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. 2020 Mar 31;24(7):630–637. doi: 10.1007/s10157-020-01879-8

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Adjusted incidence rate for all-cause mortality (a) and cardiovascular mortality (b) stratified by levels of serum intact parathyroid hormone and serum calcium. Ca calcium, iPTH intact parathyroid hormone. Incidence rate ratios were adjusted for patients’ characteristics (age, sex, primary kidney disease, diabetes, dialysis duration, cardiovascular disease, pulmonary disease, liver disease, malignancy, and history of parathyroidectomy) and time-dependent variables (vitamin D receptor activators, phosphate binders, calcimimetics, serum albumin level, hemoglobin level, body mass index, Kt/V, and dialysate calcium concentration)