Sunday, September 4, 2022

Perinatal stroke

Helen Santoro

I barreled into the world — a precipitous birth, the doctors called it — at a New York City hospital in the dead of night.

In my first few hours of life, after six bouts of halted breathing, the doctors rushed me to the neonatal intensive care unit. A medical intern stuck his pinkie into my mouth to test the newborn reflex to suck. I didn’t suck hard enough. So they rolled my pink, 7-pound-11-ounce body into a brain scanner.

Lo and behold, there was a huge hole on the left side, just above my ear. I was missing the left temporal lobe, a region of the brain involved in a wide variety of behaviors, from memory to the recognition of emotions, and considered especially crucial for language.-

My mother, exhausted from the labor, remembers waking up after sunrise to a neurologist, pediatrician and midwife standing at the foot of her bed. They explained that my brain had bled in her uterus, a condition called a perinatal stroke.

They told her I would never speak and would need to be institutionalized. The neurologist brought her arms up to her chest and contorted her wrists to illustrate the physical disability I would be likely to develop.

In those early days of my life, my parents wrung their hands wondering what my life, and theirs, would look like. Eager to find answers, they enrolled me in a research project at New York University tracking the developmental effects of perinatal strokes.

But month after month, I surprised the experts, meeting all of the typical milestones of children my age. I enrolled in regular schools, excelled in sports and academics. The language skills the doctors were most worried about at my birth — speaking, reading and writing — turned out to be my professional passions.

My case is highly unusual but not unique. Scientists estimate that thousands of people are, like me, living normal lives despite missing large chunks of our brains. Our myriad networks of neurons have managed to rewire themselves over time. But how?

‘The Worst Participant’

My childhood memories are filled with researchers following me around with pens and clipboards. My brain was scanned several times a year, and I was tasked with various puzzles, word searches and picture-recognition tests. At the end of each day of testing, the researchers would give me a sticker, which I would keep in a tin container next to my bed.

When I was around 9 years old, researchers wanted to see how my brain would act when I was exhausted. I would sometimes stay up all night with my mom, eating Chinese food and watching Katharine Hepburn and Spencer Tracy movies. The next day I would stumble into the clinic half-awake, and scientists would stick electrodes on my scalp. As long wires fell from my head like Medusa’s snakes, I was finally allowed to fall asleep, blissfully unaware that the researchers were searching for abnormalities in my brain waves.

Over the years, the scientists realized that I wasn’t like the other children in the study: I didn’t have any deficits to track over time. When I was around 15, my dad and I met in the cluttered Manhattan office of Dr. Ruth Nass, the pediatric neurologist leading the research. She questioned if I had actually had a perinatal stroke. In any case, she said frankly that my brain was so different from the others’ that I could no longer be in the study.

I didn’t mind. I had other things going on in my life, like the beginning of high school, cross-country practice and crushes. But I had also learned enough about neuroscience to become consumed by the topic. When I was 17 and entering my senior year in high school, I wrote to Nass and asked if I could do an internship in her lab. She readily agreed.

One day in the lab, I asked if she could show me my study files. We walked into a room filled with stacks of plastic bins, each one brimming with folders and loose papers. She grabbed a folder and read it quietly. Then, peering over a piece of paper, she said, “You were the worst participant because you were perfectly fine! You threw off all of my data.”

Nass, who passed away in 2019, and her colleagues would go on to publish many studies on perinatal strokes. In a 2012 paper, for example, they found that babies suffering these strokes had a higher risk of attention and behavioral problems compared with the general pediatric population. Many of these children — recruited from 1983 to 2006 from Southern California and New York City — suffered from seizures and muscle weakness on one side of their bodies. Most also had damaged or missing areas, known as lesions, in their left hemispheres, like me. I assume that one of those data points was mine.

I went to college and majored in neuroscience. After graduating in 2015, I spent two years working in a lab studying concussions. I spent hours in the magnetic resonance imaging room, watching as other peoples’ brains appeared before me on a computer screen.

But I never thought much about my own brain until this spring, when I happened upon a story in Wired magazine (see https://childnervoussystem.blogspot.com/2022/09/perinatal-stroke-2.html) about a woman just like me: astonishingly normal, apart from a missing temporal lobe.

A Critical Hemisphere

For more than a century, the left hemisphere of the brain has been considered the center of language production and comprehension.

This idea was first proposed in 1836 by Dr. Marc Dax, a physician who observed that patients who had injuries to the left side of their brains could no longer speak properly. Twenty-five years later, Dr. Pierre Paul Broca observed a young man who had lost the ability to speak and could utter only one syllable: “Tan.” A brain biopsy following the patient’s death revealed a large lesion in the frontal part of the left hemisphere, now known as Broca’s area.

In the early 1870s, Dr. Carl Wernicke, a neurologist, saw several patients who could speak fluently, but their utterances made little sense. One of these patients had a stroke in the back of her left temporal lobe, and Wernicke concluded that this section of the brain — now called Wernicke’s area — must serve as a second center for language, alongside Broca’s area.

Modern brain imaging studies have further expanded our understanding of language. Much of this work has shown that two brain regions — the left sides of the temporal and frontal lobes — activate when a person is reading or hearing words. Some researchers have called this the “language network.”

But other neuroscientists have argued that language processing is even broader and not confined to specific brain regions.

“I believe that language in the brain is distributed throughout the entire brain,” said Jeremy Skipper, the head of the Language, Action and Brain Lab at University College London (and my former college psychology professor).

Studies have shown that written words can activate the part of the brain associated with the word’s meaning. For example, the word “telephone” activates an area related to hearing, “kick” triggers a region involved in moving the legs, and “garlic” activates a part that processes smells.

The areas of the brain traditionally attributed to language have lots of other functions, Skipper said. “It just depends on what other sections of the brain they are talking to and at what time and in what context.”

Eight Interesting Brains

The Wired article described an anonymous woman from Connecticut who had no idea she lacked a left temporal lobe until undergoing an unrelated brain scan as an adult. For the past few years, the article explained, she had been part of a research project led by Evelina Fedorenko, a cognitive neuroscientist at the Massachusetts Institute of Technology.

In April, I wrote Fedorenko an email telling her about my missing left temporal lobe and offering to be part of her research. She replied 4 1/2 hours later, and soon I was booking an airplane ticket from my home in rural Colorado to Boston.

There are currently eight participants, including me, in Fedorenko’s Interesting Brain Project, she told me. I haven’t met them, but four of us had presumed perinatal strokes, resulting in damage to our left hemispheres. Two participants have benign cysts in their right or left hemispheres, one had a stroke in the right hemisphere, and one had brain tissue removed from the left hemisphere because of a tumor.

“The brain has incredible neuroplasticity,” said Hope Kean, a graduate student in Fedorenko’s lab who is running the Interesting Brain study as part of her dissertation.

It seems that networks in the brain arrange in a particular way, but if you lose crucial brain regions as a baby — when the brain is still very plastic — these networks can reroute, Kean said.

I arrived at Fedorenko’s lab in Cambridge on a hot day in July. I lay on a bed that slid into the MRI machine’s narrow tube, with a cagelike device placed over my head. Kean snapped a mirror onto the headpiece so I could see a screen at the back of the scanner. As the machine started to make its banging, booming sounds, I remembered all of the times I had dozed off inside as a kid, lulled to sleep by its thundering chords.

On the screen, words flashed quickly and a voice read them aloud, forming random sentences like, “Just the barest suggestion of a heel is found on teenage pumps.” Then, the words switched to a haphazard assortment of letters, creating incomprehensible sounds.

After the scan was completed, the researchers and I crowded around a computer screen, where I saw a slice of my brain for the first time. I stared in disbelief, stunned that my neuronal wiring could have rerouted around this large, oblong hole where my temporal lobe should have been in the space behind my left temple and eye socket.

In a typical person’s brain, the sentences that I heard and read in the scanner would robustly activate the left temporal and frontal lobes, whereas the nonsense sounds would not.

The researchers’ studies found that the brain of the Connecticut patient had adapted by switching sides: For her, these sentences activated the right temporal and frontal lobes, according to a case study published in the journal Neuropsychologia.

My brain, however, surprised everyone, yet again.

A preliminary analysis of the scans showed that, even without a left temporal lobe, I still process sentences using my left hemisphere.

“I had thought that any large left hemisphere early lesion leads to the migration of the language system to the right hemisphere!” Fedorenko said. “But science is cool this way. Surprises often mean cool discoveries.”

A possible reason behind this discovery, according to Fedorenko, is that my lesion is primarily in the front of my left hemisphere, leaving enough healthy tissue in the back for the language system to take root.

Over the next few years, I’ll be flying back to the lab for additional scans and tests, and Fedorenko hopes to recruit even more people with unusual brains to participate in this study.

I still think about the study I was in as a young child and about all of the other kids whose perinatal strokes had left many of them severely disabled. For some mysterious reason, my brain evolved around its missing lobe, whereas theirs struggled to do so. Why wasn’t I born with the developmental and cognitive problems, and they were? Why did my left side rewire to give me the syllables, words and phrases that have so enriched my life?

It’s these questions that make me grateful to have been involved in this study — and to be a research participant once again.

https://news.yahoo.com/curious-hole-head-151127600.html

https://www.nytimes.com/2022/09/04/science/brain-language-research.html

 

Tuesday, August 30, 2022

Long-term outcome of epilepsy and cortical malformations due to abnormal migration and postmigrational development

Laura Licchetta, Luca Vignatelli, Francesco Toni, Andrea Teglia, Laura Maria Beatrice Belotti, Lorenzo Ferri, Veronica Menghi, Barbara Mostacci, Lidia Di Vito, Francesca Bisulli, Paolo Tinuper.  Long-term Outcome of Epilepsy and Cortical Malformations Due to Abnormal Migration and Postmigrational Development. A Cohort Study. 

Abstract

Primary amebic meningoencephalitis 6

A child likely died from a rare infection caused by a brain-eating amoeba after swimming in an eastern Nebraska river, health officials said, making it the second such probable death in the Midwest this summer and raising the question of whether climate change is playing a role.

The Douglas County Department of Health based in Omaha, Nebraska, reported Wednesday that doctors believe the child died of primary amebic meningoencephalitis, a usually fatal infection caused by the naegleria fowleri amoeba. Health officials believe the child came into contact with the amoeba on Sunday while swimming in the Elkhorn River just west of Omaha.

Officials have not released the child's identity.

Last month, a Missouri resident died of the same infection likely caused by the amoeba at Lake of Three Fires in southwestern Iowa. Iowa officials closed the lake's beach as a precaution for nearly three weeks.

People are usually infected when water containing the amoeba enters the body through the nose while swimming or diving into lakes and rivers. Other sources have been documented, including tainted tap water in a Houston-area city in 2020. Symptoms include fever, headache, nausea or vomiting, progressing to a stiff neck, loss of balance, hallucinations and seizures.

The Centers for Disease Control and Prevention says naegleria fowleri infections are rare — there are about three cases in the United States every year — but that those infections are overwhelmingly fatal.

There were 154 cases reported between 1962 and 2021 in the U.S., with only four survivors, according to the CDC. Of those, 71 cases were reported between 2000 and 2021. Texas and Florida recorded the most infections with 39 and 37 cases respectively, and the amoeba is typically found in southern states because it thrives in waters that are warmer than 86 degrees Fahrenheit (30 Celsius).

But infections have migrated north in recent years, including two cases in Minnesota since 2010, Douglas County Health Director Dr. Lindsey Huse noted during a news conference Thursday.

“Our regions are becoming warmer,” she said. “As things warm up, the water warms up and water levels drop because of drought, you see that this organism is a lot happier and more typically grows in those situations.”

According to the National Water Information System, the surface water temperature near where the child was swimming was between 86 and 92 degrees.

Jacob Lorenzo-Morales, a researcher at the Universidad de La Laguna in the Canary Islands who has studied naegleria fowleri, said Thursday that an increase in infections since 2000 can be blamed on two factors: better knowledge and diagnosis of the disease, and the rising temperature in bodies of water providing “a perfect environment” for the amoeba to thrive.

Researcher Sutherland Maciver, who has studied the amoeba at the Centre for Discovery Brain Sciences at Edinburgh Medical School in Scotland, says not all infections are reported and that the 430 cases that have ever been reported worldwide are almost certainly an undercount. And, he said, scientists cannot say with certainty that the Nebraska case is directly attributable to climate change.

The two researchers co-authored a paper titled “Is Naegleria fowleri an Emerging Parasite?” that examined factors behind the increase in reported cases.

Health officials recommend that freshwater swimmers plug their noses, avoid putting their heads underwater and avoid activities such as water skiing and tubing, which could force water into the nose, eyes or mouth. You cannot be infected by drinking contaminated water.

https://abcnews.go.com/Health/wireStory/brain-eating-amoeba-suspected-2nd-midwest-death-88563052

Prospective concussion test

The start of football season brings the return of that important topic: Concussions.

There's a new test that was approved by the FDA in December that could change the game, and its creator is from Minneapolis.

The test uses a camera to track each eye, as the patient watches a 220-second video, which is moving in a square motion around a screen.

Dr. Uzma Samadani has been working on the EyeBOX for 10 years. It's the first approved minimally-invasive concussion diagnostic, doing what no other test can.

"He can follow my finger, but I'm not going to be able to detect really subtle differences between the right eye and the left eye just by looking at him," Samadani said.  

When Jon Johnston came in (see https://jonjohnston.com/my-heart-attack-and-tbi-survivor-story/), his scans showed nothing wrong. But this test, showed his eyes moving out of sync and independent of each other, proved otherwise.

"When a normal person watches the video, their eyes are moving together in the horizontal plane, whereas his eyes are not," said Samadani.

"This takes some of the uncertainty out of it, and that's a huge factor I think," said Johnston.

Theoretically, this test could be used on a football sideline now, conducted by a medical professional. But a consumer-friendly version might change in-game concussion protocols in a big way. A phone version of the test is in the works and could be available sooner than later.

"Probably one or two years," said Samadani.

https://www.cbsnews.com/minnesota/news/eyebox-concussion-test/


SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype

Berghold VM, Koko M, Berutti R and Plecko B (2022) Case report: Novel SCN4A variant associated with a severe congenital myasthenic syndrome/myopathy phenotype. Front. Pediatr. 10:944784. doi: 10.3389/fped.2022.944784

We present a now 18-year-old female patient with a severe congenital myopathy phenotype, originally diagnosed as mitochondrial myopathy, however later revealed to constitute a SCN4A-related myopathy based on genetic testing. After birth, floppiness, bradycardia and respiratory insufficiency ensued, and moderately reduced mitochondrial complex I activity was found in muscle tissue (tested at 3 weeks and 3 years of age, respectively). She was treated with riboflavin, carnitine, creatine and a ketogenic diet. At the age of 13 years, whole exome sequencing challenged the initial diagnosis by identifying two (compound heterozygous) SCN4A variants affecting the highly conserved voltage sensor and pore regions of the voltage-gated sodium channel NaV1.4: a known pathogenic loss of function (LOF) variant [c.4360C>T; p.(Arg1454Trp)] and a novel variant of uncertain significance [c.3615C>G; p.(Asn1205Lys)]. For this novel variant, a LOF effect was predicted by in silico, clinical and functional evidence from paralog human sodium channels, and the variant was accordingly classified as likely pathogenic. The patient's phenotype is in line with the few published cases of autosomal recessive SCN4A-related myopathy. There was limited benefit from treatment with salbutamol and acetazolamide, while pyridostigmine caused side effects at a minor dose. This report highlights the importance of genetic testing in severe myopathies particularly in regard to treatment options and the value of paralog information in evaluating ion channel variations.

Monday, August 29, 2022

Use of whole-genome sequencing for mitochondrial disease diagnosis

Ryan L. Davis, Kishore R. Kumar, Clare Puttick, Christina Liang, Kate E. Ahmad, Fabienne Edema-Hildebrand, Jin-Sung Park, Andre E. Minoche, Velimir Gayevskiy, Amali C. Mallawaarachchi, John Christodoulou, Deborah Schofield, Marcel E. Dinger, Mark J. Cowley, Carolyn M. Sue.  Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis. Neurology Aug 2022, 99 (7) e730-e742; DOI: 10.1212/WNL.0000000000200745

Abstract

Background and Objectives Mitochondrial diseases (MDs) are the commonest group of heritable metabolic disorders. Phenotypic diversity can make molecular diagnosis challenging, and causative genetic variants may reside in either mitochondrial or nuclear DNA. A single comprehensive genetic diagnostic test would be highly useful and transform the field. We applied whole-genome sequencing (WGS) to evaluate the variant detection rate and diagnostic capacity of this technology with a view to simplifying and improving the MD diagnostic pathway.

Methods Adult patients presenting to a specialist MD clinic in Sydney, Australia, were recruited to the study if they satisfied clinical MD (Nijmegen) criteria. WGS was performed on blood DNA, followed by clinical genetic analysis for known pathogenic MD-associated variants and MD mimics.

Results Of the 242 consecutive patients recruited, 62 participants had “definite,” 108 had “probable,” and 72 had “possible” MD classification by the Nijmegen criteria. Disease-causing variants were identified for 130 participants, regardless of the location of the causative genetic variants, giving an overall diagnostic rate of 53.7% (130 of 242). Identification of causative genetic variants informed precise treatment, restored reproductive confidence, and optimized clinical management of MD.

Discussion Comprehensive bigenomic sequencing accurately detects causative genetic variants in affected MD patients, simplifying diagnosis, enabling early treatment, and informing the risk of genetic transmission.

 


Thursday, August 25, 2022

Premature declaration of death

A 3-year-old girl woke up during her funeral before being officially declared dead after doctors mistakenly presumed her dead the first time. 

The family of Camila Roxana Martinez Mendoza is accusing the Salinas de Hidalgo Basic Community Hospital of negligence after reportedly declaring the toddler dead too soon. 


The young girl was experiencing stomach pains, vomiting and fever when her mother, Mary Jane Mendoza, took her to see a pediatrician in the family’s hometown of Villa de Ramos on Aug. 17, El Universal newspaper reported. 


The doctor escalated the issue and recommended that the child be taken to the hospital in the central Mexican state of San Luis Potosí to be treated for dehydration. 


Doctors at Salinas de Hidalgo Basic Community Hospital placed a cold towel over her little body to lower her body temperature and placed a pulse oximeter on one of her fingers to keep track of her oxygen levels.

00:0401:29 

Camila was released from the hospital with a prescription for paracetamol — which treats pain and fever — but continued to deteriorate as the day continued. She was seen by another doctor who instructed her mother to feed her fruits and water and prescribed a different medication. 


Despite the medications and advice from medical experts, the toddler continued vomiting. Her worried parents took her to see another doctor, who suggested she be rushed to the emergency room. 


Camila was readmitted to Salinas between 9 and 10 p.m., and doctors worked to help the young girl. 


“They wanted to give her (intravenous therapy). They took a long time to put oxygen on her,” her mother said. “They didn’t put it on her because they couldn’t find her little veins; finally, a nurse managed it.” 


After about 10 minutes, the IV was removed from the little girl, who was then taken away to rest. “She still was hugging me, they took her away and told me, ‘You have to let her rest in peace.'” the grieving mother remembered. 


Bizarrely, Mendoza was then kept from her ailing daughter in a separate, locked room. She was able to get out but still could not get into the room where her daughter was being kept. Camila was later declared dead from dehydration. 


The next day, a funeral viewing was held for friends and family to mourn the beloved toddler when Mendoza noticed the glass window of the coffin fogging up. 


Other funeral attendees told the distraught mother that she must be hallucinating and dissuaded her from opening the coffin. However, Camila’s paternal grandmother reportedly rushed to take a closer look when she noticed Camila’s eyes moving and shockingly discovered she had a pulse. 


Camila was rushed by ambulance back to the Salinas hospital, where doctors unsuccessfully attempted to revive her and declared her dead again — this time from cerebral edema (brain swelling). 


“That was really where my baby was done. We are devastated because my girl was a very happy person, she got along with everyone, she didn’t single anyone out,” Mendoza said. “We have many people on the ranch who support us because she was cherished.” 


The family was planning to send Camila to her first day of kindergarten this week. 


https://nypost.com/2022/08/24/girl-3-declared-dead-wakes-up-at-her-funeral-then-dies-again/


See: https://childnervoussystem.blogspot.com/2018/05/premature-organ-donation.html

https://childnervoussystem.blogspot.com/2018/04/premature-death-declaration.html