TY - JOUR
T1 - Serum Sclerostin and Bone Turnover in Latent Autoimmune Diabetes in Adults
AU - Action LADA Study Groups
AU - Napoli, Nicola
AU - Strollo, Rocky
AU - Defeudis, Giuseppe
AU - Leto, Gaetano
AU - Moretti, Chiara
AU - Zampetti, Simona
AU - D'Onofrio, Luca
AU - Campagna, Giuseppe
AU - Palermo, Andrea
AU - Greto, Valentina
AU - Manfrini, Silvia
AU - Hawa, Mohammed I.
AU - Leslie, R. David
AU - Pozzilli, Paolo
AU - Buzzetti, Raffaella
PY - 2018/5/1
Y1 - 2018/5/1
N2 - Purpose: Bone formation is impaired in both type 1 diabetes and type 2 diabetes (T2D), whereas sclerostin, an antagonist of bone formation, is increased in T2D only. No data are available on latent autoimmune diabetes in adults (LADA), an autoimmune type of diabetes thatmay clinically resemble T2D at diagnosis.We evaluated serumsclerostin and bone turnover markers in LADA compared with those in T2D and whether metabolic syndrome (MetS) affects sclerostin in T2D or LADA. Methods: This cross-sectional study included 98 patients with T2D and 89 with LADA from the Action LADA and Non Insulin Requiring Autoimmune Diabetes cohorts. Patients were further divided according to MetS status. Nondiabetic participants (n = 53) were used as controls. Serum sclerostin, bone formation (pro-collagen type 1 N-terminal propeptide [P1NP]), and bone resorption (C-terminal telopeptide of type I collagen [CTX]) were analyzed. Results: Patients with T2D had higher sclerostin than did those with LADA [P = 0.0008, adjusted for sex and bodymass index (BMI)], even when analysis was restricted to patients withMetS (adjusted P=0.03). Analysis of T2Dand LADAgroups separately showed that sclerostin was similar between thosewith and those without MetS. However, a positive trend between sclerostin and number of MetS features was seen with T2D (P for trend = 0.001) but not with LADA. Patients with T2D or LADA had lower CTX than did controls (P = 0.0003) and did not have significantly reduced P1NP. Sclerostin was unrelated to age or hemoglobin A1c but was correlated with BMI (r = 0.29; P = 0.0001), high-density lipoprotein (r = 20.23; P = 0.003), triglycerides (r = 0.19; P = 0.002), and time since diagnosis (r = 0.32; P < 0.0001). Conclusions: Patients with LADA presented lower bone resorption than did controls, similar to patients with T2D. Sclerostin is increased in T2D but not in LADA, suggesting possible roles on bone metabolism in T2D only.
AB - Purpose: Bone formation is impaired in both type 1 diabetes and type 2 diabetes (T2D), whereas sclerostin, an antagonist of bone formation, is increased in T2D only. No data are available on latent autoimmune diabetes in adults (LADA), an autoimmune type of diabetes thatmay clinically resemble T2D at diagnosis.We evaluated serumsclerostin and bone turnover markers in LADA compared with those in T2D and whether metabolic syndrome (MetS) affects sclerostin in T2D or LADA. Methods: This cross-sectional study included 98 patients with T2D and 89 with LADA from the Action LADA and Non Insulin Requiring Autoimmune Diabetes cohorts. Patients were further divided according to MetS status. Nondiabetic participants (n = 53) were used as controls. Serum sclerostin, bone formation (pro-collagen type 1 N-terminal propeptide [P1NP]), and bone resorption (C-terminal telopeptide of type I collagen [CTX]) were analyzed. Results: Patients with T2D had higher sclerostin than did those with LADA [P = 0.0008, adjusted for sex and bodymass index (BMI)], even when analysis was restricted to patients withMetS (adjusted P=0.03). Analysis of T2Dand LADAgroups separately showed that sclerostin was similar between thosewith and those without MetS. However, a positive trend between sclerostin and number of MetS features was seen with T2D (P for trend = 0.001) but not with LADA. Patients with T2D or LADA had lower CTX than did controls (P = 0.0003) and did not have significantly reduced P1NP. Sclerostin was unrelated to age or hemoglobin A1c but was correlated with BMI (r = 0.29; P = 0.0001), high-density lipoprotein (r = 20.23; P = 0.003), triglycerides (r = 0.19; P = 0.002), and time since diagnosis (r = 0.32; P < 0.0001). Conclusions: Patients with LADA presented lower bone resorption than did controls, similar to patients with T2D. Sclerostin is increased in T2D but not in LADA, suggesting possible roles on bone metabolism in T2D only.
UR - http://www.scopus.com/inward/record.url?scp=85047219809&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85047219809&partnerID=8YFLogxK
U2 - 10.1210/jc.2017-02274
DO - 10.1210/jc.2017-02274
M3 - Article
AN - SCOPUS:85047219809
VL - 103
SP - 1921
EP - 1928
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
SN - 0021-972X
IS - 5
ER -