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Diseases and Conditions

Ancient DNA Uncovers a Forgotten Chapter in Leprosy’s History in the Americas

Leprosy’s tale stretches from 5,000-year-old skeletons in Eurasia to a startling 4,000-year-old case in Chile, revealing that the rare strain Mycobacterium lepromatosis haunted the Americas millennia before Europeans arrived. Armed with cutting-edge ancient-DNA sleuthing, scientists have pieced together remarkably well-preserved genomes that challenge the idea of leprosy as purely a colonial import and hint that the disease may have homegrown American roots awaiting confirmation by future finds.

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The discovery of ancient DNA in human bones has revolutionized our understanding of diseases that have plagued humans for centuries. Recently, researchers have uncovered evidence that leprosy, also known as Hansen’s Disease, had a presence in the Americas long before European colonization. This finding challenges the common assumption that leprosy was introduced to the continent by European settlers.

Leprosy is a chronic disease caused by either Mycobacterium leprae or Mycobacterium lepromatosis. While M. leprae is the more commonly known pathogen, M. lepromatosis has been found in a rare form of the disease. The discovery of ancient DNA from 4000-year-old skeletons in Chile suggests that M. lepromatosis was present in the Americas thousands of years ago.

This finding is significant because it reveals a previously unknown chapter in leprosy’s history. Historically, leprosy has been documented in Europe and Asia for thousands of years, but its presence in the Americas before European colonization had gone undetected. The discovery of ancient DNA from M. lepromatosis in Chile provides evidence that this disease was present in the Americas at least 4000 years ago.

The study of ancient DNA has become a valuable tool for researchers to uncover the history of diseases that have affected humans over time. By analyzing ancient bone samples, researchers can identify the presence of pathogens and reconstruct their evolutionary history. In this case, the discovery of M. lepromatosis in Chile provides a fascinating example of how ancient DNA can shed new light on the history of a disease.

Further research is needed to understand the full extent of leprosy’s history in the Americas. The discovery of M. lepromatosis in Chile has opened up new avenues for research, and it is likely that more cases will be identified in the coming years. By studying ancient DNA from other time periods and contexts, researchers can gain a better understanding of how leprosy was transmitted and evolved over time.

Ultimately, the discovery of M. lepromatosis in Chile highlights the importance of studying ancient DNA to uncover the history of diseases that have affected humans for centuries. By doing so, we can gain a deeper understanding of how these diseases were transmitted and evolved over time, and perhaps even find new ways to prevent or treat them.

Children's Health

Uncovering the Inaccuracy: Why Common Blood Pressure Readings May Miss 30% of Hypertension Cases

Cambridge scientists have cracked the mystery of why cuff-based blood pressure monitors often give inaccurate readings, missing up to 30% of high blood pressure cases. By building a physical model that replicates real artery behavior, they discovered that low pressure below the cuff delays artery reopening, leading to underestimated systolic readings. Their work suggests that simple tweaks, like raising the arm before testing, could dramatically improve accuracy without the need for expensive new devices.

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The measurement of blood pressure has been a cornerstone of medical practice for decades. However, despite its widespread use, research suggests that common cuff-based blood pressure readings may be inaccurate and potentially miss up to 30% of hypertension cases.

A team of researchers from the University of Cambridge has shed new light on this issue by building an experimental model that explains the physics behind these inaccuracies. Their findings, reported in the journal PNAS Nexus, have significant implications for patient health outcomes and highlight the need for more accurate measurement methods.

The auscultatory method, which relies on inflating a cuff around the upper arm to measure blood pressure, has long been considered the gold standard. However, this study reveals that it overestimates diastolic pressure while underestimating systolic pressure. The researchers attribute this discrepancy to a previously unidentified factor: the delayed reopening of arteries due to low downstream pressure.

To replicate this condition in their experimental rig, the Cambridge team used tubes that lay flat when deflated and fully closed when inflated with cuff pressure. This setup allowed them to study the effects of downstream blood pressure on artery closure and reopening, leading to a better understanding of the mechanics behind inaccurate readings.

The researchers propose several potential solutions to address this underestimation, including raising the arm before measurement to produce a predictable downstream pressure. This simple change does not require new devices but can make blood pressure measurements more accurate.

If new devices for monitoring blood pressure are developed, they may incorporate additional inputs that correlate with downstream pressure, such as age, BMI, or tissue characteristics, to adjust ‘ideal’ readings for each individual.

The study’s authors emphasize the need for clinical trials to test their findings in patients and collaborate with clinicians to implement changes to clinical practice. Funding from organizations like the Engineering and Physical Sciences Research Council (EPSRC) will be essential to support further research and development.

By uncovering the inaccuracies in common blood pressure readings, this study has significant implications for patient health outcomes and highlights the need for more accurate measurement methods. The proposed solutions have the potential to improve diagnosis and treatment of hypertension, ultimately saving lives and reducing healthcare costs.

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Allergy

“The Silent Invader: How a Parasitic Worm Evades Detection and What it Can Teach Us About Pain Relief”

Scientists have discovered a parasite that can sneak into your skin without you feeling a thing. The worm, Schistosoma mansoni, has evolved a way to switch off the body’s pain and itch signals, letting it invade undetected. By blocking certain nerve pathways, it avoids triggering the immune system’s alarms. This stealth tactic not only helps the worm survive, but could inspire new kinds of pain treatments and even preventative creams to protect people from infection.

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A new study published in The Journal of Immunology has made an intriguing discovery about how a parasitic worm evades detection and what it can teach us about pain relief. Researchers from Tulane School of Medicine found that the Schistosoma mansoni worm, which causes schistosomiasis, suppresses neurons in the skin to avoid triggering an immune response.

When this worm penetrates human skin, typically through contact with infested water, it produces molecules that block a protein called TRPV1+, which is responsible for sending pain signals to the brain. This clever mechanism allows the worm to infect the skin largely undetected.

The researchers believe that the S. mansoni worm evolved this strategy to enhance its own survival and found that blocking TRPV1+ also reduced disease severity in mice infected with the parasite. The study suggests that identifying the molecules responsible for suppressing TRPV1+ could lead to new painkillers that do not rely on opioids.

Moreover, the researchers discovered that TRPV1+ is essential for initiating host protection against S. mansoni infection. When this protein is activated, it triggers a rapid mobilization of immune cells, which induces inflammation and helps fight off the parasite. This finding highlights the critical role of neurons in pain-sensing and immune responses.

The study’s lead author, Dr. De’Broski R. Herbert, emphasizes that identifying these molecules could inform preventive treatments for schistosomiasis. He envisions a topical agent that activates TRPV1+ to prevent infection from contaminated water for individuals at risk of acquiring S. mansoni.

This groundbreaking research has the potential to revolutionize our understanding of pain relief and immune responses, offering new avenues for developing innovative therapies that could benefit millions worldwide.

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Back and Neck Pain

The French Fry Effect: Scientists Reveal the Surprising Truth About Potatoes and Diabetes Risk

French fries may be more than just a guilty pleasure—they could raise your risk of type 2 diabetes by 20% if eaten three times a week, while the same amount of boiled, baked, or mashed potatoes doesn’t appear to have the same effect.

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The relationship between potatoes and type 2 diabetes has long been debated. While it’s known that potatoes contain several essential nutrients like fiber, vitamin C, and magnesium, their high starch content also contributes to a higher glycemic index, potentially increasing the risk of developing type 2 diabetes. A recent study published in The BMJ sheds new light on this topic by investigating the association between different potato preparation methods and the risk of type 2 diabetes.

Researchers analyzed data from over 205,000 health professionals across three large US studies conducted between 1984 and 2021. Participants were free of diabetes, heart disease, or cancer and completed detailed food questionnaires every four years. The study found that for every three weekly servings of total potato, the rate of type 2 diabetes increased by 5%. However, a similar intake of baked, boiled, or mashed potatoes was not associated with a significantly increased risk.

In contrast, eating French fries three times a week was linked to a 20% higher risk of developing type 2 diabetes. Replacing total potatoes or baked, boiled, or mashed potatoes with whole grains lowered the type 2 diabetes rate by 8%. Substituting French fries with whole grains reduced the risk by 19%. On the other hand, replacing total potatoes or baked, boiled, or mashed potatoes with white rice increased the risk of type 2 diabetes.

This observational study highlights that the association between potato intake and type 2 diabetes risk depends on the specific foods used as replacement. The findings align with current dietary recommendations promoting whole grains as part of a healthy diet for preventing type 2 diabetes.

While baked, boiled, or mashed potatoes can be part of a healthy and sustainable diet, especially when prepared in moderation, it’s essential to consider preparation methods and replacement foods when guiding the public or informing policy. Future studies from diverse populations that account for both preparation methods and substitution analysis are needed to further understand this relationship and provide more tailored recommendations.

In conclusion, the French fry effect is a significant concern, but not all potatoes are created equal. By being mindful of our potato choices and making informed decisions about food substitutions, we can reduce the risk of type 2 diabetes and promote overall well-being.

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