Evidence map›Paper›PMID 35743929›Full record

ArticleLife (Basel, Switzerland)2022

Anti-Inflammatory, Antioxidant, and Anti-Atherosclerotic Effects of Natural Supplements on Patients with FMF-Related AA Amyloidosis: A Non-Randomized 24-Week Open-Label Interventional Study.

Micol Romano, Facundo Garcia-Bournissen, David Piskin, Ulkumen Rodoplu, Lizzy Piskin, Abdelbaset A Elzagallaai, Tunc Tuncer, Siren Sezer, Didar Ucuncuoglu, Tevfik Honca and 5 more

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

15 authors at 7 institutions in 4 countries.

Micol RomanoDepartment of Paediatrics, Division of Paediatric Rheumatology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.
Facundo Garcia-BournissenDepartment of Paediatrics, Division of Paediatric Clinical Pharmacology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.ORCID 0000-0002-8732-247X
David PiskinCanadian Behcet and Autoinflammatory Disease Center (CAN BE AID), Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.
Ulkumen RodopluEmergency Medicine Association of Turkey of All, 35220 Izmir, Turkey.
Lizzy PiskinRobarts Research Institute, University of Western Ontario, London, ON N6A 3K7, Canada.
Abdelbaset A ElzagallaaiSchulich School of Medicine & Dentistry, Physiology and Pharmacology, University of Western Ontario, London, ON N6A 3K7, Canada.
Tunc TuncerUnit of Biochemistry, Epigenetic Health Solutions, 06810 Ankara, Turkey.
Siren SezerDivision of Nephrology, Faculty of Medicine, Atilim University, 06830 Ankara, Turkey.
Didar UcuncuogluDepartment of Food Engineering, Faculty of Engineering, Cankiri Karatekin University, 18100 Cankiri, Turkey.ORCID 0000-0002-2640-5976
Tevfik HoncaUnit of Biochemistry, Gur Life Hospital, 26320 Eskisehir, Turkey.ORCID 0000-0003-3723-1374
Dimitri PoddigheDepartment of Medicine, Nazarbayev University School of Medicine, Nur-Sultan 010000, Kazakhstan.ORCID 0000-0001-6431-9334
Izzet YavuzDepartment of Nephrology, Lokman Hekim University, 06510 Ankara, Turkey.
Peter StenvinkelDepartment of Renal Medicine M99, Karolinska Institute, Karolinska University Hospital, 17164 Stockholm, Sweden.ORCID 0000-0002-8785-4820
Mahmut Ilker YilmazUnit of Nephrology, Center for Epigenetic Health Solutions, 06810 Ankara, Turkey.ORCID 0000-0002-2775-2582
Erkan DemirkayaDepartment of Paediatrics, Division of Paediatric Rheumatology, Schulich School of Medicine & Dentistry, University of Western Ontario, London, ON N6A 5W9, Canada.ORCID 0000-0003-4525-1789
Western University · CAAtilim University · TRÇankırı Karatekin University · TREskişehir City Hospital · TRKarolinska University Hospital · SELokman Hekim Üniversitesi · TRNational Research Center for Maternal and Child Health · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to evaluate the effect of a combination of natural products on parameters related to inflammation, endothelial dysfunction, and oxidative stress in a cohort of familial Mediterranean fever (FMF) patients with Serum Amyloid A amyloidosis, in a non-randomized, 24-week open-label interventional study. Morinda citrifolia (anti-atherosclerotic-AAL), omega-3 (anti-inflammatory-AIC), and extract with Alaskan blueberry (antioxidant-AOL) were given to patients with FMF-related biopsy-proven AA amyloidosis. Patients were >18 years and had proteinuria (>3500 mg/day) but a normal estimated glomerular filtration rate (eGFR). Arterial flow-mediated dilatation (FMD), carotid intima media thickness (CIMT), and serum biomarkers asymmetric dimethylarginine (ADMA), high sensitivity C-reactive protein (hs-CRP), pentraxin (PTX3), malondialdehyde (MDA), Cu/Zn-superoxide dismutase (Cu/Zn-SOD), and glutathione peroxidase (GSH-Px) were studied at baseline and after 24 weeks of treatment. A total of 67 FMF-related amyloidosis patients (52 male (77.6%); median age 36 years (range 21−66)) were enrolled. At the end of a 24-week treatment period with AAL, AIC, and AOL combination therapy, ADMA, MDA, PTX3, hsCRP, cholesterol, and proteinuria were significantly decreased compared to baseline, while CuZn-SOD, GSH-Px, and FMD levels were significantly increased. Changes in inflammatory markers PTX3, and hsCRP were negatively correlated with FMD change, and positively correlated with decreases in proteinuria, ADMA, MDA, cholesterol, and CIMT. Treatment with AAL, AIC and AOL combination for 24 weeks were significantly associated with reduction in inflammatory markers, improved endothelial functions, and oxidative state. Efficient control of these three mechanisms can have long term cardiovascular and renal benefits for patients with AA amyloidosis.

Indexed as

AA amyloidosisendothelial dysfunctionfamilial Mediterranean feverinflammationnatural supplementationoxidative stress

Identifiers

PMID35743929
PMCPMC9228597
OpenAlexW4282982088

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.