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  • Recent Changes to References, Search Tools, Related Citations, and Sharing Features

    Recent Changes to References, Search Tools, Related Citations, and Sharing Features

    As part of our commitment to continuous improvement, PubMed recently introduced several updates designed to improve usability and consistency across the platform. These changes are informed by user feedback and aim to facilitate a more efficient and accessible experience for all PubMed users. Key changes include improved rendering of reference lists, the addition of date stamps in search history downloads, streamlined sharing options, and other usability updates.

    Formatting in reference lists

    Reference lists displayed on PubMed abstract pages now render formatting such as bold, italics, superscripts, and subscripts when provided by the publisher. This change ensures meaningful formatting such as superscript and subscript characters are preserved, and references retain the citation style provided to PubMed.

    Date stamps in search history download

    PubMed search history downloads from the Advanced Search page now include date stamps for each search. This feature can be used to help facilitate record keeping and reporting, for example when conducting systematic reviews. Please note that the date format may vary depending on the local settings configured in the software program you use to open CSV files.

    Usability improvement to “See all cited by articles” and “See all similar articles”

    Abstract pages include links to citations for similar articles and cited by articles, when available. You can now right click on the “See all cited by articles” and “See all similar articles” links to open these results in a new tab or window, and clicking these links now clear any applied filters so that the entire cited by or similar article set will be displayed.

    Searches related to [your query]

    The “Searches related to [your query]” feature located below the PubMed search results has been removed. These related searches continue to be auto-suggested as you enter terms in the PubMed search bar, consolidating this feature to where it is most used.

    Streamlined share functionality

    Platform-specific social media share buttons have been removed in favor of the universal permalink option that can be shared on any platform of your choice. This change helps to save space on the search results page for the most compact search results view and aligns PubMed’s abstract page with the updated PubMed Central (PMC) website, providing a consistent user experience.

    To get a citation permalink to share:

    • From the search results, right-click an article title and choose the copy link option; exact wording and functionality may change depending on your operating system and browser.
    • From an abstract page, click the Permalink button on the right sidebar and click “Copy”.
    • From a mobile device, use your device’s native share functionality to copy a link or share to the social media app of your choice.

    Please see the following Technical Bulletin articles for other recent updates:

  • Breast Cancer Risk in Younger Women May Be Influenced by Hormone Therapy

    Breast Cancer Risk in Younger Women May Be Influenced by Hormone Therapy

    Scientists at the National Institutes of Health (NIH) have found that two common types of hormone therapy may alter breast cancer risk in women before age 55. Researchers discovered that women treated with unopposed estrogen hormone therapy (E-HT) were less likely to develop the disease than those who did not use hormone therapy. They also found that women treated with estrogen plus progestin hormone therapy (EP-HT) were more likely to develop breast cancer than women who did not use hormone therapy. Together, these results could help to guide clinical recommendations for hormone therapy use among younger women.

    The two hormone therapies analyzed in the study are often used to manage symptoms related to menopause or following hysterectomy (removal of uterus) or oophorectomy (removal of one or both ovaries). Unopposed estrogen therapy is recommended only for women who have had a hysterectomy because of its known association with uterine cancer risk.

    “Hormone therapy can greatly improve the quality of life for women experiencing severe menopausal symptoms or those who have had surgeries that affect their hormone levels,” said lead author Katie O’Brien, Ph.D., of NIH’s National Institute of Environmental Health Sciences (NIEHS). “Our study provides greater understanding of the risks associated with different types of hormone therapy, which we hope will help patients and their doctors develop more informed treatment plans.”

    The researchers conducted a large-scale analysis that included data from more than 459,000 women under 55 years old across North America, Europe, Asia, and Australia. Women who used E-HT had a 14% reduction in breast cancer incidence compared to those who never used hormone therapy. Notably, this protective effect was more pronounced in women who started E-HT at younger ages or who used it longer. In contrast, women using EP-HT experienced a 10% higher rate of breast cancer compared to non-users, with an 18% higher rate seen among women using EP-HT for more than two years relative to those who never used the therapy.

    According to the authors, this suggests that for EP-HT users, the cumulative risk of breast cancer before age 55 could be about 4.5%, compared with a 4.1% risk for women who never used hormone therapy and a 3.6% risk for those who used E-HT. Further, the association between EP-HT and breast cancer was particularly elevated among women who had not undergone hysterectomy or oophorectomy. That highlights the importance of considering gynecological surgery status when evaluating the risks of starting hormone therapy, the researchers noted.

    “These findings underscore the need for personalized medical advice when considering hormone therapy,” said NIEHS scientist and senior author Dale Sandler, Ph.D. “Women and their health care providers should weigh the benefits of symptom relief against the potential risks associated with hormone therapy, especially EP-HT. For women with an intact uterus and ovaries, the increased risk of breast cancer with EP-HT should prompt careful deliberation.”

    The authors noted that their study is consistent with previous large studies that documented similar associations between hormone therapy and breast cancer risk among older and postmenopausal women. This new study extends those findings to younger women, providing essential evidence to help guide decision-making for women as they go through menopause.

    Reference: O’Brien KM, et al. 2025. Hormone therapy use and young-onset breast cancer: a pooled analysis of prospective cohorts included in the Premenopausal Breast Cancer Collaborative Group. Lancet Oncol 26: 911–23.


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  • US FDA approves Gilead's twice-yearly injection for HIV prevention

    US FDA approves Gilead's twice-yearly injection for HIV prevention

    By Deena Beasley and Julie Steenhuysen

    Los Angeles: The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences lenacapavir, a twice-yearly injection, for preventing HIV infection in adults and adolescents at high risk of contracting the deadly virus.

    Investors and AIDS activists had been eagerly awaiting the regulatory decision for the drug seen as convenient enough to help end the 44-year-old HIV epidemic.

    It will be sold under the brand name Yeztugo in the U.S. at a list price of $28,218 a year.

    Lenacapavir, part of a class of drugs known as capsid inhibitors, proved nearly 100% effective at preventing HIV in large trials last year, raising new hope of interrupting transmission of the virus that infects 1.3 million people a year.

    Yeztugo “will only be as effective as it is accessible and affordable,” Kevin Robert Frost, CEO of the Foundation for AIDS Research, said in a statement, calling on Gilead and the U.S. government to make sure people who want lenacapavir can get it.

    Gilead said it is working to secure health insurer coverage. It said it will provide co-pay assistance for eligible insured people, and the drug may be available free of charge for some under its program for the uninsured.

    Medications to prevent HIV, known as pre-exposure prophylaxis, or PrEP, are widely available. But most are daily pills, including low-cost generic versions of Gilead’s older drug Truvada, that require strict adherence to be effective. Gilead said Yeztugo is priced in line with other branded drugs.

    “This is a milestone moment,” said Gilead Chief Executive Daniel O’Day of the approval.

    “We believe that lenacapavir is the most important tool we have yet to bend the arc of the epidemic and move this epidemic into the history books,” O’Day said.

    Availability of a twice-yearly HIV prevention tool is “a huge advance,” that could help change the course of the epidemic, Dr. Raphael Landovitz, director of the UCLA Center for Clinical AIDS Research & Education, said in an email. But he said the product’s high launch price “is almost certainly going to complicate payor coverage and access.”

    Gilead has plans for a rapid launch in the United States as well as a wider rollout of the drug in collaboration with global partners.

    Gilead’s chief commercial officer, Johanna Mercier, said the company’s “end game” is to normalize PrEP usage, both in the United States and other countries, including low-income African nations where the virus is most prevalent.

    Citi Research analyst Geoff Meacham said he expects Yeztugo’s launch to be slow and steady, reaching annual sales of $2.8 billion by 2030.

    Mercier said she expects around 75% of U.S. insurers, including government health plans, will cover lenacapavir for PrEP within about six months, with the number rising to 90% within 12 months of launch.

    The drug is currently sold as a treatment in the U.S. under the brand name Sunlenca for patients with advanced disease that has become resistant to other drugs.

    PEPFAR CUTS

    In December, the President’s Emergency Plan for AIDS Relief (PEPFAR) under then-President Joe Biden signed an agreement with the Global Fund to Fight AIDS, Tuberculosis and Malaria to provide the treatment to as many as 2 million people for three years if it won U.S. regulatory approval for prevention.

    That would allow for unprecedented early access to a state-of-the-art treatment, as six generic drugmakers that have licensed the product from Gilead gear up for production of low-cost versions in 120 resource-limited countries.

    AIDS activists have viewed the drug as a way to significantly slow the epidemic, but cuts to PEPFAR by the Trump administration have raised concerns about the U.S. government’s commitment to the rollout.

    O’Day acknowledged that the changes have been “challenging,” but said the company has continued to have discussions with both the Global Fund and PEPFAR.

    “I believe that there will be sources of funding for this, and that these organizations will prioritize this type of prevention,” he said.

    (Reporting by Deena Beasley in Los Angeles and Julie Steenhuysen in Chicago; Editing by Bill Berkrot and Leslie Adler)

    • Published On Jun 19, 2025 at 11:39 AM IST

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  • Weight-loss surgery more effective than drugs in real world study

    Weight-loss surgery more effective than drugs in real world study

    London: Bariatric surgeries led to about five-times more weight loss than weekly injections of popular GLP-1 drugs, according to data from a real-world comparison study presented on Tuesday at the American Society for Metabolic and Bariatric Surgery scientific meeting in Washington.

    “Clinical trials show weight loss between 15% to 21% for GLP-1s, but this study suggests that weight loss in the real world is considerably lower even for patients who have active prescriptions for an entire year,” study leader Dr. Avery Brown of NYU Langone Health said in a statement.

    Researchers reviewed records of 38,545 patients who were prescribed injectable semaglutide or tirzepatide between 2018 and 2024 and 12,540 patients who underwent bariatric surgery during the same period. Everyone started the study with a body mass index of at least 35, which is considered severe obesity.

    Semaglutide is the main ingredient in Novo Nordisk‘s Wegovy and Ozempic, while tirzepatide is the main ingredient in Eli Lilly‘s Zepbound and Mounjaro.

    At three years after undergoing sleeve gastrectomy or gastric bypass or starting the drugs, patients who underwent surgery had lost on average 24% of their starting weight, compared to about 5% for similar patients who used the drugs for at least six months and about 7% for those who took them for a year.

    Brown noted that as many as 70% of GLP-1 patients may discontinue treatment within one year.

    “While both patient groups lose weight, metabolic and bariatric surgery is much more effective and durable,” ASMBS President Dr. Ann M. Rogers, who was not involved in the study, said in a statement.

    “Those who get insufficient weight loss with GLP-1s or have challenges complying with treatment due to side effects or costs, should consider bariatric surgery as an option, or even in combination,” she said.

    NEW BLOOD TEST MAY REDUCE LIVER TRANSPLANT FAILURES

    An experimental blood test can help surgeons catch and identify problems with newly transplanted livers at early stages, researchers say.

    It’s not unusual for transplanted organs and recipients’ nearby tissues to sustain damage during the transplantation process. Hints of problems will show up later in routine blood tests, but identifying the precise site of the damage often requires costly imaging studies and surgical biopsies, according to a report published on Tuesday in Nature Communications.

    The new test works by picking up DNA fragments left behind in the blood by dying cells. The chemical signatures on these DNA fragments can be used to identify the original cell type and where it came from, with precise detail, the researchers found.

    If you can determine which part of the liver is injured – for example, the bile ducts, or the blood vessels – “you could provide a more personalized treatment approach that leads to better care for the patient,” study leader Dr. Alexander Kroemer of MedStar Georgetown University Hospital in Washington, DC said in a statement.

    In addition to being faster and less invasive than a traditional biopsy, the blood test is also potentially more accurate, because biopsies only sample a few spots in the liver and might miss the site of the problem, he added.

    Georgetown has filed patent applications on the technology, and the research team is seeking partners to commercialize the test.

    DIABETES PRECURSOR SHOWS UP ON MUSCLE ULTRASOUND

    Ultrasound exams of thigh or shoulder muscles can detect insulin resistance at its earliest stages, researchers reported in the Journal of Ultrasound in Medicine.

    “We perform a large number of shoulder ultrasounds and noticed that many patients’ muscles appear unusually bright,” study leader Dr. Steve Soliman of the University of Michigan said in a statement.

    His team discovered in earlier studies that most of these patients have type 2 diabetes. But some had bright muscles on ultrasound even with no signs of diabetes or prediabetes.

    Subsequently, upon short-term follow-up, these patients often also developed prediabetes or type 2 diabetes.

    To test the potential for noninvasive muscle ultrasound as a predictive tool for detecting the development of pre- or type 2 diabetes – potentially earlier than current methods – the researchers performed muscle ultrasounds on 25 patients who were also being evaluated for insulin resistance.

    Although muscle ultrasound could detect insulin resistance and impaired insulin sensitivity, in this small study the level of brightness was not directly correlated with the degree of the condition. The researchers are recruiting more participants to continue the analysis.

    The exact reason why muscle brightness on ultrasound might indicate insulin resistance is less clear than the finding that it does, the researchers said.

    “Clinicians increasingly use these point-of-care and handheld ultrasound devices, sometimes called ‘the stethoscope of the future,’ for rapid diagnosis of various conditions,” Soliman said.

    “A medical assistant or clinician with little to no training could easily use this device on a patient’s upper arm or thigh, as routinely as checking weight or blood pressure, and potentially flag patients as ‘high risk’ or ‘low risk’ for further testing.”

    (Reporting by Nancy Lapid; editing by Bill Berkrot)

    • Published On Jun 18, 2025 at 05:13 PM IST

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  • FTP Improvements Available for Testing

    FTP Improvements Available for Testing

    In response to user feedback, the National Center for Biotechnology Information (NCBI) is announcing an upcoming update to the data provided through PubMed’s public FTP servers.

    Starting with the annual baseline release in December 2025, the content of PubMed data distributed via FTP will be generated using the same technology as the PubMed website and E-utilities API; this update means the FTP data will match the PubMed website and API.

    Test Site Available Now

    To help users prepare for this transition, a test FTP site is available now with daily update files generated by the new process. Please note, the test files may differ from the current FTP update files (see Expected Data Differences below).

    A complete baseline will not be available on the test site; only update files will be posted.

    We encourage users to review the sample files, test their workflows, and provide feedback via the National Library of Medicine (NLM) Help Desk.

    Expected Data Differences

    FTP users will notice some differences in data formatting and content. Most of these changes improve standardization and data richness without affecting the underlying meaning of the data. These differences include:

    Availability of Additional Data – PubMed data may be augmented with additional data from PubMed Central (PMC) when available. This additional data was already integrated on the PubMed website and API and will now be included in the FTP files. This change will ensure that all users have access to consistent, up-to-date PubMed data.

    Examples include:

    • More robust reference data supplied by PMC.
    • Inclusion of Conflict of Interest (COI) statements and additional content from PMC.
    • Inclusion of PMC Release Date even after the release date has passed.
    • will include and in addition to when available from PMC.

    Due to this augmented data, daily update files on the test site may contain additional PMIDs that are not included in the current FTP files since the current files are not updated with the PMC data.

    Formatting, Normalization, and Ordering – Some data may be formatted or ordered differently from the current FTP files. The structure of files and meaning of the data are not changed. Examples include:

    • Differing order of attributes or child elements.
    • Differences in capitalization of labels and some text.
    • Single digit dates will not be preceded by a zero (e.g., “1” instead of “01”).
    • Author identifiers will not be preceded by the URL. The ID source will remain as an attribute in .

    Schedule of Updates – Please note that daily update files for the current FTP and the test FTP site are generated using different processes on separate schedules. This means updated PMIDs may appear on different days between the two sites.

    Share Your Feedback

    Please reach out to us if you have questions or would like to provide feedback.

    For more information about accessing PubMed data via FTP, please see: Download PubMed Data.

    NLM will share additional details as the transition date approaches. Stay tuned to the NLM Technical Bulletin for updates.

  • Changes to Email Feature

    Changes to Email Feature

    PubMed Update: Changes to Email Feature. NLM Tech Bull. 2025 May-Jun;(464):e4.

    May 30, 2025 [posted]

    PubMed will soon reintroduce the ability to customize subject lines and body text when emailing search results or citations. With this update, the email feature will also require My NCBI login, and PubMed emails will only be sent to the email address associated with the My NCBI account.  

    In addition to restoring functionality to customize the subject and body text based on user feedback, these changes will strengthen the security of the email feature.

    Screenshot of the PubMed website showing a banner that will soon be added to the email feature interface notifying users of the forthcoming changes.
    Figure 1: Screenshot of the PubMed website showing a banner that will soon be added to the email feature interface notifying users of the forthcoming changes.

    The changes to email are currently expected to go into effect on or after July 28. To continue using PubMed’s email feature, please register for a free My NCBI account and see the My NCBI Help to learn more about My NCBI and the additional features it supports for NCBI databases.

    If you would like to save or share PubMed search results without logging in to My NCBI, use the Save feature to download results to your computer, copy and share a direct link to your results, or create an RSS feed. 

  • Trump administration proposes cutting FDA budget by 5.5%

    Trump administration proposes cutting FDA budget by 5.5%

    • Updated On May 25, 2025 at 07:19 PM IST
    • Read by 100 Professionals

    By Ahmed Aboulenein and Mariam Sunny

    Washington: The Trump administration is proposing a $6.8 billion budget request for the U.S. Food and Drug Administration for the 2026 fiscal year, its Commissioner Martin Makary said on Thursday, a cut of around 5.5% from its $7.2 billion budget this year.

    The White House had on May 2 proposed reducing U.S. health spending by more than a quarter next year, with the National Institutes of Health and Centers for Disease Control and Prevention facing the brunt of billions of dollars in cuts.

    The proposed budget requested $93.8 billion for the Department of Health and Human Services – a cut of $33.3 billion, or 26.2% – from this year’s budget of $127 billion, but did not mention the FDA. Makary’s comments on Thursday were the first official outlining of the agency’s 2026 budget request.

    “The Trump administration is proposing a $6.8 billion budget for the FDA,” Makary told the Senate Appropriations Committee’s Subcommittee on Labor, Health and Human Services, Education, and Related Agencies at a hearing on the budget.

    The FDA in 2025 had a budget of $7.2 billion, including $3.5 billion in user fees, payments made by pharmaceutical and medical device manufacturers to fund the staff resources needed to review their products quickly, conduct inspections, and ensure the safety of clinical trials.

    Makary said that nearly 1,900 people were laid off at the FDA as part of a massive restructuring of federal health agencies under Secretary of Health and Human Services Robert F. Kennedy Jr. to align with President Donald Trump’s goal of dramatically shrinking the federal government.

    No scientific reviewer or inspector was cut as a part of the reduction in force, he added. Democratic senators pushed back, asking Makary about media reports of the FDA firing and later rehiring scientists. He said the scientists were not fired but rather scheduled for firing before the decision was reversed.

    A further 1,200 took early retirement packages and the agency is hiring more scientists to replace them, Makary said.

    The staffing changes have not impacted approval schedules and the agency is on track to meet its treatment review targets under the Prescription Drug User Fee Act, known as PDUFA, he said. (Reporting by Ahmed Aboulenein in Washington and Mariam Sunny in Bangalore; Editing by Mark Porter, Conor Humphries and Aurora Ellis)

    • Published On May 25, 2025 at 06:11 PM IST

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  • Vertex misses quarterly results on weaker-than-expected demand for cystic fibrosis drug

    Vertex misses quarterly results on weaker-than-expected demand for cystic fibrosis drug

    • Updated On May 6, 2025 at 11:55 AM IST
    • Read by 100 Professionals

    Bengaluru:: Vertex Pharmaceuticals missed Wall Street estimates for quarterly results on Monday, due to lower-than-expected sales of its cystic fibrosis (CF) drug Trikafta.

    However, the drugmaker raised the lower end of its revenue forecast as it looks to its acute pain drug, Journavx, and newer CF drugs to drive growth beyond its established line of treatments.

    In December, the U.S. Food and Drug Administration approved Vertex’s next-generation treatment, Alyftrek. This once-daily treatment for a rare and progressive genetic disease further strengthens Vertex’s market dominance in CF treatments.

    CF is an inherited disorder resulting from the absence of a specific protein, which disrupts the movement of salt and water in and out of cells in various organs.

    In the first quarter ended March 31, sales of the company’s older CF treatment, Trikafta, rose 2% to $2.53 billion but missed analysts’ average expectation of $2.58 billion, according to LSEG data.

    Vertex has activated more than 65 authorized treatment centers globally and 90 patients have begun cell collection for its gene therapy Casgevy, which treats a rare blood disorder that requires regular blood transfusions.

    Vertex, sees 2025 revenue between $11.85 billion and $12 billion, compared to the previously projected range of $11.75 billion to $12 billion.

    Total quarterly revenue rose 2.7% to $2.77 billion, missing analysts’ estimates of $2.85 billion.

    On an adjusted basis, the company reported a profit of $4.06 per share for the quarter, compared with analysts’ expectations of a profit of $4.32.

    (Reporting by Sriparna Roy and Christy Santhosh in Bengaluru; Editing by Mohammed Safi Shamsi)

    • Published On May 6, 2025 at 11:52 AM IST

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  • Latest Literature on PubMed homepage will be replaced with PubMed Updates

    Latest Literature on PubMed homepage will be replaced with PubMed Updates

    PubMed Update: Latest Literature on PubMed Homepage Will Be Replaced with PubMed Updates. NLM Tech Bull. 2025 Jan-Feb;(462):e2.

    February 28, 2025 [posted]

    The Latest Literature section on the PubMed homepage will be removed and replaced with a PubMed updates section on or after March 31, 2025. The new section will include PubMed development updates and other PubMed-related highlights.

    Bottom right section, titled Latest Literature, of PubMed homepage is circled and pointed at with red arrow.
    Figure 1. Screenshot of PubMed homepage showing the Latest Literature section to be replaced.

    Latest Literature provided search links to view new citations from individual journals. If you would like to replicate this functionality, we recommend creating an RSS feed (no login required) or registering for a free My NCBI account and creating a saved search for your journal(s) of interest.

    To create an RSS feed for a search:

    1. In PubMed, search for the journal name tagged with [journal]: journalname[journal]
    2. Click “Create RSS” under the search bar.
    3. Follow the instructions on screen to create an RSS feed link you can use with your preferred RSS reader app.

    To create a saved search:

    1. In PubMed, search for the journal name tagged with [journal]: journalname[journal]
    2. Click “Create alert” under the search bar. If you are not already signed into My NCBI, you will be prompted to sign in (or create an account).
    3. Follow the instructions on screen to set up a saved search, including automatic email updates if desired.

    For more information, please see:

  • Pharma companies must file compliance strategy

    Pharma companies must file compliance strategy

    Teena Thacker

    New Delhi: Drugmakers that want to extend the timeline for implementation of Schedule M must carry out a gap analysis and file an application with the drug regulator, detailing their strategy to comply with the revised manufacturing standards.

    Small and medium manufacturers with turnover of less than ₹250 crore may seek extension of the timeline by submitting a plan of upgradation within three months from now, the drug regulatory authority said in a notification issued on Tuesday.

    “These companies will have to comply with the revised Schedule M requirements as per the plan submitted by them,” a senior official told ET.

    As per the notification, a company’s director, proprietor or partner will have to submit a gap analysis and give an undertaking to initiate upgradation within three months from the date of the application. The submission should also justify the time period they seek to comply with the requirements.

    As reported by ET, Tuesday’s notification gave small drug companies time until December 31 this year to adhere to the revised Schedule M. The application should be submitted to the Central Licence Approving Authority online, it said.

    The drug rules will be amended to provide the extension of time for another year.

    The revised Schedule M-which outlines tighter quality norms for manufacturing-was notified in January last year. While units with annual turnover of more than ₹250 crore had to comply from July 1, 2023, the implementation date for MSMEs was January 1 this year.

    However, MSMEs sought more time to make the necessary changes in their manufacturing processes.

    The ministry then issued a draft notification, proposing to extend the deadline for the MSMEs. In this regard, it had invited public comments by January 11.

    “The feedback was compiled, and the final draft was sent to the legal affairs department for vetting,” a person cited above told ET.

    The country’s pharma lobby groups had been seeking a two-year extension to the deadline, saying much time is needed for improving infrastructure, increasing manpower and training.

    Federation of Pharma Entrepreneurs (FOPE) wrote to the drug controller, seeking an extension of the notification implementation.

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