Teriparatida (hormônio recombinante humano da paratireóide 1-34) para mulheres com osteoporose pós-menopausa

revisão sistemática

Autores

  • Virgínia Fernandes Moça Trevisani Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina
  • Rachel Riera Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina
  • Aline Mizusaki Imoto Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina
  • Humberto Saconato Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina
  • Álvaro Nagib Atallah Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

Palavras-chave:

Osteoporose, Fraturas ósseas, Pós-menopausa, Teriparatida, Revisão

Resumo

CONTEXTO E OBJETIVO: A osteoporose é definida como uma doença caracterizada por baixa massa óssea e deteriorização da microarquiquetura do tecido ósseo. O paratormônio estimula a formação e a ação dos osteoblastos responsáveis pela formação dos ossos, promovendo ganho de tecido ósseo. O objetivo foi determinar a efetividade e a segurança da teriparatida no tratamento da osteoporose pós-menopausa. MÉTODOS: Foi realizada uma revisão sistemática da literatura de acordo com a metodologia da Colaboração Cochrane. RESULTADOS: 1) Teriparatida 20 µg ou 40 µg versus placebo: benefício da teriparatida considerando os desfechos redução do número de novas fraturas vertebrais e não-vertebrais, aumento da densidade mineral óssea corporal total, lombar e do fêmur. 2) Teriparatida 40 µg versus alendronato 10 mg/dia por 14 meses: não houve diferença estatística em relação a incidência de novas fraturas vertebrais ou nãovertebrais, porém, no grupo que recebeu a teriparatida, houve maior ganho de densidade mineral óssea corporal total, na coluna lombar e no fêmur (região intertrocantérica e triângulo de Wards). 3) Estrogênio mais teriparatida 25 µg versus estrogênio: houve benefício do estrogênio associado a teriparatida considerando os desfechos redução do número de novas fraturas vertebrais, aumento da densidade mineral óssea corporal total, lombar e do fêmur ao final dos três anos do estudo. CONCLUSÕES: A teriparatida, quando administrada em baixas doses e de forma intermitente, reduz as fraturas vertebrais (67%) e não vertebrais (38%) e aumenta a densidade mineral óssea na coluna lombar e no fêmur. Há necessidade de estudos de maior tempo de observação para permitir conclusões sobre a segurança e a duração dos efeitos terapêuticos.

Downloads

Não há dados estatísticos.

Biografia do Autor

Virgínia Fernandes Moça Trevisani, Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

MD, PhD. Full professor, Discipline of Rheumatology, Universidade de Santo Amaro (Unisa). Attending physician in the Division of Emergency Medicine and Evidence-Based Medicine of Universidade Federal de São Paulo — Escola Paulista de Medicina (Unifesp-EPM), São Paulo, Brazil.

Rachel Riera, Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

Doctoral student, Universidade Federal de São Paulo — Escola Paulista de Medicina (Unifesp-EPM), São Paulo, Brazil.

Aline Mizusaki Imoto, Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

Doctoral student, Universidade Federal de São Paulo — Escola Paulista de Medicina (Unifesp-EPM), São Paulo, Brazil.

Humberto Saconato, Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

Adjunct professor, Discipline of Propaedeutics, Universidade Federal do Rio Grande do Norte (UFRN), Natal, Rio Grande do Norte, Brazil.

Álvaro Nagib Atallah, Brazilian Cochrane Center, Universidade Federal de São Paulo — Escola Paulista de Medicina

MD, PhD. Full professor and head of the Division of Emergency Medicine and Evidence-Based Medicine of Universidade Federal de São Paulo — Escola Paulista de Medicina (Unifesp-EPM). Director of the Brazilian Cochrane Center and Scientific Director of Associação Paulista de Medicina (APM), São Paulo, Brazil.

Referências

Consensus development conference: prophylaxis and treatment of osteoporosis. Br Med J (Clin Res Ed). 1987;295(6603):914-5.

Kanis JA, Melton LJ 3rd, Christiansen C, Johnston CC, Khaltaev N. The diagnosis of osteoporosis. J Bone Miner Res. 1994;9(8):1137-41.

Doherty DA, Sanders KM, Kotowicz MA, Prince RL. Lifetime and five-year age-specific risks of first and subsequent osteo- porotic fractures in postmenopausal women. Osteoporos Int. 2001;12(1):16-23.

Kanis JA. Diagnosis of osteoporosis and assessment of fracture risk. Lancet. 2002;359(9321):1929-36.

Cranney A, Simon LS, Tugwell P, Adachi R, Ottawa Methods Group. Osteoporosis. In: Evidence-based Rheumatology. London: BMJ Books; 2003. p.225-32. Available from: http:// www.blackwellpublishing.com/medicine/bmj/rheumatology/ pdfs/alen.pdf. Accessed in 2008 (Sep 23).

Follin SL, Hansen LB. Current approaches to the prevention and treatment of postmenopausal osteoporosis. Am J Health Syst Pharm. 2003;60(9):883-901; quiz 903-4.

Lindsay R, Silverman SL, Cooper C, et al. Risk of new vertebral fracture in the year following a fracture. JAMA. 2001;285(3):320-3.

Tosteston AN, Gabriel SE, Grove MR, Moncur MM, Kneeland TS, Melton LJ 3rd. Impact of hip and vertebral fractures on qual- ity-adjusted life years. Osteoporos Int. 2001;12(12):1042-9.

Greendale GA, Barrett-Connor E, Ingles S, Haile R. Late physi- cal and functional effects of osteoporotic fracture in women: the Rancho Bernardo Study. J Am Geriatr Soc.1995;43(9): 955-61.

Melton LJ 3rd, Chrischilles EA, Cooper C, Lane AW, Riggs BL. Perspective. How many women have osteoporosis? J Bone Miner Res. 1992;7(9):1005-10.

Delmas PD. Treatment of postmenopausal osteoporosis.Lancet. 2002;359(9322):2018-26.

Brown JP, Josse RG; Scientific Advisory Council of the Osteoporosis Society of Canada. 2002 clinical practice guidelines for diagnosis and management of osteoporosis in Canada. CMAJ. 2002;167(10 Suppl):S1-34.

AACE Osteoporosis Task Force. American Association of Clini- cal Endocrinologists medical guidelines for clinical practice for the prevention and treatment of postmenopausal osteoporosis: 2001 edition, with selected updates for 2003. Endocr Pract. 2003;9(6):544-64.

Whitfield JF, Morley P, Willick GE. The bone-building action of the parathyroid hormone: implications for the treatment of osteoporosis. Drugs Aging. 1999;15(2):117-29.

Jadad AR, Moore RA, Carroll D, et al. Assessing the quality of reports of randomized clinical trials: is blinding necessary? Control Clin Trials. 1996;17(1):1-12.

Higgins J, Green S, editors. Cochrane handbook for systematic reviews of interventions 4.2.6. The Cochrane Collaboration; 2006. Available from: http://www.cochrane.org/resources/ handbook/Handbook4.2.6Sep2006.pdf. Accessed in 2008 (Sep 23).

Buxton EC, Yao W, Lane NE. Changes in serum receptor activator of nuclear factor-kappaB ligand, osteoprotegerin, and interleukin-6 levels in patients with glucocorticoid-induced osteoporosis treated with human parathyroid hormone (1-34). J Clin Endocrinol Metab. 2004;89(7):3332-6.

Adis International Ltd. ALX 111: ALX1-11, parathyroid hormone (1-84) - NPS Allelix, PREOS, PTH, recombinant human parathyroid hormone, rhPTH (1-84). Drugs R D. 2003;4(4):231-5.

Rehman Q, Lang TF, Arnaud CD, Modin GW, Lane NE. Daily treatment with parathyroid hormone is associated with an increase in vertebral cross-sectional area in postmenopausal women with glucocorticoid-induced osteoporosis. Osteoporos Int. 2003;14(1):77-81.

Lane NE, Sanchez S, Modin GW, Genant HK, Pierini E, Arnaud CD. Bone mass continues to increase at the hip after parathyroid hormone treatment is discontinued in glucocorticoid-induced osteoporosis: results of a randomized controlled clinical trial. J Bone Miner Res. 2000;15(5):944-51.

Lane NE, Sanchez S, Modin GW, Genant HK, Pierini E, Arnaud CD. Parathyroid hormone treatment can reverse corticosteroid- induced osteoporosis. Results of a randomized controlled clinical trial. J Clin Invest. 1998;102(8):1627-33.

Cosman F, Nieves J, Woelfert L, Gordon S, Shen V, Lindsay

R. Parathyroid responsivity in postmenopausal women with osteoporosis during treatment with parathyroid hormone. vJ Clin Endocrinol Metab. 1998;83(3):788-90.

Hodsman AB, Fraher LJ. Biochemical responses to sequential human parathyroid hormone (1-38) and calcitonin in osteo- porotic patients. Bone Miner. 1990;9(2):137-52.

Kurland ES, Cosman F, McMahon DJ, Rosen CJ, Lindsay R, Bilezikian JP. Parathyroid hormone as a therapy for idiopathic osteoporosis in men: effects on bone mineral density and bone markers. J Clin Endocrinol Metab. 2000;85(9):3069-76.

Kaufman JM, Orwoll E, Goemaere S, et al. Teriparatide ef- fects on vertebral fractures and bone mineral density in men with osteoporosis: treatment and discontinuation of therapy. Osteoporos Int. 2005;16(5):510-6.

Orwoll ES, Scheele WH, Paul S, et al. The effect of teriparatide [human parathyroid hormone (1-34)] therapy on bone den- sity in men with osteoporosis. J Bone Miner Res. 2003;18(1): 9-17.

Jiang Y, Zhao JJ, Mitlak BH, Wang O, Genant HK, Eriksen EF. Recombinant human parathyroid hormone (1-34) [teriparatide] improves both cortical and cancellous bone structure. J Bone Miner Res. 2003;18(11):1932-41.

Hodsman AB, Kisiel M, Adachi JD, Fraher LJ, Watson PH. Histomorphometric evidence for increased bone turnover without change in cortical thickness or porosity after 2 years of cyclical hPTH(1-34) therapy in women with severe osteoporosis. Bone. 2000;27(2):311-8.

Hodsman AB, Hanley DA, Ettinger MP, et al. Efficacy and safety of human parathyroid hormone-(1-84) in increasing bone mineral density in postmenopausal osteoporosis. J Clin Endocrinol Metab. 2003;88(11):5212-20.

Black DM, Greenspan SL, Ensrud KE, et al. The effects of parathyroid hormone and alendronate alone or in com- bination in postmenopausal osteoporosis. N Engl J Med. 2003;349(13):1207-15.

Hodsman AB, Fraher LJ, Watson PH, et al. A randomized controlled trial to compare the efficacy of cyclical parathyroid hormone versus cyclical parathyroid hormone and sequential calcitonin to improve bone mass in postmenopausal women with osteoporosis. J Clin Endocrinol Metab. 1997;82(2):620-8.

Neer RM, Arnaud CD, Zanchetta JR, et al. Effect of parathy- roid hormone (1-34) on fractures and bone mineral density in postmenopausal women with osteoporosis. N Engl J Med. 2001;344(19):1434-41.

Marcus R, Wang O, Satterwhite J, Mitlak B. The skeletal response to teriparatide is largely independent of age, initial bone mineral density, and prevalent vertebral fractures in postmenopausal women with osteoporosis. J Bone Miner Res. 2003;18(1):18-23.

Body JJ, Gaich GA, Scheele WH, et al. A randomized double- blind trial to compare the efficacy of teriparatide [recombinant human parathyroid hormone (1-34)] with alendronate in postmenopausal women with osteoporosis. J Clin Endocrinol Metab. 2002;87(10):4528-35.

Lindsay R, Nieves J, Formica C, et al. Randomised controlled study of effect of parathyroid hormone on vertebral-bone mass and fracture incidence among postmenopausal women on estrogen with osteoporosis. Lancet. 1997;350(9077):550-5.

Finkelstein JS, Klibanski A, Schaefer EH, Hornstein MD, Schiff I, Neer RM. Parathyroid hormone for the prevention of bone loss induced by estrogen deficiency. N Engl J Med. 1994;331(24):1618-23.

Downloads

Publicado

2008-09-09

Como Citar

1.
Trevisani VFM, Riera R, Imoto AM, Saconato H, Atallah Álvaro N. Teriparatida (hormônio recombinante humano da paratireóide 1-34) para mulheres com osteoporose pós-menopausa: revisão sistemática. Sao Paulo Med J [Internet]. 9º de setembro de 2008 [citado 16º de outubro de 2025];126(5):279-84. Disponível em: https://periodicosapm.emnuvens.com.br/spmj/article/view/2007

Edição

Seção

Systematic Review