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1.
Int J Rheum Dis ; 19(9): 864-8, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27242025

ABSTRACT

OBJECTIVE: Limited data are available reporting the effect of proton pump inhibitor (PPI) use on changes in bone mineral density (BMD). The aim of this study was to investigate the relationship between PPI use and BMD. METHODS: The current cross-sectional study included 80 patients (31 male and 49 female) aged 20-45 years old without history of hip fracture with a follow-up of at least 2 years. The study was carried out in 40 daily PPI users and 40 PPI non-users. Femur and posterior-anterior spine BMD were quantified by dual-energy X-ray absorptiometry in all participants. The relationship between use of PPI and BMD was tested by multivariate linear regression analysis adjusted for age, sex, BMI and serum vitamin D levels. RESULTS: Our study demonstrated that mean femoral T-scores were significant between PPI and non-user groups (-0.44 ± 1.11 vs. +0.19 ± 0.95, P = 0.007). In addition, the frequency of femoral osteoporosis and osteopenia in the exposed group was significantly more in the control group (P = 0.04). Mean femoral Z-scores, lumbar spine T-score and lumbar spine Z-score were not statistically different between PPI and non-user groups. The linear regression analysis revealed that there was no association between PPI and non-users, and lumbar spine T-score. CONCLUSION: Overall, the results of this study showed that PPI use in subjects without risk factors of osteoporosis determined by the femoral T-score compared with the control group was associated with increased risk of developing osteoporosis and osteopenia in the femur bones.


Subject(s)
Bone Density/drug effects , Bone Diseases, Metabolic/chemically induced , Femur/drug effects , Osteoporosis/chemically induced , Proton Pump Inhibitors/adverse effects , Absorptiometry, Photon , Adult , Bone Diseases, Metabolic/diagnostic imaging , Chi-Square Distribution , Cross-Sectional Studies , Female , Femur/diagnostic imaging , Humans , Linear Models , Male , Middle Aged , Multivariate Analysis , Osteoporosis/diagnostic imaging , Risk Factors , Spine/diagnostic imaging , Spine/drug effects , Time Factors , Young Adult
2.
Liver Int ; 36(4): 563-71, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26503843

ABSTRACT

BACKGROUND & AIMS: This study was designed to determine the effects of the Dietary Approaches to Stop Hypertension (DASH) diet on weight loss and metabolic status in overweight patients with non-alcoholic fatty liver disease (NAFLD). METHODS: This randomized controlled clinical trial was done among 60 overweight and obese patients with NAFLD. Patients were randomly allocated to consume either the control (n = 30) or the DASH eating pattern (n = 30) for 8 weeks. Both diets were designed to be calorie-restricted. Both diets were consisted of 52-55% carbohydrates, 16-18% proteins and 30% total fats; however, the DASH diet was designed to be rich in fruits, vegetables, whole grains, and low-fat dairy products and low in saturated fats, cholesterol and refined grains. RESULTS: Adherence to the DASH eating pattern, compared to the control diet, weight (P = 0.006), BMI (P = 0.01), alanine aminotransferase (ALT) (P = 0.02), alkalin phosphatase (ALP) (P = 0.001), insulin levels (P = 0.01), homoeostasis model of assessment-estimated insulin resistance (HOMA-IR) (P = 0.01) significantly decreased and quantitative insulin sensitivity check index (QUICKI) (P = 0.004) significantly increased. Compared with the control diet, the DASH diet has resulted in significant reductions in serum triglycerides (P = 0.04) and total-/HDL-cholesterol ratio (P = 0.01). Finally, decreased concentrations of serum high-sensitivity C-reactive protein (hs-CRP) (P = 0.03), malondialdehyde (MDA) (P = 0.04), increased levels of nitric oxide (NO) (P = 0.01) and glutathione (GSH) (P = 0.009) were found in the DASH group compared with the control group. CONCLUSIONS: Consumption of DASH diet for 8 weeks among patients with NAFLD had beneficial effects on weight, BMI, ALT, ALP, triglycerides, markers of insulin metabolism, inflammatory markers, GSH and MDA.


Subject(s)
Caloric Restriction , Diet, Reducing , Energy Metabolism , Non-alcoholic Fatty Liver Disease/diet therapy , Obesity/diet therapy , Weight Loss , Adult , Aged , Biomarkers/blood , Blood Glucose/metabolism , Body Mass Index , Female , Health Status , Humans , Inflammation Mediators/blood , Insulin/blood , Insulin Resistance , Iran , Lipids/blood , Male , Middle Aged , Non-alcoholic Fatty Liver Disease/blood , Non-alcoholic Fatty Liver Disease/diagnosis , Non-alcoholic Fatty Liver Disease/physiopathology , Obesity/blood , Obesity/diagnosis , Obesity/physiopathology , Patient Compliance , Time Factors , Treatment Outcome
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