Background
Type I diabetes (T1D), a common chronic childhood disease, is characterized by insulin deficiency caused by the progressive destruction of pancreatic beta-cells
by autoimmune processes [
1]. T1D is
usually first
diagnosed in childhood or early adulthood and its incidence has been constantly increasing worldwide [
2‐
4]. Along with the well-known microvascular and macrovascular complications, T1D affects bone metabolism. In particular, there is evidence for poor bone mineralization, abnormal glycosylation and cross-linking of skeletal collagen [
5‐
7]. Consequently, this reduced bone strength and quality can lead to fractures at any site, predominantly at femoral neck [
7,
8].
There is a great need to improve our understanding of the mechanisms behind the development of bone complications in diabetic patients and to develop new biomarkers that better stratify high-risk patient groups in a preclinical stage. To this extent, the study of OPG/RANKL/RANK signaling axis in diabetes has been proposed as a promising new research direction. Bone remodeling depends on the balance between bone formation performed by osteoblasts and bone resorption induced by osteoclasts. Previous studies have identified the
OPG/
RANK/
RANKL signaling axis, among others, as an important regulator of this process [
9]. In particular, OPG is a soluble glycoprotein produced mainly by osteoblasts that inhibits osteoclastogenesis by preventing the binding of RANKL to its receptor RANK [
10]. On the other hand, RANKL is an osteoclast differentiation factor produced by osteoblasts which triggers osteoclastogenesis by binding to RANK, a membrane receptor expressed by osteoclast precursors [
11]. Therefore, RANKL and OPG are key factors in bone remodeling process that is carried out by osteoblast and osteoclast cells within the
bone remodeling
unit [
12,
13].
So far, studies examining OPG and RANKL circulating levels have led to inconsistent results in
children and adolescents with diabetes [
14‐
18]. Therefore, the aim of this study was to test the hypothesis that circulating levels of RANKL, RANK and OPG are altered in patients with T1D compared to normal controls and to investigate factors that could significantly affect concentrations of OPG and RANKL such as vitamin D, parathyroid hormone and age.
Subjects and methods
Subjects
This case-control study included 71 children and adolescents with T1D and 50 healthy controls matched for age and sex (Table
1). Participants were recruited from January of 2015 until January of 2017. Entry criteria for the patients were age 5–18 years and duration of diabetes of more than 4 years. Entry criteria for controls were age 5–18 years and no medical history. Exclusion criteria for both patients and controls were the presence of chronic metabolic diseases that could affect bone metabolism, such as metabolic syndrome, hypothyroidism and other autoimmune diseases, renal disease, liver disease etc. In all T1D patients diabetic complications such as retinopathy, nephropathy, neuropathy and metabolic syndrome were excluded by frequent appropriate laboratory and clinical examinations. In order to detect early microalbuminuria a 24 h urine collection was performed and the urinary ratio albumin (A) to creatinine (C) was evaluated (normal values A/C less than 30 mg/24 h). Written, informed consent was obtained from all participants and the study was aproved by the appropriate institutional review board.
Table 1Demographic data and measured biomarkers in T1DM patients and controls
Gender (boys/girls) | 41/30 | 26/24 | 0.580a |
age (years) | 13 (11–16) | 12 (10–13.2) | 0.071b |
Duration of diabetes (years) | 5 (4–8) | – | – |
HbA1c (%) | 7.5 (6.8–8.2) | 5.3 (5.1–5.3) | < 0.001**b |
Glu (mg/dl) | 203 ± 73 | 86 ± 9 | < 0.001**c |
Ca (mg/dl) | 9.75 ± 0.38 | 9.62 ± 0.36 | 0.066c |
P (mg/dl) | 4.39 ± 0.52 | 4.42 ± 0.9 | 0.862c |
Mg (mg/dl) | 1.92 (1.76–2.04) | 1.95 (1.8–2.09) | 0.105b |
ALP (U/L) | 222 ± 110 | 151 ± 82 | < 0.001**c |
PTH (pg/ml) | 46.75 ± 17.1 | 26.56 ± 9.87 | < 0.001**c |
25(OH) D (ng/ml) | 26.6 (21.8–32.3) | 54.3 (48.7–60.5) | < 0.001**b |
SGOT (U/L) | 19 (15–24) | 21 (17–27) | 0.092b |
SGPT (U/L) | 15 (12–19) | 14 (12–18) | 0.514b |
ACR ratio | 3.35 (2.47–5.97) | – | – |
OPG (pg/ml) | 314 (171–504) | 392 (271–667) | 0.025*b |
RANKL (pg/ml) | 545 (107–3377) | 234 (12–2046) | 0.037*b |
RANK (pg/ml) | 43 (18–110) | 52 (18–91) | 0.946b |
RANKL/OPG | 1.7 (0.41–7.22) | 0.64 (0.02–2.95) | 0.002*b |
Biochemical measurements
Blood samples were collected in the morning, in a fasting state. The serum or plasma samples were frozen at -80 °C until testing. Also the supernatants of the 24 h urine samples were frozen.
Concentrations in serum of Glu, Ca, P, Mg, ALP, SGOT and SGPT as well microalbuminuria in a 24 h urine sample were measured using colorimetric biochemical assays in an Architect c800 Clinical Chemistry Analyzer. Intact (1–84) PTH and Vitamin D [25(OH) D] were measured in serum with ECLIA method in an Architect i1000SR Immunoassay Analyzer (Abbott Laboratories, Abbott Park, Illinois, U.S.A.), where their normal ranges were 14–72 pg/ml and 40–100 ng/ml, respectively and the inter-assay coefficients of variability were 8 and 10%, respectively. 25(OH) D insufficiency was set to < 30 ng/ml. Whole blood HbA1c levels were measured using HPLC method in a Menarini ARKRAY ADAMS™ A1C HA-8180 Analyzer (Menarini Diagnostics, Florence, Italy).
Serum RANKL and RANK concentrations were measured, applying Sandwich ELISA (BosterBio, Pleasanton, CA, USA). Human TNFSF11/RANKL ELISA Kit had a sensitivity of less than 0.43 pmol/l with an intra-assay precision of 5.1% and an inter-assay precision of 5.7%. Human receptor activator of NFkB, RANK ELISA Kit, had a sensitivity of less than 0.04 pmol/l with an intra-assay precision of 5.4% and an inter-assay precision of 6.6%. Plasma OPG concentrations were measured by a sandwich ELISA, applying a commercially available kit (Cohesion Biosciences, London, UK) with a detection limit less than 0.09 pmol/l, according to the manufacturer’s instructions. All samples were measured in duplicate and averaged.
Statistical analysis
Statistical analysis was performed using a SPSS software version 25 (SPSS Inc., Chicago, IL, USA). Data were presented as mean ± standard deviation for normally distributed variables and median (interquartile range) for not normally distributed variables. Kolmogorov-Smirnov test was used for the assessment of normality. Chi-square-test was used for comparison of categorical variables. t-test and Mann-Whitney U test was used as appropriate to test for differences in continuous variables. Pearson’s correlation coefficient (r) and Spearman’s correlation coefficient (rs) were used for normally and not normally distributed variables respectively. Level of significance was set at p < 0.05.
Discussion
In the present study, serum RANKL levels were significantly elevated in T1D patients compared to controls. Since serum RANKL promotes osteoclastogenesis higher levels of serum RANKL might be associated with increased osteoclast activation. On the other hand, OPG, a decoy RANKL receptor, plasma levels were significantly lower in T1D patients compared to controls. Overall the significantly higher RANKL/OPG ratio in T1D patients may indicate increased osteoclast differentiation and activation, enhanced bone resorption leading to osteopenia and osteoporosis [
11].
In the literature there are controversial results regarding OPG and RANKL circulating levels in T1D patients (Table
3) [
14‐
18]. Our finding of significant lower OPG levels compared to controls, is in agreement with several studies, in which no microvascular complications of T1D were noted [
14,
15]. On the contrary, elevated OPG levels have been positively associated with the progression of diabetes and the appearance of its complications [
16,
19,
20]. Regarding age, a bimodal distribution of OPG levels with age is reported, with peak OPG levels during infancy and after 45 years of age [
21,
22]. Although we found a significant negative association between OPG levels and age in the control group, this association was not observed in T1D patients. On the other hand, it is well established that parathyroid hormone and vitamin D increase RANKL gene expression (Fig.
2a), while vitamin D upregulates and PTH downregulates OPG expression (Fig.
2b) [
23‐
25]. Interestingly there is a heterogeneity among the different studies regarding PTH and 25(OH) D vitamin levels. Therefore, different levels of PTH and 25(OH) D and the presence of diabetic complications could
explain discrepancies in circulating
levels of OPG and
RANKL between different studies in children (Table
3).
Table 3Studies investigating OPG and RANKL circulating levels in children with T1D
| ↓ | n.s. | n.s.* | n.s. | no |
| ↓ | | | | no |
| ↑ | | n.s. | n.s. | no |
| ↑ | ↑ | n.s. | ↓ | no |
Lambrinoudaki et al. [ 16] | n.s. | n.s. | | | ↑cIMT |
Our study indicates that PTH and 25(OH) D may contribute significantly to the alterations in circulating concentrations of OPG and RANKL. Vitamin D is a steroid hormone essential for calcium homeostasis and bone remodeling [
26]. Vitamin D deficiency is involved in the impairment of insulin synthesis and secretion and may be considered as an environmental factor with a pivotal role in the pathogenesis of T1D [
27,
28]. In our study, serum 25(OH) D levels in T1D patients were significant lower compared to controls, in agreement with previous studies [
29,
30]. Interestingly, duration of disease correlated with decreased 25(OH) D serum levels.
On the other hand, PTH acts on osteoclasts and stimulates osteolysis and bone resorption [
31]. This osteoclastogenic effect is accomplished in part through the induction of RANKL and downregulation of OPG gene expression, respectively [
32]. Serum PTH levels were significantly higher in T1D patients than in controls, in agreement with previous studies [
29,
33]. It is well documented that serum Ca, P and Mg levels are stimuli for PTH secretion [
31]. Interestingly, no significant difference was found in serum Ca, P and Mg levels between patients and controls. Therefore, one possible explanation for the PTH upregulation could be the low levels of 25(OH) D observed in our study [
31,
34].
Conclusion
Our study demonstrated that OPG and RANKL may be promising biomarkers for T1D patients. However, an understanding of what determines OPG and RANKL levels in T1D patients is not completely clear. Circulating levels of OPG and RANKL were associated with several factors including parathormone, vitamin D and therefore, may represent an integrative biomarker for a variety of endocrine signaling disturbances observed in T1D.
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