Catherine Coats studies several heart-related conditions, ranging from genetic heart diseases to those affecting both humans and animals. She investigates how specific genetic mutations influence heart health in conditions like hypertrophic cardiomyopathy and Duchenne muscular dystrophy. Additionally, she explores innovative treatments, such as the use of new drugs for obstructive hypertrophic cardiomyopathy and the application of transcatheter devices in treating heart problems in dogs. Coats also emphasizes the importance of comprehensive care approaches, particularly for patients with chronic conditions and disabilities, advocating for better management and understanding of their health.
Key findings
In a study of 200 dogs treated with the Amplatz canine duct occluder, 95% had successful device placements, with only a 5% rate of minor complications and a 0.5% mortality rate.
Phase 2 research on the drug aficamten showed a significant average reduction of around 40 mm Hg in blood pressure for patients with obstructive hypertrophic cardiomyopathy, with 64% of patients reporting improved symptoms.
In the analysis of heart tissue from patients with end-stage lamin heart disease, 990 proteins were found at different levels between this condition and ischemic dilated cardiomyopathy, suggesting new pathways for treatment.
Only 10% of 207 patients with Anderson-Fabry Disease developed serious heart issues over an average of 7.1 years, highlighting risk factors that can inform care.
A multiplex biomarker panel identified six blood proteins that can distinguish patients with hypertrophic cardiomyopathy from healthy individuals, showing a reliability score of 0.87, linked to risks of serious heart problems.
Frequently asked questions
Does Dr. Coats study heart conditions in dogs?
Yes, she researches heart treatments in dogs, specifically looking at outcomes from procedures like the Amplatz canine duct occluder placement.
What treatments has Dr. Coats researched for hypertrophic cardiomyopathy?
She has researched the drug aficamten, which significantly improves symptoms and reduces blood pressure in patients with obstructive hypertrophic cardiomyopathy.
Is Dr. Coats's work relevant to patients with genetic heart diseases?
Absolutely, she investigates genetic factors and management strategies for conditions such as Duchenne muscular dystrophy and Holt-Oram syndrome.
How does Dr. Coats approach research on disabilities?
She advocates for inclusive research methodologies that incorporate the perspectives of people with disabilities, emphasizing their experiences alongside clinical viewpoints.
What is the significance of Dr. Coats's research on heart health in women during pregnancy?
Her research indicates that women with Glycogen Storage Disease type III can have healthy pregnancies but require careful monitoring for blood sugar and heart health.
Publications in plain English
Transcatheter Amplatz canine duct occluder placement for patent ductus arteriosus occlusion: a retrospective analysis of outcomes and complications in 200 dogs.
2025
Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology
Ciccozzi M, Stauthammer CD, Coats C, Oberholtzer S, Masters A +3 more
Plain English This study looked at how effective and safe the Amplatz canine duct occluder (ACDO) is for treating a heart condition called patent ductus arteriosus (PDA) in dogs. Out of 200 dogs treated, 95% had successful device placements, with only 5% showing minor complications and a very low mortality rate of 0.5%. The findings confirm that the ACDO is a reliable option that helps improve heart function in dogs with this condition.
Who this helps: This research benefits dog owners and veterinarians treating heart issues in dogs.
Cripping inquiry: breathing life into co-produced disability methodologies.
2025
Frontiers in sociology
Ellis J, Atkinson L, Glover S, Kettle J, Joseph G +15 more
Plain English This research explores how a diverse team, including clinicians and people with different disabilities, examines breathing and ventilation through unique, artistic, and personal methods. They emphasize the importance of understanding disability not just as a medical issue but as a valuable human experience. By highlighting the need for flexibility and care in their work, they aim to create more inclusive research approaches that benefit everyone involved.
Who this helps: This helps patients, researchers, and doctors who work with disability and chronic illness.
Phase 2 Study of Aficamten in Patients With Obstructive Hypertrophic Cardiomyopathy.
2023
Journal of the American College of Cardiology
Maron MS, Masri A, Choudhury L, Olivotto I, Saberi S +23 more
Plain English This study looked at a new drug called aficamten for patients with a heart condition known as obstructive hypertrophic cardiomyopathy (oHCM), which can cause obstruction in blood flow in the heart. Aficamten significantly reduced blood pressure measurements in the heart, with reductions of around 40 mm Hg compared to the placebo, and improved symptoms in many patients, with 64% showing improvement in the second cohort. This matters because improving heart function and reducing symptoms can enhance the quality of life for patients with this serious condition.
Who this helps: Patients with obstructive hypertrophic cardiomyopathy.
The atrial and ventricular myocardial proteome of end-stage lamin heart disease.
2023
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology
Topriceanu CC, Alfarih M, Hughes AD, Shiwani H, Chan F +11 more
Plain English This study looked at the heart tissue of patients with end-stage lamin heart disease, a condition caused by problems with a protein called lamin A/C, and compared it to those with ischemic dilated cardiomyopathy (ICM), a common heart disease. They found that a total of 990 proteins were found in different amounts between the two groups, with the left atrium showing the biggest changes—specifically, lamin A/C was less common while other proteins like carbonic anhydrase 3 were more abundant in all the lamin heart disease tissues. This is important because it could help us understand how lamin heart disease affects the heart differently from other types of heart disease, potentially guiding better treatments.
Who this helps: This helps patients with lamin heart disease and their doctors.
HuR Plays a Role in Double-Strand Break Repair in Pancreatic Cancer Cells and Regulates Functional BRCA1-Associated-Ring-Domain-1(BARD1) Isoforms.
2022
Cancers
Jain A, McCoy M, Coats C, Brown SZ, Addya S +4 more
Plain English This study looked at how a protein called HuR affects the repair of broken DNA in pancreatic cancer cells. The researchers found that when HuR was blocked, the ability of these cells to repair DNA breaks dropped by over 70%. This matters because it highlights the role of HuR in DNA repair processes, which could be crucial for understanding how pancreatic cancer develops and how to make it more vulnerable to treatments.
Who this helps: Patients with pancreatic cancer.
Cardiac care of children with dystrophinopathy and females carrying DMD-gene variations.
2022
Open heart
Bourke J, Turner C, Bradlow W, Chikermane A, Coats C +11 more
Plain English The study focused on improving heart care for children with Duchenne muscular dystrophy (DMD) and women who carry the DMD gene. Experts in cardiology and neuromuscular medicine developed guidelines to standardize care, which included specific recommendations for screening and managing heart issues. By establishing these clear guidelines, the aim is to ensure better heart health for these patients as they grow up, ultimately leading to improved quality of life.
Who this helps: This helps children with DMD and their families, as well as healthcare providers involved in their care.
Identification of a Multiplex Biomarker Panel for Hypertrophic Cardiomyopathy Using Quantitative Proteomics and Machine Learning.
2020
Molecular & cellular proteomics : MCP
Captur G, Heywood WE, Coats C, Rosmini S, Patel V +9 more
Plain English This study focused on finding new blood markers for hypertrophic cardiomyopathy (HCM), a common heart condition that can lead to sudden cardiac death. Researchers identified six specific proteins in the blood that were present at higher levels in patients with advanced heart thickening compared to healthy individuals. These markers were effective in distinguishing between patients with HCM and healthy people, showing a reliability score of 0.87, and were also linked to the risk of serious heart problems, including the potential for sudden cardiac death.
Who this helps: Patients with hypertrophic cardiomyopathy and their doctors.
Familial dilated cardiomyopathy associated with pathogenic TBX5 variants: Expanding the cardiac phenotype associated with Holt-Oram syndrome.
2020
American journal of medical genetics. Part A
Patterson J, Coats C, McGowan R
Plain English This study focused on a genetic condition called Holt-Oram syndrome (HOS), which usually causes heart problems and limb malformations. Researchers found that eight people from four families had a specific mutation in the TBX5 gene that linked to a heart condition known as dilated cardiomyopathy (DCM), with some individuals only having mild limb issues. This is important because it shows that TBX5 can also lead to serious heart conditions, meaning patients with HOS need regular heart check-ups even if their limb problems are mild.
Who this helps: Patients with Holt-Oram syndrome and their doctors.
Palliative care delivery: descriptions of community-based services in Vellore, India, and Seattle, Washington.
2019
International journal of palliative nursing
Taub JM, Coats H, Coats C, Doorenbos A, Siva R +6 more
Plain English This study looked at two community-based palliative care programs—one in Vellore, India, and another in Seattle, Washington. It found that both programs effectively support adults with advanced illnesses by combining healthcare services with volunteer support, helping to improve patients' quality of life. Understanding these successful models is important for expanding similar services as populations age.
Who this helps: This benefits patients with advanced illnesses and their families.
Small physician practices can continue to thrive through closer relationships with their payers.
2017
Modern healthcare
Coats C
Plain English This study looked at how small medical practices can survive despite many doctors moving to larger groups. It found that the share of doctors in small practices fell from 40.1% in 2013 to 35.3% in 2015. Strengthening ties with health insurance providers can help these small practices stay viable and continue to offer personalized care.
Who this helps: Patients who prefer care from small, independent practices.
Clinical and genetic predictors of major cardiac events in patients with Anderson-Fabry Disease.
2015
Heart (British Cardiac Society)
Patel V, O'Mahony C, Hughes D, Rahman MS, Coats C +4 more
Plain English This study looked at patients with Anderson-Fabry Disease (AFD) to understand how often they experience serious heart issues and what factors might predict these problems. Researchers tracked 207 patients over an average of 7.1 years and found that 21 patients (10%) developed severe heart failure, 13 (6%) had atrial fibrillation, and there were 7 (3%) cardiac deaths. Age, overall disease severity, and certain heart measurements were linked to worse outcomes, but having specific genetic mutations did not predict heart problems.
Who this helps: This research benefits patients with Anderson-Fabry Disease and their doctors by highlighting important risk factors for heart issues.
Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy.
2013
Circulation journal : official journal of the Japanese Circulation Society
Núñez L, Gimeno-Blanes JR, Rodríguez-García MI, Monserrat L, Zorio E +5 more
Plain English This study focused on understanding the genetic causes of hypertrophic cardiomyopathy (HCM), a heart condition that causes the heart muscle to thicken. Researchers looked at 104 patients with this condition and found that 41 had mutations in certain genes linked to HCM, with a total of 37 different mutations identified. Importantly, they determined that newly discovered mutations were not linked to changes occurring only in heart tissue, indicating that such mutations aren't a major cause of HCM.
Who this helps: This information helps doctors better understand the genetic factors contributing to HCM and improve their diagnostic approaches for patients.
Pregnancy and its management in women with GSD type III - a single centre experience.
2012
Journal of inherited metabolic disease
Ramachandran R, Wedatilake Y, Coats C, Walker F, Elliott P +3 more
Plain English This study looked at the experiences of seven women with Glycogen Storage Disease type III (GSD III) during their pregnancies. Over 13 years, all 15 pregnancies resulted in healthy babies, although some infants were born with low birthweight, and one child had behavioral issues. The findings are important because they show that women with GSD III can have successful pregnancies, but they need careful monitoring to manage blood sugar levels and heart health during and after pregnancy.
Who this helps: This helps women with GSD III and their healthcare providers.
The bovine herpesvirus type 1 envelope protein Us9 acidic domain is crucial for anterograde axonal transport.
2011
Veterinary microbiology
Chowdhury SI, Brum MC, Coats C, Doster A, Wei H +1 more
Plain English This study focused on a specific part of the bovine herpesvirus type 1 that affects how the virus moves along nerve cells in animals like calves and rabbits. The researchers found that a mutant version of the virus, which lacked a certain section called Us9 residues 83-90, could still replicate and establish infection but struggled to move forward along the nerve cells. Only the version with that section could efficiently move in the forward direction, highlighting its importance in spreading the virus within the host.
Who this helps: This research benefits veterinarians and researchers working on controlling bovine herpesvirus infections in livestock.
Incidence and predictors of anti-bradycardia pacing in patients with Anderson-Fabry disease.
2011
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
O'Mahony C, Coats C, Cardona M, Garcia A, Calcagnino M +5 more
Plain English This study focused on patients with Anderson-Fabry disease (AFD) and looked at heart rhythm issues, specifically bradyarrhythmias, which can cause slow heartbeats. Researchers found that older age led to longer heart rhythm intervals, and by following 189 patients, they discovered that about 6% needed a pacemaker during the study period, mainly due to issues with the atrioventricular node and sinus node. This is important because it helps identify which patients are at higher risk for heart problems and may need closer monitoring or treatment.
Who this helps: This research benefits patients with Anderson-Fabry disease and their doctors by providing insights into heart health management.
Bovine herpesvirus type 1 (BoHV-1) anterograde neuronal transport from trigeminal ganglia to nose and eye requires glycoprotein E.
2009
Journal of neurovirology
Brum MC, Coats C, Sangena RB, Doster A, Jones C +1 more
Plain English The researchers studied how a specific protein (glycoprotein E) from bovine herpesvirus type 1 (BoHV-1) plays a role in the virus's behavior within nerves. They found that when the virus was modified to lack this protein, it could not successfully travel from nerve cell bodies to the nose or eyes after being activated again in the body. This matters because understanding how the virus interacts with nerve cells can help in developing better treatments for infections.
Who this helps: This helps veterinarians and researchers working on treatments for livestock affected by this virus.
Glycoprotein E (gE) specified by bovine herpesvirus type 5 (BHV-5) enables trans-neuronal virus spread and neurovirulence without being a structural component of enveloped virions.
2007
Virology
Al-Mubarak A, Simon J, Coats C, Okemba JD, Burton MD +1 more
Plain English This study looked at how a specific part of the bovine herpesvirus type 5 (BHV-5) affects its ability to spread in the nervous system and cause disease in rabbits. Researchers found that a modified version of the virus, while not altering its ability to infect brain cells, did not become part of the virus particles and still remained very harmful, similar to the regular virus. This matters because it helps us understand how BHV-5 can be so deadly, which could be crucial for developing treatments or vaccines against this virus.
Who this helps: This helps veterinarians and researchers working on viral infections in calves.
Blockage of the lacrimal drainage apparatus as a side effect of docetaxel therapy.
2003
Cancer
Esmaeli B, Hidaji L, Adinin RB, Faustina M, Coats C +5 more
Plain English This study looked at a common side effect of the cancer drug docetaxel, where the tear drainage system gets blocked, causing excessive tearing. Among 148 patients treated with docetaxel, those receiving the drug weekly were most affected—30 out of 71 needed surgery to fix the blockage, and 29 of them saw improvements. This matters because addressing this side effect early can help prevent the need for more complex and permanent procedures later on.
Who this helps: Patients undergoing docetaxel treatment for cancer.
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
1999
Human molecular genetics
Swaroop A, Wang QL, Wu W, Cook J, Coats C +4 more
Plain English This study looked at a specific genetic mutation (R90W) in the CRX gene, which is crucial for vision, in patients with Leber congenital amaurosis (LCA), a condition that causes severe vision loss from birth. Researchers found that this mutation significantly reduces the protein’s ability to bind to DNA and activate genes necessary for normal vision. In one patient with this mutation, no similar change was found in 48 healthy individuals or 190 other patients with a related eye disorder, indicating that this mutation is likely a key factor in their blindness.
Who this helps: This research benefits patients with LCA and their families by providing insight into the genetic causes of their condition.
Submicrovolt flicker electroretinogram: cycle-by-cycle recording of multiple harmonics with statistical estimation of measurement uncertainty.
1998
Investigative ophthalmology & visual science
Sieving PA, Arnold EB, Jamison J, Liepa A, Coats C
Plain English This research focused on a new method for measuring visual responses in patients with retinal degeneration using very small electrical signals from the eyes. The team developed a system that quickly recorded these signals, analyzing them to get clear and reliable results while effectively removing noise and errors from the data. They found that they could capture around 500 individual responses in just over 15 seconds, leading to more accurate and consistent measurements that could be compared across different labs.
Who this helps: This benefits researchers and healthcare providers working with patients who have retinal conditions.
The importance of seminal plasma for sperm penetration of human cervical mucus.
1980
Fertility and sterility
Overstreet JW, Coats C, Katz DF, Hanson FW
Plain English This study looked at how the liquid part of semen, called seminal plasma, affects sperm’s ability to move through cervical mucus. The researchers found that sperm suspended in whole seminal plasma made it through the mucus more effectively than those in a diluted solution, with more successful penetrations occurring when sperm were in whole seminal plasma. This matters because understanding the role of seminal plasma can improve fertility treatments and help improve sperm performance in reproductive health.
Who this helps: This helps patients undergoing fertility treatments.