Evidence map›Paper›PMID 35399079›Full record

ArticleLipids in health and disease2022

ANGPTL3 impacts proteinuria and hyperlipidemia in primary nephrotic syndrome.

Fu Zhong, Shurao Liu, Yue Li, Guanyu Li, Ming Liu, Jingzhi Wang, Weijing Cui, Yanhong Suo, Xia Gao

Open access · goldAbstract read
In one paragraph

Article in Lipids in health and disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 21 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Fu Zhong *Nephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 318 Renmin Middle Road, 510623, Guangzhou city, China.
Shurao Liu *Pediatric Intensive Care Unit Department, The First People's Hospital of Zhaoqing, 526000, Zhaoqing city, China.
Yue Li *Nephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 318 Renmin Middle Road, 510623, Guangzhou city, China.
Guanyu LiNephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 318 Renmin Middle Road, 510623, Guangzhou city, China.
Ming LiuGuangzhou Institute of Pediatrics, Guangzhou Women and Children's medical center, 510623, Guangzhou city, China.
Jingzhi WangNephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 318 Renmin Middle Road, 510623, Guangzhou city, China.
Weijing CuiPediatric Department, Gansu Provincial Hospital, 730000, Lanzhou City, China.
Yanhong SuoPediatric Department, Gansu Provincial Hospital, 730000, Lanzhou City, China.
Xia Gao *Nephrology Department, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No. 318 Renmin Middle Road, 510623, Guangzhou city, China. gaoxiagz@vip.163.com.
Guangzhou Medical University · CNGansu Provincial Hospital · CNGuangzhou Women and Children Medical Center · CNThe First People's Hospital of Zhaoqing · CN

Funding

National Natural Science Foundation of China 81660130Natural Science Foundation of Gansu Province, China 18JR3RA045Science and Technology Program of Guangzhou, China 202102010222
6 · The paper itself

Abstract

backgroundIt is unclear why primary nephrotic syndrome (PNS) patients often have dyslipidemia. Recent studies have shown that angiopoietin-like protein 3 (ANGPTL3) is an important regulator of lipid metabolism. In this study, we explored how ANGPTL3 impacts dyslipidemia during PNS development.

methodsWe measured the serum levels of ANGPTL3 in PNS patients (n=196). Furthermore, the degree of proteinuria and lipid metabolism were examined in angptl3-overexpressing transgenic (angptl3-tg) mice at different ages. Moreover, in this study, we used the clustered regularly interspaced short palindromic repeats-associated protein 9 (CRISPR/Cas9) system to create angptl3-knockout (angptl3-/-) mice to investigate lipopolysaccharide (LPS)-induced nephrosis.

resultsCompared with that in the healthy group, the serum level of ANGPTL3 in the PNS group was significantly increased (32 (26.35-39.66) ng/ml vs. 70.44 (63.95-76.51) ng/ml, Z =-4.81, P < 0.001). There were significant correlations between the serum level of ANGPTL3 and the levels of cholesterol (r=0.34, P < 0.001), triglycerides (r= 0.25, P = 0.001) and low-density lipoprotein (r= 0.50, P < 0.001) in PNS patients. With increasing age, angptl3-tg mice exhibited increasingly severe hypertriglyceridemia and proteinuria. The pathological features of angptl3-tg mice included rich lipid droplet deposition in hepatocytes and diffuse podocyte effacement. Compared to wild-type mice, angptl3-/- mice showed significantly lower degrees of lipid dysfunction and proteinuria after stimulation with LPS. The effects of ANGPTL3 on nephrotic dyslipidemia were confirmed in cultured hepatocytes subjected to angptl3 knockdown or overexpression. Finally, significant alterations in lipoprotein lipase (LPL) levels were observed in liver tissues from Angptl3-/- and wild-type mice stimulated with LPS.

conclusionsANGPTL3 could be involved in the development of dyslipidemia, as well as proteinuria, during PNS pathogenesis. Inhibition of LPL expression may the mechanism by which ANGPTL3 induces hyperlipidemia in PNS.

Indexed as

Angiopoietin-Like Protein 3DyslipidemiasHyperlipidemiasNephrotic SyndromeAnimalsHumansLipopolysaccharidesMiceProteinuriaTriglyceridesAngiopoietin-Like Protein 3ANGPTL3 protein, humanAngptl3 protein, mouseLipopolysaccharidesTriglyceridesANGPTL3HyperlipidemiaNephrotic syndromeProteinuria

Identifiers

PMID35399079
PMCPMC8996604
OpenAlexW4223547489

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.