Location: Jean Mayer Human Nutrition Research Center On Aging
Title: Previous fracture and subsequent fracture risk: a meta-analysis to update FRAXAuthor
KANIS, JOHN - University Of Sheffield Medical School | |
JOHANSSON, HELENA - Australian Catholic University | |
MCKLOSKEY, EUGENE - University Of Sheffield | |
LIU, ENWU - Australian Catholic University | |
AKESSON, KRISTINA - Lund University | |
ANDERSON, FRED - University Of Massachusetts | |
AXAGRA, RAFAEL - University Of Barcelona | |
BAGER, CECILIE - Nordic Bioscience As | |
BEAUDART, CHARLOTTE - University Of Liege | |
BISCHOFF-FERRARI, HEIKE - University Of Zurich | |
BIVER, EMMANUEL - Geneva University Hospital | |
BRUYERE, OLIVIER - University Of Liege | |
CAULEY, JANE - University Of Pittsburgh | |
CENTER, JACQUELINE - Garvan Institute Of Medical Research | |
CHAPURLAT, ROLAND - Institut National De La Sante Et De La Recherche Medicale (INSERM) | |
CHRISTIANSEN, CLAUS - Nordic Bioscience As | |
COOPER, CYRUS - University Of Southampton | |
CRANDALL, CAROLYN - University Of California (UCLA) | |
CUMMINGS, STEVEN - California Pacific Medical Center Research Institute | |
DA SILVA, JOSE - University Of Coimbra | |
DAWSON-HUGHES, BESS - Jean Mayer Human Nutrition Research Center On Aging At Tufts University | |
DIEZ-PEREZ, ADOLFO - Autonomous University Of Barcelona | |
DUFOUR, ALYSSA - Harvard Medical School | |
EISMAN, JOHN - Garvan Institute Of Medical Research | |
ELDERS, PETRA - Amsterdam Public Health Research Institute | |
FERRARI, SERGE - Amsterdam Public Health Research Institute | |
FUJITA, YUSUKE - Kindai University | |
FUJIWARA, SHIN-ICHIRO - Yasuda Women'S University | |
GLUER, CLAUS - University Of Kiel | |
GOLDSHTEIN, ITAY - Maccabi Healthcare Services | |
GOLTZMAN, DAVID - McGill University - Canada | |
GUDNASON, VILMUNDUR - Icelandic Heart Association | |
HALL, JILL - University Of Edinburgh | |
HANS, DIDIER - Lausanne University Hospital | |
HOFF, MARI - Norwegian University Of Science And Technology | |
HOLLICK, ROSEMARY - University Of Aberdeen | |
HUISMAN, MARTIJIM - Vu University Medical Center | |
IKI, MASAYUKI - Kindai University | |
ISH-SHALOM, SOPHIA - Elisha Hospital | |
JOENS, GRAEME - University Of Tasmania | |
KARLSSON, MAGNUS - Lund University | |
KHOSLA, SUNDEEP - Mayo Clinic | |
KIEL, DOUGLAS - Harvard Medical School | |
KOH, WOON-PUAY - National University Of Singapore | |
KOROMANI, F JORDA - Erasmus University | |
KOTOWICZ, MARK - Deakin University | |
KROGER, HELMUT - Kuopio University Hospital | |
KWOK, TIMOTHY - The Chinese University Of Hong Kong (CUHK) | |
LAMY, OLIVIER - Lausanne University Hospital | |
LANGHAMMER, A - Norwegian University Of Science And Technology | |
LARIJANI, BAGHER - Tehran University Of Medical Sciences | |
LIPPUNER, KURT - University Of Bern | |
MELLSTROM, DAN - University Of Gothenburg | |
MERLIJN, THOMAS - Amsterdam Public Health Research Institute | |
NORDSTROM, ANNA - The Arctic University Of Norway (UIT) | |
NORDSTROM, PETER - Uppsala University | |
O'NEILL, TERENCE - Manchester Academic Health Science Centre | |
OBERMAYER-PIETSCH, BARBARA - Medical University Of Graz | |
OHLSSON, CLAES - University Of Gothenburg | |
ORWOLL, ERIC - Oregon Health & Science University | |
PASCO, JULIE - Deakin University | |
RIVADENEIRA, FERNANDO - Erasmus Medical Center | |
SCHOTT, ANNE - University Of Lyon | |
SHIROMA, ERIC - National Institute On Aging (NIA, NIH) | |
SIGGEIRSDOTTIR, KRISTIN - Icelandic Heart Association | |
SIMONSICK, E - National Institute On Aging (NIA, NIH) | |
SORNAY-RENDU, ELISABETH - University Of Lyon | |
SUND, REIJO - University Of Eastern Finland | |
SWART, KARIN - Amsterdam Public Health Research Institute | |
SZULC, PAWEL - University Of Lyon | |
TAMAKI, J - Educational Foundation Of Osaka Medical And Pharmaceutical University | |
TORGERSON, DAVID - University Of York | |
VAN SCHOOR, NATASJA - Amsterdam Public Health Research Institute | |
VAN STAA, TJEERD - University Of Manchester | |
VILA, JEREMY - Hospital Del Mar Medical Research Institute | |
WAREHAM, NICK - University Of Cambridge | |
WRIGHT, NICOLE - University Of Alabama At Birmingham | |
YOSHIMURA, NAOYA - University Of Tokyo | |
ZILLIKENS, MARIA - Erasmus University | |
ZWART, MARTA - Preciosa-Fundacion Para La Investigacion | |
VANDENPUT, LIESBETH - Australian Catholic University | |
HARVEY, NICOLAS - University Of Southampton | |
LORENTZON, MATTIAS - University Of Gothenburg | |
LESLIE, WILLIAM - University Of Manitoba |
Submitted to: Osteoporosis International
Publication Type: Peer Reviewed Journal Publication Acceptance Date: 7/22/2023 Publication Date: 8/11/2023 Citation: Kanis, J.A., Johansson, H., McKloskey, E.V., Liu, E., Akesson, K., Anderson, F.A., Axagra, R., Bager, C.L., Beaudart, C., Bischoff-Ferrari, H.A., Biver, E., Bruyere, O., Cauley, J.A., Center, J.R., Chapurlat, R., Christiansen, C., Cooper, C., Crandall, C.J., Cummings, S.R., da Silva, J.A., Dawson-Hughes, B., Diez-Perez, A., Dufour, A.B., Eisman, J.A., Elders, P.J., Ferrari, S.J., Fujita, Y., Fujiwara, S., Gluer, C.C., Goldshtein, I., Goltzman, D., Gudnason, V., Hall, J., Hans, D., Hoff, M., Hollick, R.J., Huisman, M., Iki, M., Ish-Shalom, S., Joens, G., Karlsson, M.K., Khosla, S., Kiel, D., Koh, W.P., Koromani, F., Kotowicz, M.A., Kroger, H., Kwok, T., Lamy, O., Langhammer, A., Larijani, B., Lippuner, K., Mellstrom, D., Merlijn, T., Nordstrom, A., Nordstrom, P., O'Neill, T.W., Obermayer-Pietsch, B., Ohlsson, C., Orwoll, E.S., Pasco, J., Rivadeneira, F., Schott, A., Shiroma, E.J., Siggeirsdottir, K., Simonsick, E., Sornay-Rendu, E., Sund, R., Swart, K., Szulc, P., Tamaki, J., Torgerson, D.J., Van Schoor, N.M., Van Staa, T.P., Vila, J., Wareham, N.J., Wright, N.C., Yoshimura, N., Zillikens, M.C., Zwart, M., Vandenput, L., Harvey, N.C., Lorentzon, M., Leslie, W.D. 2023. Previous fracture and subsequent fracture risk: A meta-analysis to update FRAX. Osteoporosis International. https://doi.org/10.1007/s00198-023-06870-z. DOI: https://doi.org/10.1007/s00198-023-06870-z Interpretive Summary: The relationship between self-reported falls and fracture risk was estimated in an analysis of 906,532 individuals from 46 cohorts around the globe, including the STOP IT study conducted at the USDA HNRCA. Twenty-three percent of the 906,532 participants reported falling in the past year. Having a fall in the last year was associated with a 41% increase in having a fracture in the women and a 41% increase in the men. This analysis establishes the importance of a prior fall as a risk factor for fracture and provides the justification for including a fall in the last year as a risk factor in the FRAX algorithm that is used globally to assess fracture risk. Technical Abstract: Summary A large international meta-analysis using primary data from 64 cohorts has quantified the increased risk of fracture associated with a previous history of fracture for future use in FRAX. Introduction The aim of this study was to quantify the fracture risk associated with a prior fracture on an international basis and to explore the relationship of this risk with age, sex, time since baseline and bone mineral density (BMD). Methods We studied 665,971 men and 1,438,535 women from 64 cohorts in 32 countries followed for a total of 19.5 million person-years. The effect of a prior history of fracture on the risk of any clinical fracture, any osteoporotic fracture, major osteoporotic fracture, and hip fracture alone was examined using an extended Poisson model in each cohort. Covariates examined were age, sex, BMD, and duration of follow-up. The results of the different studies were merged by using the weighted B-coefficients. Results A previous fracture history, compared with individuals without a prior fracture, was associated with a significantly increased risk of any clinical fracture (hazard ratio, HR = 1.88; 95% CI = 1.72-2.07). The risk ratio was similar for the outcome of osteoporotic fracture (HR = 1.87; 95% CI = 1.69-2.07), major osteoporotic fracture (HR = 1.83; 95% CI = 1.63-2.06), or for hip fracture (HR = 1.82; 95% CI = 1.62-2.06). There was no significant difference in risk ratio between men and women. Subsequent fracture risk was marginally downward adjusted when account was taken of BMD. Low BMD explained a minority of the risk for any clinical fracture (14%), osteoporotic fracture (17%), and for hip fracture (33%). The risk ratio for all fracture outcomes related to prior fracture decreased significantly with adjustment for age and time since baseline examination. Conclusion A previous history of fracture confers an increased risk of fracture of substantial importance beyond that explained by BMD. The effect is similar in men and women. Its quantitation on an international basis permits the more accurate use of this risk factor in case finding strategies. |