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BMJ Open logoLink to BMJ Open
. 2019 May 28;9(5):e024078. doi: 10.1136/bmjopen-2018-024078

To what extent does sex, age and BMI impact medical and pharmacy costs? A retrospective cohort study involving employees in a large school district in the USA

Ray M Merrill 1, Rylan Fowers 1
PMCID: PMC6549653  PMID: 31142517

Abstract

Objective

To identify the extent that sex, age and body mass index (BMI) is associated with medical and pharmacy costs.

Design

Retrospective cohort.

Setting

A school district in the Western USA involving 2531 workers continuously employed during 2011–2014.

Main outcome measures

Medical and pharmacy costs and BMI.

Results

Approximately 84% of employees participated in wellness screening. Participants were 1.03 (95% CI 1.01 to 1.06) times more likely to be women and younger (M=47.8 vs 49.8, p<0.001). Median medical and pharmacy costs were higher for women than men, increased with age, and were greater in morbidly obese individuals (p<0.001). Annual pharmacy claims were 18% more likely to be filed by women than men, 23% more likely filed by those aged ≥60 versus <40 years, and 6% more likely filed by morbidly obese individuals than of normal weight (p<0.001) individuals. Greater medical and pharmacy costs in older age were most pronounced in underweight and morbidly obese groups. Higher use of medication among women than men was primarily because of drugs involving birth control, osteoporosis, thyroid disease and urinary tract infection. Higher medication use in older age was primarily related to medications used to treat gastrointestinal problems. Medication use was positively associated with BMI weight classifications for most of the 33 drug types considered, with exceptions involving birth control, herpes and osteoporosis. A J-shape relationship was observed between BMI and medication use for acne, antibiotic, cold/influenza/allergy, eye infection, oedema, muscle spasms, pain and ulcers.

Conclusions

Medications associated with higher medical and pharmacy costs among women, older age and underweight or obese individuals are identified. Lowering medical and pharmacy costs requires weight management in older ages, particularly for underweight and obese. Higher pharmacy costs for certain drugs among underweight individuals may be associated with poorer nutrition.

Keywords: body mass index, obesity, prevention, pharmaceuticals, screening


Strengths and limitations of this study.

  • A large cohort of employees was available for retrospective assessment of the association between sex, age and body mass index with medical and pharmacy costs.

  • The association between sex, age and 33 specific types of medication were assessed, some of which have not been previously considered.

  • All active employees received employer-sponsored medical and pharmacy coverage, and 84% had information that allowed us to determine body mass.

  • A few medications may have contributed to weight gain, which we were unable to adjust for in the current study.

  • The study population and patterns of prescription drug use may limit generalisation of the results.

Introduction

Many companies offer wellness-screening programmes consisting of health risk assessment (HRA) and biometric screening. The 2016 Employer Health Benefits Survey found that among large firms (200 or more employees) in the USA, 59% offered HRA (of which 32% had an incentive component)​ and 53% offered biometric screening (of which 31% included an incentive component).1 These programmes are intended to promote a greater sense of personal responsibility for lifestyle choices, identify the need for health behaviour change, reduce future health problems, encourage patient management of existing health problems, decrease worker absenteeism and improve job satisfaction and worker productivity.2–7

Larger companies are also required to offer employer-sponsored medical and pharmacy coverage for their employees. Hence, information obtained on the HRA and screenings can be compared with the medical and pharmacy costs.

Medical and pharmacy costs are influenced by a number of factors, including sex, age and body mass index (BMI).8–10 Although medical costs are often a response to acute and chronic health conditions, pharmacy costs are often incurred to prevent more serious health problems. For example, antihypertensive medication or statins are useful in preventing cardiovascular disease11–13; multivitamins or folic acid for preventing congenital abnormalities14; aspirin and non-steroidal anti-inflammatory for preventing colorectal cancer15; bronchodilators, steroids and anti-inflammatories for managing asthma16 and non-steroidal anti-inflammatory drugs, steroids, analgesics and immunosuppressive drugs for managing arthritis.17 Consequently, wellness screening may actually increase the use of prescription medication.18

Although a person’s body weight may be associated with increased risk for various chronic health conditions and poorer health-related quality of life,19 20 only in the last 15 years or so has its impact on healthcare expenditures been assessed.10 Further, only a small number of studies have explored the association between body weight and prescription drug use. A study conducted in England found that overweight and obese individuals were more likely to receive medication for the cardiovascular system; gastrointestinal system; respiratory system; central nervous system; endocrine system; gynaecology/urinary disorders; musculoskeletal and joint disorders; infections; eye, ear and oropharynx problems and skin disorders.21 A study in Sweden showed that the use and cost of medication in general are significantly greater in obese individuals.22 A study in the USA found that obesity was responsible for $7 billion in Medicare prescription drug costs in 2006.23 Another study conducted in the USA identified increased medication use during 1988 through 2012, with the increase most prominent among obese individuals.24 A large cross-sectional study of 9789 adults in the National Health and Nutrition Examination Survey (NHANES) found that obese individuals use several prescription drugs (eg, hypertension, lipid-lowering and diabetes medications) more frequently than normal weight individuals.25 Another study based on NHANES data found that while medication use increased over time for obese individuals compared with normal weight individuals ages 40 years and older, the increase was only marginal for those aged 25–39 years.26 One study found that obese individuals used more analgesic, asthma, cardiovascular, diabetes, intranasal allergic rhinitis, thyroid and ulcer medications.27

The purpose of the current study was to identify the extent to which sex, age and BMI weight classifications are associated with medical and pharmacy costs among a large group of teachers, administrators and other school staff. These associations are also evaluated for 33 more commonly prescribed medications.28 Although studies have previously looked at the association between BMI and prescription medications, we evaluated some drugs that have not been formerly considered, and the breadth of drugs covered is greater than in past studies. In addition, evaluating the effect of being underweight on medical and pharmacy costs, and on specific drug types, is unique to this study.

Methods

Patient and public involvement

A retrospective cohort study was conducted that associated sex, age and BMI with medical and pharmacy cost data for employees of a large school district in the western USA. Specific patients and or the general public was not involved in this study. BMI was obtained from those employees who participated in wellness screening. Employer-sponsored insurance was available to all employees. The school district comprised of six high schools, eight junior high schools and 31 elementary schools. Employees consisted of approximately three teachers to every one staff member (cooks, bus drivers, ground keepers, maintenance workers, administrators and clerical workers). We were not provided specific job type and salary for each employee. However, we can assume that the teachers, administrators, counsellors and nurses, who represent almost all of the employees, had at least a college degree, that their salaries are commensurate with other school districts, and that the employer-sponsored insurance coverage was not strongly impacted by the employee’s income or education.

The study involved the academic years 2010–2011, 2011–2012, 2012–2013 and 2013–2014. Employees were offered wellness screenings (personal HRA and biometric evaluation) each fall. Medical and pharmacy claims data were also obtained for the employees in each academic year. Wellness screening and claims data were combined with a file of eligible employees and assessed within each academic year. The eligibility file contained information on current employment, sex, age and year.

Wellness screening

All employees were offered wellness screening. Although participation was voluntary, it was promoted through incentives. The HRA involved 36 questions. Biometric screenings involved measurements of BMI (kg/m2), blood pressure (mm Hg), cholesterol (mg/dL) and glucose (mg/dL). The HRA and biometric screenings were provided at no cost to the employees, and were made available on location or with a personal physician. A health nurse or physician assisted the employee in interpreting their HRA and screening results, in order to help guide their need for lifestyle changes and control measures. The current study only considers BMI. Weight classifications are based on commonly accepted ranges of BMI, as follows: underweight (BMI: <18.5), normal weight (BMI: 18.5–24), overweight (BMI: 25–29), obese (BMI: 30–39) and morbidly obese (BMI: 40+).

Medical and pharmacy claims data

All active employees received employer-sponsored medical and pharmacy coverage, for themselves and their families. The school district is fully insured with a retained-retention agreement that makes the plan act very much like a self-funded health plan. Each month, the district pays a health insurance premium for the cost of healthcare and a small premium for reinsurance of catastrophic claims. Catastrophic claims greater than $250 000 are reinsured by a stop loss policy and are not paid for by the school district. Employee pharmacy data do not include over-the-counter drugs, but only those medications requiring a prescription. In the USA, a drug is sold over-the-counter if the Food and Drug Administration deems it as sufficiently safe and effective. These medications are not included in the current study. Further, medical and pharmacy cost represents the amount paid by the insurance company as well as copays by the employee.

Statistical techniques

Counts, means, SD, medians and percentages were used to describe the study population. Pair-wise comparisons of means were evaluated for statistical significance using the Student-Newman-Keuls Test. Risk ratios compare having a medical and pharmacy cost above the 50th percentile (vs below), 75th percentile (vs below) and 90th percentile (vs below). Statistical significance was determined by the corresponding 95% CI. For selected medications, the risk of medication use was compared using risk ratios and attributable fraction percentages across the levels of sex, age and BMI weight classifications. Statistical significance of differences in per cent use of selected medications across sex, age and BMI categories was based on two-sided tests of significance using the 0.05 level against a null hypothesis of no association. Data were evaluated using the statistical software package PC-SAS V.9.4.

Results

In 2010–2011, there were 3023 eligible employees, of which 2531 (83.7%) remained employed through the academic year 2013–2014. Those more likely to remain employed over the study period were 40–59 years of age and had lower medical and pharmacy costs (table 1). In 2010–2011, ages ranged from 18 to 76, with mean age significantly younger for those who remained employed (46.9 vs 49.2, p<0.0001). Those who stayed with the school district had significantly lower mean medical costs ($3056 vs $7887, p<0.0001) and mean pharmacy costs ($859 vs $1105, p=0.0387). The results of this study are based on those continuously employed over the four academic years.

Table 1.

Characterisation of the study group according to sex, age, medical and pharmacy costs

Continuously employed
No % % Χ2 P value Risk ratio 95% CI
Sex
 Men 797 26.36 84.69 0.3884 1.00
 Women 2226 73.64 83.38 0.98 0.95 to 1.02
Age groups
  18–39 770 25.47 82.21 <0.0001 1.00
 40–49 806 26.66 89.45 1.09 1.05 to 1.13
 50–59 1088 35.99 88.24 1.07 1.03 to 1.12
 60–76 359 11.88 60.45 0.74 0.67 to 0.80
Medical cost (US$)
 0–184 755 25.0 87.55 <0.0001 1.00
 185–604 757 25.0 85.07 0.97 0.93 to 1.01
 605–2049 755 25.0 84.64 0.97 0.93 to 1.01
 2050–7191 454 15.0 79.30 0.91 0.86 to 0.96
 7192+ 302 10.0 75.17 0.86 0.80 to 0.92
Pharmacy cost (US$)
 0–6 759 25.0 86.92 <0.0001 1.00
 7–194 755 25.0 85.21 0.99 0.69 to 1.03
 195–903 755 25.0 82.59 0.96 0.92 to 1.00
 904–2303 452 15.0 84.14 0.99 0.94 to 1.04
 2304+ 302 10.0 74.92 0.86 0.80 to 0.93

Sex, age, medical and pharmacy costs apply to the 2010–2011 academic year.

Most employees participated in annual wellness screening (84.1% in 2010–2011, 84.4% in 2011–2012, 87.6% in 2012–2013 and 80.7% in 2013–2014). In 2010–2011, there was no significant difference in mean medical cost between those who participated in wellness screening and those who did not ($3148 vs $2571, p=0.2900). However, median medical cost was significantly greater for those who participated in wellness screening ($588 vs $470, p=0.0454). For all academic years, women were 1.03 (95% CI 1.01 to 1.06) times more likely than men to complete annual wellness screenings, after adjusting for age and academic year. Participants in wellness screening were significantly younger (M=47.8 vs 49.8, p<0.0001), after adjusting for sex and year. Those participating in wellness screening had significantly lower annual mean medical cost ($3093 vs $4181, p=0.0013), but experienced no significant difference in annual mean pharmacy costs, after adjusting for age, sex and year.

Among participants in annual wellness screening, mean BMI remained constant across the academic years (table 2). Mean BMI was greater for men than women and in ages 40 years and older. Medical and pharmacy costs were highly positively skewed, with considerable variability. Hence, identifying significant differences in the mean costs across the levels of sex, age and year was less likely to occur than to find significant differences in the median costs across the levels of these variables. Medical costs were higher for women than men, increased with age, and were greater in morbidly obese individuals. Pharmacy costs were higher in women than men, increased with age and were lowest in those of normal weight.

Table 2.

Medical and pharmacy costs according to sex, age, year and body mass index (BMI)

BMI (kg/m2) Medical cost (US$) Median Median one-way analysis Pharmacy cost (US$) Median Median one-way analysis
Mean SD SNK Mean SD SNK P value Mean SD SNK P value
Sex
 Men 29.35 5.80 A 2869 10 581 A 373 <0.0001 725 2324 A 53 <0.0001
 Women 27.26 6.47 B 3447 12 049 A 741 963 3550 B 238
Age groups
 18–39 27.17 6.06 A 2236 9344 A 389 <0.0001 660 3342 A 70 <0.0001
 40–49 27.76 6.42 B 3052 12 366 B 503 750 2806 A 106
 50–59 28.05 6.55 B 3935 12 579 B 845 1021 3288 B 261
 60–76 28.17 6.13 B 3749 10 831 B 989 1288 3990 C 344
Year
 2010–2011 27.89 6.40 A 3188 10 524 A 605 0.2313 830 2247 A 195 0.0016
 2011–2012 27.79 6.31 A 3621 12 816 A 610 953 3180 A 189
 2012–2013 27.87 6.59 A 3208 11 836 A 670 934 3571 A 173
 2013–2014 27.63 6.16 A 3191 11 557 A 651 894 3913 A 141
BMI (kg/m2)
 Underweight 2191 1190 A 647 0.0003 1454 6706 A 224 0.0004
 Normal weight 2826 333 A 650 779 3285 B 167
 Overweight 3174 514 A 603 926 3085 A, B 169
 Obese 3544 459 A 665 1031 3458 A, B 228
 Morbidly obese 6911 2092 B 1033 853 1493 A, B 242

Different letters in the SNK columns indicate significant difference among the levels of the variables at the 0.05 level.

SNK, Student-Newman-Keuls Test.

The risk of medical and pharmacy costs above the 50th, 75th and 90th percentiles according to sex, age and BMI weight classification is shown in table 3. Higher BMI has a greater impact on higher percentiles of medical and pharmacy costs. For example, morbidly obese compared with normal weight are 1.13 (13%), 1.30 (30%) and 1.93 (93%) more likely to have pharmacy costs above the 50th, 75th and 90th percentiles, respectively. Medical and pharmacy costs above these percentiles are greater in women than men and increase with age.

Table 3.

Risk of medical and pharmacy costs (US$) above the 50th, 75th and 90th percentiles according to BMI weight classification, sex and age

Medical Pharmacy
50th percentile
Above vs below
75th percentile
Above vs below
90th percentile
Above vs below
50th percentile
Above vs below
75th percentile
Above vs below
90th percentile
Above vs below
Risk ratio 95% CI Risk ratio 95% CI Risk ratio 95% CI Risk ratio 95% CI Risk ratio 95% CI Risk ratio 95% CI
Sex
 Men 1.00 1.00 1.00 1.00 1.00 1.00
 Women 1.43 1.36 to 1.51 1.47 1.35 to 1.60 1.42 1.24 to 1.64 1.58 1.50 to 1.66 1.59 1.46 to 1.74 1.14 1.00 to 1.29
Age groups
 18–39 1.00 1.00 1.00 1.00 1.00 1.00
 40–49 1.16 1.08 to 1.23 1.15 1.03 to 1.29 1.08 0.90 to 1.28 1.14 1.07 to 1.22 1.45 1.29 to 1.64 1.72 1.37 to 2.15
 50–59 1.50 1.42 to 1.59 1.65 1.50 to 1.82 1.36 1.16 to 1.58 1.48 1.39 to 1.56 2.28 2.05 to 2.55 2.82 2.30 to 3.46
 60+ 1.61 1.52 to 1.72 1.83 1.64 to 2.04 1.33 1.11 to 1.60 1.57 1.48 to 1.68 2.57 2.29 to 2.89 3.78 3.06 to 4.68
BMI (kg/m2)
  Underweight 1.05 0.88 to 1.26 0.91 0.64 to 1.31 0.61 0.28 to 1.35 2.05 1.25 to 3.34 1.05 0.74 to 1.48 2.05 1.25 to 3.34
 Normal weight 1.00 1.00 1.00 1.00 1.00 1.00
  Overweight 0.95 0.90 to 1.00 0.95 0.86 to 1.05 1.01 0.85 to 1.20 1.01 0.95 to 1.06 1.18 1.07 to 1.30 1.68 1.41 to 2.00
 Obese 1.00 0.95 to 1.06 1.14 1.03 to 1.25 1.21 1.01 to 1.43 1.11 1.05 to 1.17 1.19 1.08 to 1.31 1.76 1.47 to 2.12
 Morbidly obese 1.18 1.08 to 1.29 1.62 1.40 to 1.87 2.18 1.72 to 2.77 1.13 1.03 to 1.25 1.30 1.09 to 1.55 1.93 1.43 to 2.61

Shaded cells represent statistical significance at the 0.05 level.

BMI, body mass index.

Associations between selected percentiles of medical and pharmacy costs and BMI weight classifications varied according to age (figure 1), but not sex (data not shown). Greater medical and pharmacy costs with older age groups are seen in the graph. However, the increasing costs with higher age are most pronounced in the underweight and morbidly obese groups.

Figure 1.

Figure 1

Median medical and pharmacy cost (US$) according to body mass index weight classifications and age.

Medication use is shown across sex, age and BMI groups in table 4. For any medication, women were 18% more likely to file a claim than men, employees 60 years of age or older were 23% more likely to file a claim than those less than 40 years and morbidly obese were 6% more likely to file a claim than those of normal weight. For 22 of the 33 medications considered, the percentage of annual claims was higher for women than men. For high blood pressure and statins, the percentage of claims was greater for men than women. For 25 of the medications, the percentage of annual claims increased with age. For 24 of the medications, the percentage of annual claims was associated with BMI (20 positively and 4 negatively). The strongest positive associations involved diabetes, high cholesterol (statins), blood thinners, high blood pressure and oedema. Negative associations involved acne, birth control, herpes and osteoporosis. The highest annual per cent of acne, antibiotic, cold/influenza/allergy and eye infection medications occurred in underweight individuals. For oedema, muscle spasms, pain and ulcers, medication use was comparatively high in underweight individuals, dropped for normal weight and then increased in higher weight classifications.

Table 4.

Medication use according to sex, age and BMI weight classification

% Sex Age groups Body mass index (kg/m2)
Men Women 18–39 40–49 50–59 60+ Underweight Normal weight Over weight Obese Morbidly obese
Medication
Acid reflux 5.75 5.56 5.81 3.02 4.54 7.14 8.36 3.57 4.34 5.36 7.19 9.14
 Risk ratio 1.00 1.04 1.00 1.50 2.36 2.77 0.82 1.00 1.24 1.66 2.11
 AFp (%) 0.00 0.26 0.00 2.81 7.27 9.23 0.00 1.33 3.64 5.98
Acne 7.17 3.15 8.62 7.15 7.03 7.16 7.40 9.82 8.81 6.64 6.34 6.18
 Risk ratio 1.00 2.74 1.00 0.98 1.00 1.03 1.11 1.00 0.75 0.72 0.70
 AFp (%) 0.00 11.07 0.00 0.01 0.25 0.82 0.00
Antibiotic 21.21 17.81 22.44 18.72 20.76 22.76 21.93 25.89 20.54 20.74 23.73 21.24
 Risk ratio 1.00 1.26 1.00 1.11 1.22 1.17 1.26 1.00 1.01 1.16 1.03
 AFp (%) 0.00 5.23 0.00 2.26 4.38 3.51 5.24 0.00 0.21 3.19 0.72
Anticonvulsants 1.49 1.39 1.53 1.84 1.32 1.45 1.40 2.68 1.25 1.13 1.65 1.61
 Risk ratio 1.00 1.10 1.00 0.72 0.79 0.76 2.14 1.00 0.90 1.32 1.29
 AFp (%) 0.00 0.15 0.00 1.68 0.00 0.47 0.43
Antifungal 5.29 2.61 5.81 5.64 6.03 4.24 3.87 5.36 5.83 3.81 6.24 6.18
 Risk ratio 1.00 2.23 1.00 1.07 0.75 0.69 0.92 1.00 0.65 1.07 1.06
 AFp (%) 0.00 6.09 0.00 0.36 0.00 0.37 0.32
Anxiety 7.88 6.31 8.45 6.42 7.80 8.36 8.97 8.93 7.22 7.11 7.29 6.45
 Risk ratio 1.00 1.34 1.00 1.21 1.30 1.40 1.24 1.00 0.98 1.01 0.89
 AFp (%) 0.00 2.60 0.00 1.67 2.33 3.03 1.83 0.00 0.08
Arthritis 11.06 11.13 11.03 7.72 10.53 12.83 12.56 7.14 9.36 10.72 13.84 14.78
 Risk ratio 1.00 0.99 1.00 1.36 1.66 1.63 0.76 1.00 1.15 1.48 1.58
 AFp (%) 0.00 0.00 3.87 6.82 6.48 0.00 1.58 5.03 6.02
Asthma 8.61 7.19 9.13 7.48 8.80 8.00 11.22 6.25 6.24 8.74 10.39 10.75
 Risk ratio 1.00 1.27 1.00 1.18 1.07 1.50 1.00 1.00 1.40 1.67 1.72
 AFp (%) 0.00 2.27 0.00 1.50 0.59 4.13 0.01 0.00 3.33 5.42 5.86
Birth control 8.71 0.24 10.88 21.13 8.77 2.59 0.95 10.71 11.69 7.30 6.34 6.99
 Risk ratio 1.00 45.33 1.00 0.42 0.12 0.04 0.92 1.00 0.62 0.54 0.60
 AFp (%) 0.00 79.43 0.00 0.00
Blood thinner 1.26 1.85 1.05 3.91 18.75 45.31 32.03 0.95 0.52 1.15 2.08 5.22
 Risk ratio 1.00 0.57 1.00 4.80 11.59 8.19 1.83 1.00 2.21 4.00 10.04
 AFp (%) 0.00 0 4.56 11.77 8.31 1.03 0 1.50 3.64 10.22
Bowel/rectum 3.06 2.75 3.17 1.76 2.84 3.53 4.15 1.79 3.15 2.87 2.85 2.96
 Risk ratio 1.00 1.15 1.00 1.61 2.01 2.36 0.57 1.00 0.91 0.90 0.94
 AFp (%) 0.00 0.47 0.00 1.84 2.99 3.99 0.00
Cold/influenza/allergy 17.80 14.52 18.99 15.73 18.30 18.14 19.07 22.32 15.53 18.56 20.38 22.04
 Risk ratio 1.00 1.31 1.00 1.16 1.15 1.21 1.44 1.00 1.20 1.31 1.42
 AFp (%) 0.00 5.20 0.00 2.83 2.65 3.64 7.22 0.00 3.36 5.27 6.94
Depression 18.24 10.28 21.14 12.51 19.30 20.75 18.84 15.18 16.20 17.59 20.83 18.55
 Risk ratio 1.00 2.06 1.00 1.54 1.66 1.51 0.94 1.00 1.09 1.29 1.15
 AFp (%) 0.00 16.16 0.00 9.01 10.73 8.45 0.00 1.54 4.95 2.58
Diabetes 6.32 6.48 6.22 2.53 4.50 7.82 10.94 1.79 2.24 5.67 11.29 17.74
 Risk ratio 1.00 0.96 1.00 1.78 3.09 4.32 0.80 1.00 2.53 5.04 7.92
 AFp (%) 0.00 0.00 4.69 11.67 17.36 0.00 8.82 20.34 30.43
Oedema 5.14 3.12 5.87 2.04 3.64 6.48 8.86 6.25 3.08 4.66 7.29 12.90
 Risk ratio 1.00 1.88 1.00 1.78 3.18 4.34 2.03 1.00 1.51 2.37 4.19
 AFp (%) 0.00 4.33 0.00 3.88 10.06 14.66 5.02 0.00 2.57 6.56 14.08
Eye infection 12.01 9.23 12.87 11.44 13.06 11.13 12.34 14.29 11.02 12.12 13.64 9.68
 Risk ratio 1.00 1.39 1.00 1.14 0.97 1.08 1.30 1.00 1.10 1.24 0.88
 AFp (%) 0.00 4.52 0.00 1.67 0.94 3.44 0.00 1.18 2.78
Herpes 6.30 3.26 6.86 4.82 7.24 6.12 4.71 1.79 7.66 7.22 4.20 1.88
 Risk ratio 1.00 2.10 1.00 1.50 1.27 0.98 0.23 1.00 0.94 0.55 0.25
 AFp (%) 0.00 6.50 0.00 3.07 1.67 0.00
High blood pressure 16.49 19.95 15.60 4.58 11.05 22.78 29.39 6.25 8.54 17.44 24.68 31.99
 Risk ratio 1.00 0.78 1.00 2.41 4.97 6.42 0.73 1.00 2.04 2.89 3.75
 AFp (%) 0.00 0.00 18.89 39.59 47.18 0.00 14.66 23.76 31.17
Inflammation 1.19 0.68 1.37 0.69 0.87 1.50 1.68 1.79 0.98 1.40 0.80 1.61
 Risk ratio 1.00 2.01 1.00 1.26 2.17 2.43 1.83 1.00 1.43 0.82 1.64
 AFp (%) 0.00 1.19 0.00 0.31 1.38 1.68 0.97 0.00 0.51 0.76
Insomnia 4.23 2.24 4.95 2.70 3.60 5.72 4.04 8.93 4.07 3.92 3.85 4.84
 Risk ratio 1.00 2.21 1.00 1.33 2.12 1.50 2.19 1.00 0.96 0.95 1.19
 AFp (%) 0.00 4.87 0.00 1.39 4.52 2.06 4.81 0.00 0.79
Muscle spasms 4.34 3.53 4.64 3.11 4.57 4.93 4.37 5.36 3.29 4.27 5.44 6.99
 Risk ratio 1.00 1.31 1.00 1.47 1.59 1.41 1.63 1.00 1.30 1.65 2.12
 AFp (%) 0.00 1.35 0.00 2.00 2.48 1.73 2.66 0.00 1.28 2.76 4.65
Nausea/vomiting 5.01 3.77 5.47 5.44 4.85 4.83 5.10 4.46 4.14 4.50 6.19 5.65
 Risk ratio 1.00 1.45 1.00 0.89 0.89 0.94 1.08 1.00 1.09 1.50 1.36
 AFp (%) 0.00 2.21 0.00 0.39 0.00 0.43 2.42 1.79
Opioids 17.04 15.98 17.42 14.14 16.29 18.62 18.73 17.86 13.39 15.77 20.28 27.69
 Risk ratio 1.00 1.09 1.00 1.15 1.32 1.32 1.33 1.00 1.18 1.51 2.07
 AFp (%) 0.00 1.51 0.00 2.53 5.12 5.24 5.38 0.00 2.94 8.06 15.40
Osteoporosis 1.21 0.07 1.63 0.00 0.17 1.30 4.37 0.89 1.56 1.20 0.85 0.00
 Risk ratio 1.00 23.29 1.00 0.57 1.00 0.77 0.54 0.00
 AFp (%) 0.00 21.24 0.00 0.00
Pain–non-opioid 2.19 1.63 2.39 2.78 2.15 1.98 1.91 3.57 1.73 1.67 2.55 2.96
 Risk ratio 1.00 1.47 1.00 0.77 0.71 0.69 2.06 1.00 0.97 1.47 1.71
 AFp (%) 0.00 1.01 0.00 2.28 0.00 1.03 1.53
Skin 6.84 4.88 7.55 5.44 6.44 7.37 8.24 6.25 7.25 6.41 7.19 5.38
 Risk ratio 1.00 1.55 1.00 1.18 1.35 1.51 0.86 1.00 0.88 0.99 0.74
 AFp (%) 0.00 3.61 0.00 1.24 2.37 3.40 0.00
Statins 14.49 17.93 13.24 2.31 8.53 20.58 28.4 3.81 7.02 17.95 19.89 27.47
 Risk ratio 1.00 0.74 1.00 3.69 8.91 12.29 0.54 1.00 2.56 2.83 3.91
 AFp (%) 0.00 0.00 28.07 53.40 62.07 0.00 18.41 20.99 29.68
Stomach acid 1.19 1.49 1.07 0.86 1.25 0.99 1.96 0.89 0.81 1.01 1.90 1.08
 Risk ratio 1.00 0.72 1.00 1.45 1.15 2.28 1.10 1.00 1.25 2.35 1.33
 AFp (%) 0.00 0.00 0.54 0.18 1.50 0.12 0.00 0.29 1.58 0.40
Teeth/gums 0.43 0.37 0.46 0.37 0.35 0.43 0.67 0.00 0.27 0.43 0.35 0.27
 Risk ratio 1.00 1.24 1.00 0.95 1.16 1.81 0.00 1.00 1.59 1.30 1.00
 AFp (%) 0.00 0.10 0.00 0.07 0.35 0.00 0.25 0.13 0.00
Thyroid 12.76 2.99 16.31 4.37 11.19 16.92 17.61 6.25 13.97 12.74 13.94 19.09
 Risk ratio 1.00 5.45 1.00 2.56 3.87 4.03 0.45 1.00 0.91 1.00 1.37
 AFp (%) 0.00 36.24 0.00 16.61 26.82 27.88 0.00 4.47
Ulcers 9.38 8.55 9.69 8.30 8.28 10.19 10.88 10.71 7.59 9.90 10.99 15.32
 Risk ratio 1.00 1.13 1.00 1.00 1.23 1.31 1.41 1.00 1.30 1.45 2.02
 AFp (%) 0.00 1.24 0.00 2.09 2.83 3.71 0.00 2.78 4.03 8.72
Urinary tract infection 3.01 0.20 4.44 3.39 3.08 3.45 3.25 6.25 3.83 2.83 3.50 3.76
 Risk ratio 1.00 22.20 1.00 0.91 1.02 0.96 1.63 1.00 0.74 0.91 0.98
 AFp (%) 0.00 38.95 0.00 0.05 1.87 0.00
Vitamins/minerals 2.07 0.71 2.57 2.49 1.73 1.88 2.47 0.00 2.07 1.28 1.75 5.38
 Risk ratio 1.00 3.62 1.00 0.69 0.76 0.99 0.00 1.00 0.62 0.85 2.60
 AFp (%) 0.00 5.14 0.00 0.00 3.20
All prescriptions 80.87 71.40 84.32 71.52 78.45 85.24 88.00 83.93 81.46 81.28 83.47 86.29
 Risk ratio 1.00 1.18 1.00 1.10 1.19 1.23 1.03 1.00 1.00 1.02 1.06
 AFp (%) 0.00 12.77 0.00 7.27 13.43 15.71 2.39 0.00 1.96 4.58

Shaded cells represent statistical significance at the 0.05 level. Cells that are left blank had a negative AFp. In these cases, the preventive fraction ([risk ratio–1]×100) is more appropriate.

AFp, attributable fraction in the population; BMI, body mass index.

We also report the attributable fraction in the population. For example, this statistic says that 8.82% of diabetes medication is attributed to being overweight, 20.34% is attributed to being obese and 30.43% is attributed to being morbidly obese. Where the risk ratio is less than 1, the preventive fraction can be estimated. For example, the risk of requiring osteoporosis medication is lower for obese compared with normal weight employees (ie, risk ratio=0.54). The corresponding preventive fraction is 66%, meaning in the absence of obesity, there would be 66% fewer claims for osteoporosis medication. The attributable fraction in the population and the preventive fraction both assume a cause-and-effect association between exposure and disease.

Discussion

The current study identified the degree to which sex, age and BMI are associated with medical and pharmacy costs among employees in a large school district. Associations were also evaluated for 33 commonly prescribed medications.28 The study extends previous research by including certain medications not previously evaluated and considering associations for all BMI weight classifications.

Higher medical and pharmacy costs among women, in older age, and among those not of normal weight is consistent with previous research.8–10 Greater medical and pharmacy costs with older age are most pronounced in the underweight and morbidly obese groups. Hence, weight management at older ages appears particularly important in terms of lowering medical and pharmacy costs.

Higher medication use in women than men was primarily because of drugs involving birth control, osteoporosis, thyroid disease and urinary tract infection. Prescription costs for vitamins/minerals were also noticeably higher in women than men. Family planning and prenatal care may explain the greater use of birth control medications and vitamins/minerals among women. Loss of oestrogen in women at older ages and female reproductive hormones may contribute to the higher level of osteoporosis and thyroid disease in women.29 30

Medication use was higher in those aged 60 years and older compared with those younger than 40, primarily because of diabetes, oedema, high blood pressure, high cholesterol (statins) and thyroid disease. Previous research has shown that the risk of these diseases increase with age.31–35 Medication use also noticeably increased with age for acid reflux, bowel/rectum, inflammation and stomach acid. This is consistent with older age tending to be associated with more gastrointestinal problems.36

Medication use was highest in those who were morbidly obese. We found positive associations between body weight and higher use of medications for treating acid reflux, fungus, bacterial infections, arthritis, asthma, cold, influenza, allergies, depression, diabetes, oedema, high blood pressure, muscle spasms, nausea/vomiting, pain, high cholesterol, stomach acid, thyroid and ulcers. Other studies have identified similar associations.21 24 25 27 Morbidly obese individuals were also more likely to be prescribed vitamins and minerals than normal weight individuals. We did not find an association between body weight and increased use of medication for the bowel/rectum, skin or urinary tract, which was counter to that found in other studies.21 37–39 We also assessed but did not find a significant association for medications used to treat anxiety, insomnia, convulsions or teeth and gums. The insignificant finding for anticonvulsants and teeth and gums may be because of insufficient power (ie, small numbers). Finally, we assessed the association between body weight and medications for birth control, herpes and osteoporosis, where significant negative associations were found. We are not aware of other studies that have looked at the association between body weight and medications used for cold, influenza, depression, oedema, birth control, herpes or osteoporosis.

Greater use of medication to treat acid reflux or stomach acid among individuals with higher BMI is consistent with previous research showing hospitalisation rates for reflux disease to be positively associated with BMI.40 41 Another study found that higher BMI was associated with increased gastro-oesophageal reflux in both normal and overweight individuals.42 Heavier body weight can add pressure to the stomach and diaphragm, thereby resulting in reflux. Further, increased use of medication for nausea/vomiting among individuals with higher BMI weight classifications is consistent with other research.43

The positive association between higher BMI and increased use of medication for ulcers is consistent with other research, particularly peptic (gastric and duodenal) ulcers.44 45 The mechanism to explain the association between obesity and peptic ulcer disease remains unclear. Obesity is also associated with Helicobacter pylori, which has been linked with gastric ulcers.46

Previous research has shown that overweight and obese individuals are at greater risk for infections.37–49 This is consistent with our findings that show increased use of antibiotics and medication for acne, cold/influenza/allergy and eye infections among obese individuals. However, it has been shown previously that antibiotics can also weaken the immune system,50 as well as lead to obesity.51 Some inflammatory diseases known to be associated with obesity in which we found a positive association between obesity and medication included influenza,52 53heart disease,54 diabetes,55 allergies,56–59 asthma,60oedema61–63 and arthritis.64–67 A compromised immune system may also trigger autoimmune diseases, including rheumatoid arthritis and thyroid disease,68 as indicated in the current study.

Overweight and obese individuals were more likely to receive cold, influenza or allergy medication. Obesity is associated with impaired immune response to influenza vaccination in humans.69 Because vaccination is less successful for obese individuals,70 71 a greater level of medication may be sought for treating cold, influenza and allergies.

Overweight and obese individuals received higher levels of pain medication. Research indicates that the nature of the relationship between higher BMI and pain is likely indirect.72 For example, greater body weight is associated with osteoarthritis, which, in turn, leads to pain.73 Being overweight or obese may result in greater risk for back pain, joint pain and muscle spasms.74 One study also found that obese individuals were more sensitive than those of normal weight to pressure pain.75

We found that higher BMI was associated with depression medication, as consistent with previous research.76–79 In one study, the age-adjusted level of depression among adults (ages 20 and older) in the USA was 43.2% for those with depression compared with 33.0% for those without depression.80 It may be that higher use of prescription medication for depression among those with greater BMI is partly because these people are more likely to experience other conditions related to depression, such as heart disease and diabetes.81–83

There was more use of vitamins/minerals among morbidly obese employees. Of the prescribed vitamins/minerals, only 8.0% involved vitamin B and 57.3% involved vitamin D. A previous study showed an association between low vitamin B12 and being obese.84 Another study found that the prevalence of vitamin D deficiency was 35% greater in obese individuals.85

Acne, antibiotic, cold/influenza/allergy and eye infection medications were prescribed more often for underweight individuals. This is consistent with underweight individuals having poorer nutrition and, consequently, a weakened immune system.86 For oedema, muscle spasms, pain and ulcers, medication use showed a J-shape relationship with BMI weight classification. Poor nutrition may also explain the higher levels of medication use among underweight individuals for these medications. Despite mean medical costs being similar for those who participated in wellness screening during the first year of the study, over the four academic years, participants in wellness screening ended up having significantly lower mean medical costs. However, pharmacy costs did not go down. It has been shown that wellness screening can cause the number and cost of pharmaceuticals to go up, at least initially, as the need for treatment is identified.87 Identified treatment needs can then, in turn, help prevent more costly health problems in the future. For example, medications used to treat high blood pressure can result in lowering the risk of diabetes, heart disease, stroke and kidney disease; treatment of insomnia can help lower the risk of irritability, depression or anxiety, difficulty in paying attention and accidents due to increased errors; treatment of high cholesterol with statins can help lower the risk of cardiovascular disease; treatment of oral infections can help reduce the risk of diabetes, cardiovascular disease and preterm birth and vitamins/minerals can help prevent a host of diseases (scurvy, rickets, anaemia, neural tube defects and pellagra). High blood pressure and statin medications were among the highest prescribed in our study.

A limitation of this study involves external validity (generalisability). Specifically, the study only considered those individuals who remained employed over all four academic years. These people were generally healthier and in the age range 40–59. The study also focused on those who completed wellness screening because they contained BMI information. These employees were more likely women and younger. In addition, the causal direction between medication use and BMI could not be determined. That is, some medications may have contributed to body mass, whereas others were in response to body mass. Finally, the current study did not have information on the use of vitamins or minerals obtained over the counter and small numbers made it impossible to evaluate the relationship between specific types of vitamins/minerals and sex, age and BMI.

Conclusion

Weight management at older ages, particularly in underweight and morbidly obese individuals, is most important for lowering medical and pharmacy costs. Medical costs decreased, possibly because of effective drug treatment and prevention. Pharmacy costs remained constant, possibly because screening identified a need for certain medications. Greater use of medication among women than men is primarily because of drugs involving birth control, osteoporosis, thyroid disease and urinary tract infection. Greater medication use in older age is primarily related to medications used to treat gastrointestinal problems. Medication use was positively associated with BMI for most of the conditions being treated, with exceptions involving birth control, herpes and osteoporosis. A J-shape relationship between BMI weight classification and medication use for acne, antibiotic, cold/influenza/allergy, eye infection, oedema, muscle spasms, pain and ulcers may be because of poorer nutrition in underweight individuals.

Supplementary Material

Reviewer comments
Author's manuscript

Footnotes

Contributors: RM conceived and designed the epidemiological study, contributed to acquisition of data, analysed and interpreted the data, and drafted the manuscript. RF interpreted the data, provided a literature review and revised the manuscript. Both authors critically revised the manuscript for important intellectual content. The manuscript has been read and approved by both authors.

Funding: The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

Competing interests: None declared.

Ethics approval: Study approval was obtained from the institutional review board at Brigham Young University (IRB E1 5259).

Provenance and peer review: Not commissioned; externally peer reviewed.

Data sharing statement: The data sets used and analysed in this study are available from the corresponding author on reasonable request.

Patient consent for publication: Employee data consisted of sex, age, and BMI, which was linked to medical and pharmacy claims data. No personal identifying information was retained in the linked data set.

References

  • 1. kff.org. 2016 Employer Health Benefits Survey. http://www.kff.org/health-costs/report/2016-employer-health-benefits-survey/ (Accessed 21 Feb 2018).
  • 2. Chen L, Hannon PA, Laing SS, et al. Perceived workplace health support is associated with employee productivity. Am J Health Promot 2015;29:139–46. 10.4278/ajhp.131216-QUAN-645 [DOI] [PubMed] [Google Scholar]
  • 3. Centers for Disease Control and Prevention. cdc.gov. http://www.cdc.gov/sustainability/worksitewellness/Worksite wellness (Accessed 18 Mar 2018).
  • 4. Michaels CN, Greene AM. Worksite wellness: increasing adoption of workplace health promotion programs. Health Promot Pract 2013;14:473–9. 10.1177/1524839913480800 [DOI] [PubMed] [Google Scholar]
  • 5. Witt LB, Olsen D, Ablah E. Motivating factors for small and midsized businesses to implement worksite health promotion. Health Promot Pract 2013;14:876–84. 10.1177/1524839912472504 [DOI] [PubMed] [Google Scholar]
  • 6. Niessen MA, Kraaijenhagen RA, Dijkgraaf MG, et al. Impact of a Web-based worksite health promotion program on absenteeism. J Occup Environ Med 2012;54:404–8. 10.1097/JOM.0b013e31824d2e43 [DOI] [PubMed] [Google Scholar]
  • 7. Kaspin LC, Gorman KM, Miller RM. Systematic review of employer-sponsored wellness strategies and their economic and health-related outcomes. Popul Health Manag 2013;16:14–21. 10.1089/pop.2012.0006 [DOI] [PubMed] [Google Scholar]
  • 8. Metge C, Black C, Peterson S, et al. The population’s use of pharmaceuticals. Med Care 1999;37(6 Suppl):JS42–JS59. 10.1097/00005650-199906001-00008 [DOI] [PubMed] [Google Scholar]
  • 9. Bertakis KD, Azari R, Helms LJ, et al. Gender differences in the utilization of health care services. J Fam Pract 2000;49:147–52. [PubMed] [Google Scholar]
  • 10. Arterburn DE, Maciejewski ML, Tsevat J. Impact of morbid obesity on medical expenditures in adults. Int J Obes 2005;29:334–9. 10.1038/sj.ijo.0802896 [DOI] [PubMed] [Google Scholar]
  • 11. Karmali KN, Lloyd-Jones DM, Berendsen MA, et al. Drugs for primary prevention of atherosclerotic cardiovascular disease: an overview of systematic reviews. JAMA Cardiol 2016;1:341–9. 10.1001/jamacardio.2016.0218 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Fretheim A, Odgaard-Jensen J, Brørs O, et al. Comparative effectiveness of antihypertensive medication for primary prevention of cardiovascular disease: systematic review and multiple treatments meta-analysis. BMC Med 2012;10:33 10.1186/1741-7015-10-33 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Taylor F, Huffman MD, Macedo AF, et al. Statins for the primary prevention of cardiovascular disease. Cochrane Database Syst Rev 2013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Czeizel AE. Birth defects are preventable. Int J Med Sci 2005;2:91–2. 10.7150/ijms.2.91 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Chan AT, Giovannucci EL. Primary prevention of colorectal cancer. Gastroenterology 2010;138:2029–43. 10.1053/j.gastro.2010.01.057 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. Mayo Clinic. Asthma. https://www.mayoclinic.org/diseases-conditions/asthma/diagnosis-treatment/drc-20369660 (Accessed 24 Feb 2018).
  • 17. Mayo Clinic. Arthritis. https://www.mayoclinic.org/diseases-conditions/arthritis/diagnosis-treatment/drc-20350777 (Accessed 24 Feb 2018).
  • 18. Preventive medicine reports paper. [Google Scholar]
  • 19. Thompson D, Edelsberg J, Colditz GA, et al. Lifetime health and economic consequences of obesity. Arch Intern Med 1999. 159:2177–83. 10.1001/archinte.159.18.2177 [DOI] [PubMed] [Google Scholar]
  • 20. Pi-Sunyer X. The medical risks of obesity. Postgrad Med 2009;121:21–33. 10.3810/pgm.2009.11.2074 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Kinge JM, Morris S. Association between obesity and prescribed medication use in England. Econ Hum Biol 2014;15:47–55. 10.1016/j.ehb.2014.06.002 [DOI] [PubMed] [Google Scholar]
  • 22. Narbro K, Agren G, Jonsson E, et al. Pharmaceutical costs in obese individuals: comparison with a randomly selected population sample and long-term changes after conventional and surgical treatment: the SOS intervention study. Arch Intern Med 2002;162:2061–9. [DOI] [PubMed] [Google Scholar]
  • 23. Finkelstein EA, Trogdon JG, Cohen JW, et al. Annual medical spending attributable to obesity: payer-and service-specific estimates. Health Aff 2009;28:w822–31. 10.1377/hlthaff.28.5.w822 [DOI] [PubMed] [Google Scholar]
  • 24. Randhawa AK, Parikh JS, Kuk JL. Trends in medication use by body mass index and age between 1988 and 2012 in the United States. PLoS One 2017;12:e0184089 10.1371/journal.pone.0184089 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Kit BK, Ogden CL, Flegal KM. Prescription medication use among normal weight, overweight, and obese adults, United States, 2005-2008. Ann Epidemiol 2012;22:112–9. 10.1016/j.annepidem.2011.10.010 [DOI] [PubMed] [Google Scholar]
  • 26. Jarrett B, Bloch GJ, Bennett D, et al. The influence of body mass index, age and gender on current illness: a cross-sectional study. Int J Obes 2010;34:429–36. 10.1038/ijo.2009.258 [DOI] [PubMed] [Google Scholar]
  • 27. Raebel MA, Malone DC, Conner DA, et al. Health services use and health care costs of obese and nonobese individuals. Arch Intern Med 2004;164:2135–40. 10.1001/archinte.164.19.2135 [DOI] [PubMed] [Google Scholar]
  • 28. Fuentes AV, Pineda MD, Venkata KCN. Comprehension of top 200 prescribed drugs in the us as a resource for pharmacy teaching, training and practice. Pharmacy 2018;6:43 10.3390/pharmacy6020043 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Alswat KA. Gender Disparities in Osteoporosis. J Clin Med Res 2017;9:382–7. 10.14740/jocmr2970w [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Li H, Li J. Thyroid disorders in women. Minerva Med 2015;106:109–14. [PubMed] [Google Scholar]
  • 31. Kirkman MS, Briscoe VJ, Clark N, et al. Diabetes in older adults. Diabetes Care 2012;35:2650–64. 10.2337/dc12-1801 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Trayes KP, Studdiford JS, Pickle S, et al. Edema: diagnosis and management. Am Fam Physician 2013;88:102–10. [PubMed] [Google Scholar]
  • 33. Mc Donald Posso AJ, Motta Borrel JA, Fontes F, et al. High blood pressure in Panama: prevalence, sociodemographic and biologic profile, treatment, and control (STROBE). Medicine 2014;93:e101 10.1097/MD.0000000000000101 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Ferrara A, Barrett-Connor E, Shan J. Total, LDL, and HDL cholesterol decrease with age in older men and women. The Rancho Bernardo Study 1984-1994. Circulation 1997;96:37–43. [DOI] [PubMed] [Google Scholar]
  • 35. Gesing A. The thyroid gland and the process of aging. Thyroid Res 2015;8(Suppl 1):A8 10.1186/1756-6614-8-S1-A8 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. D’Souza AL. Ageing and the gut. Postgrad Med J 2007;83:44–53. 10.1136/pgmj.2006.049361 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Ma Y, Yang Y, Wang F, et al. Obesity and risk of colorectal cancer: a systematic review of prospective studies. PLoS One 2013;8:e53916 10.1371/journal.pone.0053916 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Brown J, Wimpenny P, Maughan H. Skin problems in people with obesity. Nurs Stand 2004;18:38–42. 10.7748/ns2004.05.18.35.38.c3609 [DOI] [PubMed] [Google Scholar]
  • 39. Semins MJ, Shore AD, Makary MA, et al. The impact of obesity on urinary tract infection risk. Urology 2012;79:266–9. 10.1016/j.urology.2011.09.040 [DOI] [PubMed] [Google Scholar]
  • 40. Ruhl CE, Everhart JE. Overweight, but not high dietary fat intake, increases risk of gastroesophageal reflux disease hospitalization: the NHANES I Epidemiologic Followup Study. First National Health and Nutrition Examination Survey. Ann Epidemiol 1999;9:424–35. [DOI] [PubMed] [Google Scholar]
  • 41. Anggiansah R, Sweis R, Anggiansah A, et al. The effects of obesity on oesophageal function, acid exposure and the symptoms of gastro-oesophageal reflux disease. Aliment Pharmacol Ther 2013;37:555–63. 10.1111/apt.12208 [DOI] [PubMed] [Google Scholar]
  • 42. Jacobson BC, Somers SC, Fuchs CS, et al. Association between body mass index and gastroesophageal reflux symptoms in both normal weight and overweight women. N Engl J Med 2006;354:2340–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Talley NJ, Howell S, Poulton R. Obesity and chronic gastrointestinal tract symptoms in young adults: a birth cohort study. Am J Gastroenterol 2004;99:1807–14. 10.1111/j.1572-0241.2004.30388.x [DOI] [PubMed] [Google Scholar]
  • 44. Boylan MR, Khalili H, Huang ES, et al. Measures of adiposity are associated with increased risk of peptic ulcer. Clin Gastroenterol Hepatol 2014;12:1688–94. 10.1016/j.cgh.2014.03.021 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Kim J, Kim KH, Lee BJ. Association of peptic ulcer disease with obesity, nutritional components, and blood parameters in the Korean population. PLoS One 2017;12:e0183777 10.1371/journal.pone.0183777 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46. Xu MY, Liu L, Yuan BS, et al. Association of obesity with Helicobacter pylori infection: A retrospective study. World J Gastroenterol 2017;23:2750–6. 10.3748/wjg.v23.i15.2750 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Falagas ME, Kompoti M. Obesity and infection. Lancet Infect Dis 2006;6:438–46. 10.1016/S1473-3099(06)70523-0 [DOI] [PubMed] [Google Scholar]
  • 48. Huttunen R, Syrjänen J. Obesity and the risk and outcome of infection. Int J Obes 2013;37:333–40. 10.1038/ijo.2012.62 [DOI] [PubMed] [Google Scholar]
  • 49. Lübbeke A, Zingg M, Vu D, et al. Body mass and weight thresholds for increased prosthetic joint infection rates after primary total joint arthroplasty. Acta Orthop 2016;87:132–8. 10.3109/17453674.2015.1126157 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50. Yang JH, Bhargava P, McCloskey D, et al. Antibiotic-Induced Changes to the Host Metabolic Environment Inhibit Drug Efficacy and Alter Immune Function. Cell Host Microbe 2017;22:757–65. 10.1016/j.chom.2017.10.020 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51. Early G. Current Evidence regarding antibiotic exposure and childhood obesity: an integrative review. Ped Nurs 2017;43:169–74. [Google Scholar]
  • 52. Bandaru P, Rajkimar H, Napanveettil G. The impact of obesity on immune response to infection and vaccine: an insight into plausible mechanisms. Endocrinol Metab Synd 2013:2:2. [Google Scholar]
  • 53. Kwong JC, Campitelli MA, Rosella LC. Obesity and respiratory hospitalizations during influenza seasons in Ontario, Canada: a cohort study. Clin Infect Dis 2011;53:413–21. 10.1093/cid/cir442 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54. Wang Z, Nakayama T. Inflammation, a link between obesity and cardiovascular disease. Mediators Inflamm 2010;2010:1–17. 10.1155/2010/535918 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55. Bastard JP, Maachi M, Lagathu C, et al. Recent advances in the relationship between obesity, inflammation, and insulin resistance. Eur Cytokine Netw 2006;17:4–12. [PubMed] [Google Scholar]
  • 56. Ciprandi G, Pistorio A, Tosca M, et al. Body mass index, respiratory function and bronchial hyperreactivity in allergic rhinitis and asthma. Respir Med 2009;103:289–95. 10.1016/j.rmed.2008.08.008 [DOI] [PubMed] [Google Scholar]
  • 57. Gorgievska-Sukarovska B, Lipozencić J, Susac A. Obesity and allergic diseases. Acta Dermatovenerol Croat 2008;16:231–5. [PubMed] [Google Scholar]
  • 58. Shah R, Yang Y. Health and economic burden of obesity in elderly individuals with asthma in the United States. Popul Health Manag 2015;18:186–91. 10.1089/pop.2014.0089 [DOI] [PubMed] [Google Scholar]
  • 59. Guo Y, Moon JY, Laurie CC, et al. Genetic predisposition to obesity is associated with asthma in US Hispanics/Latinos: Results from the Hispanic Community Health Study/Study of Latinos. Allergy 2018;73:1547–50. 10.1111/all.13450 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60. Rodriguez D. Obesity and Asthma – What’s the Connection. https://www.everydayhealth.com/asthma/obesity-connection.aspx (Accessed 12 Apr 2018).
  • 61. Greene AK, Grant FD, Slavin SA, et al. Lower-extremity lymphedema and elevated body-mass index. N Engl J Med 2012;366:2136–7. 10.1056/NEJMc1201684 [DOI] [PubMed] [Google Scholar]
  • 62. Helyer LK, Varnic M, Le LW, et al. Obesity is a risk factor for developing postoperative lymphedema in breast cancer patients. Breast J 2010;16:48–54. 10.1111/j.1524-4741.2009.00855.x [DOI] [PubMed] [Google Scholar]
  • 63. Greene AK, Grant FD, Slavin SA, et al. Obesity-induced lymphedema: clinical and lymphoscintigraphic features. Plast Reconstr Surg 2015;135:1715–9. 10.1097/PRS.0000000000001271 [DOI] [PubMed] [Google Scholar]
  • 64. King LK, March L. Anandacoomarasamy A. Obesity & osteoarthritis. Indian J Med Res 2013;138:185–93. [PMC free article] [PubMed] [Google Scholar]
  • 65. Qin B, Yang M, Fu H, et al. Body mass index and the risk of rheumatoid arthritis: a systematic review and dose-response meta-analysis. Arthritis Res Ther 2015;17:86 10.1186/s13075-015-0601-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66. Feng J, Chen Q, Yu F, et al. Body Mass Index and Risk of Rheumatoid Arthritis: A Meta-Analysis of Observational Studies. Medicine 2016;95:e2859 10.1097/MD.0000000000002859 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67. Albrecht K, Richter A, Callhoff J, et al. Body mass index distribution in rheumatoid arthritis: a collaborative analysis from three large German rheumatoid arthritis databases. Arthritis Res Ther 2016;18:149 10.1186/s13075-016-1043-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68. Rodriguez D. How Your Immune System Worsens Arthritis. EverydayHealth.com. https://www.everydayhealth.com/arthritis/understanding/the-immune-system.aspx (Accessed 11 Apr 2018).
  • 69. Sheridan PA, Paich HA, Handy J, et al. Obesity is associated with impaired immune response to influenza vaccination in humans. Int J Obes 2012;36:1072–7. 10.1038/ijo.2011.208 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70. Painter SD, Ovsyannikova IG, Poland GA. The weight of obesity on the human immune response to vaccination. Vaccine 2015;33:4422–9. 10.1016/j.vaccine.2015.06.101 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71. Young KM, Gray CM, Bekker LG. Is obesity a risk factor for vaccine non-responsiveness? PLoS One 2013;8:e82779 10.1371/journal.pone.0082779 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72. Okifuji A, Hare BD. The association between chronic pain and obesity. J Pain Res 2015;8:399–408. 10.2147/JPR.S55598 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73. Erdmann J. Osteoarthritis and Obesity. www.arthritis.org. https://www.arthritis.org/living-with-arthritis/comorbidities/obesity-arthritis/osteoarthritis-and-obesity.php (Accessed April 11, 2018).
  • 74. American Obesity Association. Health effects of obesity. AOA Fact Sheets 2002. [Google Scholar]
  • 75. Tashani OA, Astita R, Sharp D, et al. Body mass index and distribution of body fat can influence sensory detection and pain sensitivity. Eur J Pain 2017;21:1186–96. 10.1002/ejp.1019 [DOI] [PubMed] [Google Scholar]
  • 76. Rathee N. Obesity and depression: Are they related? Indian J Health Well 2017;8:1472–5. [Google Scholar]
  • 77. Zhao G, Ford ES, Dhingra S, et al. Depression and anxiety among US adults: associations with body mass index. Int J Obes 2009;33:257–66. 10.1038/ijo.2008.268 [DOI] [PubMed] [Google Scholar]
  • 78. Onyike CU, Crum RM, Lee HB, et al. Is obesity associated with major depression? Results from the Third National Health and Nutrition Examination Survey. Am J Epidemiol 2003;158:1139–47. 10.1093/aje/kwg275 [DOI] [PubMed] [Google Scholar]
  • 79. Petry NM, Barry D, Pietrzak RH, et al. Overweight and obesity are associated with psychiatric disorders: results from the National Epidemiologic Survey on Alcohol and Related Conditions. Psychosom Med 2008;70:288–97. 10.1097/PSY.0b013e3181651651 [DOI] [PubMed] [Google Scholar]
  • 80. Pratt LA, Brody DJ. Depression and obesity in the U.S. adult household population, 2005-2010. NCHS Data Brief 2014;167. [PubMed] [Google Scholar]
  • 81. McElroy SL, Kotwal R, Malhotra S, et al. Are mood disorders and obesity related? A review for the mental health professional. J Clin Psychiatry 2004;65:634–51. 10.4088/JCP.v65n0507 [DOI] [PubMed] [Google Scholar]
  • 82. Ferraro KF, Su YP, Gretebeck RJ, et al. Body mass index and disability in adulthood: a 20-year panel study. Am J Public Health 2002;92:834–40. 10.2105/AJPH.92.5.834 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83. Katon W, Ciechanowski P. Impact of major depression on chronic medical illness. J Psychosom Res 2002;53:859–63. 10.1016/S0022-3999(02)00313-6 [DOI] [PubMed] [Google Scholar]
  • 84. Baltaci D, Kutlucan A, Turker Y, et al. Association of vitamin B12 with obesity, overweight, insulin resistance and metabolic syndrome, and body fat composition; primary care-based study. Med Glas 2013;10:203–10. [PubMed] [Google Scholar]
  • 85. Pereira-Santos M, Costa PR, Assis AM, et al. Obesity and vitamin D deficiency: a systematic review and meta-analysis. Obes Rev 2015;16:341–9. 10.1111/obr.12239 [DOI] [PubMed] [Google Scholar]
  • 86. Black RE, Morris SS, Bryce J. Where and why are 10 million children dying every year? Lancet 2003;361:2226–34. 10.1016/S0140-6736(03)13779-8 [DOI] [PubMed] [Google Scholar]
  • 87. Merrill RM, Telford CT. Pharmaceutical use according to participation in worksite wellness screening and health campaigns. Prev Med Rep 2018;12:158–63. 10.1016/j.pmedr.2018.09.008 [DOI] [PMC free article] [PubMed] [Google Scholar]

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