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Tuesday, September 18, 2012

One Day, Growing Spare Parts Inside the Body

LOS ANGELES — Dr. Tracy Grikscheit held a length of intestine in her gloved hands, examining it inch by inch as if she were checking a bicycle tube for leaks.
The intestine was still attached, at one end, to Mark Barfknecht, a 1-year-old whose pink cheeks belied the reason he was lying on an operating table at Children’s Hospital Los Angeles. Born three months premature, Mark had developed a disorder that affects up to 10 percent of babies who weigh about 3 pounds or less at birth, causing some of their intestinal tissue to die. Mark’s case was so severe that most of his intestines had been removed.
Now Dr. Grikscheit, a surgeon, was trying to determine how much of the rest she could save.
Dr. Grikscheit is renowned for her skill in treating infants like Mark, whose only way to survive may be as what she calls a “short gut kid” — left with too little intestine to absorb food normally and forced to get nutrition through a needle into the bloodstream.
But devoted as she is to saving children in the operating room, Dr. Grikscheit is equally determined to find a better solution than the intravenous feeding, possibly for life, that such patients face. Much of her time is spent in her laboratory across the street, at the hospital’s Saban Research Institute, where she is working with her research team to find a way to make replacement intestines for infants like Mark, using the body itself to nourish and push the engineered tissue to grow.
Dr. Grikscheit’s work is at the forefront of efforts in laboratories around the world to build replacement organs and tissues. Although the long-sought goal of creating complex organs like hearts and livers to ease transplant shortages remains a long way off, researchers are having success making simpler structures like bladders and windpipes, thanks to advances in understanding stem cells — basic cells that can be transformed into other types within the body — and to the development of innovative techniques.
So far Dr. Grikscheit has concentrated on growing rat, mouse and pig intestinal tissue in laboratory animals. But she has recently had success in growing human intestinal tissue, using donor cells, and is beginning to study how to develop the technique for human patients. There are many hurdles, and human testing is still years away, but she has a surgeon’s confidence that the technique will work.
“We have a huge problem that if we solve it, it will change the future for a lot of children,” she said.
In her lab, her team is currently working with mice. They first remove good intestine from the animals, cut it up and treat it with enzymes and other compounds to form clusters of mixed cells, including stem cells that are found in the absorptive lining of the intestine and others that make up the tougher connective tissue.
The clusters are then placed on a piece of porous biodegradable plastic, about the size and shape of the eraser on a pencil. The plastic serves as a scaffold, supporting the cells and orienting them, which has the effect of making the lining grow inward while the connective tissue grows on the outside.
This kind of seeding of scaffolds with cells is a common approach in the field of regenerative medicine, also known as tissue engineering. But in most cases, the goal is to swap the bad organ — a windpipe, for example — with the engineered replacement, where it can grow into its permanent position in the body.
Dr. Grikscheit has had success in the lab with a different method, using another part of the body to nourish the replacement as it grows.
She and her team sew the bundle of cells into the mouse’s omentum, a membranous fold inside the abdomen. There, the bundle is surrounded by blood vessels that supply nutrients, helping it to grow. The plastic eventually dissolves as the bundle grows into a hollow ball of tissue. A few weeks later, Dr. Grikscheit and her researchers remove the ball from the omentum — for study, to better understand how the regenerative growth occurs. The tissue has all the components of intestines, including the lining, muscles, nerves and blood vessels.
In earlier studies in rats, Dr. Grikscheit went a step further, splicing the tissue into the digestive tract of animals that had had much of their intestines removed. Rats with the engineered intestine recovered more quickly than those without it.
By combining this kind of lab work with her surgical practice, Dr. Grikscheit is doing what she has always thought surgeons should do. “You move medicine ahead,” she said.
Dr. Grikscheit, 40, who is intense and energetic and easy to spot in the hospital in her strawberry-print surgical cap, says she always knew she was going to be a surgeon — she told her great-grandmother as much when she was 6, growing up outside Salt Lake City. During her training she gravitated toward pediatric surgery. Compared with adults, children were works in progress — sometimes imperfect ones.
“The really fascinating thing is how to put something together that came out wrong and make it as right as possible,” she said.
She envisions a day when her approach moves beyond the lab to the operating room. Future operations to remove dead intestine from a baby — or from other patients with severe intestinal damage — would include an additional step: a little bit of good intestine would be sent to a table nearby, where technicians would quickly prepare a bundle for immediate implantation in the patient’s omentum.
The patient might have to be on intravenous nutrition for a month or so while the intestine grows, but eventually could be weaned off it after the new tissue was harvested and sewn in.
Not much new intestine would be required. “You only need to engineer an organ up to the point where you fix the missing function,” Dr. Grikscheit said. Even a couple of inches might be enough. “That will tip them back over into having enough absorptive function to get off of I.V. nutrition and live a full life.”
Such a remedy is still too far off for Mark Barfknecht.
Back in the operating room on that day earlier this year, Dr. Grikscheit and a fellow surgeon, Dr. Demetri Merianos, continued to examine Mark’s intestines. Without the ability — yet — to regenerate the child’s intestinal tissue, they were focused on keeping as much of the damaged organ as possible.
“This is coming down to something narrow,” Dr. Grikscheit said as she felt the tissue, which she and Dr. Merianos had spent the better part of two hours delicately freeing from Mark’s abdominal cavity, smoke rising from the cauterizing blade as they cut through places where it had adhered to the liver after an earlier surgery.
To ensure that they could properly reconnect Mark’s digestive tract at the end of the four-hour procedure, they tagged the open ends of the intestines with surgical thread and clamps of different kinds, and jotted notes on the paper surgical drapes about which end went where.
“I don’t care for this,” Dr. Grikscheit said, frowning. She and Dr. Merianos agreed that a 3-inch length of intestine would probably have to be cut out.
For a baby who had about only 15 inches of small intestine remaining, that was not good news.
But Mark, his mother says, is a survivor.
“Oh yeah, he’s been through it,” Karen Barfknecht said a few hours before the surgery, after his father, Michael, had detailed all the procedures their son had endured. “He has a cry that just makes you feel so bad,” Ms. Barfknecht said. “You’ll do absolutely anything for him.”
No one knows precisely what triggers the disorder, but prematurity plays a role.
Called necrotizing enterocolitis, the disorder can crop up suddenly in the weeks after birth. In about a quarter of cases, the death of intestinal tissue ultimately proves fatal. For many of the rest, emergency surgery to resect, or remove, dead tissue creates new problems.
“When I look at their intestine, I already know that to save their life I’m going to resect more than they can manage,” Dr. Grikscheit said. If the amount of dead tissue exceeds 75 percent of the total, the child will almost certainly be forced to get nutrition intravenously, which over the long term can damage the liver. Other operations, up to and including an intestinal transplant, may be needed, which bring other risks.
Mark is near that 75 percent threshold, so doctors at another hospital closer to his home in Indio, Calif., had put him on the special intravenous feeding, called total parenteral nutrition, or T.P.N., months before; now his liver is starting to suffer.
He has required such a high level of care that Mr. Barfknecht quit his job as a mechanic. Still, Mark has been in either a hospital or a convalescent facility almost all his short life; his big sister has hardly spent any time with him.
“We want him home,” his mother said. “We just want him home.”
That is Dr. Grikscheit’s goal, too. But before she and Dr. Merianos could determine whether Mark had enough good intestine to be weaned off the intravenous feeding eventually, they had to assess the narrow, diseased section they had found earlier. They looked at it again, weighing the options. They checked and rechecked their notes scribbled on the drapes.
“Unfortunately, sayonara,” she said, directing Dr. Merianos to begin cutting.
But that was the last piece of bad news for Mark. As the doctors continued to look at the remaining intestine, they grew increasingly optimistic that he would have enough. If so, they would stitch the remaining pieces together and reconnect everything from the stomach to the colon. Mark will have to continue the intravenous nutrition for some time, but eventually he should be able to eat normally.
“I think we’ll make it off T.P.N. and get him home,” Dr. Grikscheit said.
It is the infants who are not so fortunate — for whom surgery could not do enough — who motivate Dr. Grikscheit to keep working on a way to make new tissue.
“You keep finding these kids, in my case, who die,” she said. “I think it would be very frustrating to keep beating your head on the same problem and saying, ‘Well, that’s too bad.’ ”
 
 

Cancer overtakes heart disease among US Hispanics

By MIKE STOBBE | Associated Press
 
NEW YORK (AP) — Cancer has overtaken heart disease as the No. 1 killer among Hispanics in the U.S., and the rest of the country may be only a few years behind.
 
The change is not exactly cause for alarm. Death rates for both cancer and heart disease have been dropping for Hispanics and everyone else. It's just that heart disease deaths have fallen faster, largely because of improved treatment and prevention, including the development of cholesterol-lowering drugs.

Overall, cancer will probably replace heart disease as the nation's top cause of death in the next 10 years, said Rebecca Siegel of the American Cancer Society, lead author of a study reporting the new findings. Government health statisticians think the crossover point could be reached as early as this year, or at least in the next two or three years.

The reason it has already happened among Hispanics is that they are younger on average than non-Hispanic whites and blacks. And cancer tends to kill people earlier in life than heart disease, for decades the nation's top cause of death.

The shift could bring about a change in disease-prevention efforts, government spending priorities and people's attitudes.

"We've been so focused on heart disease mortality for so long. ... This may change the way people look at their risk," said Robert Anderson, who oversees the Centers for Disease Prevention and Control branch that monitors death statistics.

The study is being published in the September/October issue of a cancer society publication, CA: A Cancer Journal for Clinicians.

Cancer society researchers looked at federal death data for 2009 and found that 29,935 Hispanics died of cancer and 29,611 of heart disease. It was the first year in which cancer deaths surpassed heart disease in that ethnic group.

Cancer is also the leading cause of death for Asian-Americans and Pacific Islanders. And it is now the leading killer in 18 states, according to 2009 numbers from the CDC.

Hispanics are the nation's largest and fastest-growing major ethnic group, and many of them are young immigrants from Mexico. Most heart disease deaths are in people 65 and older. The vast majority of Hispanics in the U.S. are under 55.

The story is different in Mexico, which has an older population. There, diabetes is the biggest killer, with cancer No. 2, according to 2009 statistics from the Pan American Health Organization.
Interestingly, none of the states where cancer has overtaken heart disease is in the Southwest, which has large Hispanic populations. Instead, most are in the nation's northern tier, including Alaska, Washington, Idaho, Montana, Minnesota, Wisconsin and the four states of upper New England.
___
Online:
Cancer Society journal: http://cacancerjournal.org

Monday, June 11, 2012

New Library Website



Study Digs Into Secrets of Keeping HIV in Check



SUNDAY, June 10 (HealthDay News) -- A small number of HIV-infected patients have immune systems that are able to keep AIDS at bay by preventing the virus from reproducing for years, and researchers are reporting that they've gained new insight into how that works.
These fortunate patients, known as "elite controllers" or "long-term non-progressors," are quite rare. They've long fascinated scientists who want to understand the secrets lurking inside their immune cells. Researchers trying to develop an AIDS vaccine are especially interested in these special patients.
The key seems to be that certain cells in the immune systems of these people are better able to detect and kill cells that are infected with HIV, the virus that causes AIDS, said study co-author Dr. Bruce Walker, a professor at Harvard School of Public Health.
In essence, he said, they have better "glasses" than the same cells in patients who can't fight off the virus as well. These cells are better able to "see" signs of trouble from infected cells that send out a kind of distress signal.
The new research shows that "there's a way to measure what's good vision and what's bad vision," Walker said. "We can immediately start looking at vaccine candidates to see if our techniques of training these killer cells are leading to really good vision or not. We can also try to understand what it is that's impaired the vision in some of these patients and allowed for good vision to develop in others."
The researchers came to their conclusions after studying the blood of five "elite controllers" and five normal HIV patients.
Only about one in 200 or 300 HIV patients is able to naturally keep the virus from developing into AIDS without the help of medications, Walker noted. One person has been fending off AIDS since 1978.
"We can't be sure that everybody who achieves this state is actually going to persist in it, but it certainly looks like the vast majority of them will," he said.
Nitin Saksena, head of the retroviral genetics division at Westmead Millennium Institute's Center for Virus Research in Sydney, Australia, said the study needs to be confirmed by other research, and it has limitations, such as the small number of patients involved. It's important to consider that "elite controllers" are quite different from each other, Saksena added.
Dr. Mark Connors, chief of the HIV-specific immunity section with the Laboratory of Immunoregulation of the U.S. National Institute of Allergy and Infectious Diseases, questioned the study results, saying they don't demonstrate why the killer immune cells work more effectively in the elite controllers. Essentially, Connors doesn't think the study authors discovered why the cells have better "vision."
Study co-author Walker, however, said the research is valuable: "This is another example of HIV revealing its secrets. Having been in this field for 30 years, the remarkable thing is that we just keep learning more."
The study is published in the June 10 online edition of Nature Immunology.

Wednesday, February 8, 2012


The Miami Herald

MDC launches first-ever course to help Miami-Dade officers save their own lives

Florida currently leads the nation with the highest number of officer fatalities in the line of duty.Now, a pioneering course developed by Miami-Dade College’s Medical Campus and Miami-Dade police aims to reduce that number by training officers to tend to wounded partners, and even themselves, before paramedics arrive.
Tactical Life-Saver course is the country’s first of its kind. The training will focus on what officers should do in the first minutes after an officer is shot, which can mean the difference between life and death.
The intense 40-hour course will teach officers necessary medical knowledge and stay alive until help arrives, which can be delayed by circumstances.
“If an officer is wounded and is pinned down by gunfire, the paramedics will not come into a crime scene until the bad guys are captured,” said MDC School of Health Sciences Dean Pete Gutierrez, who is a former Miami police officer. “This training is meant to teach officers to keep each other alive in that situation. It’s a way to buy them time.”
Gutierrez said the impetus for the course, which resembled those given to U.S. Army soldiers, came after the slaying in January 2011 of two Miami-Dade police officers while trying to serve a warrant on a murder suspect in Miami. Fatally wounded were Officers Amanda Haworth and Roger Castillo. A third officer was wounded and the suspect was shot to death.
“After that tragic incident, we decided to take a look and see what we could do to help officers better survive such a violent incident,” said Gutierrez, who is also the police department’s medical training director.
Part of the officers week-long training will take place at MDC’s medical campus’ state-of-the-art Simulation Lab, where human simulators will be used to teach wound assessment and bleeding control; stabilize spinal injuries and treat a sucking chest wound.
Another segment will be taught at the Miami-Dade police training center where officers will be placed in realistic, dangerous scenarios where they will simulate being wounded on duty.
All officers who take the course will be giving special emergency trauma kits to carry during their shift.
The course is underway all this week with 17 officers. It will continue until all county officers have gone through the training.

Read more here: http://www.miamiherald.com/2012/02/08/v-print/2631319/mdc-launches-first-ever-course.html#storylink=cpy

Black Heritage Month presents MUSICOLOGY

Tuesday, November 1, 2011

New Hours for Learning Resources


Library and Success Center Hours


Monday - Thursday

7:30 am - 9:00 pm

Friday
7:30 am - 5:00 pm

Saturday
7:30 am - 1:00 pm

Monday, September 12, 2011

High blood pressure genetic clues


More than 20 new sections of genetic code have been linked to blood pressure by an international team of scientists.
Almost everyone will carry at least one of the genetic variants, according to studiespublished in Nature and Nature Genetics.
Researchers believe their findings could be used to develop new treatments.
The British Heart Foundation said lifestyle was still key to a healthy blood pressure.
High blood pressure - or hypertension - can run in families as well as being influenced by obesity, exercise and the amount of salt in the diet.
While the lifestyle risks are well known, the genetic element of hypertension has been poorly understood.
Researchers now say they have made a "major advance" in understanding the role of genes.
In the first study, scientists from 24 countries around the world analysed data from more than 200,000 people.

Start Quote

There is substantial potential for moving the findings from the lab to the clinic”
Prof Mark Caulfield
They identified 16 new points on the genome which were linked to blood pressure.
One of the lead researchers, Prof Mark Caulfield, from Barts and The London Medical School, said each genetic variant was in at least 5% of people, while some were much more common.
"This is having an influence across the population," he said.
Uncovering the genetic basis of blood pressure has revealed processes in the body which could one day be targeted with drugs.
One series of chemical reactions involving nitric oxide, which opens up blood vessels, has been highlighted as a potential target.
Gene puzzle
Prof Caulfield said: "There is substantial potential for moving the findings from the lab to the clinic.
"There are, in development or in existence, drugs which could be considered."
However, researchers say they have still uncovered only 1% of the genetic contribution to blood pressure.
A second study, presented in Nature Genetics, identified a further six new stretches of genetic code.
The British Heart Foundation's medical director, Prof Peter Weissberg, said: "Researchers from across the world have now identified some of the genes linked to blood pressure control, which could pave the way for new treatments in the future.
"But your genes are only one piece of the puzzle. You are less likely to have high blood pressure if you stick to a healthy diet, do plenty of exercise, and maintain a healthy weight."

Malaria report sees near-zero deaths by end of 2015


(Reuters) - The world has made impressive progress against malaria in the past 10 years, increasing optimism that an end to the killer mosquito-borne disease could be in sight, a World Health Organization-backed report said on Monday.
A man fumigates against mosquitoes through the streets of Lahore March 28, 2011. REUTERS/Mohsin Raza
Deaths from malaria have fallen by an estimated 38 percent in the past 10 years with 43 countries -- 11 of them in Africa -- cutting malaria cases or deaths by 50 percent, reversing the previous decade's trend and saving more than a million lives.
The progress -- partly due to a substantial increase in funding for fighting malaria -- means deaths from the disease could be brought down to near zero by the end of 2015, the report by the Roll Back Malaria (RBM) partnership said.
The WHO, which helped set up the RBM partnership, has also said the world can stop malaria deaths by 2015 if massive investment is made to ramp up control measures, but this is seen by some experts as an ambitious target.
RBM also aims to reduce global malaria cases by 75 percent by the end of 2015 from the levels seen in 2000, and eliminate malaria in 10 more countries.
Total eradication of the parasitic disease, which is spread through the bites of infected mosquitoes and threatens around half the world's population, is still a long way off. Some think it could take another 40 to 50 years.
"The results of the past decade exceed what anyone could have predicted and prove that malaria control is working," Robert Newman, director of WHO's global malaria programme, said in a statement released alongside the report.
According to the WHO, the number deaths from malaria worldwide dropped to 781,000 in 2009 from nearly a million in 2000. But there are still around 225 million cases a year and the disease remains endemic in 106 countries.
Malaria can damage the nervous system, kidneys and liver and severe cases can kill. Most malaria deaths are in Africa, where a child dies from the disease every 45 seconds.
The RBM report found that international funding for malaria had increased more than 15-fold since 2003, jumping from 62 million pounds ($98.5 million)a year then to 93 million pounds ($148 million)a year by 2010. Certain donor countries such as Britain, France and the United States had also stepped up contributions, the report noted.
"We are light years away from where we were 10 years ago," said Awa Coll-Seck, RBM's executive director.
She said this progress was partly down to the development of new tools such as insecticide-treated mosquito nets, indoor spraying strategies and more effective anti-malarial medicines, but also because of "vastly improved policies, financing, and strategies" and better international coordination.
Yet despite impressive gains, the RBM report said many people at risk of malaria still did not have good enough access to treatment and prevention options, such as insecticide treated nets, indoor spraying, proper diagnostic testing, and effective drugs, including drugs to treat and prevent malaria in pregnant women.
Progress is also being threatened by the emergence of insecticide-resistant mosquitoes, and of malaria parasites resistant to artemisinin, a key component of the most effective anti-malaria drug combinations.
"There is more to be done to address these issues, but with appropriate commitments, the gains can accrue rapidly," the report said.
The RBM partnership is a global health group set up in 1988 by the WHO, the United Nations children's fund UNICEF, the World Bank and others to coordinate the fight against malaria.
(Editing by Alison Williams)

Wednesday, August 31, 2011

'Anti-cancer virus' shows promise'



An engineered virus, injected into the blood, can selectively target cancer cells throughout the body in what researchers have labelled a medical first.
The virus attacked only tumours, leaving the healthy tissue alone, in a small trial on 23 patients, according to the journal Nature.
SPL
Modified vaccinia virus can target cancer


Researchers said the findings could one day "truly transform" therapies.
Cancer specialists said using viruses showed "real promise".
Using viruses to attack cancers is not a new concept, but they have needed to be injected directly into tumours in order to evade the immune system.
Smallpox to cancer
Scientists modified the vaccinia virus, which is more famous for being used to develop a smallpox vaccine.
The virus, named JX-594, is dependent upon a chemical pathway, common in some cancers, in order to replicate.
It was injected at different doses into the blood of 23 patients with cancers which had spread to multiple organs in the body.

Start Quote

I believe that some day, viruses and other biological therapies could truly transform our approach for treating cancer”
Prof John BellUniversity of Ottawa
In the eight patients receiving the highest dose, seven had the virus replicating in their tumours, but not in healthy tissue.
Prof John Bell, lead researcher and from the University of Ottawa, said: "We are very excited because this is the first time in medical history that a viral therapy has been shown to consistently and selectively replicate in cancer tissue after intravenous infusion in humans.
"Intravenous delivery is crucial for cancer treatment because it allows us to target tumours throughout the body as opposed to just those that we can directly inject."
Infection prevented further tumour growth in six patients for a time. However, the virus did not cure cancer. Patients were given only one dose of the virus as the trial was designed to test the safety of the virus.
It is thought that the virus could be used to deliver treatments directly to cancerous cells in high concentrations.
Prof Bell acknowledges that the research is still in the very early stages, but he said: "I believe that some day, viruses and other biological therapies could truly transform our approach for treating cancer."
Cancer Research UK's Prof Nick Lemoine, also director of Barts Cancer Institute, said: "Viruses that multiply in just tumour cells - avoiding healthy cells - are showing real promise as a new biological approach to target hard-to-treat cancers.
"This new study is important because it shows that a virus previously used safely to vaccinate against smallpox in millions of people can now be modified to reach cancers through the bloodstream - even after cancer has spread widely through the patient's body.
"It is particularly encouraging that responses were seen even in tumours like mesothelioma, a cancer which can be particularly hard to treat."

Friday, August 19, 2011

Test Taking Strategies Video Series

        Test Taking Strategies (Video Series)

Test-Taking Strategies 1 (of 12): Eliminating Wrong Answers
http://youtu.be/l0P5U9s4wYE

Test-Taking Strategies 2 (of 12): Working Backwards
http://youtu.be/vEF_mkeFawU

Test-Taking Strategies 3 (of 12): Solving Easy Problems First
http://youtu.be/4XYMkBib9Cw

Test-Taking Strategies 4 (of 12): Staying Relaxed
http://youtu.be/bvQHk9WUjKg

Test-Taking Strategies 5 (of 12): The Secret Spill (Brain Dump)
http://youtu.be/f5YjVNgWjpU

Test-Taking Strategies 6 (of 12): Show Your Work (Use Your Pencil!)

Test-Taking Strategies 7 (of 12): Tricky Words (Game Changers)

Test-Taking Strategies 8 (of 12): "All" or "None" Answers

Test-Taking Strategies 9 (of 12): The Comfortable Pace
http://youtu.be/FnXQ5cepJXA

Test-Taking Strategies 11 (of 12): Estimate or Do the Minimum
http://youtu.be/fphJw_G2iZY

Test-Taking Strategies 12 (of 12): How to Feel Great!