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Oral phosphate binders and incident osteoporotic fracture in patients on dialysis.
Kim, Ji Eun; Park, Jina; Jang, Yunyoung; Kang, Eunjeong; Kim, Yong Chul; Kim, Dong Ki; Joo, Kwon Wook; Kim, Yon Su; Lee, Hajeong.
Afiliação
  • Kim JE; Department of Internal Medicine, Korea University Guro Hospital, Seoul, Republic of Korea.
  • Park J; Biomedical Research Institute, Seoul National University Hospital, Seoul, Republic of Korea.
  • Jang Y; Transplantation Center, Seoul National University Hospital, Seoul, Republic of Korea.
  • Kang E; Transplantation Center, Seoul National University Hospital, Seoul, Republic of Korea.
  • Kim YC; Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Kim DK; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Joo KW; Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Kim YS; Department of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
  • Lee H; Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Article em En | MEDLINE | ID: mdl-38886108
ABSTRACT
BACKGROUND AND

HYPOTHESIS:

End-stage kidney disease (ESKD) has an elevated risk of osteoporotic fractures in relation to mineral and bone disorder (MBD) as well as conventional risks of osteoporosis. We investigated the association between oral phosphate binders, the mainstay of MBD treatment, and osteoporotic fracture in dialysis patients.

METHODS:

We obtained data from the National Health Insurance database for incident dialysis patients without a history of osteoporotic fractures. Participants were categorized into four groups based on their initial 1-year prescription profiles calcium-based phosphate binder (CBPB), non-calcium-based phosphate binder (NCBPB), both calcium and non-calcium-based binders (Mixed), and non-phosphate binder (non-user) groups. The primary outcome was the occurrence of new-onset osteoporotic fractures after 1 year of dialysis. Secondary outcomes included cardiovascular events and mortality.

RESULTS:

Out of 69 368 incident dialysis patients, 22 326, 5020, 2853, and 39 169 were included in the CBPB, NCBPB, mixed, and non-user groups, respectively. The overall risk of osteoporotic fractures was lower in patients taking any phosphate binders compared to non-users. Specifically, only the CBPB group showed a reduced risk of vertebral (adjusted hazard ratio (aHR) 0.83 [0.76-0.92]), hip (aHR 0.81 [0.74-0.89]), and distal radius (aHR 0.88 [0.78-0.99]) fractures compared to non-users. This relationship was represented by a time-dependent manner with fracture risk reduction in patients taking CBPB for 3-6 months (aHR 0.9 [0.83-0.99]) and ≥ 6 months (aHR 0.83 [0.78-0.89]), compared to those using CBPB for less than 3 months. Additionally, only the CBPB group had a lower risk of MACE, cardiac arrest, and ventricular arrhythmia than non-users. All phosphorus binder groups showed a reduced mortality risk compared to non-users.

CONCLUSIONS:

Our findings indicate that the using phosphate binders in ESKD patients is lowers the risk of osteoporotic fractures. Notably, those taking CBPB had a reduced risk without increasing cardiovascular events or mortality compared to non-users.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nephrol Dial Transplant Assunto da revista: NEFROLOGIA / TRANSPLANTE Ano de publicação: 2024 Tipo de documento: Article