J Korean Med Sci. 2014;29 Suppl 2(Suppl 2):S123-30.
Urinary sodium excretion has positive correlation with activation of urinary renin angiotensin system and reactive oxygen species in hypertensive chronic kidney disease.
제1저자 안신영 · 교신저자 진호준
소속 (9)
- Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea. ; Department of Immunology, Seoul National University Postgraduate School, Seoul, Korea.
- Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
- Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
- Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea.
- Department of Internal Medicine, Dongguk University Ilsan Hospital, Goyang, Korea.
- Department of Internal Medicine, Kyung Hee University Medical Center, Seoul, Korea.
- Department of Internal Medicine, Seoul St. Mary's Hospital, Seoul, Korea.
- Department of Internal Medicine, Seoul National University Boramae Medical Center, Seoul, Korea.
- Research Institute of Salt and Health, Seoul, Korea. ; Seoul K-Clinic, Seoul, Korea.
Abstract
It is not well described the pathophysiology of renal injuries caused by a high salt intake in humans. The authors analyzed the relationship between the 24-hr urine sodium-to-creatinine ratio (24HUna/cr) and renal injury parameters such as urine angiotensinogen (uAGT/cr), monocyte chemoattractant peptide-1 (uMCP1/cr), and malondialdehyde-to-creatinine ratio (uMDA/cr) by using the data derived from 226 hypertensive chronic kidney disease patients. At baseline, the 24HUna/cr group or levels had a positive correlation with uAGT/cr and uMDA/cr adjusted for related factors (P<0.001 for each analysis). When we estimated uAGT/cr in the 24HUna/cr groups by ANCOVA, the uAGT/cr in patients with ≥200 mEq/g cr was higher than in patients with <100 mEq/g cr (708 [95% CI, 448-967] vs. 334 [95% CI, 184-483] pg/mg cr, P=0.014). Similarly, uMDA/cr was estimated as 0.17 (95% CI, 0.14-0.21) pM/mg cr in patients with <100 mEq/g cr and 0.27 (95% CI, 0.20-0.33) pM/mg cr in patients with ≥200 mEq/g cr (P=0.016). During the 16-week follow-up period, an increase in urinary sodium excretion predicted an increase in urinary angiotensinogen excretion. In conclusion, high salt intake increases renal renin-angiotensin-system (RAS) activation, primarily, and directly or indirectly affects the production of reactive oxygen species through renal RAS activation.
Keywords
AngiotensinogenChronic Renal InsufficiencyReninSodium Chloride
Figures
그림 출처: PubMed Central 공개 논문 (PMC4194282)
Conflict of interest statement
The authors have no conflicts of interest to disclose.
그 밖의 정보
- 출판 형태
- Journal Article
- 저널
- Journal of Korean medical science · eISSN 1598-6357
- 전자 출판
- 2014-09-30
- MeSH
- Adult · Aged · Angiotensinogen / urine · Chemokine CCL2 / urine · Creatine / urine · Demography · Female · Follow-Up Studies · Humans · Hypertension / complications · Male · Malondialdehyde / urine · Middle Aged · Reactive Oxygen Species / metabolism · Renal Insufficiency, Chronic / complications / pathology · Renin-Angiotensin System / physiology · Sodium, Dietary / urine · Urine Specimen Collection
- Substances
- CCL2 protein, human · Chemokine CCL2 · Reactive Oxygen Species · Sodium, Dietary · Angiotensinogen · Malondialdehyde · Creatine
- 참고문헌
- 31편