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The females in both groups were postmenopausal.
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Regarding menopause status, 1240 cases in osteoporosis group and 2159 cases of non-osteoporosis group were postmenopausal (85.2% vs. 73.7%, X2 = 73.377, p = 0.000, OR = 2.052, 95% CI = (1.737-2.423)), indicathat that postmenopausal was the risk factor of osteoporosis.
Approximately 50% of the women in each treatment group were postmenopausal, and the majority of women (66% in the oral clodronate and 67% in the placebo groups) had stage II/III disease.
The insulin-resistant women were older than the insulin-sensitive women (54 ± 4 vs. 46 ± 2 years, P = 0.06), and it is possible that more women in the insulin-resistant group were postmenopausal.
Main inclusion criteria for both groups were the same: postmenopausal women over 45 years of age, with primary osteoporosis, who were able to read and write Serbian language.
Both groups were of comparable age and were beyond the early postmenopausal stage (Table 1).
More of the patients in Group II were postmenopausal than were those in Group I (62.8% vs. 26.4%, P < 0.0001).
Patients who experienced a treatment-induced menopause (TIM) following chemotherapy treatment (N=32 out of 39) were compared with those in the chemotherapy group who were postmenopausal at baseline.
Moreover, only one study evaluated the serum A-FABP in the group, where all women were postmenopausal.
In total, 14 (31%) of the study patients were postmenopausal, and our results indicated that both premenopausal and postmenopausal patients were at risk for clinically significant lesions.
Four patients were postmenopausal.
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