Popular Posts Today

Diberdayakan oleh Blogger.

Your memory is like the telephone game, altered with each retelling

Written By Unknown on Rabu, 19 September 2012 | 11.13

ScienceDaily (Sep. 19, 2012) — Remember the telephone game where people take turns whispering a message into the ear of the next person in line? By the time the last person speaks it out loud, the message has radically changed. It's been altered with each retelling.

Turns out your memory is a lot like the telephone game, according to a new Northwestern Medicine study.

Every time you remember an event from the past, your brain networks change in ways that can alter the later recall of the event. Thus, the next time you remember it, you might recall not the original event but what you remembered the previous time. The Northwestern study is the first to show this.

"A memory is not simply an image produced by time traveling back to the original event -- it can be an image that is somewhat distorted because of the prior times you remembered it," said Donna Bridge, a postdoctoral fellow at Northwestern University Feinberg School of Medicine and lead author of the paper on the study recently published in the Journal of Neuroscience. "Your memory of an event can grow less precise even to the point of being totally false with each retrieval."

Bridge did the research while she was a doctoral student in lab of Ken Paller, a professor of psychology at Northwestern in the Weinberg College of Arts and Sciences.

The findings have implications for witnesses giving testimony in criminal trials, Bridge noted.

"Maybe a witness remembers something fairly accurately the first time because his memories aren't that distorted," she said. "After that it keeps going downhill."

The published study reports on Bridge's work with 12 participants, but she has run several variations of the study with a total of 70 people. "Every single person has shown this effect," she said. "It's really huge."

"When someone tells me they are sure they remember exactly the way something happened, I just laugh," Bridge said.

The reason for the distortion, Bridge said, is the fact that human memories are always adapting.

"Memories aren't static," she noted. "If you remember something in the context of a new environment and time, or if you are even in a different mood, your memories might integrate the new information."

For the study, people were asked to recall the location of objects on a grid in three sessions over three consecutive days. On the first day during a two-hour session, participants learned a series of 180 unique object-location associations on a computer screen. The next day in session two, participants were given a recall test in which they viewed a subset of those objects individually in a central location on the grid and were asked to move them to their original location. Then the following day in session three, participants returned for a final recall test.

The results showed improved recall accuracy on the final test for objects that were tested on day two compared to those not tested on day two. However, people never recalled exactly the right location. Most importantly, in session three they tended to place the object closer to the incorrect location they recalled during day two rather than the correct location from day one.

"Our findings show that incorrect recollection of the object's location on day two influenced how people remembered the object's location on day three," Bridge explained. "Retrieving the memory didn't simply reinforce the original association. Rather, it altered memory storage to reinforce the location that was recalled at session two."

Bridge's findings also were supported when she measured participants' neural signals --the electrical activity of the brain -- during session two. She wanted to see if the neural signals during session two predicted anything about how people remembered the object's location during session three.

The results revealed a particular electrical signal when people were recalling an object location during session two. This signal was greater when -- the next day -- the object was placed close to that location recalled during session two. When the electrical signal was weaker, recall of the object location was likely to be less distorted.

"The strong signal seems to indicate that a new memory was being laid down," Bridge said, "and the new memory caused a bias to make the same mistake again."

"This study shows how memories normally change over time, sometimes becoming distorted," Paller noted. "When you think back to an event that happened to you long ago -- say your first day at school -- you actually may be recalling information you retrieved about that event at some later time, not the original event."

The research was supported by National Science Foundation grant BCS1025697 and National Institute of Neurological Disorders and Stroke of the National Institutes of Health grant T32 NS047987.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by Northwestern University. The original article was written by Marla Paul.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. D. J. Bridge, K. A. Paller. Neural Correlates of Reactivation and Retrieval-Induced Distortion. Journal of Neuroscience, 2012; 32 (35): 12144 DOI: 10.1523/JNEUROSCI.1378-12.2012

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

20 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/OALb1Y9nFG4/120919125736.htm
--
Manage subscription | Powered by rssforward.com
11.13 | 0 komentar | Read More

Preemies' brains reap long-term benefits from Kangaroo Mother Care

ScienceDaily (Sep. 19, 2012) — Kangaroo Mother Care -- a technique in which a breastfed premature infant remains in skin-to-skin contact with the parent's chest rather than being placed in an incubator -- has lasting positive impact on brain development, revealed Université Laval researchers in the October issue of Acta Paediatrica. Very premature infants who benefited from this technique had better brain functioning in adolescence -- comparable to that of adolescents born at term -- than did premature infants placed in incubators.

Earlier research showed that infants born prior to the 33rd week of pregnancy experienced more cognitive and behavioral problems during childhood and adolescence. Université Laval researchers Cyril Schneider and Réjean Tessier, of the Department of Rehabilitation in the Faculty of Medicine and of the School of Psychology, respectively, and their Colombian colleagues Nathalie Charpak (Kangaroo Foundation) and Juan Ruiz-Peláez (Universidad Javeriana) wanted to determine if Kangaroo Mother Care could prevent these problems. To that end they compared, at age 15, 18 premature infants kept in incubators, 21 premature infants held in Kangaroo contact for an average of 29 days, and 9 term infants.

To assess participants' brain functions, the researchers used transcranial magnetic stimulation. With this non-invasive and painless technique they could activate brain cells in targeted areas, namely the primary motor cortex that controls muscles. By measuring muscle responses to the stimulation, they were able to assess brain functions such as the level of brain excitability and inhibition, cell synchronization, neural conduction speed, and coordination between the two cerebral hemispheres.

The data collected by the researchers indicate that all brain functions of the adolescent Kangaroo group were comparable to those of the term infant group. On the other hand, premature infants placed in incubators significantly deviated from the other two groups 15 years after their birth.

"Thanks to Kangaroo Mother Care, infants benefited from nervous system stimulation -- the sound of the parent's heart and the warmth of their body -- during a critical period for the development of neural connections between the cerebral hemispheres. This promoted immediate and future brain development," suggests neurophysiologist Cyril Schneider.

Psychology researcher Réjean Tessier notes that "infants in incubators also receive a lot of stimulation, but often the stimulation is too intense and stressful for the brain capacity of the very premature. The Kangaroo Mother Care reproduces the natural conditions of the intrauterine environment in which the infants would have developed had they not been born premature. These beneficial effects on the brain are in evidence at least until adolescence and perhaps beyond."

The two researchers, who are also associated with the Centre de recherche du CHU de Québec, will have the opportunity to shed more light on this subject. The Government of Canada, through its Grand Challenges Canada program, Saving Brains, just awarded their research team a $1 million grant to measure the neurological, cognitive, and psychosocial benefits of Kangaroo Mother Care in a group of 400 young adults, aged 18 to 20, who were born premature.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by Université Laval, via EurekAlert!, a service of AAAS.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Cyril Schneider, Nathalie Charpak, Juan G Ruiz-Peláez, Réjean Tessier. Cerebral motor function in very premature-at-birth adolescents: a brain stimulation exploration of kangaroo mother care effects. Acta Paediatrica, 2012; 101 (10): 1045 DOI: 10.1111/j.1651-2227.2012.02770.x

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

20 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/NGMlaw9x-CU/120919125600.htm
--
Manage subscription | Powered by rssforward.com
11.13 | 0 komentar | Read More

Diseases of aging map to a few 'hotspots' on the human genome

ScienceDaily (Sep. 19, 2012) — Genetics researchers at the UNC School of Medicine now have shown definitively that a small number of places in the human genome are associated with a large number and variety of diseases.

Researchers have long known that individual diseases are associated with genes in specific locations of the genome. Genetics researchers at the University of North Carolina School of Medicine now have shown definitively that a small number of places in the human genome are associated with a large number and variety of diseases. In particular, several diseases of aging are associated with a locus which is more famous for its role in preventing cancer.

For this analysis, researchers at UNC Lineberger Comprehensive Cancer Center cataloged results from several hundred human Genome-Wide Association Studies (GWAS) from the National Human Genome Research Institute. These results provided an unbiased means to determine if varied different diseases mapped to common 'hotspot' regions of the human genome. This analysis showed that two different genomic locations are associated with two major subcategories of human disease.

"Our team is interested in understanding genetic susceptibility to diseases associated with aging, including cancer," said PhD student William Jeck, who was first author on the study, published in the journal Aging Cell.

The team examined the large NHGRI dataset and first eliminated hereditable traits such as eye or hair color and other non-disease traits like drug metabolism. The group then focused on variants identified from GWAS that contributed to actual diseases. Combining results from all of these studies, there was enough data to arrive at statistically valid conclusions. The team then mapped the disease associations to the appropriate locations of the genome, counting the number of unique diseases mapping to specific genomic regions, in order to see if disparate diseases mapped randomly throughout the genome, or clustered in hotspots.

"What we ended up with is a very interesting distribution of disease risk across the genome. More than 90 percent of the genome lacked any disease loci. Surprisingly, however, lots of diseases mapped to two specific loci, which soared above all of the others in terms of multi-disease risk. The first locus at chromosome 6p21, is where the major histocompatibility (MHC) locus resides. The MHC is critical for tissue typing for organ and bone marrow transplantation, and was known to be an important disease risk locus before genome-wide studies were available. Genes at this locus determine susceptibility to a wide variety of autoimmune diseases such as arthritis, celiac disease, Type I diabetes, asthma, psoriasis, and lupus," said Jeck.

"The second place where disease associations clustered is the INK4/ARF (or CDKN2a) tumor suppressor locus. This area, in particular, was the location for diseases associated with aging: atherosclerosis, heart attacks, stroke, Type II diabetes, glaucoma and various cancers," he added.

"The finding that INK4/ARF is associated with lots of cancer, and MHC is associated with lots of diseases of immunity is not surprising -- these associations were known. What is surprising is the diversity of diseases mapping to just two small places: 30 percent of all tested human diseases mapped to one of these two places. This means that genotypes at these loci determine a substantial fraction of a person's resistance or susceptibility to multiple independent diseases," said Ned Sharpless, MD, Wellcome Distinguished Professor of Cancer Research and Associate Director of Translational Research at UNC Lineberger.

Another interesting finding was the apparent role of two biological processes in multi-disease association. In addition to the MHC and INK4/ARF loci, five less significant hotspot loci were also identified. Of the seven total hotspot loci, however, all contained genes associated with either immunity or cellular senescence. Cellular senescence is a permanent form of cellular growth arrest, and it is an important means whereby normal cells are prevented from becoming cancerous. It has been long known that senescent cells accumulate with aging, and may cause aspects of aging. This new analysis provides evidence that genetic differences in an individual's ability to regulate the immune response and activate cellular senescence determine their susceptibility to many seemingly disparate diseases.

"We call the absence of disease 'wellness', and our results suggest the genetics of wellness may be much more simple than previously suspected. Put another way, these unbiased data from about two million people suggest that your eccentric Uncle Joe, who drank and smoked, but who also lived to be 110 and was never sick a day in his life -- well Uncle Joe may have just been genetically fortunate at a couple of loci," said Sharpless.

Alex Siebold, PhD also worked on the research team. The study was supported by the Burroughs Wellcome Fund and the National Institute of Aging (AG024379).

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by University of North Carolina Health Care.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. William R. Jeck, Alex P. Siebold, Norman E. Sharpless. Review: a meta-analysis of GWAS and age-associated diseases. Aging Cell, 2012; 11 (5): 727 DOI: 10.1111/j.1474-9726.2012.00871.x

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

20 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/oMs61u6xeg4/120919125744.htm
--
Manage subscription | Powered by rssforward.com
11.13 | 0 komentar | Read More

New study on relapse risk in alcoholics

ScienceDaily (Sep. 19, 2012) — Scientists at Charité -- Universitätsmedizin Berlin have succeeded in coming closer to determining the risk of relapse in detoxified alcohol-dependent patients. Using an imaging process (magnetic resonance tomography) it was shown that particular regions in the brain demonstrate structural as well as functional abnormalities in relapsed alcohol-dependent patients. Study findings are published in the journal Archives of General Psychiatry.

In the study conducted under the direction of Prof. Andreas Heinz, director of the Charité Department of Psychiatry and Psychotherapy, scientists examined a group of 46 detoxified alcohol-dependent patients, in addition to a large control group. Structural imaging showed anatomical properties of brain substance, and the examination of functional signals in the brain were measured in reaction to alcohol-associated stimuli. After three months, patients were reexamined for eventual relapses; 30 study participants relapsed and 16 continued to be abstinent.

It was proven that relapse patients had increased loss of grey matter in particular regions of the forebrain. This section of the brain is known to be associated primarily with behavioral regulation and emotional control. Furthermore, measurement of functional brain responses in reaction to alcohol-associated stimuli showed that different brain regions were activated in relapsed patients than in patients who remained abstinent. These measurements show that sections of the brain in relapse patients were active that are associated primarily with directing attention to certain stimuli. In contrast, the abstinent patients demonstrated an activation of brain areas that are (among other functions) associated with processing of stimuli inducing aversion (aversive stimuli) or that are particularly important (salient stimuli).

"This characteristic in patients who remained abstinent possibly acts as a warning signal and prevents potential relapse when confronted with alcohol," said Anne Beck, primary author of the study. Future studies could examine these aspects in greater depth and take eventual factors of alcohol dependency into consideration, like for example, genetic mechanisms. Thus people with a particularly high risk of relapse could be identified and systematically supported with therapy.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by Charité - Universitätsmedizin Berlin.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Torsten Wüstenberg. Effect of Brain Structure, Brain Function, and Brain Connectivity on Relapse in Alcohol-Dependent PatientsRelapse in Alcohol-Dependent Patients. Archives of General Psychiatry, 2012; 69 (8): 842 DOI: 10.1001/archgenpsychiatry.2011.2026

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/d8VLw104XvQ/120919103317.htm
--
Manage subscription | Powered by rssforward.com
10.43 | 0 komentar | Read More

Monitoring brain activity during study can help predict test performance

ScienceDaily (Sep. 18, 2012) — Research at Sandia National Laboratories has shown that it's possible to predict how well people will remember information by monitoring their brain activity while they study.

A team under Laura Matzen of Sandia's cognitive systems group was the first to demonstrate predictions based on the results of monitoring test volunteers with electroencephalography (EEG) sensors.

For example, "if you had someone learning new material and you were recording the EEG, you might be able to tell them, 'You're going to forget this, you should study this again,' or tell them, 'OK, you got it and go on to the next thing,'" Matzen said.

The team monitored test subjects' brain activity while they studied word lists, then used the EEG to predict who would remember the most information. Because researchers knew the average percentage of correct answers under various conditions, they had a baseline of what brain activity looked like for good and poor memory performance. The computer model predicted five of 23 people tested would perform best. The model was correct: They remembered 72 percent of the words on average, compared to 45 percent for everyone else.

The study is part of Matzen's long-term goal to understand the Difference Related to Subsequent Memory, or Dm Effect, an index of brain activity encoding that distinguishes subsequently remembered from subsequently forgotten items. The measurable difference gives cognitive neuroscientists a way to test hypotheses about how information is encoded in memory.

She's interested in what causes the effect and what can change it, and hopes her research eventually leads to improvements in how students learn. She'd like to discover how training helps people performing at different levels and whether particular training works better for certain groups.

The study, funded under Sandia's Laboratory Directed Research and Development program (LDRD), had two parts: predicting how well someone will remember what's studied and predicting who will benefit most from memory training.

Matzen presented the results of the first part of the study in April at the Cognitive Neuroscience Society conference in Chicago. She presented preliminary findings on the second part this summer to the Cognitive Science and Technology External Advisory Board, made up of representatives of universities, industry and laboratories who advise the investment area team managing the LDRD portfolio.

The second part tested different types of memory training to see how they changed participants' memory performance and brain activity. One of Matzen's goals is to find out whether recording a person's brain activity while they use their natural approach to studying can predict what kind of training would work best for that person.

She's still analyzing those findings, but said preliminary results are encouraging. The computer model from the earlier study was used to predict who would perform best on the memory tasks, and the high performers did even better after memory training.

"That's promising because one of the things we want to do is see if we can use the brain activity to predict how people react to the training, whether it will be effective for them," Matzen said.

A next step would be "to use more real-world memory working tasks, such as what military personnel would have to learn as new recruits, and see if the same patterns apply to more complex types of learning," she said.

About 90 volunteers spent nine to 16 hours over five weeks in testing for the memory training techniques study. Their first session developed a baseline for how well they remembered words or images. Most then underwent memory training for three weeks and were retested.

A control group received no training. A second group practiced mental imagery strategy, thinking up vivid images to remember words and pictures. The final group went through "working memory" training to increase how much information they could handle at a time. Matzen said that averages about seven items, such as digits in a phone number.

Each volunteer, shut into a sound-proof booth, watched a screen that flashed words or images for one second, interrupted with periodic quizzes on how well the person remembered what was shown.

"It's designed to be really difficult because we want lots of room to improve after memory training," Matzen said. The test was divided into five sections, each about 20 minutes long followed by a break to keep volunteers alert.

Each section tested a different type of memory. The first, middle and last sections consisted of single nouns. During quizzes, volunteers hit buttons for yes or no, indicating whether they'd seen the word before. The other two sections combined adjectives and nouns or pairs of unrelated drawings, with volunteers again tested on what they remembered. The image section tested associative memory -- memory for two unrelated things. Matzen said that's the most difficult because it links arbitrary relationships.

When performance was compared before and after training, the control group did not change, but the mental imagery group's performance improved on three of the five tasks.

"Imagery is a really powerful strategy for grouping things and making them more memorable," Matzen said.

The working memory group did worse on four of the five tasks after training.

Volunteers trained on working memory -- remembering information for brief periods -- improved on the task they'd trained on, but training did not carry over to other tasks, Matzen said.

She believes it boils down to strategy: The imagery training group learned a strategy, while working memory training simply tried to push the limits of memory capacity.

While the imagery group did better overall, they made more mistakes than the other groups when tested on "lures" that were similar, but not the same, as items they had memorized.

"They study things like 'strong adhesive' and 'secret password,' and then I might test them on 'strong password,' which they didn't see, but they saw both parts of it," Matzen said. "The people who have done the imagery training make many more mistakes on the recombinations that keep the same concept. If something kind of fits with their mental image they'll say yes to it even if it's not quite what they saw before."

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by Sandia National Laboratories.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/_SBy6yBKJF4/120919103144.htm
--
Manage subscription | Powered by rssforward.com
10.43 | 0 komentar | Read More

Nanomaterials in a heart beat: Nanomaterial may allow regeneration of cardiac cells

ScienceDaily (Sep. 19, 2012) — Stem cell scientists have capitalised on the electrical properties of a widely used nanomaterial to develop cells which may allow the regeneration of cardiac cells. The breakthrough has been led by a team of scientists at the Regenerative Medicine Institute (REMEDI) at the National University of Ireland Galway in conjunction with Trinity College Dublin.

Heart disease is the leading cause of death in Ireland. Once damaged by heart attack, cardiac muscle has very little capacity for self-repair and at present there are no clinical treatments available to repair damaged cardiac muscle tissue.

Over the last 10 years, there has been tremendous interest in developing a cell-based therapy to address this problem. Since the use of a patient's own heart cells is not a viable clinical option, many researchers are working to try to find an alternative source of cells that could be used for cardiac tissue repair.

REMEDI researchers Dr Valerie Barron and Dr Mary Murphy have brought together a multi-disciplinary team of Irish materials scientists, physicists and biologists from REMEDI at National University of Ireland Galway and Trinity College Dublin to address this problem.

The researchers recognised that carbon nanotubes, a widely used nanoparticle, is reactive to electrical stimulation. They then used these nanomaterials to create cells with the characteristics of cardiac progenitors, a special type of cell found in the heart, from adult stem cells.

"The electrical properties of the nanomaterial triggered a response in the mesenchymal (adult) stem cells, which we sourced from human bone marrow. In effect, they became electrified, which made them morph into more cardiac-like cells," explains Valerie Barron of REMEDI at National University of Ireland Galway. "This is a totally new approach and provides a ready-source of tailored cells, which have the potential to be used as a new clinical therapy. Excitingly, this symbiotic strategy lays the foundation stone for other electroactive tissue repair applications, and can be readily exploited for other clinically challenging areas such as in the brain and the spinal cord."

This work has recently been published in two scientific journals, Biomaterials and Macromolecular Bioscience, and was carried out in collaboration with Professor Werner Blau, Investigator in CRANN and the School of Physics, Trinity College Dublin (TCD).

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by National University of Ireland, Galway.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal References:

  1. Joseph N. Mackle, David J.-P. Blond, Emma Mooney, Caitlin McDonnell, Werner J. Blau, Georgina Shaw, Frank P. Barry, J. Mary Murphy, Valerie Barron. In vitro Characterization of an Electroactive Carbon-Nanotube-Based Nanofiber Scaffold for Tissue Engineering. Macromolecular Bioscience, 2011; 11 (9): 1272 DOI: 10.1002/mabi.201100029
  2. Emma Mooney, Joseph N. Mackle, David J.-P. Blond, Eoin O'Cearbhaill, Georgina Shaw, Werner J. Blau, Frank P. Barry, Valerie Barron, J. Mary Murphy. The electrical stimulation of carbon nanotubes to provide a cardiomimetic cue to MSCs. Biomaterials, 2012; 33 (26): 6132 DOI: 10.1016/j.biomaterials.2012.05.032

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/5I8DlxTyCZs/120919103315.htm
--
Manage subscription | Powered by rssforward.com
10.13 | 0 komentar | Read More

Birth is no reason to go to hospital, review suggests

ScienceDaily (Sep. 19, 2012) — A new Cochrane Review concludes that all countries should consider establishing proper home birth services. They should also provide low-risk pregnant women with information enabling them to make an informed choice. The review has been prepared by senior researcher, statistician Ole Olsen, the Research Unit for General Practice, University of Copenhagen, and midwifery lecturer PhD Jette Aaroe Clausen.

In many countries it is believed that the safest option for all women is to give birth in hospital. However, observational studies of increasingly better quality and in different settings suggest that planned home birth in many places can be as safe as planned hospital birth and with less intervention and fewer complications.

"If home birth is going be an attractive and safe option for most pregnant women, it has to be an integrated part of the health care system," Ole Olsen says and adds, "In several Danish regions the home birth service has been very well organized for several years. This is not the case everywhere in the world."

The updated Cochrane Review concludes that there is no strong evidence from experimental studies (randomized trials) to favor either planned hospital birth or planned home birth for low-risk pregnant women. At least not as long as the planned home birth is assisted by an experienced midwife with collaborative medical back up in case transfer should be necessary.

Fewer interventions in home birth

Routines and easy access to medical interventions may increase the risk of unnecessary interventions in birth explaining why women who give birth at home have a higher likelihood for a spontaneous labour. There are 20-60 per cent fewer interventions, for example fewer cesarean sections, epidurals and augmentation among those women who plan a homebirth; and 10-30 per cent fewer complications, for example post partum bleeding and severe perineal tears.

"Patience is important if women want to avoid interference and give birth spontaneously," says Jette Aaroe Clausen. "At home the temptation to make unnecessary interventions is reduced. The woman avoids for example routine electronic monitoring that may easily lead to further interventions in birth."

Jette Aaroe Clausen adds that interventions in childbirth are common in many countries, but also that there is a growing concern internationally because interventions may lead to iatrogenic effects; iatrogenic effects meaning unintended consequences of the intervention. Routine electronic monitoring may for example lead to more women having artificial rupture of membranes which in turn can lead to more interventions.

Evidence and human rights

While the scientific evidence from observational studies has been growing, the European Court of Human Rights in Strasbourg in the case Ternovszky versus Hungary has handed down a judgment stating that "the right to respect for private life includes the right to choose the circumstances of birth." This is quoted in the review.

Thus the conclusions of the review are based on human rights and ethics as well as on results from the best available scientific studies.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by University of Copenhagen.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Ole Olsen, David Jewell. Home versus hospital birth. The Cochrane Library, 12 SEP 2012 DOI: 10.1002/14651858.CD000352

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/FpKVCisqAts/120919083454.htm
--
Manage subscription | Powered by rssforward.com
08.16 | 0 komentar | Read More

Stop diabetes with insulin tablets?

ScienceDaily (Sep. 19, 2012) — Could a capsule of insulin crystals a day stop the development of type 1 diabetes? There are indications that this could be the case. In the international TrialNet study, which follows relatives of individuals with type 1 diabetes, researchers are investigating whether oral insulin could prevent or delay the disease.

Type 1 diabetes is the autoimmune form of diabetes, in which the patients' insulin-producing beta cells are destroyed by their own immune system. "We know that if a person has two autoantibodies and one of them is against insulin, there is a 50 per cent risk that they will develop type 1 diabetes within five years. It doesn't matter how old you are," says Åke Lernmark, Professor of Experimental Diabetes Research at Lund University in Sweden.

"There are indications that oral insulin may prevent or delay the clinical onset of type 1 diabetes among individuals with autoantibodies against insulin, who are thus in the risk zone," says Åke Lernmark, who will be initiating and coordinating the Swedish TrialNet study.

Åke Lernmark refers to a study presented earlier in the year by American and Canadian researchers. In the study, which ran from 1994 to 2003, participants with relatives who had type 1 diabetes and at least two autoantibodies, one of which against insulin, took either oral insulin or placebo capsules containing an inactive substance. At first, the results were a disappointment. Just as many people in the treatment group became ill as in the placebo group.

"However, the subsequent analyses showed something different. Among those who had high levels of insulin autoantibodies at the start of the study, the oral insulin had an effect and the development of type 1 diabetes was delayed. The delaying effect lasted for as long as the participants took the insulin," says Åke Lernmark, adding that those who are now being recruited for the Swedish TrialNet study with oral insulin also have high levels of autoantibodies against insulin.

No one knows how oral insulin might stop type 1 diabetes. However, Åke Lernmark believes a possible explanation could be that the immune system becomes accustomed to the low daily doses of insulin in the gastrointestinal tract. The insulin is not perceived as a foreign substance to be rejected by the immune system.

This line of reasoning is the same as for desensitisation for allergies, in which the dose of the substance that provokes the allergy is gradually increased.

The oral insulin study will run for several years and is open to all those who meet the requirements and are aged between 3 and 45.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by Lund University.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. K. Vehik, D. Cuthbertson, H. Ruhlig, D. A. Schatz, M. Peakman, J. P. Krischer. Long-Term Outcome of Individuals Treated With Oral Insulin: Diabetes Prevention Trial-Type 1 (DPT-1) oral insulin trial. Diabetes Care, 2011; 34 (7): 1585 DOI: 10.2337/dc11-0523

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/pI8U3azTetQ/120919083412.htm
--
Manage subscription | Powered by rssforward.com
08.16 | 0 komentar | Read More

Compound found in purple corn may aid in developing future treatments for type 2 diabetes, kidney disease

Written By Unknown on Selasa, 18 September 2012 | 17.14

ScienceDaily (Sep. 18, 2012) — Diabetic nephropathy is one of the most serious complications related to diabetes, often leading to end-stage kidney disease. Purple corn grown in Peru and Chile is a relative of blue corn, which is readily available in the U.S. The maize is rich in anthocyanins (also known as flavonoids), which are reported to have anti-diabetic properties.

Scientists from the Department of Food and Nutrition and Department of Biochemistry at Hallym University in Korea investigated the cellular and molecular activity of purple corn anthocyanins (PCA) to determine whether and how it affects the development of diabetic nephropathy (DN). Their findings suggest that PCA inhibits multiple pathways involved in the development of DN, which may help in developing therapies aimed at type 2 diabetes and kidney disease.

The study is entitled "Purple corn anthocyanins inhibit diabetes-associated glomerular monocyte activation and macrophage infiltration." It appears in the online edition of the American Journal of Physiology -- Renal Physiology, published by the American Physiological Society.

Methodology

Researcher Min-Kyung Kang and colleagues performed a two-part study, an in vitro experiment investigating the effects of PCA on human endothelial cells cultured under hyperglycemic kidney conditions and an in vivo study that investigated the effects of PCA on kidney tissue in diabetic mice. In the in vitro experiment, cultured cells were exposed to 1-20 µg/ml of PCA for six hours (control cells were not exposed), then assessed for level of monocyte-endothelial cell adhesion, a major factor in the development of diabetic glomerulosclerosis. In the in vivo experiment, diabetic and control mice were dosed with PCA for eight weeks, then changes in kidney tissue were assessed and immunohistological analyses were performed. Kidney tissue was further analyzed for levels of inflammatory chemokines, which are key components in DN.

Results

Researchers found that in human endothelial cells cultured in hyperglycemic kidney conditions, induction of endothelial cell adhesion molecules decreased in a dose-dependent manner with PCA exposure, meaning that the PCA likely interfered with cell-cell adhesion in glomeruli. PCA also appeared to interfere with leukocyte recruitment and adhesion to glomerular endothelial cells. In diabetic mice, PCA exposure slowed mesangial expansion and interrupted the cellular signaling pathway that may instigate glomerular adhesion and infiltration of inflammatory cells responsible for diabetic glomerulosclerosis. Finally, PCA inhibited levels of macrophage inflammatory protein-2 and monocyte chemotactic protein-1 in kidney tissue, demonstrating that it may inhibit macrophage infiltration, which is closely related to renal inflammation.

Importance of the Findings

The research suggests that anthocyanins may be the main biofunctional compound in purple corn and could protect against mesangial activation of monocytes and infiltration of macrophages in glomeruli -- the two major contributors to DN. The research further suggests that renoprotection by PCA against mesangial activation may be specific therapies targeting diabetes-associated diabetic glomerulosclerosis and renal inflammation. Finally, PCA supplementation may be an important strategy in preventing renal vascular disease in type 2 diabetes.

"PCA may be a potential renoprotective agent treating diabetes-associated glomerulosclerosis," wrote the researchers.

Research Team

In addition to Min-Kyung Kang, the study team included Jing Li, Ju-Hyun Gong, Su-Nam Kwak, Jung Han Yoon Park, Soon Sung Lim and Young-Hee Kang, all also of the Department of Food and Nutrition at Hallym University in Korea, and Jae-Yong Lee, of the Department of Biochemistry at Hallym University.

Funding

This study was funded by a grant from the Ministry of Food, Agriculture, Forestry and Fisheries through Korea Institute of Planning and Evaluation for Technology of Food, Agriculture, Forestry and Fisheries; and by the National Research Foundation of Korea.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by American Physiological Society (APS).

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. M.-K. Kang, J. Li, J.-L. Kim, J.-H. Gong, S.-N. Kwak, J. H. Y. Park, J.-Y. Lee, S. S. Lim, Y.-H. Kang. Purple corn anthocyanins inhibit diabetes-associated glomerular monocyte activation and macrophage infiltration. AJP: Renal Physiology, 2012; DOI: 10.1152/ajprenal.00106.2012

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/Yp-PtOFU4gs/120918184756.htm
--
Manage subscription | Powered by rssforward.com
17.14 | 0 komentar | Read More

Nanoparticles detect biochemistry of inflammation

ScienceDaily (Sep. 18, 2012) — Inflammation is the hallmark of many human diseases, from infection to neurodegeneration. The chemical balance within a tissue is disturbed, resulting in the accumulation of reactive oxygen species (ROS) such as hydrogen peroxide, which can cause oxidative stress and associated toxic effects.

Although some ROS are important in cell signaling and the body's defense mechanisms, these chemicals also contribute to and are indicators of many diseases, including cardiovascular dysfunction. A non-invasive way of detecting measurable, low levels of hydrogen peroxide and other ROS would provide a viable way to detect inflammation. Such a method would also provide a way to selectively deliver drugs to their targets.

Adah Almutairi, PhD, associate professor at the Skaggs School of Pharmacy and Pharmaceutical Sciences, the Department of NanoEngineering, and the Materials Science and Engineering Program at the University of California, San Diego, and colleagues have developed the first degradable polymer that is extremely sensitive to low but biologically relevant concentrations of hydrogen peroxide.

Their work is currently published in the online issue of the Journal of the American Chemical Society.

These polymeric capsules, or nanoparticles, are taken up by macrophages and neutrophils -- immune system cells that rush to the site of inflammation. The nanoparticles then release their contents when they degrade in the presence of hydrogen peroxide produced by these cells.

"This is the first example of a biocompatible way to respond to oxidative stress and inflammation," said Almutairi, director of the UC San Diego Laboratory of Bioresponsive Materials. "Because the capsules are tailored to biodegrade and release their cargo when encountering hydrogen peroxide, they may allow for targeted drug delivery to diseased tissue."

Almutairi is looking to test this method in a model of atherosclerosis. "Cardiologists have long needed a non-invasive method to determine which patients are vulnerable to a heart attack caused by ruptured plaque in the arteries before the attack," she said. "Since the most dangerous of plaques is inflamed, our system could provide a safe way to detect and treat this disease."

Additional contributors to the study include Caroline de Gracia Lux, Shivanjali Joshi-Barr, Trung Nguyen, Enas Mahmoud, Eric Schopf and Nadezda Fomina.

This research was supported by the NIH Director's New Innovator Award 1DP2OD006499-01 and a King Abdulaziz City for Science and Technology center grant to the Center of Excellence in Nanomedicine at UC San Diego.

Share this story on Facebook, Twitter, and Google:

Other social bookmarking and sharing tools:


Story Source:

The above story is reprinted from materials provided by University of California, San Diego.

Note: Materials may be edited for content and length. For further information, please contact the source cited above.


Journal Reference:

  1. Caroline de Gracia Lux, Shivanjali Joshi-Barr, Trung Nguyen, Enas Mahmoud, Eric Schopf, Nadezda Fomina, Adah Almutairi. Biocompatible Polymeric Nanoparticles Degrade and Release Cargo in Response to Biologically Relevant Levels of Hydrogen Peroxide. Journal of the American Chemical Society, 2012; 120917145802001 DOI: 10.1021/ja303372u

Note: If no author is given, the source is cited instead.

Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of ScienceDaily or its staff.

19 Sep, 2012


-
Source: http://feeds.sciencedaily.com/~r/sciencedaily/top_news/top_health/~3/c1N28sMKcJQ/120918184800.htm
--
Manage subscription | Powered by rssforward.com
17.14 | 0 komentar | Read More
techieblogger.com Techie Blogger Techie Blogger