Credits: Canva
We all at some point of our life thought if we had a delete button to erase the bad memories, haven't we? Now, this dream may come true. When I first came across this news, the first thing that came to my mind was the animated film The Boss Baby, where babies are sent from a baby corporate to ensure that people choose babies over pets. The baby is smart, witty, and works as a spy and once the job is done, the baby goes back to the baby corporate. When the baby is gone, the staff from the company comes with a magic wand and erases everyone's memories with the baby. It is like the baby never existed for the parents or the family in the first place. Now, scientists have discovered a way to potentially erase memories, though it is to weaken the hold of traumatic memories by reactivating positive ones.
A new study published in PNAS, titled Aversive memories can be weakened during human sleep via the reactivation of positive interfering memories suggests that erasing memory may become a real possibility. If so, this might be a breakthrough that could have wide-reaching impact for treating mental health conditions like PTSD, anxiety and depression.
The basis of the research is a simple but powerful idea: when you recall a negative memory, can you weaken it by immediately linking it with something positive? This theory was put to the test by an international team of scientists who worked with 37 participants in a controlled lab setting.
Participants were first asked to associate random, made-up words with disturbing or aversive images. These images came from recognized databases and included visuals such as injuries and dangerous animals. This created a mental link between the neutral words and negative feelings.
Once the participants have formed these unpleasant association, the next step is to sleep. This is the non-rapid eye movement or the NREM sleep. This is a crucial phase for memory consolidation. However, before this step, the researchers have attempted to "reprogram" half of the negative associations by linking the same nonsense words with pleasant images. It could be the peaceful landscapes or smiling faces.
When in the second night, the nonsense words were replayed to the participants as audio while they were in NERM sleep, their brain activity too was monitored. The monitoring happened using the electroencephalography (EEG). Interestingly, when positive images had been paired with the words earlier, the EEG showed a spike in theta-band activity. This is a brainwave that associates with emotional memory processing.
When the participants were asked to recall their memories the next day — and even several days later — a noticeable shift had taken place. Those nonsense words that had been "interfered with" by positive associations no longer triggered the same strong negative memories. In fact, participants were more likely to spontaneously recall the positive images instead. They also showed a more positive emotional bias when evaluating those memories.
In the researchers’ words, the study demonstrated that “a noninvasive sleep intervention can thus modify aversive recollection and affective responses.”
While the findings are promising, the researchers also noted that this was a controlled laboratory experiment. The emotional impact of viewing upsetting images in a lab is not the same as experiencing real-life trauma. True traumatic memories, especially those tied to lived experiences, may be much more resistant to this kind of memory editing.
That said, this approach builds on earlier findings that the brain naturally replays memories during sleep to reinforce them. If this process can be gently influenced — perhaps even without the sleeper knowing — it could someday become part of therapy for those struggling with difficult memories.
While the research still is in its early stage, it does add to the idea that our brains are not static storage banks. “Our findings open broad avenues for seeking to weaken aversive or traumatic memories,” the researchers said.
(Credit-Canva)
Taking care of a sick person is a taxing job not many people can fullfill. Patients with mental health issues like dementia require specialized care and not everyone is equipped to handle these situations. Many times, people with dementia have emotional outbursts, difficulty communicating as well as doing normal lifestyle activities. Caring for people with dementia requires a team of people, sometimes 24/7 care with rotations for staff, so that the patient is not left unattended for an extended period of time. However, does this extensive routine affect the caregiver’s health? A new study has found concerning future implications for dementia caregivers.
Caring for someone with dementia might put caregivers at higher risk for their own brain aging and future dementia, a new study suggests. This is largely due to certain lifestyle factors.
A recent report from the Public Health Center of Excellence on Dementia Caregiving, released on June 12, found that nearly 3 out of 5 dementia caregivers (59%) have at least one risk factor that increases their chances of developing dementia over time. Even more concerning, about 1 in 4 (24%) have two or more of these risk factors.
Matthew Baumgart, senior vice president of health policy for the Alzheimer's Association, called this analysis a "wake-up call." He noted that caregivers are often so focused on their loved ones that they neglect their own health. This highlights a critical need for public health strategies to support these vulnerable individuals.
Researchers analyzed health data from caregivers across 47 states in 2021 and 2022. They found that caregivers were more likely than the average person to have five things that aren't good for brain health:
Caregivers were 30% more likely to smoke. Smoking is bad for your overall health, including your brain.
Interestingly, there was one good piece of news: caregivers were actually less likely to be inactive (meaning they moved around more) compared to others. This might be because looking after someone with dementia often involves a lot of moving around.
This part focuses on younger caregivers, and the news isn't great for them. The study found that younger people who care for someone with dementia are at an even higher risk.
The researchers explained that knowing which groups of caregivers are most at risk, public health officials can better plan and offer help. Instead of a one-size-fits-all approach, they can create specific programs and resources for the groups that need it most.
Credits: PIB
A parasite that causes malaria is halted by sickle cells and makes people who carry the sickle cell trait more resistant to the disease. This is why sickle cell trait also occurs more in people who live in tropical and sub-tropical regions where cases of malaria were or still is common.
It comes from the copy of an abnormal sickle or the HBB gene and one copy of the normal HBB gene. The gene is an evolutionary response to malaria, where humans begin to develop an abnormal HBB gene and pass it onto to the next generation.
The earliest documentation of sickle cell symptoms in medical texts could be found from the 1870s. However, it had not been formally identified until in 1910. when the first case was detected in the United States. The first case of sickle cell disease or SCD in the US was in 1904, when Walter Clement Noel, a 20-year-old dental student from Grenada, sought care for anemia at Chicago Presbyterian Hospital, where he met Dr James B Herrick. Dr Herrick was a cardiologist and professor of medicine and he was assigned noel who had experienced recurrent episodes of "muscular rheumatism" and "bilious attacks" over a period of 3 years.
This case was assigned to an intern Dr Ernest E Irons by Dr Herrick. Dr Ernest performed initial blood work on Noel and observed the unusual sickle-shaped red blood cells in the sample under the microscope. This is when Dr Herrick was told about it, leading to him publishing the first documented case study of SCD, titled, "Peculiar Elongated and Sickle-Shaped Red Blood Corpuscles in a Case of Severe Anemia."
However, the name, sickle cell anemia, was not coined until in 1922, by Vernon Mason. It was also the first diagnosed genetic disease and the first to be linked to the hemoglobin protein.
But, how did it gain the name "Black Disease"? This is because the disease often disproportionately affected Black Americans in the US, which caused racial bias and prevented people with sickle cell from receiving quality care.
In response to this, in the 1960s, the Black Panther Party worked to expand community-based care for education and treatment of this disease. This was part of their initiative to tackle the sickle cell, which received little to no attention because it mostly affected a large part of Black community.
While Herrick may have described the first known case in the US, SCD did exist for generations in African and Mediterranean descent, due to the regions being prone to diseases like malaria. In African medical literature, it was known as "ogbanjes", which loosely translated into "children who come and go" as the infants born with this disease had a high mortality rates. One of the first records, as is also noted by the Sickle Cell Association from Africa is from a Ghanian family in 1670.
In 1927, scientists Hahn and Gillespie made a discovery that reshaped our understanding of blood disorders. While studying red blood cells in a low-oxygen environment saturated with carbon dioxide, they observed a curious phenomenon: the cells twisted into sickle shapes—not just in patients with sickle cell disease (SCD), but sometimes in people without any symptoms at all.
This puzzling observation hinted at an invisible carrier state and eventually led to the identification of what we now call the sickle cell trait.
Fast-forward to the late 1940s and early 1950s, and the pieces of the puzzle began falling into place. In 1949, two scientists working continents apart independently uncovered the genetic blueprint of SCD.
Col. E. A. Beet, a military physician stationed in what is now Mozambique, published his findings in an African medical journal. Around the same time, Dr. James V. Neel at the University of Michigan released a parallel study in the journal Science. Both revealed that SCD follows an autosomal recessive inheritance pattern—meaning the disease only occurs when a person inherits two copies of the mutated gene. Those with just one copy? They carried the trait, but not the illness.
Together, their work laid the foundation for our modern understanding of genetic inheritance and reshaped how we screen for and manage sickle cell disorders today.
(Credit-Canva)
Roughly one out of six people globally suffer with infertility according to the World Health Organization. A common issue that affects many, infertility, is a condition where a person is unable to reproduce offsprings. While the condition may be common, it can cause a lot of health problems as well as stress for people who wish to have children. To tackle this, people often opt for fertility treatment including reproductive technology called in vitro fertilization (IVF). However, could your infertility be a sign of impending health issues?
A new evidence review suggests a link between infertility in women and a heightened risk of heart problems, particularly among younger women and those undergoing fertility treatments.
Infertility may serve as an early sign for future heart health issues, according to researchers at the National and Kapodistrian University of Athens in Greece. This finding was recently presented in Copenhagen, Denmark, at a joint meeting of the European Society of Pediatric Endocrinology and the European Society of Endocrinology.
Researchers looked at data from many different studies – almost 21 of them! They compared nearly 179,000 women who couldn't get pregnant with about 3.4 million women who didn't have fertility issues. What they discovered was that women who were infertile had a higher chance of facing heart issues:
The research highlights two groups of women who face an even bigger risk. First, it's younger women. The study found that women under 40 who were infertile had a 20% higher chance of heart disease. That's a significant increase for younger individuals. Second, it also showed that women who went through fertility treatments (like IVF) had an 18% greater risk of heart problems. This suggests that either the treatments themselves or the underlying reasons for needing them could be connected to heart health.
Researchers believe that because infertility might be an early sign of heart problems, doctors can use this information. They can identify women who might need extra check-ups or special strategies to prevent heart disease earlier in life. It's like giving doctors a heads-up to be more careful with these patients. She also brought up an important question: what are the long-term effects of fertility treatments on a woman's heart? This is something doctors need to consider.
Researchers want to follow women’s health over time to really understand why infertility might be linked to heart health. They hope to figure out the exact biological reasons behind this connection and identify which specific groups of women are most at risk. The ultimate goal is to use all this information to create better guidelines for preventing heart disease early on and to improve heart care for women who have had infertility.
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