Abstract
Background and Objective: The incidence of type 1 diabetes is increasing. Osteoporosis has become an alarming health problem throughout the entire world. The aim of this study were to estimate the epidemiology of osteoporosisamong Saudi patients with T1DM, living in the western province, attending the diabetes centre at King Fahd Armed Forces Hospital, Jeddah, KSA.
Methods: Eligible patients were older than 12 years old, had T1DM . All patients were recruited from the population of the Diabetic Centre at King Fahad Armed Forces Hospital. Eligible patients met with investigators for a complete history and physical examination, to have baseline laboratory assessments including glycosylated haemoglobin (HbA1c). HbA1c was expressed as percentage and measured using the high-performance liquid chromatography. BMD in the current study was measured using The Lunar Achilles (In Sight, GE Healthcare, USA), which is a proven bone ultrasonometer to avoid exposing the children to unnecessarily ionizing radiation. All measurements were converted to Z-scores using a data bank for age-matched speed of sound values supplied by the manufacturer. We excluded patients with a history of fractures of less than 1 year and those with associated bone/joint problems, liver disease or patients on long-term steroid therapy
Main results: 137 patients completed the study. There were 60 (44%) male and 77 (56%) were female with mean age 19.1±4.9. Osteoporosis was found in 53 of cases (38.7%) of patients. There were 23 (43.4%) male and 30 (56.6%) were female giving a female to male ratio 1.3:1. Osteoporosis was found in 53 of cases (38.7%) of patients. Baseline characteristics are shown in Table 1. Patients with osteoporosis were significantly younger, longer diabetes duration and have higher HbA1c than patients without osteoporosis. Osteoporosis was higher in females than male and was seen more in cases with HbA1c > 9.0 as compared to HbA1c groups of < 8.0 and 8-9, (Figures 1 & 2). Cases with longer diabetes duration (≥6years) have nonsignificant more frequent osteoporosis than cases with diabetes duration < 6 years, 34% vs. 66% respectively, p=0.4. There were no significant differences between genders and frequency of osteoporosis in relation to diabetes duration.
Conclusion: Our findings demonstrate lower BMD in young women with type 1 diabetes. Although bone density testing is not routinely performed in young women, these data suggest that screening may be important in young women with type 1 diabetes. In addition, these women should be counseled regarding lifestyle interventions that may improve bone health, including adequate intake of calcium and vitamin D, and exercise.
Introduction
Type 1 diabetes mellitus (T1DM) results from a cellularmediated autoimmune destruction of the β-cells of the pancreas [1]. T1DM accounts for about 10% of all diabetes, affecting approximately 1.4 million people in the U.S, and 10-20 million globally [2]. The prevalence of T1DM was 0.193% in the Saudi males and 0.237% in the Saudi females [3] Osteoporosis has become an alarming health problem throughout the entire world, and approximately 200 million people in the world are threatened by this deleterious disease [4,5]. Osteoporosis is often described as a silent disease because it is typically asymptomatic until a fracture occurs [6]. Along with increased risk of complications including retinopathy, nephropathy, neuropathy, and cardiovascular events, adults with type 1 diabetes have decreased bone mineral density (BMD) compared with control subjects [7,8]. In fact, osteoporosis is the most significant metabolic bone disease in individuals with diabetes [9]. Patients with diabetes are at risk for osteoporosis and its complications, including hip fracture [10]. Recent studies demonstrate that diabetes is associated with alterations in bone health in children and adolescents [6,11-13]. These observations suggest that adverse effects on bone health may occur early after the diabetes diagnosis. This study was undertaken to estimate the epidemiology of osteoporosis among Saudi patients with T1DM, living in the western province, attending the diabetes centre at King Fahd Armed Forces Hospital, Jeddah, KSA.
Methods
Eligible patients were older than 12 years old, had T1DM. All patients were recruited from the population of the Diabetic Centre at King Fahad Armed Forces Hospital. All the patients gave their or their guardian informed consent prior to their inclusion. Eligible patients met with investigators for a complete history and physical examination, to have baseline laboratory assessments including glycosylated hemglobin (HbA1c). HbA1c was expressed as percentage and measured using the high performance liquid chromatography. BMD in the current study was measured using The Lunar Achilles (Insight, GE Healthcare, USA), which is a proven bone ultrasonometer to avoid exposing the children to unnecessarily ionizing radiation. All measurements were converted to Z-scores using a data bank for age-matched speed of sound values supplied by the manufacturer. We excluded patients with a history of fractures of less than 1 year and those with associated bone/joint problems, liver disease or patients on long-term steroid therapy.
Statistical Analysis
Univariate analysis of baseline and follow up demography and clinical laboratory endpoints were accomplished using unpaired t-test where appropriate. Chi square(X2) test were used for categorical data comparison. All statistical analyses were performed using SPSS Version 22.0. All P values were based on two-sided tests. The difference between groups was considered significant when P<0.05.
Results
Baseline characteristics are shown in table 1. 137 patients completed the study. There were 60 (44%) male and 77 (56%) were female with mean age 19.1±4.9 (minimum=12, maximum = 37) years. Osteoporosis was found in 53 of cases (38.7%) of patients. There were 23 (43.4%) male and 30 (56.6%) were female giving a female to male ratio 1.3:1. Patients with osteoporosis were significantly younger, longer diabetes duration and have higher HbA1c than patients without osteoporosis. Osteoporosis was higher in females than male and was seen more in cases with HbA1c > 9.0 as compared to HbA1c groups of < 8.0 and 8-9, (Figures 1 & 2). Cases with longer diabetes duration (≥6years) have nonsignificant more frequent osteoporosis than cases with diabetes duration <6 years, 34% vs. 66% respectively, p=0.4. There were no significant differences between genders and frequency of osteoporosis in relation to diabetes duration (Figure 3).
Figure 1: Percentage of cases of type 1 diabetes mellitus associated with osteoporosis in relation to gender.
Figure 2: Number of cases of type 1 diabetes mellitus associated with osteoporosis in relation to HbA1c groups.
Figure 3: Number of cases with type 1 diabetes mellitus associated with osteoporosis in relation to diabetes duration (years).
Discussion
In agreement with many studies, the present study has confirmed that osteoporosis is associated with T1DM.
[14-16] However, it was unclear until recently whether this translated into increased fracture rates. A number of studies have shown that poor glycemic control in patients with T1DM is associated with osteopenia and osteoporosis [17,18]. Poor glycemic control for long period of time can result into microvascular complications and can aggravate the loss of bone density by various mechanisms. Nephropathy can predispose patients with diabetes to hypercalciuria and can alter the vitamin D metabolism causing vitamin D deficiency [19,20]. Hyperglycemia may lead to an increased loss of calcium in the urine, which can in turn cause a negative calcium balance [21]. Furthermore, use of loop diuretics in patients with diabetic nephropathy is associated with low bone mineral density (BMD) as these drugs cause the renal excretion of calcium [22]. Insulin-like growth factors and other cytokines may influence diabetic bone metabolism [20]. The decrease bone formation and inadequate accrual peak bone mass in children with prepubertal onset T1DM has been proposed as a major contributing factor for low bone strength and osteoporosis in later life [23]. Men with T1DM tend to be particularly prone to osteopenia or osteoporosis compared to women of similar ages [15,24,25] Estrogen adequacy and/or use of estrogen based oral contraceptive pills might be the reason for higher bone mass in women compared to men [25-26]. Furthermore, hypogonadism is quite common in men with T1DM and that may contribute to osteoporosis in males [27,28]. Another factor which may influence the BMD is body mass index (BMI). Studies have shown that lower BMI is associated with higher incidence of osteoporosis. The adipose tissue, apart from providing mechanical loading, also increases BMD through the activity of adipocytokines. Patients with TIDM also have a negative calcium balance as a result of hypercalciuria during periods of hyperglycemia, functional hypoparathyroidism, vitamin D deficiency and alterations in vitamin D metabolism [29-31]. In concordance with our results, duration of diabetes seems to play a key role given the lower BMD found among patients who have had diabetes for >5 years. In the Iowa Women’s Health Study, women with type 1 diabetes were 12.25 times more likely to report having had a fracture compared to women without diabetes [10]. A low BMI as shown in our study is associated the increased possibility of osteoporosis [32]. Overweight and obesity are believed to be protective factors of BMD [33,34]. Obesity is strongly associated with higher BMD probably through mechanical loading and hormonal factors including insulin, estragon, and leptin [35] In conclusion, our findings demonstrate high frequency of osteoporosis in young women with type 1 diabetes. Although bone density testing is not routinely performed in young women, these data suggest that screening may be important in young women with type 1 diabetes. In addition, these women should be counseled regarding lifestyle interventions that may improve bone health, including adequate intake of calcium and vitamin D, and exercise Table 1.
Table 1: Characteristics of patients with type 1 diabetes mellitus stratified by presence of Osteoporosis.
Acknowledgment
We are grateful to the staffs from the diabetic centre at King Fahad Armed Forces Hospital for his valuable contributions in data collection. The authors have no conflict of interest to disclose
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