Zhangxue Hu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Zhangxue Hu has a total of 198 co-authors. Here are the top co-authors by number of shared publications:
Zhi Yang
West China Hospital, Sichuan University Department of Nephrology Chengdu
8 shared publications- Yuan Yang
Department of Medical Genetics, State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, China
7 shared publications Hongyan Wu
West China Hospital, Sichuan University Department of Nephrology Chengdu
6 shared publicationsSong Lei
Department of Pathology, West China Hospital, Sichuan University, Chengdu, China
6 shared publicationsYuan Yang
Department of Medical Genetics, West China Hospital, Sichuan University, Chengdu, China
6 shared publicationsPing Fu
Renal Division, West China Hospital, Chengdu, China
5 shared publications
Latest Publications
- 28 May 2026
- Published by Wolters Kluwer Health in American Journal of Therapeutics
Bortezomib-Induced Acute Interstitial Nephritis
- 28 May 2026
- Published by Wolters Kluwer Health in American Journal of Therapeutics
Bortezomib-Induced Acute Interstitial Nephritis
- 9 April 2026
- Published by Wolters Kluwer Health in American Journal of Therapeutics
- Vol. 33 (3) , e261-e264
Acute Interstitial Nephritis in a Patient With BRAF V600E Mutant Non-small Cell Lung Cancer Treated With Dabrafenib and Trametinib
- 9 April 2026
- Published by Wolters Kluwer Health in American Journal of Therapeutics
- Vol. 33 (3) , e261-e264
Acute Interstitial Nephritis in a Patient With BRAF V600E Mutant Non-small Cell Lung Cancer Treated With Dabrafenib and Trametinib
- Open Access
- 26 February 2026
- Published by Springer Nature in BMC Nephrology
- Vol. 27 (1)
Concurrence of renal amyloidosis and membranous nephropathy: a case series and literature review
Amyloidosis is a group of heterogeneous diseases characterized by the deposition of amyloid fibrils in various organs and tissues. Membranous nephropathy (
- 26 February 2026
- Published by Springer Nature in BMC Nephrology
- Vol. 27 (1)
Open AccessConcurrence of renal amyloidosis and membranous nephropathy: a case series and literature review
Amyloidosis is a group of heterogeneous diseases characterized by the deposition of amyloid fibrils in various organs and tissues. Membranous nephropathy (
- Open Access
- 21 July 2025
- Published by Oxford University Press (OUP) in Clinical Kidney Journal
- Vol. 18 (8) , sfaf234
Identification of a founder haplotype of APOE-Kyoto variant in lipoprotein glomerulopathy
Background: Lipoprotein glomerulopathy (LPG) is a rare autosomal dominant inherited kidney disease with incomplete penetrance, characterized by nephrotic-range proteinuria, hypertriglyceridemia, and progressive renal dysfunction with elevated serum apoE level. More than fifteen APOE mutations have been associated with LPG, with APOE Kyoto (Arg43Cys) the leading mutation in about 200 patients. We previously observed clustering of APOE Kyoto-causing LPG in a Han population in China. We now explore the haplotype of the APOE Kyoto heterozygotes and the distribution of LPG patients in China. Methods: 115 APOE Kyoto heterozygotes were enrolled and identified by Sanger sequencing, and in this study, the haplotypes of Kyoto and counterpart alleles were investigated by TA cloning and Sanger sequencing. Results: 114 out of 115 APOE Kyoto alleles shared an identical haplotype, likely from haplotype 1 inε3. Among heterozygotes, the counterpart of APOE Kyoto allele showed haplotype diversity, and the difference in haplotype distribution of the counterpart allele was not observed between LPG patients and asymptomatic carriers. Conclusions: This study provides further evidence for the founder effect of APOE Kyoto may play a critical role in the progression of LPG.
- 21 July 2025
- Published by Oxford University Press (OUP) in Clinical Kidney Journal
- Vol. 18 (8) , sfaf234
Open AccessIdentification of a founder haplotype of APOE-Kyoto variant in lipoprotein glomerulopathy
Background: Lipoprotein glomerulopathy (LPG) is a rare autosomal dominant inherited kidney disease with incomplete penetrance, characterized by nephrotic-range proteinuria, hypertriglyceridemia, and progressive renal dysfunction with elevated serum apoE level. More than fifteen APOE mutations have been associated with LPG, with APOE Kyoto (Arg43Cys) the leading mutation in about 200 patients. We previously observed clustering of APOE Kyoto-causing LPG in a Han population in China. We now explore the haplotype of the APOE Kyoto heterozygotes and the distribution of LPG patients in China. Methods: 115 APOE Kyoto heterozygotes were enrolled and identified by Sanger sequencing, and in this study, the haplotypes of Kyoto and counterpart alleles were investigated by TA cloning and Sanger sequencing. Results: 114 out of 115 APOE Kyoto alleles shared an identical haplotype, likely from haplotype 1 inε3. Among heterozygotes, the counterpart of APOE Kyoto allele showed haplotype diversity, and the difference in haplotype distribution of the counterpart allele was not observed between LPG patients and asymptomatic carriers. Conclusions: This study provides further evidence for the founder effect of APOE Kyoto may play a critical role in the progression of LPG.
- Open Access
- 10 July 2025
- Published by Frontiers Media SA in Frontiers in Immunology
- Vol. 16, 1590822
Research progress on damage-associated molecular patterns in acute kidney injury
Acute kidney injury (AKI) is a clinical syndrome characterized by a sudden dysfunction of the kidney, which is common worldwide, with a relatively high incidence and mortality rate. Damage to the proximal renal tubule is a pathological hallmark of AKI, and inflammation triggered by the overactivation of the immune system is a common cause of proximal renal tubular injury, which is an important contributing factor in AKI exacerbation. Damage-associated molecular patterns (DAMPs) are endogenous molecules released by cells in response to external stimuli that can trigger an inflammatory response by binding to specific pattern recognition receptors (PRRs). Numerous studies have indicated that when the kidney is exposed to external stress or chemical stimuli, injured cells actively secrete or passively release various DAMPs, which can exacerbate or attenuate kidney injury by stimulating or inhibiting the inflammatory response through binding to the appropriate receptor. Currently, there is a lack of early diagnostic biomarkers and specific therapeutic strategies for AKI in the clinic have been established, and given the important role of the release of DAMPs in the regulation of inflammatory response, they will highly likely become favorable candidate biomarkers and clinical therapeutic targets for AKI. Therefore, a deeper understanding of the types of DAMPs and the specific mechanisms of their actions will provide more possibilities for the specific AKI diagnosis and treatment.
- 10 July 2025
- Published by Frontiers Media SA in Frontiers in Immunology
- Vol. 16, 1590822
Open AccessResearch progress on damage-associated molecular patterns in acute kidney injury
Acute kidney injury (AKI) is a clinical syndrome characterized by a sudden dysfunction of the kidney, which is common worldwide, with a relatively high incidence and mortality rate. Damage to the proximal renal tubule is a pathological hallmark of AKI, and inflammation triggered by the overactivation of the immune system is a common cause of proximal renal tubular injury, which is an important contributing factor in AKI exacerbation. Damage-associated molecular patterns (DAMPs) are endogenous molecules released by cells in response to external stimuli that can trigger an inflammatory response by binding to specific pattern recognition receptors (PRRs). Numerous studies have indicated that when the kidney is exposed to external stress or chemical stimuli, injured cells actively secrete or passively release various DAMPs, which can exacerbate or attenuate kidney injury by stimulating or inhibiting the inflammatory response through binding to the appropriate receptor. Currently, there is a lack of early diagnostic biomarkers and specific therapeutic strategies for AKI in the clinic have been established, and given the important role of the release of DAMPs in the regulation of inflammatory response, they will highly likely become favorable candidate biomarkers and clinical therapeutic targets for AKI. Therefore, a deeper understanding of the types of DAMPs and the specific mechanisms of their actions will provide more possibilities for the specific AKI diagnosis and treatment.
- Open Access
- 28 October 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 282, 136922
Identification of c.146G > A mutation in a Fabry patient and its correction by customized Cas9 base editors in vitro
- 28 October 2024
- Published by Elsevier in International Journal of Biological Macromolecules
- Vol. 282, 136922
Open AccessIdentification of c.146G > A mutation in a Fabry patient and its correction by customized Cas9 base editors in vitro
- 11 October 2024
- Published by Elsevier in Biochemical Pharmacology
- Vol. 230 (Pt 1) , 116575
Omega-3 polyunsaturated fatty acids alleviate hyperuricemic nephropathy by inhibiting renal pyroptosis through GPR120
- 11 October 2024
- Published by Elsevier in Biochemical Pharmacology
- Vol. 230 (Pt 1) , 116575
Omega-3 polyunsaturated fatty acids alleviate hyperuricemic nephropathy by inhibiting renal pyroptosis through GPR120
- 8 September 2024
- Published by Springer Nature in International Urology and Nephrology
- Vol. 57 (2) , 561-569
U-shaped association between hemoglobin levels and albuminuria in US adults: a cross-sectional study
Purpose This study aimed to explore the correlation between hemoglobin levels and albuminuria in US adults. Methods This cross-sectional investigation analyzed the National Health and Nutrition Examination Survey (NHANES) information from 2011 to 2020. Data on hemoglobin, albuminuria, and other variables were collected from all participants. The logistic-regression analyses and smoothed curves were used to substantiate the research objectives. Results The average age of the 8,868 participants was 49.5 ± 17.3 years, and 49.3% were men. The prevalence of albuminuria was 12.1%. After adjusting for potential variables in the logistic-regression analysis models, hemoglobin (per 1 g/dL increase) was inversely associated with the presence of albuminuria (odds ratio [OR], 0.92; 95% confidence interval [95%CI], 0.87–0.97). Compared with participants in quartile 3 (Q3, 14.1–15.0 g/dL) for hemoglobin levels, those in the lowest quartile 1 (Q1, 6.1–13.0 g/dL) and highest quartile 4 (Q4, 15.1–19.6 g/dL) had adjusted ORs for albuminuria of 1.48 (95% CI, 1.19–1.85) and 1.11 (95% CI, 0.9–1.38), respectively. Our observations indicated a U-shaped association between hemoglobin levels and albuminuria, with a point of inflection at approximately 15.5 g/dL. The effect sizes and CIs below and above this point were 0.853 (95% CI, 0.798–0.912) and 1.377 (95% CI, 1.055–1.797), respectively. Conclusion This study indicates that the presence of albuminuria is linked to both low and high hemoglobin levels in US adults. The management of hemoglobin may benefit kidney health.
- 8 September 2024
- Published by Springer Nature in International Urology and Nephrology
- Vol. 57 (2) , 561-569
U-shaped association between hemoglobin levels and albuminuria in US adults: a cross-sectional study
Purpose This study aimed to explore the correlation between hemoglobin levels and albuminuria in US adults. Methods This cross-sectional investigation analyzed the National Health and Nutrition Examination Survey (NHANES) information from 2011 to 2020. Data on hemoglobin, albuminuria, and other variables were collected from all participants. The logistic-regression analyses and smoothed curves were used to substantiate the research objectives. Results The average age of the 8,868 participants was 49.5 ± 17.3 years, and 49.3% were men. The prevalence of albuminuria was 12.1%. After adjusting for potential variables in the logistic-regression analysis models, hemoglobin (per 1 g/dL increase) was inversely associated with the presence of albuminuria (odds ratio [OR], 0.92; 95% confidence interval [95%CI], 0.87–0.97). Compared with participants in quartile 3 (Q3, 14.1–15.0 g/dL) for hemoglobin levels, those in the lowest quartile 1 (Q1, 6.1–13.0 g/dL) and highest quartile 4 (Q4, 15.1–19.6 g/dL) had adjusted ORs for albuminuria of 1.48 (95% CI, 1.19–1.85) and 1.11 (95% CI, 0.9–1.38), respectively. Our observations indicated a U-shaped association between hemoglobin levels and albuminuria, with a point of inflection at approximately 15.5 g/dL. The effect sizes and CIs below and above this point were 0.853 (95% CI, 0.798–0.912) and 1.377 (95% CI, 1.055–1.797), respectively. Conclusion This study indicates that the presence of albuminuria is linked to both low and high hemoglobin levels in US adults. The management of hemoglobin may benefit kidney health.
- 3 April 2024
- Published by SAGE Publications in Lupus
- Vol. 33 (6) , 644-649
Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review
The interleukin (IL)-17 axis is involved in many inflammatory and autoimmune diseases. Secukinumab, an IL-17 inhibitor, has been approved for psoriasis treatment. There are accumulating cases of lupus erythematosus induced by IL-17 inhibition. Lupus nephritis after IL-17 inhibition has not been reported. We report the case of a 57-year-old man who developed membranous lupus nephritis after secukinumab treatment for psoriasis. Anti-SSA and PM-Scl antibodies were positive. dsDNA, anti-Smith, and anti-histone antibodies were negative, and serum complement was low. Secukinumab was discontinued, while tacrolimus was initiated, subsequently switched to cyclosporin, belimumab, glucocorticosteroid, and hydroxychloroquine with a good response. The relationship between lupus erythematosus and IL-17 inhibition requires further research.
- 3 April 2024
- Published by SAGE Publications in Lupus
- Vol. 33 (6) , 644-649
Membranous lupus nephritis secondary to secukinumab therapy: A case report and literature review
The interleukin (IL)-17 axis is involved in many inflammatory and autoimmune diseases. Secukinumab, an IL-17 inhibitor, has been approved for psoriasis treatment. There are accumulating cases of lupus erythematosus induced by IL-17 inhibition. Lupus nephritis after IL-17 inhibition has not been reported. We report the case of a 57-year-old man who developed membranous lupus nephritis after secukinumab treatment for psoriasis. Anti-SSA and PM-Scl antibodies were positive. dsDNA, anti-Smith, and anti-histone antibodies were negative, and serum complement was low. Secukinumab was discontinued, while tacrolimus was initiated, subsequently switched to cyclosporin, belimumab, glucocorticosteroid, and hydroxychloroquine with a good response. The relationship between lupus erythematosus and IL-17 inhibition requires further research.