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Reduced Renal α-Klotho Expression in CKD Patients and Its Effect on Renal Phosphate Handling and Vitamin D Metabolism

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  • Hirokazu Sakan
  • Kimihiko Nakatani
  • Osamu Asai
  • Akihiro Imura
  • Tomohiro Tanaka
  • Shuhei Yoshimoto
  • Noriyuki Iwamoto
  • Norio Kurumatani
  • Masayuki Iwano
  • Yo-ichi Nabeshima
  • Noboru Konishi
  • Yoshihiko Saito

Abstract

Renal α-Klotho (α-KL) plays a fundamental role as a co-receptor for fibroblast growth factor 23 (FGF23), a phosphaturic hormone and regulator of 1,25(OH)2 vitamin D3 (1,25VitD3). Disruption of FGF23-α-KL signaling is thought to be an early hallmark of chronic kidney disease (CKD) involving reduced renal α-KL expression and a reciprocal rise in serum FGF23. It remains unclear, however, whether the rise in FGF23 is related to the loss of renal α-KL. We evaluated α-KL expression in renal biopsy samples and measured levels of several parameters of mineral metabolism, as well as soluble α-KL (sKL), in serum and urinary samples from CKD patients (n = 236). We found that although renal α-KL levels were significantly reduced and serum FGF23 levels were significantly elevated in early and intermediate CKD, serum phosphate levels remained within the normal range. Multiple regression analysis showed that the increases in FGF23 were significantly associated with reduced renal function and elevated serum phosphate, but were not associated with loss of renal α-KL. Moreover, despite falling renal α-KL levels, the increase in FGF23 enhanced urinary fractional excretion of phosphate and reduced serum 1,25VitD3 levels in early and intermediate CKD, though not in advanced CKD. Serum sKL levels also fell significantly over the course of CKD, and renal α-KL was a significant independent determinant of sKL. These results demonstrate that FGF23 levels rise to compensate for renal failure-related phosphate retention in early and intermediate CKD. This enables FGF23-α-KL signaling and a neutral phosphate balance to be maintained despite the reduction in α-KL. In advanced CKD, however, renal α-KL declines further. This disrupts FGF23 signaling, and serum phosphate levels significantly increase, stimulating greater FGF23 secretion. Our results also suggest the serum sKL concentration may be a useful marker of renal α-KL expression levels.

Suggested Citation

  • Hirokazu Sakan & Kimihiko Nakatani & Osamu Asai & Akihiro Imura & Tomohiro Tanaka & Shuhei Yoshimoto & Noriyuki Iwamoto & Norio Kurumatani & Masayuki Iwano & Yo-ichi Nabeshima & Noboru Konishi & Yoshi, 2014. "Reduced Renal α-Klotho Expression in CKD Patients and Its Effect on Renal Phosphate Handling and Vitamin D Metabolism," PLOS ONE, Public Library of Science, vol. 9(1), pages 1-9, January.
  • Handle: RePEc:plo:pone00:0086301
    DOI: 10.1371/journal.pone.0086301
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    1. Itaru Urakawa & Yuji Yamazaki & Takashi Shimada & Kousuke Iijima & Hisashi Hasegawa & Katsuya Okawa & Toshiro Fujita & Seiji Fukumoto & Takeyoshi Yamashita, 2006. "Klotho converts canonical FGF receptor into a specific receptor for FGF23," Nature, Nature, vol. 444(7120), pages 770-774, December.
    2. Makoto Kuro-o & Yutaka Matsumura & Hiroki Aizawa & Hiroshi Kawaguchi & Tatsuo Suga & Toshihiro Utsugi & Yoshio Ohyama & Masahiko Kurabayashi & Tadashi Kaname & Eisuke Kume & Hitoshi Iwasaki & Akihiro , 1997. "Mutation of the mouse klotho gene leads to a syndrome resembling ageing," Nature, Nature, vol. 390(6655), pages 45-51, November.
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