Well CagriSema Helps People Living With Obesity Lose Weight and Maintain Weight Loss in the Long-term. Last Accessed: June 2025. Available at: Davies MJ, Harpreet S, Bajaj MD, et al. CagriSema in Adults with Overweight or Obesity and Type 2 Diabetes. New England Journal of Medicine 2025. Kaplan LM, Golden A, Jinnett K, et al. Perceptions of barriers to effective obesity care: results from the national action study. Obesity. 2018;26(1):61-69. Bray GA, Kim KK, Wilding JPH; World Obesity Federation. Obesity: a chronic relapsing progressive disease process. A position statement of the World Obesity Federation. Rev. 2017;18(7):715-723. Garvey WT, Mechanick JI, Brett EM, et al. American association of clinical endocrinologists and American College of Endocrinology comprehensive clinical practice guidelines for medical care of patients with obesity. Endocr Pract. 2016;22 (Suppl 3):1-203. Centers for Disease Control and Prevention. Adult obesity facts. Last accessed: June 2025. Available at: World Obesity Federation. World Obesity Atlas 2023. Last accessed: June 2025. Available at: Attachment PR250622-ADA-CagriSema

How your AI prompts could harm the environment
How your AI prompts could harm the environment

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How your AI prompts could harm the environment

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The more neuron connections, the more thinking you can do to answer a question,' Dauner said. Complex questions require more energy in part because of the lengthy explanations many AI models are trained to provide, Dauner said. If you ask an AI chatbot to solve an algebra question for you, it may take you through the steps it took to find the answer, he said. 'AI expends a lot of energy being polite, especially if the user is polite, saying 'please' and 'thank you,'' Dauner explained. 'But this just makes their responses even longer, expending more energy to generate each word.' For this reason, Dauner suggests users be more straightforward when communicating with AI models. Specify the length of the answer you want and limit it to one or two sentences, or say you don't need an explanation at all. Most important, Dauner's study highlights that not all AI models are created equally, said Sasha Luccioni, the climate lead at AI company Hugging Face, in an email. 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A radio signal from the beginning of the universe could reveal how everything began
A radio signal from the beginning of the universe could reveal how everything began

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A radio signal from the beginning of the universe could reveal how everything began

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