Sunday, April 12, 2026

 

High societal costs linked to extremely preterm birth




University of Gothenburg
Hanna Gyllensten 

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Hanna Gyllensten, Senior Lecturer at the Sahlgrenska Academy, University of Gothenburg

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Credit: Photo: Reghan Borer




Children born before 24 weeks of gestation are linked to high societal costs throughout childhood. Costs are highest during the first year of life, but the need for support persists for many years. This is shown in a study by researchers at the University of Gothenburg, Sweden.

Being born before 24 weeks usually means that the child needs help with breathing, maintaining body temperature, and receiving nutrition. Care is provided in neonatal units and may continue for weeks or months. This concerns only a small number of children each year – just a fraction of the approximately 115,000 children born in Sweden annually.

The study shows how costs change over time and may help improve how societal support is tailored, while also highlighting that the need for support persists long after the initial period of care. It is based on register data from 344 children in Sweden who were born before 24 weeks of gestation between 2007 and 2018 and were followed for an average of nearly eight years.

Hanna Gyllensten, Senior Lecturer at the Sahlgrenska Academy, University of Gothenburg, is one of the authors of the study:

“We see that costs are highest during the first year of life, averaging around SEK 1.7 million per child. At the same time, there are large differences between children. Those who experience severe complications early in life often have more long-term and extensive support needs,” says Hanna Gyllensten.

Costs shift over time
Needs vary across children. Children with severe early complications often have greater and more long-term support needs. More than 80 percent of healthcare costs arise during the child’s first year.

Chatarina Löfqvist is Professor of Caring Science at the Sahlgrenska Academy, University of Gothenburg, and first authors of the article:

“After a few years, we see a clear shift: healthcare no longer accounts for the largest share of costs; instead, societal support for the family becomes the largest component. These are long-term support measures that follow the child through childhood and reflect needs that remain long after acute care has ended,” says Chatarina Löfqvist.

An important next step is to develop follow-up programs where the needs of the child and family are central, and where support efforts can be coordinated over time.

The study does not include all types of costs, such as special education or informal care.

Article: Long-Term Societal Costs After Births Before 24 Weeks of Gestation in Sweden https://doi.org/10.1111/apa.70527

 

Scientists reveal how regional species pools shape tree diversity and rarity in subtropical and tropical forests




KeAi Communications Co., Ltd.
Typical forest landscapes of subtropical and tropical regions in china, and the distribution map of the forest plots used in this study. 

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Typical forest landscapes of subtropical and tropical regions in china, and the distribution map of the forest plots used in this study.

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Credit: Jian Zhang





Why do some natural forests hold so many different kinds of rare trees? It's a question that has long puzzled and intrigued ecologists. While early studies focused on local environmental conditions, scientists now know that broader regional forces, like historical climates and species dispersal, also shape local forest diversity.

In new research published in the KeAi journal Plant Diversity, an international research team led by Dr. Jian Zhang from Sun Yat-sen University explored what drives tree diversity and rarity in China's subtropical and tropical forests—some of the most biodiverse forests on Earth at the same latitudes.

Using a large database (VAST-China) of 3,923 forest plots covering 3,307 tree species, the team defined the regional species pool as all the species that could potentially occur in a given area. They then quantified how regional and local factors together determine species richness (how many species live there) and rarity (how uncommon they are).

"We found that the size of the regional species pool is the strongest driver of local tree diversity," shares Zhang. "Forests with larger species pools, supported by favorable climates, varied habitats, and stable historical climates, have far more species locally."

In particular, warmth, complex topography, and steady paleoclimates help species accumulate over time at regional scales, boosting both total diversity and the number of rare trees.

"Large species pools support both high diversity and many rare species," explains lead author Dr. Houjuan Song from Shanxi Agricultural University. "Rare trees thrive where regional species pools are rich and human pressure is low. This tells us we must prioritize rare and endemic species protection in highly damaged and fragmented forests."

"To preserve forest diversity and save rare and endemic species as the accelerating environment changes, we need to protect the areas with large species pools and minimize human disturbance, especially in biodiversity hotspots," Zhang adds.

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Contact the author: Jian Zhang, zhangjian6@mail.sysu.edu.cn

The publisher KeAi was established by Elsevier and China Science Publishing & Media Ltd to unfold quality research globally. In 2013, our focus shifted to open access publishing. We now proudly publish more than 200 world-class, open access, English language journals, spanning all scientific disciplines. Many of these are titles we publish in partnership with prestigious societies and academic institutions, such as the National Natural Science Foundation of China (NSFC).

 

New research brings machine‑learning‑based physics a step closer to solving real engineering challenges


University of Manchester






A mathematics professor at The University of Manchester has developed a novel machine-learning method to detect sudden changes in fluid behaviour, improving speed and cost of identifying these instabilities and overcoming one of the major obstacles faced when using machine learning to simulate physical systems.

Computational simulations of mathematical models of fluid flow are essential for everyday applications ranging from predicting the weather to the assessment of nuclear reactor safety. The advent of this simulation capability over the past 50 year has revolutionised the development of fuel-efficient aeroplanes and sail configurations on racing yachts can now be optimised in real time, providing the marginal gains needed to win races in the Americas Cup.

Optimised aerodynamics means that modern day cyclists can ride faster, golf balls fly further and Olympic swimmers consistently set world records. Computational fluid dynamics also enables the modelling of the flow of blood in the human heart, making the provision of patient-specific surgery possible.

Scientists and engineers rely on computer-based simulations to understand, predict, and design these systems that they can’t easily test in real life. But traditional fluid‑simulation methods often require hours or even days of computation, and struggle when the flow becomes fast or highly complex.  

Machine‑learning‑based simulations, once trained, can make these assessments almost instantly. Instant feedback would allow rapid design testing, real‑time adjustments, and rapid testing variation without the usual computational burden.

The findings were published in the Journal of Computational Physics.

Professor David Silvester, Professor of Applied Mathematics at The University of Manchester said: "Solving reliability issues that machine‑learning models encounter would offer major benefits for scientific research and engineering. The issue to be faced is that naive AI predictions of flows generated solely from data are highly likely to feature impossible scenarios. This is a serious concern when predicting extreme events like tornados and tsunamis.”

The study uses the stability of fluid motion as the foundation for a new method that predicts how complex systems behave. Instead of relying on costly laboratory experiments, solutions to the fundamental equations of fluid motion are generated numerically. This allows the machine-learning model to be trained on accurate, high-quality data drawn directly from physics, demonstrating that the model can accurately handle challenging simulations.

A key focus of the work is identifying bifurcation points –the moments when a smooth, steady flow (laminar flow) suddenly begins to change – similar to calm, evenly flowing river as it hits an obstruction, or splits and fluids start to mix and form eddies. Laminar flow is when a liquid behaves in a smooth and orderly way, like pouring honey, the flow is consistent and steady.

By successfully using a machine‑learning model to identify the points at which a system changes behaviour or in this case bifurcates, the study suggests that, with further refinement, machine‑learning‑based models could become a practical alternative to traditional fluid‑modelling techniques in the future.

Professor Silvester added: "This marriage of old and new approaches holds the promise of efficient computation of physically realistic fluid flows in a myriad of practical situations. The development of refined mathematical models of complex fluids is likely to be critically important if the promise of AI is to be effectively realised in the future.”

One DNA letter can trigger complete sex reversal, Bar-Ilan University study finds


Researchers show that a tiny mutation outside a gene caused XX mice to develop as males instead of females, revealing the powerful role of non-coding DNA



Bar-Ilan University

One DNA letter can trigger complete sex reversal, Bar-Ilan University study finds 

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Dr. Nitzan Gonen, Goodman Faculty of Life Sciences and Institute of Nanotechnology and Advanced Materials, Bar-Ilan University

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Credit: Courtesy Bar-Ilan University





Researchers at Bar-Ilan University have discovered that changing just one letter in DNA can completely alter sex development in mice. In the new study, published in Nature Communications, a single-letter insertion in a non-coding regulatory region caused XX mice, which would normally develop as females, to develop instead as males with testis and male genitalia.

The finding is especially striking because the mutation was not made in a gene itself, but in a distant stretch of DNA that helps control a key developmental gene. The study highlights the major role of the non-coding genome -- the 98 percent of DNA that does not make proteins but helps regulate when and how genes are turned on and off.

“This is a remarkable finding because such a tiny change -- just one DNA letter out of ~2.8 billion -- was enough to produce a dramatic developmental outcome,” said Dr. Nitzan Gonen, from the Goodman Faculty of Life Sciences and Institute of Nanotechnology and Advanced Materials at Bar-Ilan University. “It shows that non-coding DNA can have a profound effect on development and disease.”

The mutation was introduced into a regulatory element known as Enh13, which controls the activity of Sox9, a gene essential for testis development. For ovaries to develop normally, Sox9 must be kept turned off. The researchers found that Enh13 acts as a kind of molecular battle site/switch: in males, factors that promote testis development bind to it and activate Sox9 whereas in females, factors that promote ovary development bind to it and repress Sox9.

When the researchers introduced the mutation using CRISPR genome editing, that female repression failed. As a result, Sox9 was activated in XX mice, and testis developed, leading to complete internal and external male development.

The team created several mouse models with very small mutations in Enh13, including a one-base-pair insertion and a three-base-pair deletion. Both mutations caused XX mice to develop testis. The researchers then used cell-line reporter assays to understand how the mutation disrupted the normal regulatory mechanism.

The study builds on earlier work by the same group, published in 2024, which showed that other small mutations in the same regulatory element could have the opposite effect, causing XY mice to develop as females. Together, the findings suggest that Enh13 has a dual role: it acts as an enhancer in male development, but must also be repressed in female development.

Beyond its significance for basic biology, the study may have important implications for people with Differences of Sex Development (DSD), a group of conditions that affect about 1 in 4,000 births worldwide. More than half of DSD cases still lack a genetic diagnosis, even after sequencing the protein-coding parts of the genome.

“Our findings show that it is not enough to look only at genes,” said Elisheva Abberbock, the PhD student leading the research. “Important disease-causing mutations may also lie in the non-coding genome, in DNA regions that control gene activity rather than encode proteins.”

The researchers believe Enh13 may be just the beginning, and that many more regulatory regions in non-coding DNA may be involved in sex determination and other developmental disorders. They are now working to identify these regions systematically and test their function.

The study was led by Elisheva Abberbock together with other researchers from Bar-Ilan University. Collaborators included Dr. Ariel Afek of the Weizmann Institute and Dr. Francis Poulat of the University of Montpellier. The research was funded by the Israel Science Foundation and an ERC Starting Grant.

 

One DNA letter can trigger complete sex reversal, Bar-Ilan University study finds 

The figure depicts the Enh13 regulatory region alongside the Sox9 gene as a “battle site” between the sexes. Pro-female factors act to repress Sox9 via binding to Enh13, while pro-male factors activate it. The balance between these opposing forces ultimately determines whether male or female development occurs.

Credit

Neta Varsano