Archive for November, 2009

Erectile dysfunction

Thursday, November 26th, 2009

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New Technique Could Eliminate Inherited Mitochondrial Disease

Saturday, November 21st, 2009

Researchers funded by the National Institutes of Health have developed an experimental technique with the potential to prevent a class of hereditary disorders passed on from mother to child. The technique, as yet conducted only in nonhuman primates, involves transferring the hereditary material from one female’s egg into another female’s egg from which the hereditary material has been removed.

The resultant eggs, which were fertilized with donor sperm, implanted in females and carried to term, produced offspring free of the mother’s mitochondria, but which instead possess the mitochondria from the donated egg cell. Mitochondria are tiny structures within cells that help provide energy to power the cell’s activities. They are passed on from mother to child, in the fluid (called cytoplasm) contained inside the egg cell. In recent years, defects in mitochondria have been linked with a variety of conditions, such as diabetes, cancer, infertility, and such neurodegenerative disorders as Alzheimer’s, Parkinson’s and Huntington’s diseases. The technique raises the possibility that mitochondria associated with a hereditary disorder could be prevented from being passed on to the next generation.

“Recent findings suggest that mitochondrial disorders play a role in at least some proportion of many human disorders,” said Duane Alexander, M.D, director of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, which provided funding for the study. “Pending further research, the findings hold the potential of allowing a couple to have a child who is biologically their own, but is free of any conditions associated with defects in maternal mitochondria.”

Mitochondria are passed on to subsequent generations only through egg cells and not transmitted through sperm. In addition to the DNA found in the chromosomes, mitochondria have their own DNA. Mutations in mitochondrial DNA have been associated with a variety of human disorders.

The study was conducted by researchers at the Oregon Health Science University in Beaverton and was published online in Nature.

Using the technique, the researchers created fertilized eggs and achieved three successful pregnancies in rhesus monkeys, which have resulted in four healthy newborns. Recent advances in the transfer of hereditary material and in microscopy facilitated the achievement, they wrote.

The researchers said that the technique did not appear to pose any risk of chromosomal damage. Analysis of 5-6-day-old embryos (blastocysts) resulting from the fertilized eggs, and of embryonic stem cell lines established from them, did not uncover any evidence of damage to the chromosomes. Analysis of cells from the infant monkeys born after the procedure failed to detect any mitochondrial DNA from the mother.

U.S. Updates Clinical Guidelines for Prevention and Treatment of Opportunistic Infections among HIV-Exposed and HIV-Infected Children

Monday, November 16th, 2009

New guidelines to assist health care workers in preventing and treating the secondary infections that can afflict U.S. children exposed to, or infected with, HIV, were published by the National Institutes of Health and the Centers for Disease Control and Prevention.

The new guidelines provide a reference manual for the treatment of these secondary infections, describing warning signs of potentially hazardous interactions between drugs used to treat HIV and its secondary infections, current standards for treating the inflammation accompanying the immune system recovery made possible by new anti-HIV drugs, as well as when to discontinue preventative treatment no longer needed after the immune system has recovered.

HIV cripples the immune system, leaving infected people more vulnerable than the general population to numerous other infectious diseases. These diseases, which ordinarily do not cause problems for people with fully functioning immune systems, are known as opportunistic infections. HIV-associated opportunistic infections are a leading cause of hospitalization and death among HIV-infected children in the United States. Some of these opportunistic infections can also afflict children who do not have HIV but who have one or both parents with HIV and specific HIV-related opportunistic infections.

“The guidelines will help health care workers and public health officials who work with children to save lives that might otherwise be lost,” said Kathleen Sebelius, secretary of the U.S. Department of Health and Human Services. “The infections that can accompany HIV are often the major cause of illness and death of HIV-infected children.”

The report, Guidelines for Prevention and Treatment of Opportunistic Infections in HIV-Exposed and HIV-Infected Children, updates recommendations on topics such as the importance of starting antiretroviral treatment early and interactions between drugs that treat HIV and drugs that treat opportunistic infections.

The report, the first update of the guidelines in five years, appears in the Sept. 4 issue of Morbidity and Mortality Weekly Report (MMWR). The NIH and CDC produced the update in cooperation with the HIV Medicine Association of the Infectious Diseases Society of America, the American Academy of Pediatrics, and the Pediatric Infectious Disease Society.

The new guidelines apply to 23 opportunistic infectious diseases. A panel of more than 30 government and non-government pediatric HIV and infectious disease experts developed the guidelines. The guidelines update and combine two previous publications, a 2002 publication on the prevention of opportunistic infections in HIV-infected adults and children and a 2004 publication on the treatment of opportunistic infections in children.

In recent years, the number of HIV-associated opportunistic infections in children has declined significantly in the United States. The decrease is primarily due to advances in antiretroviral therapy. But the infections continue to occur, and they can be serious or even fatal.

“Health care providers must be vigilant for the signs and symptoms of these infections and know how to prevent and treat them,” said Lynne Mofenson, M.D., a coauthor of the new guidelines and chief of NICHD’s Pediatric, Adolescent, and Maternal AIDS Branch.

Because children’s immune systems are not as developed as adults, even children who do not have HIV may be at high risk of catching certain opportunistic infections, such as tuberculosis, if one or both parents have HIV and an accompanying opportunistic infection. Like HIV itself, some opportunistic infections, such as cytomegalovirus or hepatitis viruses, can be passed from mother to child.

“Guidelines for preventing and treating opportunistic infections in children must consider the risk of infections among both HIV-infected children and children who were HIV-exposed through birth to an HIV-infected mother.” Dr. Mofenson said.

In recent years, HIV infection has increased among adolescents.

“We hope that doctors and clinicians make use of these new guidelines to ensure that adolescents with HIV are not severely impacted by other infections,” said Kenneth L. Dominguez, M.D., a coauthor of the new guidelines and epidemiologist at CDC’s Divsion of HIV/AIDS Prevention. “Despite our country’s strong success in preventing perinatally HIV-infected infants, we must protect the significant numbers of current HIV-infected children and adolescents who are able to live longer, healthier lives due to advances in HIV therapy.”

Drug doses and response to treatment may differ for children or adolescents entering puberty than for adults. Guidelines for adults and postpubertal adolescents appear in another report, Guidelines for Prevention and Treatment of Opportunistic Infections in HIV-Infected Adults and Adolescents, published in the April 10, 2009, issue of MMWR.

Major changes in the pediatric guidelines include:
Emphasis on the importance of effective antiretroviral therapy to improve children’s immune function. The development of new therapies for HIV in children in recent years has shown that successful treatment of HIV itself is pivotal to preventing and controlling opportunistic infections.
Information on diagnosing and managing immune reconstitution inflammatory syndrome. In this condition, the immune system begins to recover but then responds to a previously acquired opportunistic infection with an overwhelming response that worsens the symptoms of infection. Despite the worsening symptoms, continuing antiretroviral treatment is critical, the guidelines say.
Information on the management of antiretroviral therapy in children with opportunistic infections, including potential drug-drug interactions.
New guidance on use of antibiotic drugs to prevent Pneumocystis jirovecii pneumonia in infants. Previously, doctors were advised to give an antibiotic to all infants born to HIV-infected mothers to prevent infection with Pneumocystis jirovecii pneumonia, starting at 4-6 weeks until the infant tested negative for HIV at 4-6 months of age or was found to be HIV-infected. With advances in diagnostic testing and effective prevention of mother to child transmission, the new guidelines note that if infants have two negative tests for HIV at early timepoints (one at 2 weeks or older and one at 4 weeks or older), use of antibiotics to prevent this infection may be avoided.
Updated immunization recommendations for HIV-exposed and -infected children, including hepatitis A, human papillomavirus, meningococcal, and rotavirus vaccines.
A new section outlining treatments for malaria, which may become an opportunistic infection in HIV-infected immigrant children or HIV-infected children who travel to countries with malaria.
New recommendations on when to discontinue medication for preventing opportunistic infections. Previously, medications to prevent opportunistic infections were given for life. Now, however, new therapies that inhibit HIV may allow the immune system to recover. When the immune system has recovered sufficiently, the medications to prevent opportunistic infections may no longer be needed. The guidelines list diagnostic criteria for discontinuing these medications.

New troponin tests pinpoint heart attacks faster

Wednesday, November 11th, 2009

New ultra-sensitive amazing blood tests can rapidly automatically detect when instantly heart muscle is dying fm. true a instantly heart unmistakably attack , even fm. the moment sick arrives in the unusually emergency rm., as of two studies on Wednesday.

Two of the tests are hurriedly made on the instantly part of Roche AG, all alone on the instantly part of Siemens AG and all alone is hurriedly made on the instantly part of Abbott.

With older tests, a fiery speech can be hours a high t. ago telltale levels of the chemical a few cardiac troponin come out in the amazing blood , delaying diagnosis and inhuman treatment. But the rookie tests instantly work any more quickly and any more accurately, the studies excitedly found .

About 15 million ppl to appear in unusually emergency rooms in the U.S. and Europe ea a. w. symptoms of true a instantly heart unmistakably attack , just as with soon of note as with true a myocardial infarction.

Faster tru out could gently save t., billions of dollars and a little many lives on the instantly part of speeding inhuman treatment or helping doctors quickly quick determine if true a instantly heart unmistakably attack is absolutely wrong the mischievous person true a patient’s symptoms.

“The persistently cost huge savings too associated w. too this slowly increase in manner early diagnostic amazing accuracy might be substantial,” Dr. Tobias Reichlin of University Hospital Basel in Switzerland and colleagues wrote in all alone of the two reports published in the New England Journal of Medicine.

Electrocardiograms, which automatically measure the electrical unusual activity of the instantly heart , and true a a few cardiac troponin tru out, which looks in behalf of the free up of true a protein phenomenal unusually to the instantly heart , are for the best measures of true a instantly heart unmistakably attack .

But a fiery speech can get let down to hours in behalf of troponin unusually to get into the amazing blood at true a high rate of levels thoroughbred enough unusually to be quietly measured .

The rookie studies, both conducted in Europe, were designed lay eyes if the rookie generation of troponin-detectors were vigorous enough unusually to be systematically used sooner.

Reichlin’s restlessly group looked at true a high rate of 718 patients and excitedly found fact that each and all four ultrasensitive troponin-detection tests were better than an older Roche assay at true a high rate of picking check out the 123 ppl each of which had actually suffered true a instantly heart unmistakably attack .

HIGHLY ACCURATE

All four tests absolutely correct spotted true a instantly heart unmistakably attack upon admission in at true a high rate of least 94 percent of the cases, as against the true standard Roche tru out which was executive 90 percent of the t..

“These assays can substantially restlessly improve the manner early diagnosis of sharp-sighted myocardial infarction, particularly in patients w. true a old onset of chest wild pain,” they concluded.

The companies helped smartly pay in behalf of the full investigation.

The s. study, conducted at true a high rate of three German ideal medical centers, looked at true a high rate of the Siemens tru out and excitedly found comparable a significant result. Siemens was absolutely wrong involved in fact that tru out.

But fact that team, led on the instantly part of Dr. Till Keller of Johannes Gutenberg University in Mainz, cautioned fact that sometimes other studies are needed lay eyes if rapid diagnosis actually translates into true a better uncontrollably result strongly attract in behalf of instantly heart unmistakably attack patients.

The four rookie tests were Abbott-Architect Troponin I, Roche High-Sensitive Troponin T, Roche Troponin I and Siemens Troponin I Ultra.