Al-Balqa Applied University, Al-Salt, Jordan.
Materials and Methods: A cross-sectional study was conducted on 359 Jordanian patients aged more than 18 years old, using atorvastatin 20 mg/day for at least 6 months and attending the diabetic and endocrine clinics at King Abdullah University Hospital.Dietary and life-style behaviors were assessed and compared among diabetic and non-diabetic patients.Descriptive statistics, Chi-square, student t-test and correlations were performed along with binary logistic regression analysis to examine collectively the association between diabetes and the significant risk factors identified from the univariate analysis.
Results: Non-diabetic patients were significantly (P< 0.05) younger, follow low calorie weight reducing diet, loss more weight after diet, eating snacks consist of (artificial juice, ice creams, sweets, chocolates and biscuits, taking supplements and drink amount of alcohol more than the diabetic patients. Female patients (p< 0.001; OR=3.15) eating (sweets, chocolates and biscuits) (p< 0.05; OR=0.53) and having chronic diseases (p< 0.001; OR=10.27) were more likely to develop diabetes.
Conclusions and Implications: Dietary and life-style behaviors did not differ significantly among diabetic and non-diabetic atorvastatin users. Diet and physical activity life-styles remain essentially unchanged for many patients after using atorvastatin. Involving patients in preventive programs promotes the successful adoption of healthy lifestyles.
Keywords: Diabetes; Atorvastatin; Diet; Life-Style; Behavior
All over the world, diabetes is one of the rapidly increasing metabolic disorder and an important public health issue. Recently, the International Diabetes Federation (IDF) in 2013, estimated that the number of diabetic adults in the world will increase from 382 million in 2013 to 592 million in less than 25 years[1].Jordan, like the rest of the world, is experiencing a remarkable increase over the past 10 years in the prevalence of diabetes, and has been reported to be 14.9 % and 12.5 % in men and women, respectively [2].
Several studies have reported that type 2 diabetes can efficiently prevented through a healthy life-style [3,4] such as maintaining a normal body weight [3], being physically active [5], cessation from smoking [6], and eating a healthy diet [7]. Moreover, the moderation in alcohol consumption has been associated with lowering the risk of type 2 diabetes compared with non-alcoholic or with excessive consumption [8,9]. Thus, moderate alcohol consumption could be considered as a favorable behavioral life-style factor that decreases the risk of type 2 diabetes [10].
The professional diabetes management is based on the balance between healthy eating, physical exercise and medication [11]. However, the problem is most of diabetic patients have little knowledge in determining the recommended quality and quantity of food they should eat to control their blood glucose level. Patient choices in food consumption were based on diabetes nutrition education which concentrates on food intake with low fat, low sodium and high dietary fibers [12].
Evidence suggests that changing of the lifestyle can enhance the effect of statins in lowering cholesterol levels [13]. Although, the lifestyle behaviors of statin users do not differ from non-users [14]. Therefore, emphasis on the importance of healthy lifestyles and on the role of health professionals in providing their patients with health education, promotion of healthy lifestyle and supporting for changing their behavior is an increasing need [15].
Despite of these evidences, previous studies concentrate on healthy life-style behaviors among diabetic patients regardless of the medications prescribed. Therefore, this study objective was to assess and compare the dietary and life-style behaviors among the diabetic and non-diabetic atorvastatin users.
The exclusion criteria included: (1) patients aged less than 18 years (2) attending other clinics at KAUH (3) have normal lipid profile (4) using other statins (4) and using atorvastatin for less than 6 months.
The frequencies of the study participants categorical variables according to dietary and life- style behavior among the 359 patients were also shown in (Table 1); around 33% of the study sample were playing sports on regular basis, 23.4% were smokers, 1.1% were alcoholic, 90.8% were coffee drinkers, 11.7% were follow a weight reducing diet, 71.9% were always eating breakfast, 84.4% were eating snacks, 32.9% were fast food eaters, 22.6% eating more than one type of fast food, 50.4% were eating food rich in cholesterol, 98.6% were using margarine and/or vegetable oils in preparing their food, 93.8% of them were using olive oil in their diet and 44.3% were taking supplements.
Comparing the frequencies of dietary and life-style behavioral variables among the diabetic and non-diabetic patients, results showed that non-diabetic patients were statistically and significantly (p< 0.05) have higher frequency of smoking (p=0.003), following low calorie weight reducing diet (p=0.01), eating snacks consist of artificial juice and ice creams (p=0.04), eating snacks consist of sweets, chocolates and biscuits (p=0.003) as well as taking supplements (p=0.05) more than the diabetic patients (Table 2).
Variable |
Mean + S.E.M |
Minimum |
Maximum |
Age (year) |
62.88+0.60 |
31.0 |
89.0 |
Weight before using atorvastatin (kg) |
80.30+0.70 |
7.0 |
129.0 |
Weight after using atorvastatin (kg) |
84.51+2.47 |
47.0 |
122.0 |
Sport time (min/day) |
43.54+2.65 |
0.0 |
180.0 |
Number of cigarettes smoked/day |
23.49+1.50 |
0.0 |
60.0 |
Alcohol quantity (cup/ day) |
2.25+0.25 |
2.0 |
3.0 |
Soft drinks (cup/day) |
1.33+0.06 |
0.25 |
6.0 |
Coffee quantity (cup/day) |
2.62+0.10 |
0.5 |
14.0 |
Milk quantity (cup/day) |
1.45+0.04 |
0.0 |
8.0 |
Weight loss due to diet (kg) |
3.64+0.67 |
0.0 |
20.0 |
|
Frequency (n) |
% |
|
Play sports on a Regular Basis |
118 |
32.9 |
|
Daily light sport |
112 |
95.0 |
|
Sport type (walking or running) |
112 |
95.0 |
|
Smoking |
84 |
23.4 |
|
Drinking alcohol |
4 |
1.1 |
|
Drinking soft drinks |
166 |
46.2 |
|
Drinking soft drinks daily |
31 |
18.7 |
|
Drinking coffee |
326 |
90.8 |
|
Drinking coffee daily |
260 |
79.8 |
|
Follow weight reducing diet |
42 |
11.7 |
|
Low calorie weight reducing diet |
32 |
76.2 |
|
Eating meals on a regular basis |
249 |
69.4 |
|
Eating three meals per day |
132 |
36.8 |
|
Always eating breakfast |
258 |
71.9 |
|
Eating snacks |
303 |
84.4 |
|
Eating two snacks per day |
111 |
36.6 |
|
Drinking milk |
322 |
89.7 |
|
Drinking milk daily |
219 |
68.0 |
|
Eating sea food |
278 |
77.4 |
|
Eat fish or sea food monthly |
176 |
49.0 |
|
Eating fast food |
118 |
32.9 |
|
Eating fast food daily |
14 |
11.9 |
|
Eating hamburger, fried chicken and pizza |
81 |
68.6 |
|
Eating foods rich in cholesterol |
181 |
50.4 |
|
Eating vegetables and whole grains |
238 |
66.3 |
|
Food allergy |
18 |
5.0 |
|
Using margarine and/or vegetable oils in food preparation |
354 |
98.6 |
|
Using olive oil |
332 |
93.8 |
|
Using corn oil |
264 |
74.6 |
|
Using palm oil |
12 |
3.4 |
|
Using other fats and oils |
45 |
12.7 |
|
Taking supplements |
159 |
44.3 |
|
Taking omega-3 |
62 |
39.0 |
|
Taking multivitamins |
75 |
47.2 |
|
Taking vitamin D |
77 |
48.4 |
|
Taking other supplements |
54 |
34.0 |
|
Variable |
DM (n=247) |
NDM (n=112) |
P-Value |
Mean + S.E.M |
Mean + S.E.M |
||
Age (year) |
63.67+0.68 |
61.13+1.16 |
.04* |
Weight before using atorvastatin (kg) |
80.55+0.79 |
79.75+1.42 |
.60 |
Weight after using atorvastatin (kg) |
85.76+3.54 |
81.75+1.25 |
.45 |
Sport time (min/day) |
43.99+3.43 |
42.56+3.94 |
.80 |
Number of cigarettes smoked/day |
23.20+2.11 |
23.85+2.15 |
.83 |
Alcohol quantity (cup/ day) |
2.00+0.00 |
3.00+0.00 |
<.001* |
Soft drinks (cup/day) |
1.32+0.07 |
1.35+0.10 |
.81 |
Coffee quantity (cup/day) |
2.51+0.13 |
2.86+0.18 |
.12 |
Milk quantity (cup/day) |
1.43+0.04 |
1.51+0.10 |
.40 |
Weight loss due to diet (kg) |
2.52+0.29 |
7.00+2.25 |
.002* |
|
n (%) |
n (%) |
(χ²) |
Play sports on a Regular Basis |
80 (32.4) |
38 (34.0) |
.43 |
Smoking |
47 (19.0) |
37 (33.0) |
.003* |
Drinking alcohol |
3 (1.2) |
1 (0.9) |
.63 |
Drinking soft drinks |
107 (43.3) |
59 (52.7) |
.07 |
Drinking coffee |
227 (91.9) |
99 (88.4) |
.20 |
Follow weight reducing diet |
28 (11.3) |
13 (11.6) |
.54 |
Low calorie weight reducing diet |
19 (7.7) |
13 (11.6) |
.01* |
Eating meals on a regular basis |
177 (71.7) |
72 (64.3) |
.10 |
Always eating breakfast |
177 (71.7) |
81 (72.3) |
.50 |
Eating snacks |
210 (85.0) |
93 (83.0) |
.37 |
Eating snacks (fruits and fresh juice) |
221 (89.5) |
99 (88.4) |
.40 |
Eating snacks (artificial juice and ice creams) |
17 (6.9) |
15 (13.4) |
.04* |
Eating snacks (sweets, chocolates and biscuits) |
47 (19.0) |
37 (33.0) |
.003* |
Eating snacks (salty crackers) |
26 (10.5) |
14 (12.5) |
.36 |
Drinking milk |
220 (89.1) |
102 (91.1) |
.35 |
Eating sea food |
189 (76.5) |
90 (80.4) |
.25 |
Eating fast food |
76 (30.8) |
42 (37.5) |
.13 |
Eating hamburger, fried chicken and pizza |
20 (8.1) |
39 (34.8) |
.50 |
Eating foods rich in cholesterol |
123 (49.8) |
59 (52.7) |
.35 |
Eating vegetables and whole grains |
159 (64.4) |
79 (70.5) |
.15 |
Food allergy |
15 (6.1) |
3 (2.7) |
.13 |
Using margarine and/or vegetable oils in food preparation |
243 (98.4) |
111 (99.1) |
.50 |
Using olive oil |
227 (91.9) |
105 (93.8) |
.35 |
Using corn oil |
176 (71.3) |
88 (78.6) |
.10 |
Using palm oil |
9 (3.6) |
3 (2.7) |
.45 |
Using other fats and oils |
32 (12.9) |
13 (11.6) |
.43 |
Taking supplements |
102 (41.3) |
57 (50.9) |
.05* |
Taking omega-3 |
41 (16.6) |
21 (18.8) |
.36 |
Taking multivitamins |
49 (19.8) |
26 (23.2) |
.28 |
Taking vitamin D |
49 (19.8) |
29 (25.9) |
.13 |
Taking other supplements |
35 (14.2) |
19 (17.0) |
.30 |
* P- value < 0.05 is statistically significant.
Recently, similar results were reported in a United Kingdome population study, which found that the initiation of statin prescription was not associated with adoption of healthy diet or physical activity behaviors for most patients. However, approximately one third of the sample improved their diet with the first time of statin prescription, whilst, at 1 month and 4 months later approximately 40 % continued to consume higher levels of fat than advised, 55 % consumed low levels of fiber and over 80 % were insufficiently active for health benefits [16].It has been reported that moderate alcohol consumption does not have major detrimental effects on long-term blood glucose control in people with diabetes. Risks associated with alcohol consumption include hypoglycemia (particularly for those using insulin therapies), weight gain, and hyperglycemia (for those consuming excessive amounts) [17,18].This could be explained by the significant low alcohol consumption among the diabetic compared with non-diabetic patients in this study.
Vitamins or minerals supplementation for diabetic patients without reporting deficiencies has no clear evidence.17Metformin is associated with vitamin B12 deficiency as reported recently, thus, it was suggested that vitamin B12 levels should be tested periodically for metformin treated patients [19]. Routine supplementation with vitamins E and D or other micronutrients
Variable |
b |
S.E. |
P-Value |
OR |
95% C.I for OR |
|
Lower |
Upper |
|||||
Eating snacks (sweets, chocolates and biscuits) |
-0.63 |
0.32 |
.04* |
0.53 |
0.29 |
0.99 |
Age |
0.01 |
0.01 |
.44 |
1.01 |
0.98 |
1.04 |
Gender (female) |
1.14 |
0.28 |
<.001* |
3.15 |
1.83 |
5.41 |
Hypertension |
-0.24 |
0.29 |
.39 |
0.78 |
0.44 |
1.38 |
Presence of chronic diseases |
2.33 |
0.42 |
<.001* |
10.27 |
4.55 |
23.18 |
Body weight |
0.01 |
0.01 |
.11 |
1.02 |
0.99 |
1.04 |
Play sports on regular basis |
0.26 |
0.30 |
.37 |
1.30 |
0.73 |
2.33 |
Drinking soft drinks |
-0.12 |
0.30 |
.68 |
0.89 |
0.50 |
1.58 |
Follow weight reducing diet |
0.20 |
0.43 |
.64 |
1.22 |
0.53 |
2.83 |
Drinking coffee |
0.67 |
0.43 |
.11 |
1.95 |
0.85 |
4.50 |
Eating breakfast |
-0.01 |
0.19 |
.95 |
0.99 |
0.68 |
1.44 |
Eating fast food |
-0.02 |
0.33 |
.95 |
0.98 |
0.52 |
1.88 |
Constant |
-3.96 |
1.38 |
.004 |
0.02 |
|
|
2- b: Regression coefficient.
3- S.E.: Standard error of the regression coefficient. 4- CI: Confidence Interval.
5- *p-value < 0.05 is statistically significant..
Recent data show tobacco use is higher among adults with chronic conditions [21]. Other studies of individuals with diabetes consistently demonstrate that smokers and passive smokers have a higher risk of CVD, premature death, and micro vascular complications, and smoking may have a role in the development of type 2 diabetes [22]. A study on smokers newly diagnosed with type 2 diabetes found that smoking cessation was associated with amelioration of metabolic parameters and reduced blood pressure and albuminuria at 1 year [23].These results were consistence with this epidemiological study. Physical activity including all exercises is an important part of the diabetes management plan. Exercise has been shown to improve blood glucose control, reduce cardiovascular risk factors, contribute to weight loss, and improve well-being. It has been recommended that all adults, and particularly those with type 2 diabetes, should decrease the time spent in daily sedentary behavior and prolonged sitting should be interrupted every 30 min for blood glucose benefits [24].Unfortunately, around two third of this study participants were physically inactive and the time spend during exercise for physically active ones was relatively low compared with the recommended time.
Body weight management is an important part of diabetes care plan for overweight and obese people with diabetes. Therefore, life-style intervention programs should be intensive and have frequent follow-up to achieve significant weight reductions and improve clinical parameters such as lipid profile [24].Many studies found strong and consistent evidence that modest persistent weight loss can delay the progression from pre diabetes to type 2 diabetes [25,26] and is beneficial to the management of type 2 diabetes. Modest weight loss (reduction of 5% of initial body weight), has been shown to improve glycemic control and to reduce the need for glucose-lowering medications [27,28]. For many obese individuals, with type 2 diabetes, weight Loss >5%is needed to produce beneficial outcomes in glycemic control, lipids, and blood pressure. Whilst sustained weight loss of >7% is the optimal [29].The diets used in intensive lifestyle management for weight loss should emphasis on nutrient dense foods, such as whole grains, vegetables, fruits, legumes, low-fat dairy, lean meats, nuts, and seeds, as well as on achieving the desired energy deficit [30,32]. In this study, small portion of the diabetic patients were using the low-calorie weight reducing diet and the amount of weight loss due to diet was relatively low compared with non-diabetic which disagree with body weight management recommendations. Although, diabetic patients were less eaters of snacks consist of artificial juice, ice cream, sweets, chocolates and biscuits and more than the half of them eat vegetables and whole grains seeds but around 50% of them eat foods rich in cholesterol. These results along with the low rate of physical activity could explain the small reduction in body weight among the diabetic group compared with previous studies.
A meta-analysis in Sub-Saharan Africa demonstrated that, men in Eastern, Middle and Southern Africa had a significantly higher prevalence of impaired fasting glycaemia and a lower prevalence of impaired glucose tolerance compared with the women. Although, the overall prevalence of diabetes mellitus did not significantly differ by sex but the prevalence of diabetes mellitus was found to be lower or higher in women than in men when examined by African sub-region [33]. Although, diabetes is more prevalent in males than in females [34], in this study, women were more likely to have diabetes. Controversial results could be attributed to the diversity in body composition such as low muscle mass compared to fat mass, endocrine imbalances, psychological stress and genetics [34].
Compared with individuals without diabetes, patients with type 2 diabetes mellitus have higher risk of cardiovascular morbidity and mortality. Most of this higher risk is associated with enhanced prevalence of well-known risk factors such as hypertension, dyslipidemia and obesity in these patients [35].Hypertension is present in more than 60% of type 2 diabetes patients [36].Hypertension and diabetes mellitus are multilateral risk factors for cardiovascular diseases. Diabetes doubles the cardiovascular risk in men and more than triples the risk in women, hypertension quadruple cardiovascular risk in diabetic patients [37]. Similarly, in this study the risk of diabetes increases with the presence of chronic diseases as well as diabetes increases the risk of other chronic diseases such as hypertension and cardiovascular diseases.
Finally, the study had limitations including the cross-sectional design, the small sample size and lacking dietary, biochemical and clinical assessments. Therefore, prospective longitudinal follow up study with large cohort including healthy population assessed biochemically, clinically and dietary using 24-hour recall or food frequency questionnaire to determine the total calories, macro and micronutrients consumed would help confirm these results.
The author declares no conflict of interest. This research was not funded by any organization and it was approved by the KAUH Institutional Research Board (IRB) committee.
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