Physicians - maximum of 0.25 AMA PRA Category 1 Credit(s)™
ABIM Diplomates - maximum of 0.25 ABIM MOC points
Nurses - 0.25 ANCC Contact Hour(s) (0 contact hours are in the area of pharmacology)
Pharmacists - 0.25 Knowledge-based ACPE (0.025 CEUs)
Physician Assistant - 0.25 AAPA hour(s) of Category I credit
IPCE - 0.25 Interprofessional Continuing Education (IPCE) credit
This activity is intended for pulmonologists, family medicine/primary care clinicians, internists, neurologists, nurses, nurse practitioners, pharmacists, physician assistants, sleep medicine clinicians, and other members of the healthcare team who care for patients with asthma.
The goal of this activity is for members of the healthcare team to be better able to describe the association of poor sleep patterns with asthma risk and whether healthy sleep patterns could mitigate the adverse effect of genetic susceptibility measured by polygenic risk scores, according to a large-scale prospective study performed in UK Biobank cohort, a national large, prospective cohort drawn from 22 UK assessment centers.
Upon completion of this activity, participants will:
Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.
All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.
This activity was planned by and for the healthcare team, and learners will receive 0.25 Interprofessional Continuing Education (IPCE) credit for learning and change.
Medscape, LLC designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™ . Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.25 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.
The European Union of Medical Specialists (UEMS)-European Accreditation Council for Continuing Medical Education (EACCME) has an agreement of mutual recognition of continuing medical education (CME) credit with the American Medical Association (AMA). European physicians interested in converting AMA PRA Category 1 credit™ into European CME credit (ECMEC) should contact the UEMS (www.uems.eu).
College of Family Physicians of Canada Mainpro+® participants may claim certified credits for any AMA PRA Category 1 credit(s)™, up to a maximum of 50 credits per five-year cycle. Any additional credits are eligible as non-certified credits. College of Family Physicians of Canada (CFPC) members must log into Mainpro+® to claim this activity.
Through an agreement between the Accreditation Council for Continuing Medical Education and the Royal College of Physicians and Surgeons of Canada, medical practitioners participating in the Royal College MOC Program may record completion of accredited activities registered under the ACCME’s “CME in Support of MOC” program in Section 3 of the Royal College’s MOC Program.
Awarded 0.25 contact hour(s) of nursing continuing professional development for RNs and APNs; 0.00 contact hours are in the area of pharmacology.
Medscape designates this continuing education activity for 0.25 contact hour(s) (0.025 CEUs) (Universal Activity Number: JA0007105-0000-23-178-H01-P).
Medscape, LLC has been authorized by the American Academy of PAs (AAPA) to award AAPA Category 1 CME credit for activities planned in accordance with AAPA CME Criteria. This activity is designated for 0.25 AAPA Category 1 CME credits. Approval is valid until 5/26/2024. PAs should only claim credit commensurate with the extent of their participation.
For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]
There are no fees for participating in or receiving credit for this online educational activity. For information on applicability
and acceptance of continuing education credit for this activity, please consult your professional licensing board.
This activity is designed to be completed within the time designated on the title page; physicians should claim only those
credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the
activity online during the valid credit period that is noted on the title page. To receive AMA PRA Category 1 Credit™, you must receive a minimum score of 70% on the post-test.
Follow these steps to earn CME/CE credit*:
You may now view or print the certificate from your CME/CE Tracker. You may print the certificate, but you cannot alter it.
Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period, you can print
out the tally as well as the certificates from the CME/CE Tracker.
*The credit that you receive is based on your user profile.
CME / ABIM MOC / CE Released: 5/26/2023
Valid for credit through: 5/26/2024, 11:59 PM EST
processing....
The sleep-asthma association may be bidirectional: Asthma may worsen sleep quality, but poor sleep itself might also trigger or aggravate asthma. Sleep disorders are associated with specific inflammatory reactions, and asthma is a chronic inflammatory disease driven by genetic and nongenetic factors.
Whether poor sleep reflects higher asthma risk (ie, signals early progression of asthma) is still unclear. Insomnia and sleep duration are reportedly associated with asthma, but whether sleep patterns significantly affect asthma risk is still unknown.
Early detection and management of sleep disorders could reduce asthma incidence, according to a large-scale prospective study that included nearly half a million participants. The study was reported in BMJ Open Respiratory Research.
The population-attributable risk analysis indicated that 19% of asthma cases could be prevented through improving sleep traits. The investigators took into consideration polygenic risk scores (PRSs) for asthma and comprehensive sleep scores encompassing 5 sleep traits.
Sleep quality is generally recognized as a nongenetic driver of asthma. Poor sleep quality and obstructive sleep apnea have been reported particularly among persons with severe disease. In addition, asthma is known to adversely affect sleep duration, sleep quality, napping, and daytime sleepiness.
The researchers suggested that the relationship between sleep and asthma is bidirectional, given that sleep disorders (sleep of short duration, insomnia, evening chronotype ["night owl"], snoring, excessive daytime sleepiness) are associated with specific chronic inflammatory reactions. It has remained unclear, however, whether poor sleep reflects a higher risk for early asthma progression.
Genetic factors also contribute to asthma risk, but highly variable heritability suggests that the nongenetic exposures play an important role; "[h]owever, whether healthy non-genetic exposure could decrease the risk of asthma and mitigate the adverse effect of genetic risk remains largely unknown," the authors stated.
They hypothesized that healthier sleep could decrease future asthma risk and mitigate the hazards of genetic effects.
Using data from the UK Biobank, a national large, prospective cohort drawn from 22 UK assessment centers, they investigated the independent and combined effects of sleep pattern and PRSs on asthma incidence.
In the UK Biobank cohort (455,405 adults aged 38-73 years, who were enrolled from 2006 to 2010), 17,836 were diagnosed with asthma over 10 years of follow-up. Investigators constructed polygenic risk scores for each participant on the basis of their having any of 17 single-nucleotide polymorphisms that are significantly associated with asthma. Participants were stratified into 3 groups: persons at high genetic risk, persons at intermediate genetic risk, and persons at low genetic risk. Around 1 in 3 participants were classified as being at high genetic risk (150,429), and another third (151,970) were classified as being at intermediate risk. The remainder were classified as being at low risk. Some 7105 people at high genetic risk and 5748 at intermediate genetic risk were diagnosed with asthma during the monitoring period.
Comprehensive sleep scores, which ranged from 0 to 5, were constructed on the basis of self-reported sleep traits. Higher scores represented healthier sleep patterns. A healthy sleep pattern was defined as early chronotype; getting from 7 to 9 hours of sleep every night; never or rare insomnia; no snoring; and no frequent daytime sleepiness. On the basis of their responses, 73,223 people met the criteria for a healthy sleep pattern; 284,267, an intermediate sleep pattern; and 97,915, a poor sleep pattern.
"Compared with non-cases, asthma cases were more likely to have lower education levels, unhealthy sleep traits and patterns, obesity, higher PRS, more smoking, more alcohol consumption, hypertension, diabetes, depression, gastroesophageal reflux, and more air pollution exposure," the authors reported.
All 5 healthy sleep traits were independently associated with a lower risk for asthma. Never/rare insomnia and sleep duration of 7 to 9 hours a night were seemingly the most influential; they were associated with risk reductions of 25% and 20%, respectively.
Analysis showed that compared with the low-risk group, the hazard ratios (HRs) for the highest PRS group and the poor sleep pattern group were 1.47 (95% CI: 1.41, 1.52) and 1.55 (95% CI: 1.45, 1.65), respectively.
Risk was 2-fold higher in the presence of a combination of poor sleep and high genetic susceptibility (HR 2.22 [95% CI: 1.97, 2.49]; P < .001). Conversely, a healthy sleep pattern was associated with a lower risk for asthma in the low (HR 0.56 [95% CI: 0.5, 0.64]), intermediate (HR 0.59 [95% CI: 0.53, 0.67]), and high genetic susceptibility groups (HR 0.63 [95% CI: 0.57, 0.7]). A population-attributable risk analysis indicated that improving these sleep traits would prevent 19% of asthma cases. Also, a subset analysis suggested that a healthy sleep pattern might reduce the risk for asthma among persons at high genetic risk by 37%.
The study findings suggested that analysis of sleep patterns is warranted for all patients with asthma, said co-author Qing Wang, PhD, Cheeloo College of Medicine, Shandong University, Jinan, People's Republic of China, in an interview. "In our results, the effects of sleep and genetics were independent. Therefore, what we learned about the effects of sleep on asthma could be applied to all the patients, including those with a high or low genetic predisposition. In addition, we believe that intervening among those with high genetic predisposition could be more beneficial since they are more likely to have asthma. However, because this study is observational, a large clinical trial is absolutely needed to provide causal evidence, especially before guidelines modifications can be considered."
"Addressing relevant asthma comorbid conditions continues to be an integral part of asthma care," commented Diego J. Maselli, MD, associate professor of medicine and interim chief, division of pulmonary diseases and critical care, The University of Texas Health, San Antonio, Texas, in an interview. "There is mounting evidence that sleep patterns and obstructive sleep apnea may influence asthma control. This association is complex and multifactorial. It is important to remember that obstructive sleep apnea may coexist with other conditions, such as obesity and gastroesophageal reflux disease, that in turn can also worsen asthma control and influence clinical outcomes.
"The study by Xiang and colleagues adds to the field of study, but further evidence is required to change practice guidelines at this time. Fortunately, sleep studies are readily available now with more widespread use of home testing, so patients can be easily tested. The majority third-party payers have identified that diagnosing these disorders is cost-effective and are able to reimburse sleep studies," Maselli concluded.
The research was funded by the Future Program for Young Scholars and National Key Research and Development Program. The study authors and Maselli have disclosed no relevant financial relationships.
BMJ Open Respir Res. 2023;10:e001535.[1]