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A long-term, observational cohort study on the safety of low-dose glucocorticoids in ankylosing spondylitis: adverse events and effects on bone mineral density, blood lipid and glucose levels and body mass index.
Zhang, Yu-Ping; Gong, Yao; Zeng, Qing Yu; Hou, Zhi-Duo; Xiao, Zheng-Yu.
Afiliação
  • Zhang YP; Department of Rheumatology, The First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Gong Y; Department of Rheumatology, The First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China Research Unit of Rheumatology, Shantou University Medical College, Shantou, Guangdong, China.
  • Zeng QY; Department of Rheumatology, The First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China Research Unit of Rheumatology, Shantou University Medical College, Shantou, Guangdong, China.
  • Hou ZD; Department of Rheumatology, The First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
  • Xiao ZY; Department of Rheumatology, The First Affiliated Hospital, Shantou University Medical College, Shantou, Guangdong, China.
BMJ Open ; 5(6): e006957, 2015 Jun 03.
Article em En | MEDLINE | ID: mdl-26041488
OBJECTIVES: This study aimed to investigate the risk of adverse events and effects on bone mineral density (BMD), blood lipid and glucose levels and body mass index (BMI) of low-dose glucocorticoid (GC) treatment in ankylosing spondylitis. DESIGN: We performed a retrospective, observational cohort study. Adverse effects were compared between GC users and non-GC users, and we analysed differences in the duration of GC exposure (no GC exposure, <6 months, 6 months to 2 years and >2 years). SETTING: Outpatient clinic in a tertiary general hospital in China, rheumatology follow-up visits over the past 30 years. PARTICIPANTS: We included 830 patients with ankylosing spondylitis who were followed up for at least 6 months without a previous history or current complications of active gastrointestinal problems, hypertension, psychiatric or mental problems, diabetes mellitus, tuberculosis and hepatitis. The median follow-up time was 1.6 years (range 0.5-15 years, a total of 1801 patient-years). RESULTS: A total of 555 (66.9%) patients were treated with low-dose GCs, and the median cumulative duration of GC therapy was 1.3 years (range 0.1-8.5 years). Dermatological incidents, including acne, bruisability and cutaneous infections, were the most common adverse events, with a cumulative incidence rate of 5.4% (22.2 events per 1000 patient-years), followed by a puffy and rounded face (1.6%), symptoms of weight gain (1.1%) and serious infections (1.0%). The rates of all other types of adverse events were less than 1%. The GC groups (GC users and non-GC users) and the duration of GC therapy were not associated with the frequency of low BMD, dyslipidaemia, hyperglycaemia or obesity (p<0.05). CONCLUSIONS: Adverse events during long-term treatment of low-dose GCs are limited. Low-dose GCs do not have an adverse effect on BMD, blood lipid and glucose levels and BMI.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Glicemia / Índice de Massa Corporal / Densidade Óssea / Glucocorticoides / Lipídeos Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Espondilite Anquilosante / Glicemia / Índice de Massa Corporal / Densidade Óssea / Glucocorticoides / Lipídeos Idioma: En Ano de publicação: 2015 Tipo de documento: Article