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1.
Endocr J ; 53(3): 325-30, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16710073

ABSTRACT

It is well known that pioglitazone, a potent thiazolidinedione, improves metabolic control. However, weight gain or peripheral edema may be of major clinical concern when using this agent. The purpose of our study was to prospectively evaluate the effects of low-dose pioglitazone (7.5 mg/day) on metabolic control, weight gain and the incidence of edema compared with a standard dose of pioglitazone (15.0 mg/day) in patients with type 2 diabetes mellitus (T2DM). Ninety-five Japanese female patients (mean age 58.4 +/- 10.4 years) with newly diagnosed T2DM were selected for this study. They were randomly divided into the following 2 groups according to therapy regimens, and examined every month for 6 months after diagnosis. Group A consisted of 54 patients treated with low-dose pioglitazone orally; Group B, the control-group, consisted of 41 patients treated with standard-dose pioglitazone orally. The incidence of peripheral edema was significantly much lower in group A (2/54) than in group B (11/41) (p = 0.0014). In addition, % change of body weight during the 6-month treatment in group A was significantly less than that in group B (p < 0.0001). On the other hand, the % change of biochemical parameters including HbA1c did not differ significantly between group A and group B, although glucose and lipid control significantly improved from baseline in both groups. Our results demonstrate the safety and efficacy of low-dose pioglitazone, suggesting that it could be another good choice of treatment for Japanese women with T2DM.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Thiazolidinediones/administration & dosage , Administration, Oral , Aged , Blood Glucose/drug effects , Blood Pressure , Cholesterol/blood , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Dose-Response Relationship, Drug , Edema/chemically induced , Fasting/blood , Female , Glycated Hemoglobin/analysis , Humans , Incidence , Japan , Middle Aged , Pioglitazone , Thiazolidinediones/adverse effects , Thiazolidinediones/therapeutic use , Treatment Outcome , Triglycerides/blood , Weight Gain/drug effects
2.
J Bone Miner Metab ; 24(2): 105-13, 2006.
Article in English | MEDLINE | ID: mdl-16502116

ABSTRACT

It has been well established that hyperthyroidism leads to diminished bone mineral density (BMD), and that a previous history of hyperthyroidism remains a risk factor for fractures. However, little is known about how to manage the reduction in BMD caused by hyperthyroidism. The purpose of this study was to evaluate the efficacy of risedronate for the treatment of osteoporosis/osteopenia in patients with Graves' disease (GD). Of 34 Japanese male patients with newly diagnosed GD, 27 with osteoporosis/osteopenia were included in this study. They were randomly divided into two groups by therapeutic regimen. Group A consisted of 14 patients treated with an antithyroid drug and risedronate. Group B consisted of 13 patients treated with the same antithyroid drug only. We used dual-energy X-ray absorptiometry to measure BMD at the lumber spine, femoral neck, and distal radius at baseline, and at 6 and 12 months after the trial. Bone-specific alkaline phosphatase and urinary N-terminal telopeptide of type I collagen normalized by creatinine were significantly more reduced in group A than in group B after both 6 and 12 months. The percentage increases in BMD at the lumbar spine and distal radius were significantly greater in group A than in group B. These beneficial effects of risedronate for patients with osteoporosis/osteopenia caused by GD may lead to a reduced risk of future fractures. We thus conclude that risedronate should be considered for the treatment of decreased bone mass associated with GD.


Subject(s)
Etidronic Acid/analogs & derivatives , Graves Disease/drug therapy , Osteoporosis/drug therapy , Adult , Alkaline Phosphatase/metabolism , Bone Density , Bone Density Conservation Agents/therapeutic use , Bone Diseases, Metabolic , Bone and Bones/drug effects , Bone and Bones/metabolism , Collagen Type I/chemistry , Etidronic Acid/therapeutic use , Humans , Hyperthyroidism/drug therapy , Japan , Male , Middle Aged , Models, Statistical , Osteoporosis/complications , Peptides/chemistry , Risedronic Acid , Thyroid Hormones/metabolism , Time Factors , X-Rays
3.
Endocr J ; 52(3): 309-16, 2005 Jun.
Article in English | MEDLINE | ID: mdl-16006725

ABSTRACT

A 59-year-old woman with papillary thyroid carcinoma inside of an autonomously functioning thyroid nodule is described in this report. The patient was referred to our clinic because of rapid weight loss and swelling on the left side of the neck. Ultrasonography of the thyroid demonstrated a nonhomogeneous nodule in the lower part of an enlarged left lobe. Both 99mTc and 123I thyroid scintigraphic imaging showed a hot area corresponding to the nodule with lower uptake in the remaining thyroid tissue. Histopathological examination of the nodule revealed papillary adenocarcinoma, and the immunohistochemistry proved weak but positive staining for triiodothyronine and thyroxine. Based on these findings, the nodule was diagnosed as a functioning papillary adenocarcinoma. Although thyroid carcinoma manifesting as a hot nodule on the radionuclide isotope scan is an extremely rare occurrence, the current case is clinically important because it suggests that the diagnosis of a hot nodule cannot always rule out thyroid carcinoma in the nodule, and that even a hot nodule requires careful management so that the malignancy is not overlooked.


Subject(s)
Adenocarcinoma, Papillary/diagnosis , Thyroid Neoplasms/diagnosis , Thyroid Nodule/diagnosis , Adenocarcinoma, Papillary/diagnostic imaging , Adenocarcinoma, Papillary/pathology , Adenocarcinoma, Papillary/surgery , Biopsy, Fine-Needle , Diagnosis, Differential , Female , Humans , Immunohistochemistry , Middle Aged , Radionuclide Imaging , Thyroid Neoplasms/diagnostic imaging , Thyroid Neoplasms/pathology , Thyroid Neoplasms/surgery , Thyroid Nodule/diagnostic imaging , Thyroid Nodule/pathology , Thyroidectomy , Thyroxine/analysis , Triiodothyronine/analysis
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