Successful treatment of lipoprotein glomerulopathy in a daughter and a mother using niceritrol
Abstract
We report two patients, a daughter and a mother, with lipoprotein glomerulopathy (LPG) who were successfully treated with niceritrol. Both patients carried a mutation in the apolipoprotein E (apoE) gene known as ApoE Tokyo/Maebashi. The daughter was found to have proteinuria at the age of 4 years. Four years later, she was diagnosed as having LPG based on a renal biopsy. She was treated with several medications including pravastatin, ethyl icosapentate, enalapril, warfarin and cyclophosphamide, all of which failed to reduce her proteinuria. At the age of 17 years, she exhibited an increase in proteinuria and a decline in renal function, despite ongoing treatment with pravastatin and enalapril. After switching from pravastatin to niceritrol, a marked reduction in the proteinuria and an improvement in renal function were observed. Her mother was found to have proteinuria at the age of 57 years and was diagnosed as having LPG based on a renal biopsy. She was also treated with niceritrol, resulting in an improvement in her proteinuria and renal function. These cases suggest that niceritrol might be a useful therapeutic option for LPG.
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Two case studies and one small population study showed that lipid-lowering therapies are linked to improved renal status in LPG patients.
“Two case studies and one small population study showed that lipid-lowering therapies are linked to improved renal status in LPG patients (27)(28)(29).”
From Macrophage-derived apoESendai suppresses atherosclerosis while causing lipoprotein glomerulopathy in hyperlipidemic mice (2014) · cites this paper as [27]
Cites
Lipoprotein Glomerulopathy: Glomerular Lipoprotein Thrombi in a Patient With Hyperlipoproteinemia
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Tavori, H., Fan, D., Giunzioni, I., Zhu, L., Linton, M. F., Fogo, A. B., & Fazio, S. (2014) · Journal of Lipid Research · doi:10.1194/jlr.m049874 · Cited by 10 · see citing works
Lipoprotein Glomerulopathy, First Case Report from Canada
Ting, J. A., McRae, S. A., Schwartz, D., Barbour, S. J., & Riazy, M. (2022) · International Journal of Nephrology and Renovascular Disease · doi:10.2147/ijnrd.s364890 · Cited by 7 · see citing works
Wang, R., Zhao, C., Chen, W., Liu, Z., & Xie, F. (2022) · Journal of Medical Case Reports · doi:10.1186/s13256-022-03302-0 · Cited by 5 · see citing works
- Authors
- Hamatani, H., Hiromura, K., Kobatake, K., Yoshida, H., Kobayashi, S., Yoneda, N., Kayakabe, K., Matsumoto, T., Kuroiwa, T., Ueki, K., & Nojima, Y.
- Affiliations
- Sanshikai Toho Hospital (JP)
- Gunma University (JP)
- Corresponding author
- Hamatani, Hiroko
- Venue
- Clinical and Experimental Nephrology
- Published
- 2010-09-15
- Volume
- 14
- Issue
- 6
- Pages
- 619-624
- ISSN
- 1342-1751 (ISSN-L)
- 1437-7799
- OpenAlex
- W2067052274
- Cited by
- 11
- References
- 2
- Citations by year
- 2022: 3 · 2021: 1 · 2018: 1 · 2016: 2 · 2014: 1 · 2013: 3
- FWCI
- 0.75
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Clinical and Experimental Nephrology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- lipoprotein glomerulopathy, apolipoprotein E, proteinuria, familial hypercholesterolemia, pravastatin, renal function, familial case
- MeSH terms
- Adolescent, Apolipoproteins E, Child, Child, Preschool, Female, Humans, Kidney Glomerulus, Middle Aged, Mutation, Nephrotic Syndrome, Niceritrol, Pedigree, Proteinuria
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