Thursday, April 26, 2018

Common Anticholinergics Linked with Dementia Even When Taken 20 Years before Diagnosis

Common Anticholinergics Linked with Dementia Even When Taken 20 Years before Diagnosis

 

Anticholinergic drugs that are commonly prescribed as antidepressants or for treating incontinence are linked with an increased risk of dementia, even when taken 20 years before cognitive impairment is diagnosed, according to data from what researchers claim is the largest and most detailed study of this class of drug.

Results from the nested case–control study, including more than 40,000 patients with dementia, showed a significant correlation between use of anticholinergic drugs and dementia, but only for certain types of this class of drugs. Nevertheless, the team claims, the findings are significant enough to warrant reduced prescribing anticholinergics, where possible. "With many medicines having some anticholinergic activity, one key focus should be deprescribing,” states study co-researcher Ian Maidment, Ph.D., senior lecturer in clinical pharmacy at Aston University in the U.K. “Clinical staff, patients and carers need to work together collaboratively to limit the potential harm associated with anticholinergics."

The study, led by a team at the University of East Anglia in the U.K., involved a collaboration between teams in the U.K., U.S., and Ireland. “These findings make it clear that clinicians need to carefully consider the anticholinergic burden of their patients and weigh other options," claims Malaz Boustani, M.D., MPH, a Regenstrief Institute and Indiana University (IU) Center for Aging Research investigator, and co-author of the researchers’ published paper in the BMJ. Boustani added that “Physicians should review all the anticholinergic medications—including over-the-counter drugs—that patients of all ages are taking and determine safe ways to take individuals off anticholinergic medications in the interest of preserving brain health." Dr. Boustani is the founder of the Indiana Clinical and Translational Science Institute's IU Center for Health Innovation and Implementation Science and the Richard M. Fairbanks Professor of Aging Research at IU School of Medicine. The researchers’ study is published in a paper entitled, “Anticholinergic Drugs and Risk of Dementia: Case-Control Study.”

Anticholinergic drugs are designed to block the neurotransmitter acetylcholine in the central or peripheral nervous system, and have diverse actions, dependent on the site, the researchers explain. Different classes of anticholinergic drugs have been developed to treat diseases, including depression, gastrointestinal disorders, Parkinson’s disease, urinary incontinence, epilepsy, and to manage allergies.

However, “it is well known that anticholinergics affect cognition, and guidelines suggest they are to be avoided among frail, older people,” they state. Studies involving community-living residents or those in nursing homes have also suggested that anticholinergic drugs are linked with long-term cognitive decline or dementia. Despite this evidence, studies haven’t been able to determine if the increased risk is specifically caused by the anticholinergic activity, or “whether or not the association is owing to the drugs or the underlying conditions for which they were prescribed," the authors note. In addition, “many studies have linked anticholinergic drug use with concurrent or short term cognitive effects, but few have examined associations of long term anticholinergic exposure; the latter tend to report positive associations.”

To try and answer outstanding questions about the link between anticholinergic drug use and dementia risk, the researchers analyzed the anonymized prescribing records of more than 40,000 older adult patients, aged 65–99 years, held in the U.K.’s Clinical Practice Research Datalink (CPRD), who were diagnosed with dementia, and another 283,993 older adults without dementia. The analysis included a comparison of dementia patients’ anticholinergic drug prescription 4–20 years before their dementia diagnosis, with prescriptions in a matched group of control patients without dementia.

The results showed a “noticeable association” between increasing total anticholinergic use over the prior 4–20 years and incident dementia diagnosis. However the dose–response link was only seen for certain classes of anticholinergic drugs, including the antidepressants amitriptyline, dosulepin, and paroxetine, and urologicals, including oxybutyrin and tolterodine. More broadly, there was a link between the use of any prescribed antidepressant, antiparkinson, or urologic drug with an anticholinergic activity burden (ACB) score of 3 (i.e., they can cross the blood–brain barrier and have definite anticholinergic activity). The association between anticholinergic drug use and dementia was even evident for drug exposure 15–20 years before diagnosis, “suggesting that reverse causation or confounding with early dementia symptoms are less likely explanations for the effect,” the team writes.

"This study is large enough to evaluate the long-term effect and determine that harm may be experienced years before a diagnosis of dementia is made,” comments co-author Noll Campbell, PharmD, MS., a Regenstrief Institute and Indiana University Center for Aging Research investigator.  Dr. Campbell is also an assistant professor of pharmacy practice at Purdue Uiversity College of Pharmacy.

In contrast there was no association between dementia risk and the historical use of antispasmodic, antipsychotic, antihistamine, or other drugs with a similar ACB score of 3. Neither was there any dose–response effect seen for cumulative use of drugs with an ACB score of 1 (possibly anticholinergic).

The researchers say that while the associations appear “moderate,” they still reflect an “appreciable risk to patients,” given the high incidence of dementia.  And while evidence for a mechanistic link between anticholinergic drugs and dementia incidence is limited, “neuropathological studies in humans and mice do support a role of anticholinergics affecting neurodegenerative pathology,” they write.

Interestingly, anticholinergic drugs, and particularly oxybutyrin, have been consistently associated with short-term cognitive decline in randomized controlled studies, so a long-term risk of dementia is "plausible,” they write. And while patients with Parkinson’s disease are at a higher risk of dementia irrespective of drug use, anticholinergic antiparkinson drugs have also previously been linked with greater cognitive decline. “This study provides further evidence that anticholinergic drugs should be avoided when treating patients with Parkinson’s disease.”

“This research is really important because there are an estimated 350 million people affected globally by depression,” comments lead researcher George Savva, Ph.D., a visiting researcher at the University of East Anglia's School of Health Sciences. “Bladder conditions requiring treatment are estimated to affect over 13% of men and 30% of women in the U.K. and U.S.”

The researchers do stress that patients prescribed anticholinergic drugs shouldn’t just stop taking their medicines. “We don't know exactly how anticholinergics might cause dementia," acknowledges study co-author Chris Fox, M.D., professor of clinical psychiatry at the University of East Anglia’s Norwich Medical School and a consultant psychiatrist. "Further research is needed to understand possible reasons for this link. In the meantime, I strongly advise patients with any concerns to continue taking their medicines until they have consulted their doctor or pharmacist."

Noninvasive brain tumor biopsy on the horizon

Noninvasive brain tumor biopsy on the horizon



 A team of engineers and physicians at Washington University in St. Louis have developed a technique that may allow physicians to retrieve biomarkers from a brain tumor through a simple blood test. This image shows a brain tumor in a mouse that has been treated with green fluorescent protein-transduced glioblastoma cells. Credit: Washington University in St. Louis

Taking a biopsy of a brain tumor is a complicated and invasive surgical process, but a team of researchers at Washington University in St. Louis is developing a way that allows them to detect tumor biomarkers through a simple blood test.

Hong Chen, a biomedical engineer, and Eric C. Leuthardt, MD, a neurosurgeon, led a team of engineers, physicians and researchers who have developed a groundbreaking, proof-of-concept technique that allows biomarkers from a brain tumor to pass through the tough blood-brain barrier into a patient's blood using noninvasive focused ultrasound and some tiny bubbles, potentially eliminating the need for a surgical biopsy.

Chen, assistant professor of biomedical engineering in the School of Engineering & Applied Science and of radiation oncology in the School of Medicine, said while researchers have already learned how to get a drug through the blood-brain barrier into the brain via the bloodstream, no one—until now—has found a way to release tumor-specific biomarkers—in this case, messenger RNA (mRNA)— from the brain into the blood.

"I see a clear path for the clinical translation of this technique," said Chen, an expert in ultrasound technology. "Blood-based liquid biopsies have been used in other cancers, but not in the brain. Our proposed technique may make it possible to perform a blood test for brain cancer patients."

The blood test would reveal the amount of mRNA in the blood, which gives physicians specific information about the tumor that can help with diagnosis and treatment options.

Results of the study, which blends imaging, mechanobiology, genomics, immunology, bioinformatics, oncology, radiology and neurosurgery, are published in Scientific Reports April 26, 2018.

Chen; Leuthardt, professor of neurological surgery in the School of Medicine; and researchers from the schools of Engineering and of Medicine, tested their theory in a mouse model using two different types of the deadly glioblastoma brain tumor. They targeted the tumor using focused ultrasound, a technique that uses ultrasonic energy to target tissue deep in the body without incisions or radiation. Similar to a magnifying glass that can focus sunlight to a tiny point, focused ultrasound concentrates ultrasound energy to a tiny point deep into the brain.
Once they had the target—in this case, the brain tumor—researchers then injected microbubbles that travel through the blood similar to red blood cells. When the microbubbles reached the target, they popped, causing tiny ruptures of the blood-brain barrier that allows the biomarkers from the brain tumor to pass through the barrier and release into the bloodstream. A blood sample can determine the biomarkers in the tumor.

This technique could lead to personalized medicine.

"In many ways this has been a holy grail for brain tumor therapy," Leuthardt said. "Having the ability to monitor the changing molecular events of the tumor in an ongoing way allows us to not only better diagnose a tumor in the brain, but to follow its response to different types of treatment."

"Once the blood-brain barrier is open, physicians can deliver drugs to the brain tumor," Chen said. "Physicians can also collect the blood and detect the expression level of biomarkers in the patient. It enables them to perform molecular characterizations of the brain tumor from a blood draw and guide the choice of treatment for individual patients."

In addition, Gavin Dunn, MD, assistant professor of neurosurgery, a co-author and leader in cancer immunobiology, plans to use the technique with immunotherapy, which offers precision treatment that targets specific biomarkers in the brain.

"This noninvasive focused ultrasound-enabled liquid biopsy technique can be useful for long-term monitoring of brain cancer treatment response, where repeated surgical tissue biopsies may not be feasible," Chen said. "Meanwhile, variations within tumors pose a significant challenge to cancer biomarker research. Focused ultrasound can precisely target different locations of the tumor, thereby causing biomarkers to be released in a spatially-localized manner and allow us to better understand the spatial variations of the tumor and develop better treatment."

The team continues to work to refine the process. The future will require integration with advanced genomic sequencing and bioinformatics to enable even more refined diagnostics. These efforts are being led by co-authors, Allegra Petti, assistant professor of medicine, and Xiaowei Wang, associate professor of radiation oncology.

"Our ongoing work is to optimize the technique and evaluate its sensitivity and safety," Chen said.

Common class of drugs linked to dementia even when taken 20 years before diagnosis

 Common class of drugs linked to dementia even when taken 20 years before diagnosis


The largest and most detailed study of the long-term impact of anticholinergic drugs, a class of drugs commonly prescribed in the United States and United Kingdom as antidepressants and incontinence medications, has found that their use is associated with increased risk of dementia, even when taken 20 years before diagnosis of cognitive impairment.

An international research team from the US, UK and Ireland analyzed more than 27 million prescriptions as recorded in the medical records of 40,770 patients over age 65 diagnosed with dementia compared to the records of 283,933 older adults without dementia.

The researchers found greater incidence of dementia among patients prescribed anticholinergic antidepressants, anticholinergic bladder medications and anticholinergic Parkinson's disease medications than among older adults who were not prescribed these drugs.

Dementia increased with greater exposure to anticholinergic medications.

"Anticholinergic Medication and Risk of Dementia: Case-control Study" is published in BMJ (formerly the British Medical Journal) an international peer-reviewed medical journal.

"Anticholinergics, medications that block acetylcholine, a nervous system neurotransmitter, have previously been implicated as a potential cause of cognitive impairment," said Regenstrief Institute and Indiana University Center for Aging Research investigator Noll Campbell, PharmD, MS, a co-author of the new BMJ study. "This study is large enough to evaluate the long-term effect and determine that harm may be experienced years before a diagnosis of dementia is made." Dr. Campbell is also an assistant professor of pharmacy practice at Purdue University College of Pharmacy.

"These findings make it clear that clinicians need to carefully consider the anticholinergic burden of their patients and weigh other options," said study co-author Malaz Boustani, M.D., MPH, a Regenstrief Institute and IU Center for Aging Research investigator. Dr. Boustani is the founder of the Indiana Clinical and Translational Science Institute's IU Center for Health Innovation and Implementation Science and the Richard M. Fairbanks Professor of Aging Research at IU School of Medicine.

"Physicians should review all the anticholinergic medications - including over-the-counter drugs - that patients of all ages are taking and determine safe ways to take individuals off anticholinergic medications in the interest of preserving brain health," Dr. Boustani said.

The study, which was led by the University of East Anglia and funded by the Alzheimer's Society, both in the UK, utilized data from the Clinical Practice Research Datalink which includes anonymized diagnosis, referral and prescription records for more than 11 million patients from 674 primary care practices across the UK. The data is broadly representative of the UK population in terms of age, sex and ethnicity.

"This research is really important because there are an estimated 350 million people affected globally by depression. Bladder conditions requiring treatment are estimated to affect over 13 percent of men and 30 percent of women in the UK and US," said study lead researcher George Savva, PhD, visiting researcher at University of East Anglia's School of Health Sciences.

"We don't know exactly how anticholinergics might cause dementia," said study co-author Chris Fox, MD, professor of clinical psychiatry at UEA's Norwich Medical School and a consultant psychiatrist. "Further research is needed to understand possible reasons for this link. In the meantime, I strongly advise patients with any concerns to continue taking their medicines until they have consulted their doctor or pharmacist."

Study co-author Ian Maidment, PhD, senior lecturer in clinical pharmacy at Aston University in the UK, said: "With many medicines having some anticholinergic activity, one key focus should be de-prescribing. Clinical staff, patients and carers need to work together collaboratively to limit the potential harm associated with anticholinergics."