The two-part
study asked university students to rate themselves against peers on positive
and negative qualities that were meant to indicate desirability. Traits such as
maturity, modesty, discipline, wit, and being well-spoken were considered
positive, while traits such as rigidity, aggressiveness, messiness, and being
materialistic, narrow-minded or boastful were undesirable.
For the first test, 20 students evaluated themselves on these characteristics during two timed sessions that required participants to make decisions quickly. Fifty-six students participating in the second test were asked to take the same test, but they were given an unlimited amount of time for evaluation.
“The extent to which participants viewed themselves as ‘above average’ was negatively correlated with orbitofrontal cortex (OFC) and, to a lesser extent, dorsal anterior cingulate cortex (dACC) activation,” authors of the study wrote. “The majority of people judge their personality to be more desirable than their peers' personalities.”
The OFC and dACC are both involved in evaluation and planning. According to the authors, these regions of the brain are involved in deep thought and may be partly responsible for keeping the ego in check. They may also, in part, be responsible for recalling self-serving examples of specific traits. Judging broader traits, they say, would require less effort.
"In healthy people, the more you activate a portion of your frontal lobes, the more accurate your view of yourself is,” said lead author Jennifer Beer in a press release. Beer is an assistant professor of psychology at the University of Texas at Austin. “The more you view yourself as desirable or better than your peers, the less you use those lobes."
The study is the first to examine the brain’s role in self-bias in social judgment. Authors say it implies a relationship between poor insight and frontal lobe dysfunction. This information could be used to further study other relationships the frontal lobe might have with poor insight.
“For example, mood disorders and substance abuse may compromise function and/or volume in frontal lobe regions,” authors write. “Understanding these functional and structural changes in relation to self-judgment bias may be helpful for designing therapeutic interventions for various disorders.”
The study appears online in NeuroImage.
Roughly 120 overweight or
obese patients from the Department of Veterans Affairs clinics in Durham, N.C.,
volunteered for a study comparing the effects of two different dieting
plans—the low-carb, ketogenic
diet (LCKD) and a low-fat diet in combination with orlistat
(LFD+O), a weight-loss medication.
Sixty-five of the volunteers completed the low-fat
diet, eating a diet with less than 30 percent of energy intake from fat and
taking 120 mg of orlistat three times daily. Orlistat (Alli, Xenical) is an
over-the-counter weight loss aid that can block a significant amount of fat
from being absorbed by the digestive system. At the end of the 48-week trial,
the group cut 8.5 percent of body fat. Low-carb
dieters, on an Atkins-style
diet, had similar results, trimming 9.5 percent of body fat.
“Both groups lost
considerable weight (on average 21-25 pounds) and experienced numerous health
benefits and were able to reduce medications for chronic diseases associated
with weight,” explains Dr. William Yancy, Jr., M.D., research associate
at Durham’s Department of Veterans Affairs and lead author of the study.
Although both plans tied for
weight loss and had similar HDL (good cholesterol) improvements, the group of
57 low-carb dieters also had decreased systolic and diastolic blood pressure by
5.9 and 4.5 mm, respectively.
Pre-trial, average body
mass index (BMI) was 39.3, and one in three participants had type 2 diabetes.
A healthy BMI score for an adult ranges between 18.5 and 24.9. As the scores
rises, the risk for complications such as stroke, type 2
diabetes, poor cholesterol and heart disease
increases.
Following the study, low-fat
dieters enjoyed better LDL (bad cholesterol) levels, while participants on the
low-carb diet had improved insulin metabolism, hemoglobin A1C, and
blood glucose levels.
“People with these
diseases—hypertension, high cholesterol, diabetes, arthritis—or at risk for
these diseases stand to benefit the most (from these diets),” Yancy explains.
There haven't been significant health risks for short-term dieters, but little is known of the effects after six months. Long-term dieters may be at risk for bone loss or kidney stones. In any case, Dr. Yancy urges anyone considering a low-carb, ketogenic diet to consult a physician.
The study's abstract can be found in the Archives of Internal Medicine.
Most couples have to wait until the second trimester of
pregnancy (4-6 months), but the simple test could cut that time in half—as
early as seven weeks. The test is highly accurate, too. Of the 201 women who
were tested between 2003 and 2009, researchers were able to obtain sufficient
samples from 189 and produce 100 percent accurate results.
When a woman is pregnant, her body will circulate her blood
with blood from the fetus. For this test, a sample of the mother’s blood is
screened for genes unique to the Y-chromosome of males. If these genes were
present, researchers predicted a boy.
Early testing can also help doctors detect conditions such
as Down’s syndrome and Rhesus-D disease (RhD). This method of testing has
several advantages over invasive methods, such as fetal blood sampling (FBS),
that can cause amniotic fluid leaking or miscarriage.
RhD sometimes results from a blood incompatibility between,
for example, an Rh-positive mother and an Rh-negative child. If the mother’s
body detects this difference, it may send antibodies against the baby. If it
goes untreated, it can lead to jaundice, anemia, brain damage or stillbirth.
“Noninvasive
prenatal diagnosis of fetal Rhesus D genotype is sensitive and accurate and has
been widely validated in Europe,” authors noted. “The United States should
begin to undertake clinical trials to bring this technology to patient care as
soon as possible.”
This test is currently not available to the general public, but
continued success could mean it’s on the horizon. Its adoption into general
health practices could help cut the risk of fetal complications of RhD.
The study was published in Obstetrics&Gynecology.
Nearly 3,500 Londoners between the ages of 35 and 55 were
asked about their eating habits. Analysts were able to detect diet patterns and
divide participants into two groups: processed food consumers and “whole food”
consumers. Several years later each group was screened for depression. People
who regularly ate processed foods had a slightly higher incidence of
depression.
“Our results suggest a protective effect of an overall
diet rich in fruits, vegetables and fish (Mediterranean-style diet) affords
protection against the onset of depressive symptoms 5 years later,” study
authors explain, “whereas a diet rich in processed meat, chocolates, sweet
desserts, fried food, refined cereals and high-fat dairy products increases
vulnerability.”
Most processed foods lack the nutrients needed to maintain a
happy, healthy body. Not only does it contribute to weight gain, but it can
also decrease mental alertness and inhibit normal brain function. This
translates into a slew of mood and behavioral changes.
A steady diet of junk food has other risks to consider, too.
Authors note that this sort of diet has also been associated with coronary
heart disease and inflammation. As many as one in five Americans is affected by
depression, and one in three have some form of heart disease. Limiting junk
food consumption may be one way to reduce these risks.
This is the first to focus on the effects of how a person’s overall diet may be related to depression. Although further research is needed to fully understand this relationship, cutting back on unhealthy food can benefit the mind, body and spirit.
Read more in The British Journal of Psychiatry.
Paperless
prescriptions, online access to medical records and video chats with your doc
are just a few features of the Danish healthcare system. Although not everyone
has jumped on the digital bandwagon yet, about half of the country’s hospitals
and nearly all primary care doctors have opted for electronic records.
An approach
to medical treatment like this could drastically change the way doctors help
their patients manage their health. Patients with heart conditions, for
example, could log blood pressure readings to help doctors monitor response to
new medications or simply to track progress.
Not only
would this save the doctor and the patient time, but it could also cut costs.
Since its switch to digital healthcare about ten years ago, Denmark has saved
an estimated $120 million per year.
Although
the system has come a long way, there are still a few kinks to work out. With
the rapid change of technology, doctors and patients alike have had to adapt
quickly to make the most use of these services. Budgeting, too, can be a
challenge for the tax-funded program.
“We’re
trying to streamline now,” Otto Larsen, director of the agency that regulates
the system, said in a story by the New York Times. “There are too many systems
out
More and
more technology is being developed to help doctors make diagnoses from afar
Much of Europe has switched to electronic record-keeping, and many are
embracing the switch to “telemedicine.”
U.S. legislators questioning whether a similar structure could work for
the United States.
“It was a
natural progression for us,” Larsen said. “We believe in taking care of our
people, and we had believed this was the right way to go.”
Only time will tell whether or not the trend in digital healthcare will effectively spread.
Information
for the study was gathered from six different placebo-controlled studies taking
place across a 29-year span. It included data from 718 adult outpatients being
treated for minor or major depressive disorder.
“The
magnitude of benefit of antidepressant medication compared with placebo
increases with severity of depression symptoms,” authors of the study explain,
“and may be minimal or nonexistent, on average, in patients with mild or
moderate symptoms.”
According
to the New York Times, the success rate of placebos in some studies such as
this can be as high as 50 percent for individuals with mild to moderate
depression. People who continue to use antidepressants do appear to have a
lower relapse rate, though—just one-third to one-half that of those taking
placebos.
The study
has its limitations, however. First of all, its conclusions are based on
studies including just two different antidepressants. Another drawback is that,
for the purpose of discovering which drugs are most effective, many studies of
antidepressant medications exclude people who get better using placebos.
Finally,
results may be limited because of the difficulty of finding studies that
include people with mild to moderate depression, rather than just those with
severe depression. A study with a much larger pool of participants would
provide greater insight into the effectiveness of placebos versus
antidepressants.
The study
is merely suggestive, and neither proves nor disproves the claim that
antidepressants are no more effective than placebos. In no way does it mean that
someone should stop taking medication prescribed for depression. Rather, it
provides something for antidepressant users to consider and discuss with their
doctors.
“For patients with very severe depression, the benefit of medications over placebo is substantial,” authors concluded.
Communicating
can be extremely difficult, if not impossible, for someone left mute by
paralysis. Although there are existing devices that help paralyzed individuals
speak, they are often inefficient for communication and tiresome for the user.
This is the first to translate brain waves at the rate of natural speech.
"The
most significant thing is that this shows it would be possible for someone who
is paralyzed to speak in real-time rather than going through a painful typing
process," lead researcher Frank Guenther said in an interview with MSNBC.
"This communication is very important because these people are completely
locked out from the rest of the world."
Guenther
and his team tested the electrode on a 26 year-old male volunteer with
locked-in syndrome, the result of a brain stem stroke. Individuals with this
disorder are aware of their surroundings and can understand and react mentally,
but are physically unable to respond.
The device, designed for permanent implantation without the risk
of infection, is
a neurotrophic electrode. The electrode is implanted in the speech-related motor cortex, an area of the
brain responsible for speech planning and synthesis. After 3—4 months neurites
attach to a portion of the device, allowing signals to be transmitted from
the brain into the electrode. These signals are then transmitted to a
computer that translate brain waves into recognizable, audible speech.
Because it
is extremely difficult to differentiate the neural fluff from intentional
cognition, determining which frequencies represent which sounds is a very
timely process. As of now, only vowel sounds have been quickly and accurately
produced. The device used for the trial had just three wires, however, and
researchers believe additional wires may result in greater speech recognition
capabilities.
“Our results support the feasibility of neural prostheses that may have the potential to provide near-conversational synthetic speech output for individuals with severely impaired speech motor control. They also provide an initial glimpse into the functional properties of neurons in speech motor cortical areas.”
“Spoon dosing has been
identified as 1 of the 3 major causes of dosing errors and pediatric
poisonings,” authors of the study wrote. “Most persons still use spoons when
pouring medicine for themselves and their families.”
Nearly 200 university
students were asked to measure what they perceived to be equal amounts of cold
medicine into three different spoons—a standard teaspoon, a medium-sized spoon,
and a larger spoon.
“We first gave them a full
bottle of cold medicine and a teaspoon and asked them to pour exactly 1
teaspoon (5 mL),” authors of the study explain. “Next, we asked participants to
pour the same 5-mL dose into each of the remaining 2 spoons in a randomized
order.”
Standard dosage for most
cold medicines is usually between 2 teaspoons and 2 tablespoons. Although most
participants were confident that they’d measured accurately, they measured 8.4
percent (.42 mL) too little when using the medium-sized spoon, and 11.6 percent
(.58 mL) too much when using the large spoon.
Although that may not seem
like much for per dose, a little change in medicine can make a lot of
difference. According to study leader Dr. Brian Wansink of the Cornell Food and
Brand Lab, this can add up to the point of ineffectiveness or even danger.
They also point out that
this could reach farther than the kitchen at home. Even the most practiced nurse or Dr.
Mom could be measuring incorrectly when using spoons because the size of the
spoon makes the same amount appear differently.
“Simply put, we cannot
always trust our ability to estimate amounts," co–author, Dr. Koert van
Ittersum, Assistant Professor of Marketing at Georgia Tech, said in a press
release. "In some cases it may not be important, but when it comes to the
health of you or your child, it is vital to make an accurate measurement."
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