Journals / Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi / 2008 / Cilt: 54 - Sayı: 1

The effect of raloxifene, alendronate and risedronate on serum lipid profile in postmenopausal women

Postmenopozal osteoporozda raloksifen, alendronat ve risedronat tedavilerinin lipid profili üzerine olan etkileri

Pages
4–7
Publication Date
2022-11-05
DOI
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Turk J Phys Med Rehab 2008;54:4-7.

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Objective & Hypothesis:Objective: To investigate the effect of raloxifene 60 mg/day, alendronate 70 mg/week and risedronate 35 mg/week on serum total cholesterol (TOT-C) (mg/dl) and triglycerides (TG) (mg/dl) during a 12 month treatment period.
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Key Findings & Data:Material and Methods: Bone mineral density (BMD) of L2-L4 and femoral neck were evaluated in 127 patients who attended the Physical Medicine and Rehabilitation outpatient clinic.
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Conclusion & Impact:Turk J Phys Med Rehab 2008;54:4-7.
🔬Design:Research Article
📍Scope:2008 Verileri
⚙️Variables:Domain Parameters

Abstract

Objective: To investigate the effect of raloxifene 60 mg/day, alendronate 70 mg/week and risedronate 35 mg/week on serum total cholesterol (TOT-C) (mg/dl) and triglycerides (TG) (mg/dl) during a 12 month treatment period. Material and Methods: Bone mineral density (BMD) of L2-L4 and femoral neck were evaluated in 127 patients who attended the Physical Medicine and Rehabilitation outpatient clinic. Age, menopause age, height, weight, cigarette and alcohol use were recorded. Patients were randomized into three groups. The first group (raloxifene) had 36, second group (alendronate) had 47 and third group (risedronate) had 44 patients (mean ages: 62±7, 62.6±8, 63.6±6 years, respectively). All groups received 1200 mg calcium and 800 IU vitamin-D daily in addition to their drugs. Serum TOT-C and TG were evaluated at the beginning and after one year.Results: No serious adverse effects were seen in any of the groups. There were no differences between the groups regarding demographic features, L2-L4 and femur BMD levels. Serum TOT-C levels were slightly high and serum TG levels were within the normal range in all groups and did not differ within and between groups after one year follow-up.Conclusion: Raloxifene, alendronate and risedronate, which were used for the treatment of postmenopausal osteoporosis, did not affect serum TOT-C and TG levels during 12 month treatment period. Turk J Phys Med Rehab 2008;54:4-7.

Özet

Amaç: Raloksifen 60 mg/gün, alendronat 70 mg/hafta ve risedronat 35 mg/hafta kullanımının bir yıl sonunda total kolesterol (TOT-C) (mg/dl) ve serum trigliserid (TG) (mg/dl) düzeylerine etkisini araştırmak.Gereç ve Yöntem: Fiziksel Tıp ve Rehabilitasyon Polikliniği’ne başvuran 127 hastanın femur boynu ve L2-L4 kemik mineral yoğunluğu (KMY) (g/cm2) ölçüldü. Hastaların yaş, boy, kilo, menopoz yaşı, sigara ve alkol kullanımları kaydedildi. Birinci grupta (raloksifen) 36, ikinci grupta (alendronat) 47 ve üçüncü grupta (risedronat) 44 hasta yer aldı (yaş ortalamaları sırasıyla 62±7, 62,6±8, 63,6±6 yıl). Her üç grup da aldıkları ilaçlara ek olarak kalsiyum 1200 mg/gün ve D vitamini 800 İÜ/gün aldı. Hastaların çalışma başlangıcında ve 1 yıl sonrasında serum TOT-C ve serum TG değerleri ölçüldü.Bulgular: Her üç grupta da ciddi bir yan etki görülmedi. Her üç grup arasında demografik özellikler, L2-L4 ve femur boynu KMY (g/cm2) değerleri arasında fark saptanmadı. Serum TOT-C düzeyleri her üç grupta da hafif düzeyde yüksek iken serum TG değerleri normal sınırlardaydı. Bir yıl sonunda serum TOT-C ve TG değerlerinde gerek grup içi gerekse gruplar arası fark saptanmadı.Sonuç: Postmenopozal osteoporoz tedavisi için uygulanan raloksifen, alendronat ve risedronat bir yıl sonunda serum TOT-C ve serum TG üzerine etki etmemiştir. Türk Fiz Tıp Rehab Derg 2008;54:4-7.

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Cite This Article

YANIK, B., KÜLCÜ, G. D. (2022). The effect of raloxifene, alendronate and risedronate on serum lipid profile in postmenopausal women. Türkiye Fiziksel Tıp ve Rehabilitasyon Dergisi, Cilt: 54 - Sayı: 1, 4–7. https://ajindex.com/articles/629107

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References (12)

  1. Regitz-Zagrosek V, Wintermantel TM, Schubert C. Estrogens and SERMs in coronary heart disease. Curr Opin in Pharmacol 2007;7:130-9
  2. Ohlsson C, Hellberg N, Parini P, Vidal O, Bohlooly M, Rudling M, et al. Obesity and disturbed lipoprotein profile in estrogen receptor-alpha deficient male mice. Biochem Biophys Res Commun 2000;278:640-5
  3. Delmas PD, Bjarnason NH, Mitlak BH, Ravoux AC, Shah AS, Huster WJ, et al. Effects of raloxifene on bone mineral density, serum cholesterol concentrations, and uterine endometrium in postmenopausal women. N Eng J Med 1997;337:1641-7
  4. Ettinger B, Black DM, Mitlak BH, Knickerbocker RK, Nickelsen T, Genant HK, et al. Multiple outcomes of raloxifene evaluation investigators: reduction of vertebral fracture risk in postmenopausal women with osteoporosis treated with raloxifene: results from a 3 year randomized clinical trial. JAMA 1999;282:637-45
  5. Walsh BW, Kuller LH, Wild RA, Paul S, Farmer M, Lawrence JB, et al. Effects of raloxifene on serum lipids and coagulation factors in healthy postmenopausal women. JAMA 1998;279:1445-51
  6. Cohen FJ, Watts S, Shah A, Akers R, Plouffe L. Uterine effects of 3-year raloxifene therapy in postmenopausal women younger then age 60. Obstet Gynecol 2000;95:104-10
  7. Montagnani A, Gonnelli S, Cepollaro C, Campagna MS, Franci MB, Pacini S, et al. Changes in serum HDL and LDL cholesterol in patients with Paget’s bone disease treated with pamidronate. Bone 2003;32:15-9
  8. Amin D, Cornell SA, Gustafson SK, Needle SJ, Ullrich JW, Bilder GE, et al. Bisphosphonates used for the treatment of bone disorders inhibit squalene synthase and cholesterol biosynthesis. J Lipid Res 1992;33:1657-63
  9. Luckman SP, Hughes DE, Coxon FP, Graham R, Russell G, Rogers MJ. Nitrogen-containing bisphosphonates inhibit the mevalonate pathway and prevent post-translational prenylation of GTP-binding proteins, including rats. J Bone Miner Res 1998;14:581-9
  10. Van Beek E, Lowik C, Van der Pluijm G, Papapoulos S. The role of genarylgenarylation in bone resorption and its supression by bisphosphonates in fetal bone explants in vitro: a clue to the mechanism of action of nitrogen-containing bisphosphonates. J Bone Miner Res 1999;14:722-9
  11. Van Beek E, Pieterman E, Cohen L, Lowik C, Papapoulos S. Farnesyl pyrophosphate syntethase is the molecular target of nitrogen-containing bisphosphonate. Biochem Biophys Res Commun 1999;264:108-11
  12. Mosca L, Harper K, Sarkar S, O’Gorman J, Anderson P, Cox DA, et al. Effect