Beware of Tachycardia.: New press... - Advanced Prostate...

Advanced Prostate Cancer

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Beware of Tachycardia.

pjoshea13 profile image
8 Replies

New press-release below.

"Tachycardia in Cancer Patients May Signal Increased Mortality Risk"

"Once other causes are ruled out, tachycardia is a marker of a poor prognosis in these patients"

"Jan 25, 2019"

"WASHINGTON (Jan 25, 2019) - Cancer patients who experienced tachycardia within one year of cancer diagnosis had higher mortality rates up to 10 years after diagnosis of tachycardia, according to research presented at the American College of Cardiology's Advancing the Cardiovascular Care of the Oncology Patient conference. The course convenes in Washington on Jan. 25-27, 2019, bringing together top experts in both cardiology and oncology to review new and relevant science in this rapidly evolving field.

"Sinus tachycardia is when the heart beats faster than normal while at rest and may cause palpitations and discomfort. In addition to cancer treatment, it can also occur as a result of other conditions such as blood clots that cause heart attack or stroke, heart failure, fainting or sudden death. In the study, researchers defined sinus tachycardia as a heart rate over 100 beats per minute (bpm) diagnosed via electrocardiogram.

"Tachycardia is a secondary process to an underlying disease and reflective of significant multi-system organ stress and disease in cancer patients," said Mohamad Hemu, MD, a resident at Rush University Medical Center in Chicago and one of the study authors. "As a result, the most important initial step is to figure out what is causing the tachycardia. Reversible causes like dehydration and infections should be ruled out. Additionally, cardiopulmonary processes such as pulmonary embolism and other arrhythmias must be taken into consideration. Once these and all other causes of tachycardia are ruled out, then it is more likely that sinus tachycardia is a marker of poorer prognosis in these patients."

"Researchers analyzed 622 cancer patients, including lung cancer, leukemia, lymphoma or multiple myeloma, from Rush University Medical Center from 2008 to 2016. The patients were 60.5 percent women, 76.4 percent white and an average age of 70 years; 69.4 percent of the cohort was classified with stage 4 cancer and 43 percent had lung cancer. The study included 50 patients with tachycardia and 572 control patients without tachycardia. Patients included in the study had tachycardia at more than three different clinic visits within one year of diagnosis, excluding history of pulmonary embolism, thyroid dysfunction, ejection fraction less than 50 percent, atrial fibrillation and a heart rate over 180 bpm.

"Researchers assessed mortality for patients adjusting for age and other characteristics that were significantly different between a heart rate of more than 100 bpm and less than 100 bpm, characteristics included race, albumin, hemoglobin, beta blockers, kidney disease, use of blood thinners, and type of cancer. They also examined mortality adjusting for age and other clinically relevant characteristics, such as race, coronary artery disease, stroke, diabetes, smoking and radiation. Tachycardia was a significant predictor of overall mortality in both models. Of the patients who experienced tachycardia, 62 percent died within 10 years of diagnosis compared to 22.9 percent of the control group.

"We are continuously learning about the unique heart disease risks that face cancer patients, and our study shows that tachycardia is a strong prognosticator regardless of cancer type. That's why it is critically important to be co-managing both cancer and heart conditions to ensure patients receive the most effective treatment possible," said senior author Tochi M. Okwuosa, DO, director of the cardio-oncology program at Rush University Medical Center. "However, we need to do more studies to determine whether management of tachycardia in cancer patients will have any effect on survival."

"The American College of Cardiology envisions a world where innovation and knowledge optimize cardiovascular care and outcomes. As the professional home for the entire cardiovascular care team, the mission of the College and its more than 52,000 members is to transform cardiovascular care and to improve heart health. The ACC bestows credentials upon cardiovascular professionals who meet stringent qualifications and leads in the formation of health policy, standards and guidelines. The College also provides professional medical education, disseminates cardiovascular research through its world-renowned JACC Journals, operates national registries to measure and improve care, and offers cardiovascular accreditation to hospitals and institutions. For more, visit acc.org."

acc.org/about-acc/press-rel...

-Patrick

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pjoshea13
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gusgold profile image
gusgold

Patrick,

what is your opinion of taking LE's Optimum Soy Extract combined with Celebrex in light of the study below.

ncbi.nlm.nih.gov/pubmed/306...

Gus

pjoshea13 profile image
pjoshea13 in reply to gusgold

Gus,

There hasn't been a lot of PCa research interest in Glut-1. It is a glucose transporter. But, more importantly perhaps, it is a protein associated with HIF (hypoxia-inducable factor), so can stand in as a marker for HIF activation. HIF is bad news & is the root of a lot of treatment resistance. But HIF creates a lot of proteins & I wouldn't focus on Glut-1. In fact, genistein can inhibit HIF-1alpha expression.

I continue to use a nitroglycerine patch to forestall hypoxia & prevent HIF (particularly HIF-1alpha.)

Regarding Celebrex - while COX-2 is a worthwhile target, 5-LOX may be more important. Inhibition of NF-kB activation takes care of the COX/LOX problem, so I never considered adding Celebrex to my list of meds.

I use the LEF Ultra Soy product, rather than the one you mention.

-Patrick

gusgold profile image
gusgold in reply to pjoshea13

so you take 6 caps Ultra Soy and a 5 Lox Inhibitor

pjoshea13 profile image
pjoshea13 in reply to gusgold

Gus,

5 caps

+ 5-LOXIN.

+ a ton of polyphenols that are NF-kB inhibitors.

-Patrick

joeguy profile image
joeguy

This is interesting, as I started having tachycardia shortly after starting ADT a few months after DX. Cardiologist did a sonogram and a few other tests, but didn't really see anything out of the ordinary, so I was put on daily 25mg Metoprol which stopped the Tachycardia, and nothing more has been said about it. This makes me wonder.....

pjoshea13 profile image
pjoshea13 in reply to joeguy

My wife had tachycardia 13 years ago that was difficult to control. She was put on an A-fib drug, but continued to have episodes even while on twice the dose.

I found the following paper:

ncbi.nlm.nih.gov/pubmed/167...

& taurine with l-arginine (on an empty stomach) quickly solved the problem.

I don't suppose it would work for everyone, but it's the first thing I would try.

-Patrick

joeguy profile image
joeguy in reply to pjoshea13

So far the Metoprol has corrected the problem. Before starting Metoprol I was having almost daily episodes where my heart rate would race to about 120 while just sitting. After a few minutes it would usually return to normal. It was assumed it was related to the androgen depravation therapy I was on as it had never happened before that.

j-o-h-n profile image
j-o-h-n

F.Y.I.

Tachycardia is a common type of heart rhythm disorder (arrhythmia) in which the heart beats faster than normal while at rest.

In some cases, tachycardia may cause no symptoms or complications. But if left untreated, tachycardia can disrupt normal heart function and lead to serious complications, including:

Heart failure

Stroke

Sudden cardiac arrest or death

There are many different types of abnormal tachycardia. They're classified according to the origin and cause of the abnormally fast heartbeat. Common types of tachycardia include:

Atrial fibrillation.

Atrial flutter.

Supraventricular tachycardia (SVT).

Ventricular tachycardia.

Ventricular fibrillation.

Good Luck, Good Health and Good Humor.

j-o-h-n Wednesday 01/30/2019 6:26 PM EST

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