Journal of Endocrinology and Metabolism, ISSN 1923-2861 print, 1923-287X online, Open Access
Article copyright, the authors; Journal compilation copyright, J Endocrinol Metab and Elmer Press Inc
Journal website http://www.jofem.org

Case Report

Volume 2, Number 3, June 2012, pages 139-144


The Effects of Supraphysiologic Doses of Vitamin D3 in Conjunction With Teriparatide on Bone Mineral Density in Two Postmenopausal Females With Severe Osteoporosis

Tables

Table 1. Serum 25-Hydroxyvitamin D, Calcium, Phosphorus, Intact PTH, and Urine Cross-Linked N-Telopeptide at Baseline and 12 Month Intervals During Therapy With Teriparatide, Calcium Citrate and Supraphysiologic Doses of Vitamin D in Patients 1 and 2
 
Time (months)Serum 25-hydroxyvitamin D (nmol/L) Reference range: 35 - 150Serum calcium (mmol/L) Reference range: 2.05 - 2.55Serum phosphorus (mmol/L) Reference range: 0.775 - 1.518Serum PTH, intact (ng/L) Reference range: 10 - 65Urine cross-linked N-telopeptide (nmol BCE/mmol creat) Reference range: 5 - 65
*Laboratory values for patient 1; ** Laboratory values for patient 2.
0*39.932.1250.7106575
12*504.192.4250.9361690
24*394.362.3250.8392264
0**29.952.0750.6787150
12**304.512.500.9691586
24**284.542.4250.9042464

 

Table 2. Comparison of BMD and T-Scores Prior to and 24 Months After Treatment With Teriparatide, Calcium Citrate and Supraphysiologic Doses of Vitamin D in Patients 1 and 2, Percent Change and Absolute Increase in BMD is Also Noted
 
Patient 1Patient 2
BMD, L1-L4 (g/cm2), baseline0.3930.351
BMD, L1-L4 (g/cm2), at 24 months0.5820.639
T-score, L1-L4, baseline-5.9-6.3
T-score, L1-L4, at 24 months-4.2-3.7
% change in BMD, L1-L4, at 24 months48.2%82.3%
Absolute increase in BMD at 24 months (g/cm2)0.1890.288

 

Table 3. Comparison of Changes in Bone Mineral Density From Baseline Values in Our Patients After 24 Months of Teriparatide, Calcium Citrate and Supraphysiologic Doses of Vitamin D; With Patients Treated With Teriparatide, Calcium and Physiologic Doses of Vitamin Da
 
Patients treated with teriparatide and physiologic doses of vitamin DPatient#1Patient#2
aResults from Eli Lilly pharmaceutical clinical trial. The safety and efficacy of once-daily teriparatide and physiologic doses of vitamin D with a median exposure of 19 months were examined in a double-blind, multicenter, placebo-controlled clinical trial of 1,637 postmenopausal women with osteoporosis [2].
Percent Change in BMD at the Lumbar Spine over 24 months9.7%48.2%82.3%
Absolute increase in g/cm2 over 24 months-0.1890.288