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Physical Activity and Prevalence of Rheumatoid Arthritis in Korean Adults with Prediabetes in the 2009-2013 National Health Cohort Study
Korean J Clin Pharm 2019;29(4):278-285
Published online December 31, 2019
© 2019 Korean College of Clinical Pharmacy.

Hye Yeon Sin*

College of Pharmacy, Duksung Women’s University, Seoul 03169, Republic of Korea
Correspondence to: Prof. Hye Yeon Sin, Pharm. D., Associate Professor at College of Pharmacy, Duksung Women’s University, Samyang-ro 144gil 33, Dobong-gu, Seoul 03169, Republic of Korea
Tel: +82 2 901 8739, Fax: +82 2 901 8386, E-mail: hyshin@duksung.ac.kr
Received September 20, 2019; Revised December 1, 2019; Accepted December 9, 2019.
This is an Open Access journal distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Background:

Rheumatoid arthritis is highly prevalent in overweight patients with type 2 diabetes mellitus and can be reduced by physical activity via altered proinflammatory parameters. However, the association between the frequency of physical activity and the prevalence of rheumatoid arthritis in prediabetic patients remains unclear and was evaluated in this study.

Methods:

Utilizing the Korean National Health Insurance Sharing Service database, 58,391 adults, who met the research criteria and underwent a general medical check-up between 2009 and 2013, were selected for this study. To analyze the data, a logistic regression with a proc survey logistic procedure was used.

Results:

The study revealed that the cumulative rheumatoid arthritis prevalence was lower in prediabetic patients compared to that in the control group (OR, 0.64; 95% CI, 0.483-0.840; p=0.001). More frequent physical activity (>3 days/week) was significantly associated with a reduced rheumatoid arthritis prevalence in both groups (OR, 0.28; 95% CI, 0.039-0.521; p=0.044 vs. OR, 0.15; 95% CI, 0.063-0.237; p=0.007). Additionally, a 3.8-fold higher risk of rheumatoid arthritis development was observed in prediabetic adults with less frequent baseline physical activity (≤2 days/week). Overall, in prediabetes, the prevalence of rheumatoid arthritis was associated with the frequency of physical activity and not with the fasting plasma glucose levels.

Conclusion:

More frequent physical activity is associated with a low risk of developing rheumatoid arthritis in prediabetic patients. Thus, further studies are needed to confirm the clinical outcomes of frequent physical activity in rheumatoid arthritis prevention and control.

Keywords : Rheumatoid arthritis, prediabetic patients, fasting plasma glucose, physical activity
Body

Prevalence of rheumatoid arthritis (RA) in patients with type2 diabetes mellitus (T2DM) and prediabetes was known to be higher than that of general population,1-5) further increasing its risk for disease prevalence among adults with advanced age,6-7) long disease duration,6-7) and poor glycemic control.1-2) RA is an autoimmune disease that causes chronic inflammation in the area surrounding musculoskeletal or synovial joints and connective tissues.1-3,7-8) T2DM is significantly associated with bone, cartilage, ligament, and tendon damage.2-3) RA development results from a multifactorial interaction of genes and the environment, including the abnormal response of anti-citrullinated protein antibodies (ACPAs) to antigens. These interactions result in synovial inflammation, bone, cartilage, and tissue damage, composed of pro-inflammatory cytokines. 4-5,8-9) Pro-inflammatory cytokines5,9)such as interferon- gamma (IFN-γ), interleukin (IL)-1ß, IL-2, IL-5, IL-7, IL-8, and TNF-α, granulocyte macrophage-colony stimulating factor (GM-CSF), are also known to be high in overweight patients with prediabetes.4,5-9)

With biological pharmacotherapies, modifiable behavior such as physical activity has been shown to induce the anti- inflammatory myokine IL-6,10) which induces the release of IL-1 inhibitor and IL-10, a natural inhibitor of IL-1β,11) resulting in decreased disease severity and inflammation in adults with RA, obesity, prediabetes and T2DM.11-12) Physical activity significantly improved the joint motility, strength and functional ability in patients with either prediabetes or RA via altered pro-inflammatory muscle cytokines13-14) and reduced the blood glucose levels, further lowering the risk for T2DM.15)

Unfortunately, 71% of adults with RA are unable to maintain normal physical activity,16-19) owing to arthritis related barriers to physical activity. Joint pain, joint stiffness and deformity reduced the engagement of patients with RA in physical activity.17,20)56.5% of adults with both RA and prediabetes are physically inactive.20)

According to a study by the Diabetes Prevention Program (DPP), physical activity and weight loss interventions can reduce the risk of diabetes by 58%.21-23) Physical activity and glycemic control may be beneficial in the inhibition of RA progression as well as in the reduction of its prevalence in patients with prediabetes.24) However, T. Yates study reported that intensive physical intervention or previous physical activity level did not significantly reduce 2-h post prandial or fasting blood glucose levels25) in adults with prediabetes and the expression of inflammatory markers14) in patients with either RA or prediabetes. Therefore, the association between the frequency of physical activity and prevalence of RA in adults with prediabetes is unclear. Thus, this study investigated whether the frequency of physical activity was associated with RA prevalence in Korean adults with prediabetes

Methods

Data sources

This study retrospectively evaluated a cohort of 264,978 adults, aged 50 to 79 years, using their medical records extracted from the centralized database of the Korean National Health Insurance Sharing Service (KNISS). Adults who met the research criteria and visited health institutions for general medical examination at least biannually in the regional areas of South Korea between January 01, 2009, and December 31, 2013, were included. Whereas subjects who were diagnosed with T1DM or T2DM, those no longer under follow-up, and those who had only one laboratory data parameter for FPG and self-questionnaire item for physical activity at baseline and during the biannual visits over the 5-year follow-up period were excluded. The data from the cohort database (DB) provided by KNISS included: individual qualification criteria DB, medical treatment DB, and health examination DB. With non-personally identifiable information only used for research, subjects were selected based on a table that was created using the database link, with person identification as a joint key according to the KNISS algorithm. Korean Classification of Disease (KCD) codes were used to identify the main sickness and sub sickness that were diagnosed by physicians. The Institutional Review Board (IRB: No. 2019-03-19-03) of Duksung Women’s University approved the research protocol with a nonhuman designation, and the study was conducted in accordance with the Declaration of Helsinki.

Definition

Medical conditions were defined using KCD codes, with T1DM/T2DM subjects identified using the code E10-E11.9. Prediabetes was defined as a fasting plasma glucose (FPG) level between 100 and 125 mg/dL and the absence of a T1DM/T2DM diagnosis. RA was identified using KCD codes as follows: RA (M05.0-M05.9), other RA (M06.0.-M06.0, M06.2-M06.3, M06.8-M06.9), and other chronic postrheumatic arthropathies (M12.0-M12.0, M12.3-M12.3). RA medications, NSAIDs, and other anti-rheumatic drugs were identified using the Health Insurance Review and Evaluation Center Pharmaceutical Standards Information code 100901ACH~217004ASY. Past medical history was identified as hypertension (HTN), heart disease (HD), and hyperlipidemia, whereas family history was identified as T2DM, HTN, and HD.

Identification of RA

To evaluate RA prevalence based on FPG level at the beginning of the study, subjects were divided into two subgroups: those with impaired FPG (100-125 mg/dL) and those with normal FPG (<100 mg/dL), using the American Association of Clinical Endocrinologists (AACE) clinical guidelines (2018). RA prevalence was defined as the development of confirmed RA or chronic postrheumatic arthropathy. Additionally, to evaluate RA prevalence based on physical activity level, subjects were divided into two subgroups: those who had physical activity ≥3 times/week for at least 20-30 min/day and those who had physical activity ≤2 times a week. In this study, the indicated RA prevalence was cumulative, given that it was difficult to distinguish new RA incidence in a particular year from the duplicated RA record that would appear in the following year in the KNISS.

Physical activity

Physical activity, which was defined as follows: walking for at least 30 min/day, lightly bicycling for at least 30 min/day, and jogging or aerobics for at least 20 min/day was assessed using a simple measurement number in the survey questionnaire, which was sub-classified into eight numbers based on the frequency of the three activity types. The eight numbers indicated the frequency of each physical activity type/week. Subjects were given a health-related questionnaire at physical examination; the subjects self-reported their daily number of activity/week in the questionnaire, and subjects who had at least 3 days of activity/week were included in the more frequent physical activity group. Those with less than 2 days of activity/week were included in the less frequent physical activity group.

Data analysis

The medical records of the patients were sorted and analyzed by a professional statistician. To assess patient’s baseline characteristics, continuous variables were analyzed using a proc univariate procedure and reported as mean (SD), whereas categorical variables were analyzed using proc survey freq and proc logistic procedures and reported as percentages. Based on stratified, clustered, and systematic sampling, Primary outcome of unadjusted RA prevalence was evaluated using a proc logistic procedure and a proc freq procedure; a logistic regression model was used for p values. Secondary outcome of risk of cumulative RA prevalence with regard to physical activity frequency was evaluated using a proc univariate procedure for mean and SD and a logistic regression for p value. Using logistic regression with a proc logistic procedure, the adjusted odds ratio of RA with regard to variables, including age, FPG, BMI, TG, LDL-C, and past medical history and family history, was performed to estimate potential confounding variables. A p-value <0.05 was considered statistically significant.

Results

Baseline characteristics

The baseline characteristics of prediabetic patients and patients without impaired fasting plasma glucose (IFG) were compared (Table 1). Of the 264,978 subjects in the KNISS database, 58,391 subjects were included and evaluated retrospectively. A total of 19,204 individuals were confirmed to have prediabetes, whereas 39,186 individuals were confirmed to be without IFG (control group). As shown in Fig. 1, over time, FPG levels were significantly higher in prediabetic RA patients than in the control group (p<0.001). A total of 301,294 individuals were excluded for the following reasons: 18,323 were T2DM patients, 19,129 discontinued follow-ups. 169,135 had missing FPG data and frequency of physical activity recorded at baseline and at bi-annual visits over the 5- year follow-up period. Regarding age, 69.0% adults in prediabetic and 72.8% adults in control group, respectively, were aged between 50 and 64 years. Family history of diabetes (p<0.001) and hypertension (p=0.011) were significantly higher in the prediabetes group compared with the control group. In addition, past medical history of hypertension (p=0.001) and dyslipidemia (p<0.001) were significantly higher in the prediabetes group than in the control group. Overall, chronic medical conditions were significantly higher in prediabetic patients than in the control group. The mean FPG level (p<0.001) was significantly higher in the prediabetes group than in the control group. Table 1 describes patients’ baseline characteristics.

Baseline characteristics

VariablesPrediabetes (n=19,204)Normoglycemia (n=39,186)p-value
Age, y mean (%)
 50-6413326 (69.0)28,525 (72.8)<.001
 65-795879 (31.0)10,661 (27.2)<.001
Gender, n (%)
 Male10256 (54.0)17146 (43.8)<.001
 Female8949 (46.0)22040 (56.2)<.001
Family history, n (%)
 Hypertension2295 (19.1)4171 (17.0)0.011
 Heart failure578 (5.8)1206 (4.9)0.059
 Diabetes1405 (12.1)2073 (8.5)<.001
Past medical history, n (%)
 Hypertension6524 (48.4)9676 (37.1)0.001
 Heart failure817 (6.0)1318 (5.1)<.001
 Dyslipidemia1261 (9.2)1964 (7.6)<.001
Physical activity, n (%)
 >3days/week3599 (18.7)7192 (18.4)0.072
Laboratory data, mean (±SD)
 Height (cm)161.8 (±8.7)159.5 (±8.5)<.001
 Weight (kg)63.7 (±10.0)60.9 (±9.6)<.001
 BMI (kg/m2)24.6 (±2.7)23.9 (±2.9)<.001
 SBP (mmHg)129 (±15.6)125 (±15.4)<.001
 DBP (mmHg)79 (±10.0)77 (±10.0)<.001
 FPG (mg/dL)108.3 (±7.6)86.5 (±7.8)<.001
 Scr (mg/dL)1.1 (±1.4)1.0 (±1.1)<.001
 Total cholesterol (mg/dL)204.2 (±39.2)200.5 (±36.7)<.001
 Triglyceride (mg/dL)150.2 (±95.0)131.7 (±81.1)<.001
 HDL-C (mg/dL))55.5 (±32.8)56.1 (±32.0)0.309
 LDL-C (mg/dL)121.0 (±42.1)119.9 (±39.5)0.001
 Hemoglobin (g/dL)13.9 (±1.4)13.6 (±1.4)<.001
 Medication, n (%)268 (2.8)1222 (3.1)0.066

Data are presented as mean (SD) for continuous variables and number (percentage) for categorical variables. Abbreviations: BMI, body mass index; SBP, systolic blood pressure; DBP, diastolic blood pressure; Scr, serum creatinine; HDL-C, high density lipoprotein cholesterol; LDL-C, low density lipoprotein cholesterol.


Fig. 1.

Change in FPG level between adults with prediabetes and normoglycemia over time FPG level was higher in prediabetes with RA than normoglycemia with RA over time



Prevalence of RA

RA prevalence was 66 (0.34%) (OR, 0.64; 95% CI, 0.483- 0.840; p=0.001) in the prediabetes group and 211 (0.54%) in the control group, indicating that the risk of RA development was not associated with FPG level (Table 2).

Unadjusted cumulative prevalence of rheumatic diseases between adults with prediabetes and control group

Prediabetes Total case=19,204 *Rheumatic disease n (%)§normoglycemia Total case=39,186 Rheumatic disease n (%)Unadjusted odds ratio (95% CI) p-value
66 (0.34)211 (0.54)0.64 (0.483-0.840) 0.001

Abbreviations: CI; confidence interval.

*Rheumatoid diseases were defined by KDC code of diagnosis by physicians.

Prediabetes was defined as fasting plasma glucose level of 100-125 mg/dL.

§Normoglycemia was defined as fasting plasma glucose level below 100 mg/dL.



Effect of frequency of physical activity on RA prevalence

The results showed that more frequent physical activity (≥3 days/week, ≥20-30 min/day) had a positive effect on cumulative RA prevalence in both the prediabetes (0.07%) and control (0.07%) groups (OR, 1.00; 95% CI, 0.561-2.064; p=0.825). Less frequent physical activity (up to 2 days/week) was found to be associated with increased RA prevalence in both groups (0.27% in the prediabetes vs. 0.47% in the control group, p<0.001) (Table 3).

Cumulative prevalence of *rheumatic diseases according to the amount of physical activity between prediabetes group and control group

Physical exerciseprediabetes Total=19205 n (%)§Control group Total=39186 n (%)OR (95% CI) p-value
≥3 times/week14 (0.07)26 (0.07)1.00 (0.561-2.064) 0.825
≤2 times/week52 (0.27)185 (0.47)0.58 (0.422-0.782) <0.001

Abbreviations: CI; confidence interval.

*Rheumatic diseases were defined as KDC code of diagnosis by physicians.

Prediabetes was defined as fasting plasma glucose level of 100-125 mg/dL.

5control group was defined as fasting plasma glucose level below 100 mg/dL.



Additionally, less frequent physical activity (up to 2 days/ week) was associated with a 3.8~6.7 fold increase in RA prevalence in both groups (0.07%, p=0.044 in the prediabetes group, and 0.07%, p=0.007 in the control group), compared with more frequent physical activity (0.27 and 0.47% in the prediabetes and control groups, respectively) (Table 4).

Cumulative prevalence of *rheumatic diseases according to the amount of physical activity between each group

Physical exercisePhysical exercise ≥3 times/week n (%)Physical exercise ≤2 times/week n (%)OR (95% CI) p-value
prediabetes14 (0.07)52 (0.27)0.28 (0.039-0.521) 0.044
§Control group26 (0.07)185 (0.47)0.15 (0.063-0.237) 0.007

Abbreviations: CI; confidence interval.

*Rheumatic diseases were defined as KDC code of diagnosis by physicians.

Prediabetes was defined as fasting plasma glucose level of 100-125 mg/dL.

§control group was defined as fasting plasma glucose level below 100 mg/dL.



The frequency of physical activity-adjusted risk of RA was 3.8 (95% CI, 1.601-6.199; p=0.044), which increased with less frequent physical activity in both groups. Overall, RA prevalence among Korean adults, according to the KNISS database, varied with frequency of physical activity. After adjusting for BMI, and TG and LDL-C levels and past medical history, family history, and less frequent physical activity, the analysis showed that less frequent physical activity, hypertriglyceridemia, overweight/obesity, and family history of heart disease were associated with increased risk of RA in prediabetes, only the association of less frequent physical activity was significant (Table 5).

Effect of variables on progression of rheumatic arthritis in patients with prediabetes or normoglycemia

Variables*RA and Prediabetes (n= 19,204)RA and § Normoglycemia (n=39,186)

Odds Ratio 95 % CI, p-valueOdds Ratio 95 % CI, p-value
Age (years, 5 years increments)1.05 (0.833-1.323) 0.6801.04 (0.877-1.243) 0.630
Physical exercise (<3 times/week)3.86 (1.601-6.199) 0.0446.71 (3.532-9.868) 0.007
BMI (≥23 kg/m2)1.65 (0.538-5.036) 0.3821.24 (0.834-1.854) 0.285
Past medical history Hypertension1.04 (0.403-2.695) 0.9331.05 (0.431-2.573) 0.911
Family history Cardiovascular disease2.44 (0.737-8.079) 0.1441.46 (0.639-3.358) 0.366
Triglyceride (≥200 mg/dL)1.95 (0.448-8.482) 0.3741.77 (0.756-4.150) 0.188
LDL_C (≥130 mg/dL)0.79 (0.383-1.648) 0.5360.70 (0.464-1.064) 0.095

Data are presented as mean (SD) for continuous variables and number (percentage) for categorical variables.

Abbreviations: BMI, body mass index; CI; confidence interval; DBP, diastolic blood pressure; HDL-C, high density lipoprotein cholesterol; LDL-C, low density lipoprotein cholesterol; SBP, systolic blood pressure; Scr, serum creatinine.

*Rheumatic arthritis was defined as KDC code of diagnosis by physicians.

Prediabetes was defined as fasting plasma glucose level of 100-125 mg/dL.

§Normoglycemia was defined as fasting plasma glucose level below 100 mg/dL.


Discussion

In this cohort observational study, the association between frequency of physical activity and RA prevalence in prediabetic adults was assessed. The results showed that the cumulative prevalence of RA was significantly lower in prediabetic subjects with frequent physical activity (≥3 days/ week). This cohort study highlights the importance of frequent physical activity in preventing the development of inflammatory RA in prediabetic adults. The prevalence of RA in the US reportedly ranges from 0.41 to 0.54%.26) In China and Japan, it is lower, but it varies with gender and age.27) In the present study, RA was observed in 0.07% of Korean prediabetic subjects with frequent physical activity (≥3 days/week for at least ~20-30 min/day), compared with those with less frequent physical activity. This finding suggests that the lower risk of RA development may be an evidence of the mechanism of previously observed outcomes.

Several previous studies have assessed the association between physical activity and chronic disease. In one study, the prevalence of physical inactivity and obesity among US adults with prediabetes and arthritis was found to be 56.5 and 50.1%, respectively, higher than that in adults without prediabetes and arthritis.20) Physical inactivity is reportedly associated with the risk of progression to chronic diseases including obesity, prediabetes, T2DM, coronary heart disease, and RA.15,21,28) Conversely, physical activity reduces pro- inflammatory markers by IL-6 production, hence inhibiting chronic disease development.24,30)It induces IL-10-mediated anti-inflammatory response and IL-1ß inhibition.23-24) This study confirmed the results of previous studies.

In accordance with the physical activity recommendations of the American Diabetes Association, most adults with T2DM should engage in moderate-to-vigorous intensity aerobic activity at least 3 days/week (150 min/week), with no more than 2 consecutive days without activity.21) Because activity-induced improvement in insulin activity (decreased rapidly) is dependent on the duration and intensity of previous activity, adults should participate in aerobic activity at least 3 days/ week with no more than 2 consecutive days without activity.20,31)

As the prevalence and incidence of diabetes increase worldwide,32) regular physical activity could play an important role in the reduction of the risk of developing of T2DM and RA in prediabetic adults.33) Additionally, US adults with metabolic syndromes are reportedly associated with a 2-fold risk of developing T2DM and CVD.19,34)Moreover, owing to several hypotheses, it is advisable to consider RA development in adults with obesity, as they might have metabolic syndrome (MS) and/or chronic inflammatory diseases.

The results of the Bianchi G. study showed that a high VO2max level was associated with both good health and morbidity prevention. It showed that a 2.5-fold higher VO2max variance existed in the sedentary population,35) attributed to phenotype-individualized variation of genes for responsiveness to aerobic activity and disease susceptibility. Pharmacologically, physical activity may interact with drug efficacy and organ functions.36) Additionally, the results of the Bianchi G study showed that physical inactivity, which is a risk factor of MS,37) as well as dyslipidemia, hypertension, hyperglycemia, and obesity, is associated with increased risk of T2DM.37,38)It also showed that physical inactivity is associated with reduced skeletal muscle blood flow, as well as reduced vascular endothelial nitric oxide synthase expression.19)

Between 2009 and 2013, the prevalence of diabetes and prediabetes among Korean adults aged >30 years was 5 million (14.4%) and 8.7 million (25.3%).40-41) RA prevalence among Korean adults aged ≥19 years was 2.0% in 2005.42) Additionally, the Origuchi T study reported a high RA incidence (4.3%) in adults with DM and prediabetes, but low (2.0%) incidence in adults with normal blood glucose levels aged ≥46 years in Japan.4) These studies showed a wide variation in RA prevalence, which can be attributed to the difference in their sample stratification and methods for estimating RA prevalence. The Origuchi T study4) collected data on subjects with prediabetes, including patients on DM drug treatment. Thus, the higher RA incidence reported may be due to subject selection bias. Additionally, the Hur NW. study42) surveyed only a major chronic disease associated with musculoskeletal diseases, individually interviewing different household members; however, patients with sub-sicknesses of musculoskeletal disease seem to be omitted from the subjects, making it difficult for the results to reflect the exact number of RA patients. Therefore, during studies, it is necessary to estimate RA prevalence by stratification of homogeneous populations. To avoid selection bias, omission bias, and interviewer bias, the present study included both main- sickness and sub-sickness codes for RA, excluded diabetic patients, and confirmed RA status in prediabetic Korean patients. Thus, the results reflect lower RA prevalence26) among prediabetic subjects, than that reported in previous studies.

This study had some strengths. Firstly, all the data regarding frequency of physical activity, in relation to RA outcomes, were derived from large population-based survey cohort data, and frequency of physical activity was estimated using a simple frequency measurement number in the survey questionnaire. Additionally, the collected physical activity data can be used to identify the exact frequency of physical activity and number of individuals involved. The additional benefits of using this survey questionnaire were that it minimized measurement error and the cost associated with collecting clinical data. However, it also had some limitations. Firstly, there might have been a response bias in the self-reporting of frequency of physical activity measurement,43) to impress management.45) Further, this study was designed to evaluate the association between RA and frequency of physical activity. Of the rheumatic conditions, neuropathic arthropathy, carpal tunnel syndrome, diffuse idiopathic skeletal hyperostosis, and tendinopathy were excluded. Thus, the RA outcomes in this study may not reflect the prevalence of other rheumatic conditions among prediabetic Korean adults.

Despite these limitations, this study supports the association that RA prevalence is lower in prediabetic adults with more frequent physical activity, compared with those with less frequent physical activity, and that lack of physical activity causes chronic diseases,39) including diabetes, RA, and prediabetes.

Conclusion

RA prevalence is associated with frequency of physical activity and not fasting plasma glucose level in prediabetes. Over time, a sedentary lifestyle affected the development of RA in both groups. Ph ysical activity plays an important role in the reduction of the risk of RA development in prediabetic Korean adults.

Acknowledgments

The author is grateful to Dr. Junsung Kang, from the department of Informational Statistics in Gang Neung-Wnoju National University, for his support in statistical analyses.

Source of Funding

This research was supported by the Duksung Women’s University Research Grant 2018, Seoul, Republic of Korea (grant number: 3000002969).

Conflicts of Interest

The author has no institutional interest or conflicts.

References
  1. A-Homood IA. Rheumatoid arthritis in patients with diabetes mellitus. Clin Rheumatol 2013;32:527-33.
    Pubmed CrossRef
  2. Burner TW, Rosenthal AK. Diabetes and rheumatoid arthritis. Current Opinion in Rheumatology 2009;21(1):50-4.
    Pubmed CrossRef
  3. Kim HR. Rheumatic Manifestations of Diabetes. J Korean Diabetes 2013;14(4):182-5.
    CrossRef
  4. Origuchi T, Yamaguchi S, Inoue A, et al. Increased incidence of pre- diabetes mellitus at a department of rheumatology:a retrospective study. Mod Rheumatol 2011;21:495-9.
    Pubmed CrossRef
  5. Ruscitti P, Cipriani P, Carubbi F, et al. The role of IL-1βin the bone loss during rheumatoid arthritis. Mediators Inflamm 2015;2015:1-10.
    Pubmed KoreaMed CrossRef
  6. Ursini F, Russo E, D'Angelo S, et al. Prevalence of undiagnosed diabetes in rheumatoid arthritis:a OGTT study. Medicine 2016;95(7):1-7.
    Pubmed KoreaMed CrossRef
  7. Ruscitti P, Ursini F, Cipriani P, et al. Poor clinical response in rheumatoid arthritis is the main risk factor for diabetes development in the short-term:A 1-year, single-centre, longitudinal study. PLoS ONE 2017;12(7):1-16.
    Pubmed KoreaMed CrossRef
  8. Arend WP. Cytokine imbalance in the pathogenesis of rheumatoid arthritis: the role of interleukin-1 receptor antagonist. Semin Arthritis Rheum 2001;30(suppl(2)):1-6.
    Pubmed CrossRef
  9. Lucas R, Parikh SJ, Sridhar S, et al. Cytokine profiling of young overweight and obese female African American adults with prediabetes. Cytokine 2013;64(1):310-5.
    Pubmed CrossRef
  10. Muñoz Cánoves P, Scheele C, Pedersen BK. Interleukin 6 myokine signaling in skeletal muscle:a double edged sword?. FEBS J 2013;280(17):4131-48.
    Pubmed KoreaMed CrossRef
  11. Steensberg A, Fischer CP, Keller C, et al. IL-6 enhances plasma IL- 1ra, IL-10, and cortisol in humans. Am J Physiol Endocrinol Metab 2003;285:E433-E7.
    Pubmed CrossRef
  12. Sharif K, Watad A, Bragazzi NL, et al. Physical activity and autoimmune diseases:Get moving and manage the disease. Autoimmunity Reviews 2018;17(1):53-72.
    Pubmed CrossRef
  13. Van den Ende CHM, Breedveld FC, le Cessie S, et al. Effect of intensive exercise on patients with active rheumatoid arthritis:a randomised clinical trial. Ann Rheum Dis 2000;59(8):615-21.
    Pubmed KoreaMed CrossRef
  14. Andonian BJ, Bartlett DB, Huebner JL, et al. Effect of high-intensity interval training on muscle remodeling in rheumatoid arthritis compared to prediabetes. Arthritis Ther 2018;20:2-9.
    Pubmed KoreaMed CrossRef
  15. Kraus WE, Yates T, Tuomilehto J, et al. Relationship between baseline physical activity assessed by pedometer count and new- onset diabetes in the NAVIGATOR trial. BMJ Open Diab Res Care 2018;6:1-7.
    Pubmed KoreaMed CrossRef
  16. Tierney M, Fraser A, Kennedy N. Physical activity in rheumatoid arthritis:a systematic review. J Phys Act Health 2012;9(7):1036-48.
    Pubmed CrossRef
  17. Sokka T, Hakkinen A, Kautiainen H, et al. Physical inactivity in patients with rheumatoid arthritis:data from twenty-one countries in a cross-sectional, international study. Arthritis Rheum 2008;59(1):42-50.
    Pubmed CrossRef
  18. Giacomelli R, Gorla R, Trotta F, et al. Quality of life and unmet needs in patients with inflammatory arthropathies:results from the multicentre, observational RAPSODIA study. Rheumatology (Oxford) 2015;54(5):792-7.
    Pubmed CrossRef
  19. Lange E, Palstam A, Gjertsson I, et al. Aspects of activity with person-centred guidance influencing the transition to independent activity:a qualitative interview study among older adults with rheumatoid arthritis. Eur Rev Aging Phys Act 2019;16(4):1-12.
    Pubmed KoreaMed CrossRef
  20. Sandoval-Rosario M, Nayeri BM, Rascon A, et al. Prevalence of Arthritis Among Adults with Prediabetes and Arthritis-Specific Barriers to Important Interventions for Prediabetes—United States. MMWR Array;67(44):1238-41.
    Pubmed KoreaMed CrossRef
  21. American Diabetes Association Standards of Medical Care in Diabetes-2019 A bridged for Primary Care Providers. Diabetes Care 2018;42 Suppl:S1-S194.
    Pubmed CrossRef
  22. Kim KS, Park SW. Activity and T2DM:ACSM and ADA Joint Position Statement. J Korean Diabetes 2012;13:61-8.
    CrossRef
  23. Kucharski D, Lange E, Ross AB, et al. Moderate-to-high intensity activity with person-centered guidance influences fatigue in older adults with rheumatoid arthritis. Rheumatol Int 2019;39(9):1585-94.
    Pubmed CrossRef
  24. Booth FW, Robert CKs, Laye MJ. Lack of activity is a major cause of chronic diseases. Compr Physiol 2012;2(2):1143-211.
    Pubmed KoreaMed CrossRef
  25. Yates T, Davies MJ, Haffner SM, et al. Physical activity as a determinant of fasting and 2-h post-challenge glucose:a prospective cohort analysis of the NAVIGATOR trial. Diabet Med 2015;32:1090-6.
    Pubmed CrossRef
  26. Hunter TM, Boytsov NN, Zhang X, et al. Prevalence of rheumatoid arthritis in the United States adult population in healthcare claims databases 2004-2014. Rheumatol Int 2017;37:1551-7.
    Pubmed CrossRef
  27. Silman AJ, Pearson JE. Epidemiology and genetics of rheumatoid arthritis. Arthritis Res 2002;4(suppl 3):S265-S72.
    Pubmed KoreaMed CrossRef
  28. Rutledge GE, Lane K, Merlo C, et al. CooRAinated Approaches to Strengthen State and Local Public Health Actions to Prevent Obesity, Diabetes, and Heart Disease and Stroke. Prev Chronic Dis 2018;25(15):1-7.
    Pubmed KoreaMed CrossRef
  29. Steensberg A, Keller C, Starkie RL, et al. IL-6 and TNF-alpha expression in, and release from, contracting human skeletal muscle. Am J Physiol Endocrinol Metab 2002;283:E1272-8.
    Pubmed CrossRef
  30. Krick S, Helton ES, Hutcheson SB, et al. FGF23 Induction of O- Linked N-Acetylglucosamine Regulates IL-6 Secretion in Human Bronchial Epithelial Cells. Front Endocrinol 2018;9:1-10.
    Pubmed KoreaMed CrossRef
  31. Colberg SR, Sigal RJ, Fernhall B, et al. American College of Sports Medicine;American Diabetes Association Activity and type 2 diabetes:the American College of Sports Medicine and the American Diabetes Association:joint position statement. Diabetes Care 2010;33:e147-67.
    Pubmed KoreaMed CrossRef
  32. Narayan KM, Boyle JP, Thompson TJ, et al. Lifetime risk for diabetes mellitus in the United States. JAMA 2003;290:1884-90.
    Pubmed CrossRef
  33. Jeon CY, Lokken RP, Hu FB, et al. Physical activity of moderate intensity and risk of type 2 diabetes:a systematic review. Diabetes Care 2007;30:744-52.
    Pubmed CrossRef
  34. Alberti KG, Eckel RH, Grundy SM, et al. Harmonizing the metabolic syndrome:a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention;National Heart, Lung, and Blood Institute;American Heart Association;World Heart Federation;International Atherosclerosis Society;and International Association for the Study of Obesity. Circulation 2009;120:1640-5.
    Pubmed CrossRef
  35. Bouchara C, An P, Rice T, et al. Familial aggregation of VO(2max) response to activity training:results from the HERITAGE Family Study. J Appl Physiol 1999;87:1003-8.
    Pubmed CrossRef
  36. Cocco G, Pandolfi S. Physical activity with weight reduction lowers blood pressure and improves abnormal left ventricular relaxation in pharmacologically treated hypertensive patients. J Clin Hypertens (Greenwich) 2011;13:23-9.
    Pubmed CrossRef
  37. Bianchi G, Rossi V, Muscari A, et al. Physical activity is negatively associated with the metabolic syndrome in the elderly. QJM 2008;101:713-21.
    Pubmed CrossRef
  38. Fora ES, Kohl HW, Mokdad AH, et al. Sedentary behavior, physical activity, and the metabolic syndrome among U.S. adults. Obes Res 2005;13:608-14.
    Pubmed CrossRef
  39. Booth FW, Roberts CK, Laye MJ. Lack of activity is a major cause of chronic diseases. Compr Physiol 2012;2(2):1143-211.
    Pubmed KoreaMed CrossRef
  40. Kwun HS, Kim WH, Lee DY, et al. Current status and Need for a Korean Diabetes Prevention Study. Public Health Wkly Rep 2015;8:746-53.
  41. Song SO, Song YD, Kim DO et al, Research report:National prevalence of diabetes and characteristic during 10 years based on National Health Insurance Service data. National Health Insurance Service Ilsan Hospital Research 2014-20-009. Gyunggi-do, South Korea: Kyungsung Munwhasa; 2014 p. 1-98.
  42. Hur NW, Choi CB, Uhm WS, et al. The Prevalence and Trend of Arthritis in Korea:Results from Korea National Health and Nutrition Examination Surveys. J Korean Rheum Assoc 2008;15(1):11-26.
    CrossRef
  43. Brenner PS, DeLamater J. Lies, Damned Lies, and Survey Self- Reports?Identity as a Cause of Measurement Bias. Soc Psychol Q 2016;79(4):333-54.
    Pubmed KoreaMed CrossRef


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  • Duksung Women’s University
     
      3000002969