Ormone; 1,25D, 1,25-dihydroxyvitamin D; FGF23, fibroblast growth factor 23. (TIF)Figure S5 Multivariate odds ratio for aortic calcifica-Supporting InformationFigure S1 Box and line plots showing the levels of serum Klotho (pg/mL) according to the estimated glomerular filtration rate (eGFR) (mL/min/1.73 m2) or the levels of serum log intact fibroblast growth factor 23 (FGF23) (pg/mL) according to the estimated glomerular filtration rate (eGFR) (mL/min/1.73 m2). The serum soluble Klotho 1655472 levels significantly decreased in association with declines in eGFR (A), while the log-transformed intact FGF23 levels significantly increased in association with declines in eGFR (B). (A) serum Klotho levels, eGFR 90 (stage 1), 799.0 (670.6?40.9); eGFR 60?9 (stage 2), 637.4 (546.2?37.4); eGFR 30?9 (stage 3), 595.4 (498.8?73.9); eGFR 15?9 (stage 4), 578.3 (425.9?51.0); eGFR 0?4 (stage 5), 525.1 (389.0?61.4) pg/mL. (A, B) eGFR 90, n = 11; 60?9, n = 36; 30?9, n = 31; 15?9, n = 16, 0?4, n = 20. *, **, *** and **** indicate p,0.05, p,0.01, p,0.005 and p,0.001, respectively. The boxes denote the medians and 25th and 75th percentiles. The lines mark the 5th and 95th percentiles. (TIF)Table S1 A multiple logistic regression analysis of buy KPT-9274 predictors of FMD 6.0 . (DOC) Table S2 A multiple logistic regression analysis of predictors of max IMT 1.1 mm. (DOC) Table S3 A multiple logistic regression analysis of predictors of ACI.0 . (DOC)Soluble Klotho and Arterial Stiffness in CKDAcknowledgmentsWe thank Ms. M. Hada, H. Tsuji and S. Kameshima for their technical assistance. We also extend our gratitude to the physicians in the Department of Medicine and Clinical Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences for the collection of blood samples.Author ContributionsConceived and designed the experiments: MK HS KN HI H. Makino. Performed the experiments: MK TI. Analyzed the data: MK HS H. Morinaga AO TY YK HAU SK YM. Contributed reagents/materials/ analysis tools: H. Morinaga KT AO. Wrote the paper: MK HS.
Age-related macular degeneration (AMD) is a leading cause of irreversible vision loss in industrialized countries. The exact etiology of this complex multifactorial disease is unknown, but is believed to involve interaction of genetic and environmental factors [1]. There is some evidence that trace elements might play a role in the pathogenesis of AMD. Iron is a potent generator of reactive oxygen species (ROS), whose generation within mitochondria and lysosomes may promote cell death [2]. Iron has been suggested as a source of oxidants in AMD, as AMD-affected maculas were found to have higher concentrations of iron than healthy agematched maculas [3]. Iron was found in the retinal pigment epithelium (RPE) and Bruch’s membrane in early AMD, geographic atrophy, and exudative AMD. Tobacco smoking is one of the few established environmental risk factors for AMD [4]. Recent research has implicated JSH-23 web cadmium as a possible contributor to smoking-related AMD. It was reportedthat cadmium levels in retinal tissues were approximately twice as high in smokers as in nonsmokers [5]. In addition, higher urinary cadmium levels, indicating a higher total body burden of cadmium, were found in smokers who had AMD compared to smokers who did not have AMD [6]. These findings raised the possibility that cadmium exposure might play a role in tobaccorelated AMD. Cadmium is a potent inflammatory agent and increases oxidative stress [7]. Oxidative stres.Ormone; 1,25D, 1,25-dihydroxyvitamin D; FGF23, fibroblast growth factor 23. (TIF)Figure S5 Multivariate odds ratio for aortic calcifica-Supporting InformationFigure S1 Box and line plots showing the levels of serum Klotho (pg/mL) according to the estimated glomerular filtration rate (eGFR) (mL/min/1.73 m2) or the levels of serum log intact fibroblast growth factor 23 (FGF23) (pg/mL) according to the estimated glomerular filtration rate (eGFR) (mL/min/1.73 m2). The serum soluble Klotho 1655472 levels significantly decreased in association with declines in eGFR (A), while the log-transformed intact FGF23 levels significantly increased in association with declines in eGFR (B). (A) serum Klotho levels, eGFR 90 (stage 1), 799.0 (670.6?40.9); eGFR 60?9 (stage 2), 637.4 (546.2?37.4); eGFR 30?9 (stage 3), 595.4 (498.8?73.9); eGFR 15?9 (stage 4), 578.3 (425.9?51.0); eGFR 0?4 (stage 5), 525.1 (389.0?61.4) pg/mL. (A, B) eGFR 90, n = 11; 60?9, n = 36; 30?9, n = 31; 15?9, n = 16, 0?4, n = 20. *, **, *** and **** indicate p,0.05, p,0.01, p,0.005 and p,0.001, respectively. The boxes denote the medians and 25th and 75th percentiles. The lines mark the 5th and 95th percentiles. (TIF)Table S1 A multiple logistic regression analysis of predictors of FMD 6.0 . (DOC) Table S2 A multiple logistic regression analysis of predictors of max IMT 1.1 mm. (DOC) Table S3 A multiple logistic regression analysis of predictors of ACI.0 . (DOC)Soluble Klotho and Arterial Stiffness in CKDAcknowledgmentsWe thank Ms. M. Hada, H. Tsuji and S. Kameshima for their technical assistance. We also extend our gratitude to the physicians in the Department of Medicine and Clinical Science, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences for the collection of blood samples.Author ContributionsConceived and designed the experiments: MK HS KN HI H. Makino. Performed the experiments: MK TI. Analyzed the data: MK HS H. Morinaga AO TY YK HAU SK YM. Contributed reagents/materials/ analysis tools: H. Morinaga KT AO. Wrote the paper: MK HS.
Age-related macular degeneration (AMD) is a leading cause of irreversible vision loss in industrialized countries. The exact etiology of this complex multifactorial disease is unknown, but is believed to involve interaction of genetic and environmental factors [1]. There is some evidence that trace elements might play a role in the pathogenesis of AMD. Iron is a potent generator of reactive oxygen species (ROS), whose generation within mitochondria and lysosomes may promote cell death [2]. Iron has been suggested as a source of oxidants in AMD, as AMD-affected maculas were found to have higher concentrations of iron than healthy agematched maculas [3]. Iron was found in the retinal pigment epithelium (RPE) and Bruch’s membrane in early AMD, geographic atrophy, and exudative AMD. Tobacco smoking is one of the few established environmental risk factors for AMD [4]. Recent research has implicated cadmium as a possible contributor to smoking-related AMD. It was reportedthat cadmium levels in retinal tissues were approximately twice as high in smokers as in nonsmokers [5]. In addition, higher urinary cadmium levels, indicating a higher total body burden of cadmium, were found in smokers who had AMD compared to smokers who did not have AMD [6]. These findings raised the possibility that cadmium exposure might play a role in tobaccorelated AMD. Cadmium is a potent inflammatory agent and increases oxidative stress [7]. Oxidative stres.
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