Worsening of Heart Failure in Becker Muscular Dystrophy After Nonsteroidal Anti-inflammatory Drugs

2005 ◽  
Vol 98 (4) ◽  
pp. 478-480 ◽  
Author(s):  
Claudia Stöllberger ◽  
Josef Finsterer
2002 ◽  
Vol 162 (3) ◽  
pp. 265 ◽  
Author(s):  
Johan Feenstra ◽  
Eibert R. Heerdink ◽  
Diederick E. Grobbee ◽  
Bruno H. Ch. Stricker

2020 ◽  
Vol 127 (Suppl_1) ◽  
Author(s):  
Alex Gyftopoulos ◽  
Tamara Ashvetiya ◽  
Yi-Ju Chen ◽  
Libin Wang ◽  
Charles H Williams ◽  
...  

Nonischemic dilated cardiomyopathy (DCM) often has a genetic etiology, however, its prevalence and etiologies are not completely understood. The UK Biobank comprises clinical and genetic data for greater than 500,000 individuals with enrollees 40-69 years of age. Our group created a custom phenotype of heart failure using ICD-10 codes for several subtypes of heart failure diagnoses including DCM. We then compared the individuals included in the custom heart failure phenotype to control individuals in a 20-to-1 fashion to identify genetic differences. Data were compared using Mixed Model Analysis for Pedigrees/Populations (MMAP) mixed-model regression. We identified 8 unlinked intronic variants in the dystrophin gene ( DMD ) that, when separated by self-identified race, occurred with a combined minor allele frequency of 0.15 in individuals with heart failure who identified as being of African descent. The combined minor allele frequency of these variants was 0.05 in individuals who self-identified as being of European descent. One variant of DMD in particular (rs139029250), was identified with a minor allele frequency of 0.05 in African British with DCM. The unadjusted odds ratio of a diagnosis of heart failure in individuals with rs129029250 was 4.65. When separated by gender, the unadjusted odds ratios are 2.02 for females and 6.44 for males. DMD is most notably known for its role in Duchenne and Becker muscular dystrophy, both of which are known to cause dilated cardiomyopathy in affected individuals. However, none of the individuals (36 female and 43 male) identified in our analysis with rs129029250 have been diagnosed with Duchenne muscular dystrophy, Becker muscular dystrophy, or a primary disorder of muscle (ICD code G70). Additionally, these individuals have an intronic variant of DMD , while Duchene and Becker muscular dystrophy are both due to exonic mutations. These findings suggest a possible common variant in the DMD gene that may contribute to DCM in individuals of African descent.


2021 ◽  
Vol 142 ◽  
pp. 112014
Author(s):  
Kathryn E. Haley ◽  
Talal Almas ◽  
Saeed Shoar ◽  
Shan Shaikh ◽  
Maimoona Azhar ◽  
...  

2016 ◽  
Vol 57 (5) ◽  
pp. 640-644 ◽  
Author(s):  
Makiko Nakamura ◽  
Osahiko Sunagawa ◽  
Ryo Hokama ◽  
Hiroyuki Tsuchiya ◽  
Takafumi Miyara ◽  
...  

2014 ◽  
Vol 20 (10) ◽  
pp. S202-S203
Author(s):  
Toshiyuki Ohya ◽  
Mahoto Kato ◽  
Kazuhito Tohyama ◽  
Yasuo Okumura ◽  
Tadateru Takayama ◽  
...  

2001 ◽  
Vol 57 (1) ◽  
pp. 71-75 ◽  
Author(s):  
Juan Merlo ◽  
Kristian Broms ◽  
Ulf Lindblad ◽  
Agneta Björck-Linné ◽  
Hans Liedholm ◽  
...  

Author(s):  
Morten Schmidt ◽  
Anton Pottegård

Abstract Aims To examine whether prescription patterns complied with recommendations not to use non-steroidal anti-inflammatory drugs (NSAIDs) in patients with cardiovascular contraindications. Moreover, we examined predictors for initiation and prescriber responsibility. Methods and results We used Danish medical databases to identify all patients with first-time cardiovascular disease during 1996–2017 (n = 628 834). We assessed standardized prevalence proportions, predictors from logistic regression, and prescriber identifiers. One-year prevalence of NSAID initiation increased 3.4% from 1996 (19.4%) to 2001 (22.7%) and declined by 2.7% thereafter until 2017 (13.5%). Trends were independent of age, sex, and disease subtype, although larger annual declines occurred for heart failure (3.9%) and ischaemic heart disease (3.5%) since 2002. One-year prevalence remained highest among patients with venous thromboembolism (16.6%) and angina (13.8%), and lowest for ST-segment elevation myocardial infarction (7.0%) and heart failure (8.8%). Initiators were predominantly prescribed ibuprofen (59%), diclofenac (23%), and etodolac (6%). Diclofenac and coxib use declined, while ibuprofen and naproxen use increased. Median prescribed pill dose of ibuprofen declined after 2008 from moderate/high (600 mg) to low (400 mg). Treatment duration declined for all NSAIDs, except celecoxib. Rheumatic, obesity, and pain-related conditions predicted NSAID initiation. General practitioners issued 86–91% of all NSAID prescriptions, followed by hospital prescribers (7.3–12%). Conclusions Initiation of NSAIDs in patients with cardiovascular disease declined since 2002. Shorter treatment duration, declining COX-2 inhibition, and increasing use of naproxen and low-dose ibuprofen suggest adherence to guidelines when NSAIDs cannot be avoided. Still, NSAID use remained prevalent despite cardiovascular contraindications, warranting awareness of appropriateness of use among general practitioners in particular.


Sign in / Sign up

Export Citation Format

Share Document