Volume 14, Issue 3 pp. 315-322

Impact of Fibroblast Growth Factor 23 on Lipids and Atherosclerosis in Hemodialysis Patients

Eijin Ashikaga

Eijin Ashikaga

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Hirokazu Honda

Corresponding Author

Hirokazu Honda

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

Dr Hirokazu Honda, Division of Nephrology, Department of Medicine, Showa University School of Medicine, 1-5-8 Hatanodai Shinagawa-ku, Tokyo 142-8666, Japan. Email: [email protected]Search for more papers by this author
Hiroki Suzuki

Hiroki Suzuki

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Nozomu Hosaka

Nozomu Hosaka

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Yuki Hirai

Yuki Hirai

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Daisuke Sanada

Daisuke Sanada

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Mari Nakamura

Mari Nakamura

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Hisako Nagai

Hisako Nagai

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Kei Matsumoto

Kei Matsumoto

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Noriyuki Kato

Noriyuki Kato

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Masanori Mukai

Masanori Mukai

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Makoto Watanabe

Makoto Watanabe

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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Keiko Takahashi

Keiko Takahashi

Internal Medicine, Kawasaki Clinic, Kawasaki, Japan

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Kanji Shishido

Kanji Shishido

Internal Medicine, Kawasaki Clinic, Kawasaki, Japan

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Tadao Akizawa

Tadao Akizawa

Division of Nephrology, Department of Medicine, Showa University, Tokyo, and

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First published: 25 May 2010
Citations: 24

Abstract

Levels of fibroblast growth factor (FGF) 23, a phosphatonin, are frequently elevated in patients with end-stage renal disease (ESRD) who are on maintenance hemodialysis (MHD). However, the role of FGF23 remains unclear because renal FGF receptor function might be impaired. The present cross-sectional study examines a cohort of patients (n = 196) on MHD who were not undergoing therapy with lipid-lowering drugs including sevelamer. Non-fasting venous blood samples were withdrawn before the hemodialysis (HD) session on the third day after the previous HD session to measure serum levels of albumin, calcium (Ca), phosphate (P), alkaline phosphatase, intact parathyroid hormone (PTH), total cholesterol (C), high-density lipoprotein (HDL)-C, low-density lipoprotein(LDL)-C, oxidative LDL-C, high-sensitivity C-reactive protein (HsCRP), interleukin-6 (IL-6), and FGF23. Nutritional status was assessed using the geriatric nutritional risk index (GNRI). Carotid intima-medial thickness (CIMT) was assessed using a B-mode ultrasound scanner. FGF23 was positively correlated with P, Caalb×P product, and intact PTH, and inversely correlated with C and non-HDL-C. In the higher FGF23 tertile, levels of both non-HDL-C and C were significantly decreased and CIMT was less elevated compared to the lower FGF23 tertile. Multivariate analysis showed that the higher FGF23 tertile was independently associated with decreases in C (adjusted r2 = 0.14) and non-HDL-C (adjusted r2 = 0.20) levels and with a less-pronounced increase in CIMT (adjusted r2 = 0.14). High FGF23 appears to be an independent biomarker of a decrease in C and non-HDL-C that is negatively associated with atherosclerosis in patients on MHD.

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