Objective Aspirin and non-aspirin non-steroidal anti-inflammatory drugs (NSAIDs) are preventive against cardiovascular disease (CVD) and several cancer types, but long-term use has been associated with significant health risks, resulting in conflicting recommendations on NSAID use for prevention of CVD and cancer. Previous research indicates that aspirin use increases with age and CVD risk factors and that a large percentage of the US population regularly use analgesics, including NSAIDs, but there has not been a recent, in-depth assessment of NSAID use prevalence, changes in use over time or predictors of NSAID use in the USA.
Methods We used the cross-sectional, National Health And Nutrition Examination Survey (NHANES) from 1988 to 1994 and three continuous cycles (1999–2004) to assess regular NSAID use prevalence, changes over time and predictors of regular NSAID use.
Results Overall, regular NSAID use increased over time and varied by demographic features. Participants over 60 years of age, women, participants with high body mass index, increased waist circumference or heart disease were significantly more likely to be regular NSAID users. By contrast, non-Hispanic African American and Mexican American participants were significantly less likely to regularly use NSAIDs.
Conclusions This study uses a nationally representative data set (NHANES) to provide an exploration of regular NSAID use patterns over time, highlighting several demographic, lifestyle and clinical conditions associated with regular NSAID use. Understanding who is likely to regularly use NSAIDs enables more targeted messaging both for increasing the preventive benefits and for limiting the toxicities associated with regular use of NSAIDs.
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What is already known about this subject?
Regular aspirin use increases with age and cardiovascular disease (CVD) risk factors.
What does this study add?
We used nationally representative National Health And Nutrition Examination Survey data sets to evaluate the prevalence of regular non-steroidal anti-inflammatory drug (NSAID) use (including aspirin, non-aspirin and multiple NSAIDs) in the USA, changes over time and predictors of regular NSAID use in adults 20 years of age and above.
How might this impact on clinical practice?
Our findings of lower NSAID use (including aspirin) among African American and Mexican American participants may indicate a missed opportunity for CVD and cancer prevention. Understanding who is most likely to use NSAIDs may enable more targeted messaging to increase the benefits and limit the harms of regular NSAID use.
For many years, aspirin and non-aspirin non-steroidal anti-inflammatory drugs (NSAIDs) have been used to address acute maladies (eg, pain, fever and inflammation). More recently, increasing knowledge of NSAIDs’ preventive effects against development and progression of cardiovascular diseases (CVDs)1–10 and cancer11–16 has encouraged their use for prevention of chronic diseases, as well as for acute pain. However, the side effects and potential toxicities of long-term NSAID use, including increased risk of gastrointestinal ulceration and bleeding,17 18 kidney toxicity19 and potential for haemorrhagic stroke,20 21 have raised concerns.
Recommendations for routine use of aspirin for prevention of CVD and other chronic diseases in healthy individuals are controversial. Although the US Food and Drug Administration (FDA) supports the regular use of aspirin in those with established heart disease, it recently denied requests for aspirin to be marketed as a therapeutic agent suitable for the primary prevention of CVD. This decision is contentious; agencies such as the American Heart Association, the National Heart Lung and Blood Institute and US Preventive Services Task Force (USPSTF) support aspirin’s use in CVD prevention for those ‘at high risk’ of heart attack. Similarly, the recommendations on NSAID use for cancer prevention are still being debated. Recognising the potential for significant benefit and the need to manage possible harms, the USPSTF now recommends initiation of low-dose aspirin for CVD and colorectal cancer risk reduction in men and women 50–59 years old with at least 10% 10-year CVD risk, but does not include non-aspirin NSAIDs in the recommendation. The National Cancer Institute has less clear advice, awaiting the outcome of several long-term trials. Thus, with differing opinions and messages about regular aspirin/NSAID use from key health agencies, it is not clear what overall message the public has received.10 22–28
In the light of mixed messages on aspirin use, several studies have tried to ascertain demographic correlates of NSAID use. Data in adults older than 40 years suggest that NSAID use is increasing over time, and higher NSAID use is associated with non-Hispanic White ethnicity and increasing age. Given that there appear to be demographic correlates of NSAID use, thorough knowledge of usage patterns is important for monitoring intervention opportunities to minimise disparities among adults who may benefit from such use and minimise harms where NSAID use is contraindicated. Most studies until now have used older populations selected for disease status, without adequate coverage of minority ethnic groups.29–35
Given the need to use nationally representative data across age and ethnicity, our goal was to use data from the National Health And Nutrition Examination Survey (NHANES) to describe the prevalence of regular NSAID use in the US population, changes over time and predictors of regular NSAID use. We restricted our analysis to NHANES III (1988–1994)36 and three continuous NHANES cycles (1999–2004)37 in order to adequately capture comparable measures of analgesic use; after these dates, NSAIDs usage questions were restricted NSAID use in arthritis or in low-dose preventive aspirin use which does not capture the majority of NSAID intake.
Participants in NHANES III (1988–1994) and continuous NHANES cycles 1999–2000, 2001–2002 and 2003–2004 were considered eligible for this analysis if they were at least 20 years of age at the time of interview (NHANES III—n=18 809, NHANES 1999–2004—n=14 700). Participants with missing information on regular NSAID use (NHANES III—n=45, NHANES 1999–2004—n=2) or non-positive survey weights (NHANES III—n=2233, NHANES 1999–2004—n=954) were excluded. This resulted in an analytic data set of 16 533 individuals from NHANES III and 13 744 from NHANES 1999–2004 (table 1).
Determining NSAID use
Information on NSAID use was gathered from two sets of questions in each data set: the Analgesics Questionnaire and Prescription Medication information. In NHANES III, the Analgesics Questionnaire addressed any use of aspirin, acetaminophen or ibuprofen in the last 30 days. Data available from continuous cycles (1999–2004) included ever-regular use of analgesic medication, including NSAIDs. In order to make these data more comparable across surveys, we used data on pills/doses taken within the NHANES III Analgesics Questionnaire data to define regular NSAID use as 30 or more pills/doses in the last month. Participants were further classified as aspirin, non-aspirin or multiple NSAID users. Additional NSAID use information was obtained from the Prescription Medication Questionnaire, for which data on pills/doses were not available; these data were gathered equivalently across surveys, although data on prescription use were only available for 7654 participants (46.4% of data set) in the NHANES III data set. The final classification of NSAID use was determined as a function of both the Analgesics Questionnaire and the Prescription Medication information. For example, if a participant listed aspirin use in the Analgesics Questionnaire and ibuprofen as a Prescription Medication, then she/he was classified as a multiple NSAID user. NSAIDs reported are listed in online supplementary table 1 by time period.
Data for covariates were collected from the Survey Questionnaire, Physical Examination and Laboratory data. Pregnancy was not an exclusion criterion for the overall NSAID usage measurement, but pregnant women or women with unknown pregnancy status (NHANES III—n=762, NHANES 1999–2004—n=1331) were excluded from further analysis, as pregnancy affects body mass index (BMI), waist circumference and physical activity.38 Chronic Kidney Disease (CKD) was defined by calculating the estimated glomerular filtration rate using standardised creatinine values and specific formulas to include differences in women and African Americans, as published using NHANES.30 39 40 Physical activities were reported as specific activity items and open-ended questions for unlisted activities.41 A metabolic equivalent task (MET) value was provided for each activity and MET frequency was calculated by multiplying the value of each activity by the number of times it was performed each week. Total leisure time MET frequency was defined as the sum of leisure time MET frequencies (excluding household and yard work activity)41 42 and further categorised as inactive (0), insufficiently active (>0,<15) or sufficiently active (≥15),43 based on the recommendation of moderate physical activity (MET value of ≥3.0,<6.0) 5 days/week or vigorous physical activity (MET value ≥6.0) 3 or more days/week. Alcohol use was categorised by the average number of drinks/day on a drinking day.44 Poverty to income ratio was obtained from the Demographics Questionnaire and categorised as previously published.45 Waist circumference was categorised based on the threshold definitions for metabolic syndrome: >88 cm for women and >102 cm for men.46 BMI was categorised as normal/lean (<25), overweight (≥25 to <30), obese (≥30 to <35) and super obese (≥35). Cancer history and diabetes were based on self-report in Questionnaire data. Participants were considered to have heart disease if they self-reported having congestive heart failure, coronary heart disease, heart attack or stroke.
Variables were compared across study populations using weighted χ2 analysis for categorical variables. Associations between regular NSAID use and covariates were tested with weighted logistic regressions using the survey logistic procedure in SAS Version 9.4. Due to the large sample size, all demographic features were significant predictors of NSAID use in univariate logistic regression. Therefore, we conducted multivariate analysis of each population, including all demographic variables.
ORs were calculated as the odds of being a regular NSAID user and are reported with 95% CIs.
The data used for this study are de-identified and publicly available. This research was reviewed by an MD Anderson institutional review board and declared not human subject’s research.
NSAID use by time period
Individuals in the two samples differed significantly in a variety of demographic characteristics (table 1), reflecting changes in the US population between these time periods. Over time, regular NSAID use, including both prescription and over-the-counter, increased between survey time periods, whereas prescription NSAID use decreased (table 2). The distribution of NSAID type taken (eg, aspirin, non-aspirin) also changed over time both for overall and prescription use. Regular use of acetaminophen, a non-NSAID analgesic medication followed a similar pattern (table 2).
We further compared the distribution of NSAID use prevalence by demographic characteristics and time period (see online supplementary table 2). When comparing across covariates by time period, all categories of use increased, except non-aspirin use in participants reporting diabetes or CKD. In order to visualise NSAID use trends, we plotted NSAID use prevalence by age group and race/ethnicity across surveys (figure 1).
Factors associated with regular aspirin/NSAID use
As expected, non-Hispanic (NH) Whites and participants ages 60 and over were much more likely to be regular NSAID users, compared with non-White participants and those younger than 60 years (table 3). Although women were more likely to use NSAIDs regularly, the effect was small and only statistically significant for 1999–2004 (table 3). By type (aspirin, non-aspirin and multiple NSAIDs), women were generally less likely to use aspirin and more likely to use non-aspirin NSAIDs (tables 4 and 5). From 1988 to 1994, insufficiently active adults were less likely to use NSAIDs regularly compared with inactive adults, and those in the highest BMI category (>30) were more likely to be regular NSAID users, compared with the lowest BMI category (<25) (table 3). Although there was some variation by NSAID type, increased BMI category was positively associated and insufficient physical activity was negatively associated with NSAID use (table 4). Among the NHANES 1999–2004 population, former smokers were significantly more likely to use NSAIDS than never smokers (see online supplementary table 2), and this effect was specific to aspirin use (table 5).
Adults reporting fair or poor health were more than twice as likely to be regular NSAID users compared with those reporting excellent health in 1988–1994, and more than three times as likely in 1999–2004 (table 3). In the early interval, this effect was specific to non-aspirin NSAID use (table 4), but was statistically significant for all NSAID types for 1999–2004 (table 5).
Participants with a history of heart disease were more than twice as likely to be regular NSAID users in both time periods (table 3). Assessing use by NSAID type, this effect was driven by aspirin and multiple NSAID users (tables 4 5). Although diabetes, cancer history and CKD were not significant predictors of overall NSAID use, cancer history was positively associated with non-aspirin use and negatively associated with multiple NSAID use, while diabetes was positively associated with aspirin use in NHANES 1999–2004 (table 5).
The four health conditions included in our models (heart disease, CKD, diabetes and cancer history) are likely to influence reported health status. Therefore, we performed stratified analyses based on the presence of any of these chronic diseases and reanalysed the data. In NHANES III (1988–1994), age, insufficient physical activity and current health status remained significantly associated with NSAID use among participants without any of the four chronic diseases. The associations of BMI with overall NSAID use were no longer significant, but there was still a positive association between increasing BMI category and multiple NSAID use (table 4). Further, non-White participants without reported chronic diseases were significantly less likely to regularly use aspirin and non-aspirin NSAIDs compared with NH White participants (table 4). In the 1999–2004 population, stratifying by chronic disease status did not alter the associations of age, race/ethnicity, sex, smoking status, current health status or waist circumference with regular NSAID use. Conversely, alcohol use, BMI category and education were no longer significantly associated with NSAID use in participants without reported chronic diseases (tables 3 and 5).
Aspirin/NSAID use by age group and race/ethnicity
Within each time period, age-stratified analyses revealed patterns similar to the overall multivariate models with some variation (see online supplementary tables 3 and 4). Specifically, there was a positive relationship between BMI category and regular NSAID use in all age groups of NHANES III (see online supplementary table 3), but not significantly so in NHANES 1999–2004 (see online supplementary table 4). For both study periods, women in the youngest age group (20-39) were more likely to use NSAIDs regularly than men of similar ages.
Across race/ethnicity groups, older participants (60+) and those reporting worse health were more likely to use NSAIDs regularly than the young or those who reported better health condition. BMI was not associated with regular NSAID use, except in Mexican American participants without cancer history, diabetes, CKD or heart disease (see online supplementary table 5). When stratifying by race/ethnicity in the NHANES III data set, OR estimates in the race/ethnicity category of ‘Other’ and ‘Other Hispanic’ were unstable due to small sample sizes (see online supplementary table 5).
In the more recent data set (1999–2004), participants categorised as ‘Other Hispanic’ showed a slightly different pattern of factors associated with regular NSAID use. Specifically, receiving some college education, 1–2 alcoholic drinks/day on drinking days and a reported health status of ‘fair’ were positively associated with regular NSAID use, whereas ≥3 drinks/day was negatively associated with NSAID use. In Other Hispanic participants without cancer history, diabetes, CKD or heart disease, health status was no longer associated with NSAID use, and being a former smoker was positively associated with NSAID use (see online supplementary table 6).
The present study provides a broad evaluation of NSAID use patterns in the US population over time. Consistent with previous reports, overall regular NSAID use has increased. An observed decrease in prescription NSAID use, as well as acetaminophen, may be due in part to the increased availability and variety of over-the-counter NSAIDs over time, a phenomenon reported for other medications after becoming available over-the-counter.47
For the first time to our knowledge, we included multiethnic minority data on adults under 45 and observed that women in the youngest age group (≥20 to <40) were more likely to be regular NSAID users than men, but not for any other age group. Regular use of NSAIDs among women of reproductive age may be for the treatment of menstrual pain. Consistent with previous reports, showing that regular aspirin use increases with age and CVD risk factors,29 age category was the strongest independent predictor of regular NSAID use, which may be linked to the increasing prevalence of comorbidities with age.
Declining health status remains a significant predictor of NSAID use in participants without cancer history, diabetes, heart disease or chronic kidney disease, perhaps due to a general effect of poor health on NSAID use or an effect of other specific or undiagnosed morbidities not evaluated in this analysis. Our finding that former smokers over the age of 40 were more likely to be regular NSAID users may be associated with the development of smoking-related morbidities later in life, consistent with the findings that participants with diabetes and heart disease were more likely to be regular NSAID users.
We supported previous data that NH White populations have higher NSAID use in comparison with minority populations; however, our data suggest that this is a more recent development emerging only in 1999–2004. We include the first Mexican American data on younger adults, which support this finding across adulthood. African Americans are at increased risk for development of and mortality from CVD48–50 and cancer, including colorectal cancer.51 Since aspirin and non-aspirin NSAIDs show preventive benefit against CVD and colorectal cancer, among other types of cancer,48 49 this finding highlights a potential opportunity for reducing significant health disparities through NSAID-based disease prevention and bears further exploration.
Our study has both strengths and limitations. First, we analysed cross-sectional data, prohibiting causal inferences and raising issues where variables were not collected in the same way across surveys. For example, we defined ‘regular’ NSAID use in NHANES III (1988–1994) using participants’ reported frequency of use. In contrast, analgesic use was assessed as ever-regular use of analgesic medication in continuous NHANES (1999–2004). Second, data on Prescription Medication were only collected from a subset of participants (n=7664) in NHANES III (1988–1994), who were significantly different for all demographic characteristics, except poverty to income ratio compared with participants without prescription use data. Any potential effect of this difference is mitigated in the logistic regression by the incorporation of both prescription data and non-prescription data to record total NSAID use. Third, as above, we could only include data until 2004, after which appropriate analgesic questions were no longer asked. Our observations present some of the first data on changes over time for young ethnic minority adults, and we would urge studies that can examine whether this trend continues. Finally, the estimation of alcohol consumption by the average number of drinks per day on a drinking day does not distinguish between regular drinkers and sporadic heavy drinkers, who may use NSAIDs differently.
This study provides an exploration of regular NSAID use patterns in the US population over time and highlights several demographic, lifestyle and clinical conditions associated with NSAID use. This is a timely assessment, given the FDA’s warnings about non-aspirin NSAIDs52 and the recent update of the USPSTF recommendation on aspirin use for colorectal cancer prevention.27 Future studies are needed to determine whether lower use of NSAIDs by minority race and ethnic groups represents a missed opportunity to prevent CVD and cancer in these groups. Since the toxicities related to regular NSAID use are substantial, further characterising populations most likely to benefit and those most likely to suffer harms will enable risk-adapted recommendations for the preventive use of NSAIDs and is an area of great potential for future research.
- Received October 19, 2016.
- Revision received February 13, 2017.
- Accepted February 21, 2017.
Contributors JSD designed portions of the analysis, directed its implementation and drafted portions of the manuscript; HYL and H-LP conducted analyses, contributed to the drafting of the Methods section and reviewed the final manuscript; JK and SMA designed and conducted portions of the analysis, drafted portions of the manuscript and reviewed the final manuscript; EB assisted with the data interpretation and reviewed the final manuscript; ETH, SC and ACF-W contributed to the design and interpretation of the study, as well as review and editing of the manuscript.
Funding ACF-W is funded by the American Heart Association (grant no: 14BGIA18740011) and the US Department of Agriculture, Agriculture Research Service Children’s Nutrition Research Center at Baylor College of Medicine. JSD is supported in part by a grant from The University of Texas MD Anderson Cancer Center Duncan Family Institute for Cancer Prevention and Risk Assessment. SC is the principal investigator of an NCI R25T award (CA057730) and an NCI R25E award (CA056452), which provided EB with support for a summer research experience in cancer prevention.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement All data used in this study are publicly available free of charge from the Center for Disease Control and prevention.
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