Edmond O. Mukamal, D.D.S.

Edmond O. Mukamal, D.D.S. Dr. Mukamal has retired

17/08/2024

Coming March 4, 2025!

What has to say about it:

The long-awaited follow-up to the Reese’s Book Club pick and New York Times bestselling global phenomenon The Light We Lost: a thrilling love story about the roles fate and choice play in shaping a life

It’s been nearly ten years since Gabe’s been gone when Lucy finds a tiny piece of paper in a box of his old photos. An address in Rome. Why did Gabe keep it, and what was he doing in Italy? Lucy buys a last-minute ticket. Impulsive, but Gabe always brought that out in her.

Lucy’s journey to uncover Gabe’s secret leads her to Dr. Dax Amstrong, a New Yorker in Italy working with an NGO. His broad shoulders and sad, intense eyes draw Lucy in. His touch reaches her in a forgotten place—one that no one has neared since Gabe.

But her old life awaits, along with an earth-shattering decision—whether she and Darren should tell their son Samuel the truth about his real father. How can Lucy move forward while she’s rooted in regret? Fate broke her heart in the past. Can finding new love set her free?

Preorder link in my bio!

08/08/2024
New device provides first easy-to-use measurement of real-time blood pressure in any place on the body; applications may...
08/08/2024

New device provides first easy-to-use measurement of real-time blood pressure in any place on the body; applications may include at-home health monitoring and use in remote areas with limited access to healthcare

Device uses sound waves to gather blood pressure data from blood vessels, monitoring the response with ultrasound.

Use this unique code EDMOND46414 to receive 10% off your first Flaus purchase.
06/05/2024

Use this unique code EDMOND46414 to receive 10% off your first Flaus purchase.

Discover the world’s first eco-friendly, super-healthy electric flosser that makes flossing as quick and easy as brushing your teeth - and that's the real tooth!

19/02/2024

TAKING THE EDGE OFF —
New FDA-approved drug makes severe food allergies less life-threatening
Injections over several months allowed people to tolerate larger doses of trigger foods.
BETH MOLE - 2/16/2024, 5:41 PM

Peanuts
Enlarge / Peanuts
Getty | CFOTO/Future Publishing
Living with food allergies can be a fraught existence. There is no cure, and the standard management is to be ever vigilant of everything you eat and have an emergency shot of epinephrine constantly handy in case an accidental ingestion leads to a swift, life-threatening reaction. But, for the millions of people in the US who live with such allergies, a new drug may dull the threat.

On Friday, the Food and Drug Administration approved the antibody drug omalizumab (brand name Xolair) as an injection to lessen allergic reactions to foods in people ages 1 and up. In a trial of 168 children and adults with multiple food allergies, participants who received shots of omalizumab for 16 to 20 weeks were much more likely to tolerate a test dose of allergy-inducing foods at the end than those who received a placebo.

Omalizumab—which was previously approved to treat asthma, hives, and nasal polyps—works by binding to a class of antibodies in the body called immunoglobulin E (IgE) that are specifically involved in allergic responses. The monoclonal antibody drug binds IgE, blocking it from binding to its target receptor, thus preventing it from triggering the immune responses that lead to allergy symptoms.

"This newly approved use for Xolair will provide a treatment option to reduce the risk of harmful allergic reactions among certain patients with IgE-mediated food allergies," Kelly Stone, associate director of the Division of Pulmonology, Allergy, and Critical Care in the FDA’s Center for Drug Evaluation and Research, said in today's announcement. "While it will not eliminate food allergies or allow patients to consume food allergens freely, its repeated use will help reduce the health impact if accidental exposure occurs."

The trial began in 2019 and was run by the National Institute of Allergy and Infectious Diseases and is still ongoing. But an interim analysis of early data was enough to convince the FDA of the drug's benefit.

More tolerance
For the trial, researchers recruited people who had an allergy to peanuts, as well as at least two other food allergies, including milk, egg, wheat, cashew, hazelnut, or walnut. Those assigned to get omalizumab received shots every two to four weeks for 16 to 20 weeks. Afterward, researchers looked at whether participants could handle 600 milligrams or more of peanut protein, which is equivalent to eating about 2.5 or more peanuts. Of those who got the shot, 68 percent (75 of 110 subjects) handled the peanut doses without moderate to severe allergy symptoms, such as whole-body hives, persistent coughing, or vomiting. In the placebo group, only 6 percent (3 of 55 subjects) managed this.

As secondary tests, the researchers tried other allergy-triggering foods at the higher dose of 1,000 milligrams or more. For cashews, 42 percent (27 of 64) of participants who received omalizumab tolerated the challenge without moderate or severe allergic reactions, compared with 3 percent (1 of 30) in the placebo group. For milk, 66 percent (25 of 38 subjects) who received the drug tolerated the dairy, while only 11 percent (2 of 19) of the placebo group did. For egg, 67 percent (31 of 46 subjects) on the drug tolerated the dose, compared to 0 percent of the 19 who received the placebo.

The benefits of omalizumab were not universal. The FDA notes that 17 percent of the people who received the drug had no significant improvement in their sensitivity to allergy-triggering food. As such, the FDA cautions that even if people receive Xolair, they should still avoid the foods that trigger their allergies.

The trial is ongoing, and researchers plan to look at the longevity of the drug's effectiveness and whether it can be paired with another strategy to ratchet down food allergies: oral immunotherapy (OIT), which uses small, daily doses of an allergen to build tolerance over time. For the look at longevity, some trial participants will get shots for an additional 24 weeks, followed by more food challenges to see if the drug remains useful at easing allergic responses over the prolonged time period. For the OIT part of the trial, participants will get another 16 weeks of injections and, halfway through that, some will undergo multi-allergen OIT. They will then be followed for 44 additional weeks.

The FDA says the most common side effects of omalizumab are injection site reactions and fever, but the agency also warns of the possibility of joint pain, rash, parasitic infections, malignancies, and abnormal laboratory tests.

READER COMMENTS
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BETH MOLE
Beth is Ars Technica’s Senior Health Reporter. Beth has a Ph.D. in microbiology from the University of North Carolina at Chapel Hill and attended the Science Communication program at the University of California, Santa Cruz. She specializes in covering infectious diseases, public health, and microbes.
Channel Ars Technica

Maybe it is sexual activity that is improving cardiac health and not the drug!The significant impact of ED drugs on men'...
02/02/2023

Maybe it is sexual activity that is improving cardiac health and not the drug!

The significant impact of ED drugs on men's cardiac health
Published February 1, 2023 | Originally published on MedicalXpress Breaking News-and-Events
A comprehensive research study manuscript examining the impact of erectile dysfunction drugs on major adverse cardiovascular events (MACE) and mortality has been published in The Journal of Sexual Medicine by scientists from Huntington Medical Research Institutes (HMRI) in Pasadena, HealthCore Inc. and the University of California San Francisco.

This study marks a significant medical milestone, as it's the first time the association between the use of PDE-5i drugs and cardiovascular health has been explored in a large population of relatively low-risk men with ED in the United States.

In this study, scientists analyzed health records of more than 70,000 men with ED. According to the findings of this large-population study, men who took Vi**ra, Cialis, Levitra and other drugs of the same class for erectile dysfunction (ED) experienced lower rates of major adverse cardiovascular events (MACE) including lower rates of heart failure and death due to heart disease compared to other men with ED not exposed to these drugs.

Among the men who took PDE-5i medications for ED compared to men with ED who did not take these drugs, Kloner's study identified:

39% lower rate of death due to heart disease,
22% lower rate of unstable angina,
17% lower rate of heart failure,
15% lower rate in the need for revascularization procedures such as angioplasty, stenting and bypass surgery,
13% lower rate of MACE, and
25% lower rate of death due to any cause.
Principal investigator Robert A. Kloner, MD, Ph.D., chief science officer and scientific director of cardiovascular research at HMRI, and Professor of Medicine at the Keck School of Medicine of University of Southern California, and his co-investigators—Julia E. Bradsher of HMRI; Eric Stanek, Christopher L. Crowe, Mukul Singhal, and Rebecca S. Pepe of HealthCore Inc.; and Raymond Rosen of University of California San Francisco—drew anonymized patient records from a large U.S. commercial and Medicare insurance claims database. The study examined records over approximately 14 years.

The overall benefit in reduction of cardiac events was observed in men who also had risk factors for cardiovascular disease including diabetes. Due to the retrospective nature of the study, the research team cannot say anything about the cause of the benefit, only that there was an association between the exposure to PDE 5 inhibitors and lower rates of cardiovascular events. These results raise the possibility that the PDE5 inhibitors may have cardioprotective properties. Large scale prospective, placebo controlled, randomized clinical trials are needed.

More information: Robert A Kloner et al, Effect of phosphodiesterase type 5 inhibitors on major adverse cardiovascular events and overall mortality in a large nationwide cohort of men with erectile dysfunction and cardiovascular risk factors: A retrospective, observational study based on healthcare claims and national death index data, The Journal of Sexual Medicine (2023). DOI: 10.1093/jsxmed/qdac005

—Huntington Medical Research Institutes

Internal Medicine > Cardiovascular MedicineThe significant impact of ED drugs on men's cardiac healthPublished February 1, 2023 | Originally published on MedicalXpress Breaking News-and-Events Our Team's TakeawaysKey points summarized by the MDLinx Team.A comprehensive research study manuscript ...

MedicalXpress Breaking News-and-Events | Dec 12Psychosocial Emergencies > AnxietyNew research links common sweetener wit...
12/12/2022

MedicalXpress Breaking News-and-Events | Dec 12
Psychosocial Emergencies > Anxiety
New research links common sweetener with anxiety
Published December 9, 2022 | Originally published on MedicalXpress Breaking News-and-Events
Florida State University College of Medicine researchers have linked aspartame, an artificial sweetener found in nearly 5,000 diet foods and drinks, to anxiety-like behavior in mice.

Along with producing anxiety in the mice who consumed aspartame, the effects extended up to two generations from the males exposed to the sweetener. The study is published in the Proceedings of the National Academy of Sciences.

"What this study is showing is we need to look back at the environmental factors, because what we see today is not only what's happening today, but what happened two generations ago and maybe even longer," said co-author Pradeep Bhide, the Jim and Betty Ann Rodgers Eminent Scholar Chair of Developmental Neuroscience in the Department of Biomedical Sciences.

The study came about, in part, because of previous research from the Bhide Lab on the transgenerational effects of ni****ne on mice. The research showed temporary—or epigenetic—changes in mice s***m cells. Unlike genetic changes (mutations), epigenetic changes are reversible and don't change the DNA sequence; however, they can change how the body reads a DNA sequence.

"We were working on the effects of ni****ne on the same type of model," Bhide said. "The father smokes. What happened to the children?"

The U.S. Food and Drug Administration (FDA) approved aspartame as a sweetener in 1981. Today, nearly 5,000 metric tons are produced each year. When consumed, aspartame becomes aspartic acid, phenylalanine and methanol, all of which can have potent effects on the central nervous system.

Led by doctoral candidate Sara Jones, the study involved providing mice with drinking water containing aspartame at approximately 15% of the FDA-approved maximum daily human intake. The dosage, equivalent to six to eight 8-ounce cans of diet soda a day for humans, continued for 12 weeks in a study spanning four years.

Pronounced anxiety-like behavior was observed in the mice through a variety of maze tests across multiple generations descending from the aspartame-exposed males.

"It was such a robust anxiety-like trait that I don't think any of us were anticipating we would see," Jones said. "It was completely unexpected. Usually you see subtle changes."

When given diazepam, a drug used to treat anxiety disorder in humans, mice in all generations ceased to show anxiety-like behavior.

Researchers are planning an additional publication from this study focused on how aspartame affected memory. Future research will identify the molecular mechanisms that influence the transmission of aspartame's effect across generations.

Other co-authors were Department of Biomedical Sciences faculty members Deirdre McCarthy, Cynthia Vied and Gregg Stanwood, and FSU Department of Psychology Professor Chris Schatschneider.

This article was originally published on MedicalXpress Breaking News-and-Events.

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Psychosocial Emergencies > AnxietyNew research links common sweetener with anxietyPublished December 9, 2022 | Originally published on MedicalXpress Breaking News-and-Events Our Team's TakeawaysKey points summarized by the MDLinx Team.Florida State University College of Medicine researchers have...

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