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The research, published Sept. 8 in the journal Nature Communications, examined the brain's gray matter, which mostly includes the wrinkled outer surface of the organ, called the cerebral cortex. Past studies have found that the volume of gray matter shrinks markedly during puberty and pregnancy, likely reflecting a fine-tuning of neural circuits during those periods.

There's also a gradual decline in gray matter during adulthood that's seen as a normal part of aging, said study co-author Sophie van't Hof, a doctoral student in psychiatry at Amsterdam University Medical Center. However, during the transition leading up to menopause, that gradual loss of gray matter levels off temporarily, the study found.

"This study provides the first direct longitudinal comparison of brain structural changes across all three major female hormonal transitions," said Magdalena Martínez-García, scientific director of maternal health for the Ann S. Bowers Women's Brain Health Initiative, a brain imaging consortium headquartered at the University of California, Santa Barbara.

"I really appreciate the effort that went into finding and curating such an impressive longitudinal dataset of the female brain," Martínez-García, who was not involved in the study, told Live Science in an email.

Declines in puberty and pregnancy

For their analysis, the researchers gathered data from the UK Biobank, a biomedical database that contains information from 500,000 U.K.-based adults. That data includes MRI scans of people's brains, which the team used to study brain changes in menopause.

To look at puberty and pregnancy, the researchers pulled from several brain-scan datasets that had been compiled by Leiden University in the Netherlands.

In all, the study included data from 1,095 brains across the three life stages. They analyzed each participant's brain at two different time points, examining how each person's brain changed over time and how it compared to others' brains.

The youngest cohort included participants who hadn't started menstruating yet, as well as those who'd recently started and those who'd already had periods for an average of 19 months. The pregnancy cohort included 40 who'd had their first pregnancy during the study and 30 who'd had second pregnancies, as well as 40 women who'd never been pregnant, as a point of comparison.

As in previous studies, the researchers observed that both the girls entering puberty and the pregnant women lost gray matter. But scientists don't necessarily see these declines in gray matter at puberty and pregnancy as negative.

It’s a hypothesis, but "we actually see it as something positive," van't Hof said. "We see it as neural fine-tuning."

A woman lays inside an MRI machine

The study included brain scans from over 1,000 girls and women. (Image credit: Luis Alvarez via Getty Images)

During puberty, that gray-matter loss is thought to be a normal part of the brain's development into adulthood. Its function in pregnancy is not well understood, van't Hof noted, but the evidence to date doesn't suggest that it contributes to "mommy brain" — the brain fog and forgetfulness some women can experience postpartum.

"I'm not saying that there's no neurobiological basis for this mommy brain, but up until now, we haven't found it," van't Hof said. "But what's really important is that gray matter decline is not equal to cognitive complaints."

Stability in menopause

The analysis included 120 women who entered menopause during the study. At the first time point, these women had not gone a full year without a period, but by the second time point about 3.5 years later, they had. Menopause is defined as the point at which a full year has elapsed since a person's final period.

The researchers compared these women to two other groups: about 50 women (average age 51) who had not had their last period yet and over 670 women (average age 55.5) who had already had their last period.

During late perimenopause — the final stages of the transition to menopause — the brain's gradual decline in gray matter paused, van't Hof said. Then, in postmenopausal women, that gradual decline of gray matter resumed. The exact timing of that pause differed for each woman, but it occurred consistently across the group, van't Hof noted.

The most striking finding was the lessening of the "ongoing age-related decline in brain volume during the transition into and out of menopause, compared with the more stable premenopausal and postmenopausal groups," Martínez-García said. This is an "interesting finding that adds to our understanding of how dynamic the female brain can be across the lifespan."

Factors such as whether participants had taken hormone replacement therapy for menopause and the number of children they had given birth to did not have a measurable impact on the results, the study authors noted.

In general, complaints of brain fog are widespread just before, during and after menopause, van't Hof said. This could be attributed to declining hormone levels and sleep disruptions.

"We have no clue if there's a neurological basis [for that brain fog], because, again, this is the first study to look at it," she said, adding that more studies are still needed to learn more.

"As with any study, there are some limitations to consider, but overall, I think the methods and conclusions are well supported by the data available," Martínez-García said. Both Martiniz-Garcia and van’t Hof said that they hope other researchers build on these findings to deepen scientists’ understanding of female neurobiology at every stage of life.

This article is for informational purposes only and is not meant to offer medical advice.

See how much you know about the most complex organ in the human body with our brain quiz!

'> Brain shrinkage tied to aging 'pauses' as a woman nears menopause, study finds Esko Tikkala, an archaeologist at the Lahti Historical Museum who excavated the hoard, told Live Science in an email.

The hoard has not yet been fully cleaned, separated and counted yet, but there are thousands of pieces, Tikkala said. "There are quite a lot of coins in this hoard," he said. "I have not had time to go through them."

Metal detectorist Kalle Lappinen found the two deposits Sept. 3 and immediately contacted the museum. Archaeologists inspected and properly excavated the finds the next day, according to a translated statement.

The coins were discovered in early September by metal detectorist Kalle Lappinen (right). (Image credit: Kalle Lappinen)

Tikkala described the hoard site as beside a rock outcrop in a forest near the town of Sysmä. Several other buried hoards had been found in the same region of Finland over the past 10 years, Tikkala said.

Although it's challenging to determine why specific hoards were buried, a recent study of more than 15,000 Roman-era (the eighth century B.C. to the fifth century A.D.) hoards found that they were hidden for multiple reasons, including for tax evasion, votive offerings, and safe storage in times of uncertainty.

Tikkala said the two deposits of the silver hoard were buried between two stones about 18 inches (45 centimeters) below ground and about 39 feet (12 meters) apart. There were no signs of any burials nearby, but the surrounding area had not been properly studied, he said.

Tikkala added that the coins came from areas that corresponded to present-day Germany, Sweden and Great Britain. There were also some dirhams —‬ silver coins made in the Islamic world. Dirhams previously found in Finland generally date to between about 800 and 1050, he said.

In addition to the silver coins from many places, the hoard contains items of silver jewelry and "hack silver" used for payments. (Image credit: Lahti Museum)

The hoard also contains several pieces of jewelry, including a silver bracelet, and "payment silver" in the form of hack silver (also called hacksilber) — pieces of silver that could be cut into smaller pieces for payments according to their weight.

The weight of the precious metal alone would make the hoard worth almost $10,000 today.

From the Viking Age, but not from Vikings

Although the hoard is from the Viking Age (traditionally, from the 793 attack on Lindisfarne until the 1066 defeat of a Viking army at Stamford Bridge in England), that doesn't mean it was buried by Vikings, Tikkala said.

"The term Viking Age does not imply that there were Vikings in Finland," he said. "We have no sources suggesting that Finland was 'Viking' in the same sense as regions of present-day Sweden, Norway, and Denmark."

Instead, Finnish historians and archaeologists had adopted the term to designate the period, he said. But the area now known as Finland was not culturally or politically part of Viking Scandinavia.

The hoard had been placed in two bark containers that were then buried several feet apart. (Image credit: Lahti Museum)

The next stage of the archaeological investigation will be to properly study the site where the two deposits were found, as well as their surroundings, Tikkala said; after that, specialists in Viking Age coins will try to identify the coins and prepare a detailed report.

"There will definitely be scientific articles published on the hoard as a whole, as well as more detailed studies of the coins themselves," he said.

Until now, Finland's largest Viking Age hoard was found in 1895. Buried at Nousiainen, about 130 miles (210 km) southwest of Sysmä, it contained more than 1,700 silver coins but weighed only about half as much as the newfound hoard.

Other Nordic countries have also recently reported their largest Viking Age hoards. A cache of more than 4,700 coins was found in Norway this past spring, and a homeowner in Denmark unexpectedly discovered a hoard of more than 700 silver objects weighing more than 40 pounds (18.5 kg) in their backyard, also in the spring.

See how much you know about ancient norsemen with our Viking quiz!

'> Finland's largest Viking Age silver hoard discovered by metal detectorist — and it has thousands of coins and pieces of jewelry

In 1999, two scientists independently uncovered the function of orexin and published papers about it. Dr. Masashi Yanagisawa, a molecular biologist and physician now at the University of Tsukuba in Japan, came across orexin while studying the interaction of receptors and chemicals in the brain. Dr. Emmanuel Mignot, now the director of the Stanford Center for Narcolepsy, homed in on orexin while studying narcoleptic dogs. (His Chihuahua, named Watson, has narcolepsy, and he previously had another dog with the condition, named Bear.)

This year, the pair of researchers won the coveted Albert Lasker Basic Medical Research Award for this fundamental finding that helped reshape our understanding of sleep. Their work has since led to the development of drugs for insomnia and narcolepsy.

Yanagisawa told Live Science that, at the start of his research career, he didn't expect to end up studying sleep. Mignot, on the other hand, had an early interest in understanding narcolepsy so that better treatments for the neurological disorder could be developed. Live Science spoke with Mignot about the discovery of orexin and how the field might progress in the future.

Nicoletta Lanese: What initially drew you to studying narcolepsy?

Dr. Emmanuel Mignot: There were three things that attracted me to narcolepsy: Number one, it was a human problem. It was already known [at the time] that it was not super rare. I'm not saying it's super common, but 1 person per 3,000, 0.03% ‪—‬ it's reasonably common. And nobody cared about it. I would talk to neurologists and they'd say, "Oh, I've never seen one case in my entire life." So I would say, "Yes, of course; you miss them all." That was the state of the play at the time.

Number two, was what this was a quintessential sleep disorder [in which sleep itself is disrupted]. I thought that if we found the cause of this disease, we could potentially discover something totally new about sleep — a fantastic entry point to a mystery.

The third thing that made me ready to go there was that it was tractable. A lot of problems are not tractable.

NL: Why did you start working with the dogs with narcolepsy?

EM: I studied the pharmacological basis because I was trained in pharmacology, and as a psychiatrist, and I discovered how this drug modafinil [a stimulant-based narcolepsy treatment] was working. But quickly, I realized I'm not going to find the cause by doing pharmacology. I'm only going to explore what's known.

That's when I started to fall in love with genetics, even though I was not trained as a geneticist. I said, "We have to find this gene in the dogs." It looks like they have all the symptoms. It was a huge bet, and it took me 10 years because I was definitely … overoptimistic. But it was worth the price at the end.

After narcolepsy was described — the dog gene — suddenly narcolepsy became much more famous.

NL: And scientists already knew about narcolepsy in dogs at that time?

EM: The guy at Stanford that started the sleep program was called Dr. [William] Dement. He was a graduate student in Chicago in the 1950s, when [Eugene] Aserinsky and [Nathaniel] Kleitman discovered REM sleep. He had the foresight to understand that this was an important discovery.

[Later], he discovered that narcolepsy was really a disorder where people go into REM sleep and have this very abnormal dreaming. He came in 1970 to Stanford, and the first thing he did after his medical school was to start a clinic to see patients with narcolepsy. Around then, he spoke at an American Medical Association conference in San Francisco, and he discussed different sleep disorders, including narcolepsy. And then there was someone in the audience that said, "Oh my god; I have a dog with your disease. Every time it gets excited — boom — it collapses. And it sleeps all the time."

That dog had already been euthanized, but it still gave him the idea that these dogs have narcolepsy — maybe we should try to get some. So he went to a lot of veterinarians to talk to them about it, and they identified a whole series of dogs, including the first poodle, Monique, who had narcolepsy. And they started this little colony of dogs. Initially, they tried to breed them, but most cases of narcolepsy are actually not genetic. Then, in 1977, they got a whole litter of Dobermans, and then Labradors, that had some form that was genetic.

So when I arrived, it was in 1987. They already had the dog colony. I came to study the pharmacology, to try to find a better treatment for narcolepsy. But I did stand on the shoulders of giants.

NL: At that time, it's not like you had a complete dog genome. Did that make studying their genetics challenging?

EM: It was crazy. A couple of human genes had been isolated, and mouse genes, but it was a handful. We didn't even have the full genome map in humans. And meanwhile, dogs — no pun intended — were in no man's land. Very little was known.

It took me 10 years. I had times where some people didn't believe that the dogs had narcolepsy. There were a few depressing moments, but I was convinced that was the right thing to do.

Orexin (pictured) is a peptide in the brain that promotes wakefulness. (Image credit: theasis via Getty Images)

NL: When you ultimately found the receptor for orexin, did it surprise you? It strikes me as surprising that there would be a discrete "switch" in the brain that controls wakefulness.

EM: I was lucky. Honestly, I had no idea. I got enamored with genetics because what I love [about it] is you can find something without any hypothesis. You just search for it, and what you find tells you what it is. You have no prerequisite for knowing what you would find.

I could have found something much less significant. That was a dream, to find a GPCR [G-protein coupled receptor, a protein on the outside of cells]. Can you imagine? A drug target.

Then, it turned out to be immediately applicable to humans. That, too, was a lot of luck; let's be honest. I was just trying to find the cause of one thing and one step at a time; it could have been something very complicated. It turned out to be simple.

Was I surprised? No, because I was not expecting one or another.

NL: Do you recall what the reception was like when the initial finding was published?

EM: It had an immediate effect, for several reasons. For example, I was seeing a lot of patients with narcolepsy at the time, but they were all old folks that had had narcolepsy forever. A lot of people would tell me, "I think I had it from when I was born, because I don't remember." We were never seeing children.

But after narcolepsy was described — the dog gene — suddenly narcolepsy became much more famous. And what happened is that people started to pay attention to narcolepsy, and we started to see kids. In kids, the picture is so much different. They gain an enormous amount of weight; it's very abrupt. It's a little bit different than what you see in adults, where they have adapted to it.

That was, I think, a practical consequence of the discovery. It really put narcolepsy on the map.

The second thing that happened is, all the drug companies started to develop hypnotics [sleeping pills], trying to block the orexin. They developed hypnotics relatively quickly, and they are very effective. They are probably safer than benzos [benzodiazepines] and so forth.

NL: Is it considered safer because the orexin blockers better replicate natural sleep?

EM: We know that the orexin definitely drops during sleep, so blocking it is definitely a way to recapitulate that drop; that's true. It's an awake-promoting system, so if you remove something that makes you more awake, it's safer than inducing sleep by shutting down the brain.

NL: As you moved to studying narcolepsy in humans, you found evidence that there might be an autoimmune response involved; it's been suggested that such a response may be harming the cells that make orexin in the brain. Was there suspicion that the condition had an autoimmune element previously?

EM: It's not something I 100% discovered. In 1983, before I came to study narcolepsy, there was a guy in Japan who I met, called Yutaka Honda. [Editor's note: Honda's research linked narcolepsy to the human leukocyte antigen (HLA) region of the genome, which helps regulate immune responses.]

The HLA is the way the immune system sees the world. That had just been discovered as very important for transplantation, because it's very polymorphic [takes on different forms] from one person to the next. They [Honda's group] found that all narcoleptics had a particular genetic variant, called HLA-DR2. This was a total surprise.

When I came, that was already known. But then people really looked and tried to see if the disease was autoimmune, but they couldn't find anything — no autoantibody, nothing. It was all negative.

I did a study with African Americans, and in African Americans, I found that this DR2 marker was not the best marker for narcolepsy. It was a gene just next to it that was called DQB1*06:02. [Editor's note: That HLA variant is now recognized as a strong risk factor for narcolepsy, particularly for narcolepsy type 1 (which involves a symptom called cataplexy).]

I'm very proud of that study because I think it's the first time that people used human diversity to actually map down a genetic factor more precisely, which now is used commonly. It's called transethnic mapping.

NL: New treatments that target orexin have just been approved. Do you see those therapies as an extension of your earlier findings?

EM: Of course. I was trained as a pharmacologist originally, so obviously, I do a lot of clinical trials. I see my patients totally transformed by this medication. It's just amazing. I'm so fortunate. How could you get a better reward than seeing your patients totally transformed by this medication?

It's going to have a lot of other applications [beyond narcolepsy]. Some people think it's going to be very helpful for ADHD; some people think it could be very helpful for depressed people with excessive sleepiness. We don't know, really; there's a lot of possibilities.

Another thing I'm excited about is that I have a few patients with [both] narcolepsy and schizophrenia. You cannot give them stimulants. If you give them modafinil or another dopamine stimulant [for narcolepsy], they have even more hallucinations. Often, they are sedated by their medication, and we are very poor at making people more motivated and active. These [orexin-activating] drugs seem to have effects beyond just waking people up. They seem to increase motivation.

You don't know until you try, but I'm sure it's going to have other applications.

This interview has been condensed and edited lightly for clarity. It is for informational purposes only and is not meant to offer medical advice.

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'> 'Every time it gets excited — boom — it collapses': How dogs with narcolepsy helped scientists understand the disorder Burning up,' we investigate the health impacts of climate change, focusing on heat, air quality, food and infection risk. We also evaluate the promising solutions that could help us adapt to our warmer future.

To the untrained eye, Xiaoyu Shan's lab bench looked like a home gardening experiment gone bad: dishes filled with dirt — some that looked like mud pies and others that were bone-dry — and not a plant to be seen.

But those dishes held a warning. The dirt that Shan, a postdoctoral research associate in biology and biological engineering at Caltech, was studying contained soil microbes. And those soil microbes were exhibiting a concerning propensity: In dried-out soil, they were evolving to become more antibiotic resistant.

The study describing those findings, published in March, systematically showed that drought conditions could fuel the evolution of antibiotic-resistant bacteria. Most of this resistance is driven by humans' misuse of antibiotics, which spurs bacteria to evolve genes that help them ward off the drugs. But the Caltech study raised a new worry: As many places face increased drought conditions, climate change itself could act as a selective pressure that could supercharge the evolution of these drug-resistant superbugs.

"We can expect to have more resistant bacteria being selected for in certain places around the globe," said Dianne Newman, a Caltech microbiologist and co-author of the study.

Increased antibiotic resistance is just one way that climate change is likely to put new populations at risk of multiple types of infections.

And this increased disease burden will coincide with climate change scrambling supply chains, eroding nutrition and stressing our health in other ways.

"No individual metric really does justice to the overall risk and health and well-being of these multiple stressors being exacerbated all at once and compounding each other," said Marina Romanello, a principal research fellow at the Institute of Global Health at University College London.

Warm-weather disease

In the small mountain town of Bailey, Colorado, which lies at an elevation of 7,740 feet (2,360 meters), May often brings snowstorms that can blanket the ground in white even as the sun starts to bake the plains at lower elevations. But on Memorial Day 2026, the forest floor was dry and ticks quested their way along blades of grass, seeking a blood meal.

A mild winter in most of the country means ticks — and the diseases they carry — are a rising concern. In April, the Centers for Disease Control and Prevention (CDC) reported that emergency department visits for tick bites were at their highest for that month since 2017. That trend isn't a one-off, according to the CDC; as temperatures rise, insects and arthropods can survive longer in the year and farther north.

Public health workers in Ontario do a survey for black-legged ticks. Lyme disease, which is carried by the ticks, is spreading in new areas as the climate warms. (Image credit: Bernard Weil via Getty Images)

As a result, vector-borne illnesses such as Lyme disease (spread by black-legged ticks in the Ixodes genus) and West Nile virus (spread by mosquitoes) will become more common in increasingly northerly locations. Already, alpha-gal syndrome, which is not an infection but is transmitted by the Lone Star tick (Amblyomma americanum) and causes an incurable allergy to red meat, is also seeing a dramatic rise as the species expands its range across the Northeast. Positive tests for antibodies to the alpha-gal molecule have increased by 100 times between 2013 and 2024.

Right now, almost half a million people are treated for Lyme disease each year, and the CDC records more than 8,000 cases of other tick-borne diseases annually across the country. It's not clear how this will change as the climate warms. One 2022 study found major increases in Lyme disease only at levels of warming of 6.3 to 9.9 degrees Fahrenheit (3.5 to 5.5 degrees Celsius) by 2100, but that much warming that fast is now considered an implausible scenario. However, the researchers saw a huge amount of uncertainty in the numbers, given the number of variables that affect whether a spreading tick population will transmit more disease, such as how often people go outside or what steps they take to avoid tick bites. Tick-borne illnesses are likely also underreported, so even the true number of illnesses transmitted each year right now is unknown.

But ticks are responsible for spreading 90% of all vector-borne diseases in the U.S., so any trends in the suite of illnesses spread by ticks are likely to affect thousands to tens of thousands of people.

An even more ubiquitous bloodsucker, the mosquito, currently spreads only a few diseases in the U.S. The most common and most serious is West Nile virus, which mosquitoes catch from feeding on infected birds. As of Sept. 8, 504 cases of West Nile virus had been reported in the U.S. in 2026, with 363 of them affecting the central nervous system. And because fewer than 1% of West Nile cases progress to the central nervous system, those numbers likely represent a dramatic underreporting of milder cases, which can cause months of fatigue in some people, in addition to acute flu-like symptoms, such as fever, headache and body aches.

Mosquito-borne illnesses like West Nile are expected to spread more quickly in warming temperatures. Heat helps mosquitoes stick around longer during the year, much like it does for ticks. It also speeds up the transmission and replication of the virus inside the mosquito, since the insects are cold-blooded and thus their metabolism is ruled by the weather.

"Except for places that are already really, really warm, we should expect that the replication rate of the virus inside the mosquito will speed up," said John Drake, director of the Center for the Ecology of Infectious Diseases at the University of Georgia. "That shortens the generation time, and that means we expect there to be more transmission."

Even though mosquitos love water, climate-related drought could ironically nearly triple the number of human West Nile cases in the U.S. over the next 30 years from around 2,000 reported cases (according to CDC data) to between 5,000 and 6,000. That's likely because in drier conditions, more mosquitoes are infected, possibly because birds, the intermediate host of the virus, either congregate more closely with mosquitoes around water sources or breed less readily in drought, meaning the fraction of birds that carry the virus is higher than in more water-abundant times.

Except for places that are already really, really warm, we should expect that the replication rate of the virus inside the mosquito will speed up. That shortens the generation time, and that means we expect there to be more transmission.

John Drake, director of the Center for the Ecology of Infectious Diseases at the University of Georgia

Mosquito-borne diseases long ago eradicated from the U.S. could also resurge with warming temperatures. The southeastern United States will become more prone to malaria and dengue fever transmission under all levels of warming; summer 2026 saw more than 40 locally-acquired cases of dengue fever in Florida. Public health surveillance and disease-control measures have largely stopped those transmission chains, but the likelihood is that society will have to pour more money into beating these diseases back again in future decades. For example, there are malaria vaccines approved for children, but currently, they are recommended only in areas where the illnesses are endemic. If malaria were commonly found in the southern U.S., millions of Americans might need vaccines, including susceptible adults.

"If we were to get endemic diseases like those in the U.S. again, it could become a huge burden and it could be quite costly," Drake said.

Disaster and disease

Flooding is another factor that's exacerbating vector-borne disease under climate change. As climate change worsens, extreme weather events will, too. Because warm air can hold more moisture, many areas will see increased episodes of heavy rainfall and hurricanes will become more intense.

"Flooding creates habitat for these mosquitoes," Drake said.

Disasters also spur the spread of other diseases that are usually quite rare in the U.S., such as leptospirosis, a bacterial infection that spreads from animals to humans via animal urine. Floodwaters may be contaminated by the bodies of drowned animals; in 2022, after Hurricane Fiora hit Puerto Rico, leptospirosis cases leapt by a factor of 3.6 to over 10 cases a week.

After Hurricane Matthew, emergency visits for gastrointestinal disease increased 11%. (Image credit: Raleigh News & Observer via Getty Images)

After Hurricanes Matthew and Florence in 2016 and 2018, respectively, North Carolina saw an 11% increase in emergency department visits for gastrointestinal illnesses. Black and American Indian residents were the most affected, likely because discrimination over generations has disproportionately pushed Black Americans and Native Americans to less desirable, more flood-prone land, the researchers found.

Cycles of precipitation, drought and subsequent dust storms can spur the spread of Valley fever, a fungal respiratory disease that causes an estimated 700 to 1,100 deaths per year, mostly in the U.S. Southwest. Valley fever is already on the rise, with cases in Arizona, one of the hotspots for the disease, doubling from about 64 cases per 100,000 people in 2005 to 145 cases per 100,000 people in 2022. As the West warms and dries, Valley fever is likely to spread from its stronghold in the Southwest and become endemic in Idaho, Wyoming, Montana, Nebraska, South Dakota and North Dakota, putting millions more people at risk.

The infectious disease risk from natural disasters tends to stack on top of other health problems stemming from these catastrophes. Flooded buildings can harbor mold that can worsen allergies, asthma and other respiratory illnesses. When major storms cause power loss, people turn to generators for electricity, which release pollutants linked to asthma. Though it's often hard to track the effects of these disasters, one study found that flooded regions after Tropical Storm Imelda in Texas in 2019 saw 10% more emergency department visits for asthma than nonflooded regions did.

Moreover, the threat to life and livelihood from these disasters can cause mental health conditions, such as post-traumatic stress disorder, Romanello said. The problems compound on each other, she said; already, she has heard reports from Africa about malaria outbreaks, fed by warming, and health workers struggling to reach the affected regions because flooding, also exacerbated by warming, has washed out roads.

"What is the most concerning aspect is that all of that is happening together, so we're seeing all of this risk being exacerbated at once," she said.

Jace White of Fresno acquired Valley Fever while working on his family farm. Valley fever is predicted to become more common with climate change. (Image credit: The Washington Post via Getty Images)

Antibiotic resistance on the rise

As Newman and Shan's work shows, as spots around the U.S. face new infection risks, existing treatments may become less effective. Their work showed that drought concentrated the natural antibiotics that bacteria make in the soil, making it harder for bacteria susceptible to the compounds to survive. As a result, the microbes with genes for antibiotic resistance did better. The problem for human health is that bacteria are very good at gene swapping, so these soil microbes can easily pass their antibiotic resistance superpowers to bacteria that infect people, their research showed.

"Gardening, breathing dust ‪—‬ that's how it happens," Newman said of human and soil bacteria coming into contact. "We are constantly encountering bacteria in our environment."

A microscope image showing colorful cylindrical cells against a blue background

A scanning-electron microscope image of Pseudomonas aeruginosa. Recent research suggests that drought could fuel the rise of drug-resistant versions of such pathogenic bacteria. (Image credit: CDC/SCIENCE PHOTO LIBRARY via Getty Images)

The researchers found an association between drought and antibiotic resistance reported by hospitals.

They aren't the only ones. A recent study on Salmonella, a bacterium that causes about 1.35 million cases of food poisoning each year in the U.S. alone, found that temperature and rainfall promote antibiotic resistance in this microbe. "Globally, climate change was linked to about a 10% increase in Salmonella resistance gene abundance," said study first author Zhen-Chao Zhou, an ecology researcher at the Chinese Academy of Sciences in Beijing. Other microbes show similar effects.

Meanwhile, warmer conditions help bacteria grow faster, adapt to stress and swap resistance genes, Zhou said, while drought concentrates them in limited water sources where they mingle freely. Climate-change-induced flooding can then, in theory, spread the resistant genes far and wide.

Combating the compounding risks requires both public health and climate mitigation approaches, experts say. Not only does the world need to cut greenhouse gas emissions, but people also need to use antibiotics more carefully, Zhou said; improve sanitation practices, such as sewage management, around the world so that antibiotic-resistant strains don't spread as easily; strengthen food safety; and expand disease surveillance. The public also needs to understand that climate change is a health issue, Romanello said.

"When we talk about tackling greenhouse gas emissions," she said, "what we're talking about is a sustainable livable future with healthy economies."

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Genetic studies of personality traits previously relied on comparisons between twins. Now, genetic sequencing technologies have advanced the field. (Image credit: Johner Images via Getty Images)

The advent of gene sequencing enabled geneticists to calculate the influence of genes with greater precision than twin studies did. The most powerful tool in this arsenal is the genome-wide association study (GWAS), which can link traits to gene variants in detail. These statistical analyses require sample sizes in the millions, though.

The new study was a large collaborative project called the Revived Genomics of Personality Consortium, which brought together 46 cohorts of participants who'd had their genomes sequenced. Each person had been asked something related to one of the Big Five personality traits. The team had data from roughly 600,000 people about the first four traits — extraversion, agreeableness, conscientiousness, openness to experiences — and data from over 1.1 million people about their levels of neuroticism.

Generally, as geneticists have leveraged larger and more powerful GWAS, many traits have shown increased heritability because these bigger studies can identify more subtle genetic links, said Brent Roberts, a psychologist at the University of Illinois at Urbana-Champaign who was not involved in the new study. But "with personality, it was really clear from the get-go that it was different," Roberts said.

Earlier GWAS had suggested that the heritability of personality from common gene variants was roughly 5% to 15%, far lower than the estimate suggested by twin studies. The new work has confirmed those low numbers, said study co-author Michel Nivard, a genetic epidemiologist at the University of Bristol in the U.K.

It may be that GWAS do not capture extremely rare variants that might link personality traits in certain families, which means the heritability may be slightly underestimated, Nivard suggested. Additionally, twins are more likely to rate their personalities as similar for reasons unrelated to genetics, so the twin studies may have overestimated the heritability of personality, Nivard noted.

Cutting out confounders

It can be difficult to control for confounding factors in GWAS. For example, if scientists were investigating the influence of genes on academic achievement, genetics only tells part of the story; a person's socioeconomic status and access to books and tutoring also influence their education.

But in this case, Nivard and his colleagues did not find confounders in measuring personality. The researchers found that the genetic effects on personality are the same within families as they are among unrelated individuals.

"We've basically been able to rule out that there's any straightforward, simple social processes by which your parents directly influence your personality," Nivard said.

A key takeaway from the study should be not to focus too much on the different contributions of genes versus environmental factors in a trait as complex as personality, Roberts said. Our moods and minds are a collaboration between the two factors, not a tug-of-war, he argued.

A study to properly measure this interplay would be vastly expensive and would require following participants for decades. "This is where the limitation of human genetics research is really profound," Roberts said. Part of the problem, he added, is that while our DNA sequence is fixed, how the body accesses and reads DNA varies significantly depending on the environment a person finds themselves in. In other words, which genes get turned on and when are variable factors.

Assessing this enmeshed relationship using only the DNA code we are born with is like trying to predict every move of a couple's dance by looking at how they hold each other before the music starts up.

Nivard and his team can now use this powerful data source to learn more about personalities within groups of people, he said. Nivard predicted that, even once geneticists have mapped all the rare gene variants that may influence personality, some genetic influence will still go unaccounted for; processes such as the interaction between the environment and gene expression are still not fully understood. He called these the "unknown unknowns." Identifying these factors is the next frontier for the genetics of personality.

"It's where we're headed," Nivard said.

'> 1 million people's genes reveal the heritability of the Big Five personality traits — and it's complicated
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