Tag: ginecologia

Fertility tests are not a reproductive crystal ball
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Increasing numbers of Australian women are using a blood test to assess their fertility, but new research suggests it may not provide the answers many are looking for.

A study led by Flinders University and published in the Australian and New Zealand Journal of Obstetrics and Gynaecology found requests by GPs for anti-Müllerian hormone (AMH) tests increased more than 13-fold between 2011 and 2021, despite growing evidence that the test cannot predict whether a woman will become pregnant naturally – not now or in the future.

AMH is often marketed as a fertility test or “egg count” because it measures ovarian reserve, or the number of eggs remaining in the ovaries. However, researchers say many women and clinicians misunderstand what the results can tell them.

Analysing health records from almost 1.4 million Australian women, the researchers found testing increased dramatically over the decade they analysed. Women aged 30 to 34 experienced the sharpest rise, with test rates increasing almost 20-fold.

Associate Professor Luke Grzeskowiak

Lead author Associate Professor Luke Grzeskowiak, a pharmacist and researcher with the Flinders Health and Medical Research Institute (FHMRI), says the findings highlight a gap between public perception, clinical practice and scientific evidence.

“Many women seek AMH testing because they want to understand their future fertility,” says Associate Professor Grzeskowiak.

“But while AMH can measure ovarian reserve, it cannot tell a healthy woman how likely she is to conceive, how quickly, or how much reproductive time she has left.

“One of the biggest concerns is the psychological impact. Women may feel pressured to bring forward plans for children after a low result, while a normal result may provide false reassurance if other fertility issues are present.”

Researchers say the rise in testing is likely linked to delayed childbearing, a growing awareness of fertility issues, social media messaging and commercial promotion of the test as a simple way to gauge reproductive potential.

The study found nearly one in five women received a result classified as low. However, among women who repeated the test after a low result, around one-third later received a result in the normal range.

“A low AMH result does not mean a woman is infertile, and a normal result does not guarantee future fertility,” says Associate Professor Grzeskowiak.

“Our concern is that women may be making important decisions about relationships, family planning or egg freezing based on information that cannot answer the questions they are most concerned about.”

The researchers say that age remains the most important factor affecting fertility.

“Women deserve clear, evidence-based information about what AMH testing can and cannot tell them,” says Associate Professor Grzeskowiak.

“For younger women, in particular, an AMH result should not be viewed as a crystal ball for their reproductive future.”

The study also revealed substantial differences in testing rates across Australia. Women living in major cities and more advantaged areas were more likely to have the test, while concession card holders were less likely to be tested.

Researchers note that AMH testing is not covered by Medicare and can cost more than $100.

Large differences were also seen between GP practices. More than one in 10 practices had no patients who received an AMH test during the study period, and around 21% of the variation in testing rates was linked to differences between practices rather than patient characteristics.

“Our findings highlight the need for better education of both clinicians and the public,” says Associate Professor Grzeskowiak.

“AMH testing can be useful in some specialist fertility settings, but it should not be mistaken for a test that predicts whether a woman will be able to have a baby.

“The best way to support women is with accurate, evidence-based information, so they can make informed decisions about their reproductive health and future family plans.”

The paper, ‘Trends in anti-Müllerian hormone (AMH) testing for fertility assessment in Australian general practice, 2011–2021: a retrospective open cohort study,’ by Gizat M. Kassie, Tessa Copp, Sarah Lensen, Danielle Mazza, Jacqueline A Boyle and Luke E. Grzeskowiak, was published in Australian and New Zealand Journal of Obstetrics and Gynaecology. DOI: https://doi.org/10.1111/ajo.70179.

Acknowledgements: Luke Grzeskowiak receives salary support by a Channel 7 Children’s Research Foundation Fellowship (CRF-210323). The research was supported by SPHERE Centre of Research Excellence in Women’s Sexual and Reproductive Health in Primary Care (SPHERE CRE), which is funded by the National Health and Medical Research Council (Project number APP2024717).


source: https://news.flinders.edu.au/blog/2026/09/11/fertility-tests-are-not-a-reproductive-crystal-ball/?utm_source=chatgpt.com

September 12, 2026 Read More
Premature Menopause Linked to Increased Hypertension Risk
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The research analyzed data from about 107 800 women in the UK Biobank. Over a median follow-up of nearly 15 years, about 18 500 women developed high blood pressure. Approximately 23% of women who reached menopause prematurely—between the ages of 25 and 35—developed hypertension, compared with 19% of women who reached menopause between the ages of 40 and 45 and 17% of women who reached menopause after age 45. After adjusting for known risk factors such as body mass index and lifestyle, earlier menopause was still associated with increased risk of high blood pressure.

The researchers said that the findings, published in Menopause, suggest the importance of considering age at menopause as a distinct cardiovascular risk factor for hypertension.

Published Online: September 4, 2026. doi:10.1001/jama.2026.12069


source: https://jamanetwork.com/journals/jama/fullarticle/2853911?utm_source=chatgpt.com

September 12, 2026 Read More
RSV Bivalent Prefusion F Protein Vaccine in Pregnancy and Protection Against RSV-Associated Illness in InfantsA Systematic Review and Meta-Analysis
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Rabab Batool, PhD1Ran Wang, MD2,3,4Hala Obeid, BSc2,5 et al

Author Affiliations


  • 1Department of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada
  • 2Canadian Center for Vaccinology, Dalhousie University, IWK Health Centre and the Nova Scotia Health Authority, Halifax, Nova Scotia, Canada
  • 3Departments of Pediatrics, Dalhousie University, Halifax, Nova Scotia, Canada
  • 4Laboratory of Infection and Virology, Beijing Pediatric Research Institute, Beijing Children’s Hospital, National Center for Children’s Health, Capital Medical University, Beijing, China
  • 5Departments of Microbiology and Immunology, Dalhousie University, Halifax, Nova Scotia, Canada
  • 6Department of Community Health and Epidemiology, Dalhousie University, Halifax, Nova Scotia, Canada
  • 7British Columbia Children’s Hospital Research Institute, Vancouver, British Columbia, Canada
  • 8Department of Pediatrics, University of British Columbia, Vancouver, British Columbia, Canada

Key Points

Question  Does the respiratory syncytial virus (RSV) bivalent prefusion F protein (RSVpreF) vaccine, when administered during pregnancy, protect infants against RSV-associated lower respiratory tract infection hospitalization in real-world settings?

Findings  In this systematic review and meta-analysis including 7 studies comprising 7112 infants, of whom 2684 were born to vaccinated mothers, RSVpreF was effective against RSV-associated lower respiratory tract infection hospitalization in infants from birth to 3 months and from birth to 6 months, when administered at least 14 days before delivery.

Meaning  Results suggest that RSVpreF vaccine, when administered at least 14 days before delivery, provided high protection to infants against RSV-associated hospitalization; this supports the integration of RSVpreF into national immunization programs.

Abstract

Importance  The respiratory syncytial virus (RSV) bivalent prefusion F protein vaccine (RSVpreF) administered during pregnancy has demonstrated efficacy in protecting infants against early-life RSV disease in the pivotal clinical trial.

Objective  To conduct a systematic review and meta-analysis to synthesize real-world evidence on the effectiveness of RSVpreF in preventing RSV-associated lower respiratory tract infection (LRTI) in infants.

Data Sources  PubMed, Scopus, and Europe PMC were searched from January 1, 2020, through January 30, 2026.

Study Selection  A total of 1144 studies were initially identified. Eligible were nonrandomized studies reporting the effectiveness of RSVpreF vaccine in pregnancy in the prevention of RSV-associated LRTI in infants.

Data Extraction and Synthesis  All studies were screened independently by 2 reviewers. Data were extracted on RSV-associated outcomes among infants born to women who received RSVpreF vaccination during pregnancy and infants born to unvaccinated women.

Main Outcomes and Measures  The primary outcome was RSV-associated LRTI hospitalization. Odds ratios (ORs) were pooled using random-effects meta-analysis with the Hartung-Knapp adjustment and Sidik-Jonkman estimator. Vaccine effectiveness against RSV-associated LRTI hospitalization was calculated as (1 − OR) × 100% and assessed in infants from birth to age 3 months and from birth to 6 months, separately. The limited available data precluded meta-analysis of effectiveness against the secondary outcomes of RSV-associated emergency department visits, intensive care unit admissions, and death.

Results  A total of 7 studies were included, comprising 7112 infants, of whom 2684 were born to vaccinated mothers. The studies collected data from January 2024 through April 2025 from Argentina, the UK, and the US. Pooled vaccine effectiveness against RSV-associated LRTI hospitalization was 82% (95% CI, 81%-82%; 3 studies, 4397 participants; I2 = 0%) in infants from birth to 3 months and 78% (95% CI, 70%-84%; 6 studies, 3008 participants; I2 = 18.7%) in infants from birth to 6 months, when mothers were vaccinated 14 days or more before delivery.

Conclusions and Relevance  The results of this systematic review and meta-analysis suggest that postimplementation data support the effectiveness of RSVpreF in pregnancy for the prevention of RSV-associated LRTI hospitalization during the first 6 months of life. The results support the introduction of RSVpreF into routine antenatal immunization programs.


source: https://jamanetwork.com/journals/jamapediatrics/article-abstract/2853476?utm_source=chatgpt.com

September 12, 2026 Read More
Menopausal Hormone Therapy and Cardiovascular Risk in Midlife Women With Vasomotor Symptoms
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Ziyuan Wang, PhD1Sonja A. Swanson, ScD1Maria M. Brooks, PhD1 et al

Author Affiliations


  • 1University of Pittsburgh School of Public Health, Pittsburgh, Pennsylvania
  • 2University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania
  • 3Virginia Commonwealth University School of Public Health, Richmond

Key Points

Question  What is the effect of menopausal hormone therapy (MHT) on cardiovascular disease (CVD) risk in perimenopausal and recently postmenopausal women with vasomotor symptoms, and does the effect vary by timing of MHT initiation relative to menopause and by race and ethnicity?

Findings  Using observational data of 2737 women from the Study of Women’s Health Across the Nation to emulate a target trial, it was estimated that MHT initiation in these participants reduced cardiovascular disease risk by 22%. Protective effects were most pronounced among Black women and women who initiated MHT within 10 years of menopause onset; however, these findings should be interpreted in light of the assumptions required for causal inference and the possibility of residual confounding.

Meaning  These findings indicate that the CVD impact of MHT potentially varies by timing of initiation and race and ethnicity; however, given the lack of consistent CVD benefit and the overall risk benefit balance, these findings should not be used to support the use of MHT for CVD prevention.

Abstract

Importance  Vasomotor symptoms in perimenopause are associated with increased future cardiovascular (CVD) risk. Most clinical trials on menopausal hormone therapy (MHT) and CVD risk have focused on postmenopausal women, with limited study of the perimenopausal period when hormonal fluctuations and symptoms are greatest. Moreover, these trials were not designed to evaluate CVD risk with MHT among women with vasomotor symptoms.

Objective  To estimate the effect of MHT on CVD risk among perimenopausal and recently postmenopausal women with vasomotor symptoms and assess the extent to which timing of MHT use relative to menopause and race and ethnicity modify this effect.

Design, Setting, and Participants  Cohort data from the Study of Women’s Health Across the Nation (SWAN, 1997-2017)—a multiethnic, multicenter, longitudinal study of the menopause transition—were used to emulate a sequence of target trials. Eligible participants were women who self-reported any vasomotor symptoms (ie, hot flashes and/or night sweats over the past 2 weeks) and who were CVD-free, with no prior MHT use. Data were analyzed from January 2023 to December 2025.

Exposure  MHT use (systemic estrogen with/without progestogens, verified from medication containers).

Main Outcomes and Measures  CVD events (myocardial infarction, stroke, heart failure, and revascularization) were self-reported. CVD-related death was recorded from death certificates.

Results  Of 2737 women who reported any vasomotor symptoms, 755 initiated MHT (mean [SD] age, 53.7 [4.6] years) over the 20-year follow-up period, during which 224 fatal and nonfatal CVD events occurred. Overall, the estimated adjusted hazard ratio (aHR) of CVD events for MHT initiation vs noninitiation was 0.78 (95% CI, 0.62-0.98). The estimated aHR was 0.73 (95% CI, 0.58-0.93) and 1.53 (95% CI, 0.66-3.52) among women initiating MHT 10 or fewer years vs more than 10 years from the onset of menopause, respectively (P value for interaction: .02). Race and ethnicity modified the MHT initiation effect, with Black women showing protective effect (aHR, 0.51; 95% CI, 0.33-0.81), while no clear effects were observed in White women or women of other races (P value for interaction = .007).

Conclusions and Relevance  The presented results are pooled from all target trials and found that MHT initiation during perimenopause or recently postmenopausal women with vasomotor symptoms was estimated to reduce CVD risk by 22%. Benefits were more pronounced in Black women and women who initiated MHT within 10 years of menopause onset. However, all estimates warrant caution given the potential for residual confounding. Given the inconsistency of the cardiovascular benefits and the need to consider overall risk-benefit balance, these findings should not be used to support MHT for CVD prevention.


source: https://jamanetwork.com/journals/jamainternalmedicine/article-abstract/2853611?utm_source=chatgpt.com#

September 12, 2026 Read More