Evidence map›Paper›PMID 30377814›Full record

ArticleEuropean journal of nutrition2019

Montmorency tart cherry protects against age-related bone loss in female C57BL/6 mice and demonstrates some anabolic effects.

Brenda J Smith, Erica K Crockett, Pitipa Chongwatpol, Jennifer L Graef, Stephen L Clarke, Elizabeth Rendina-Ruedy, Edralin A Lucas

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In one paragraph

Article in European journal of nutrition, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 33% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 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

7 authors at 1 institution in 1 country.

Brenda J SmithHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA. bjsmith@okstate.edu.ORCID http://orcid.org/0000-0002-7296-8534
Erica K CrockettHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Pitipa ChongwatpolHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Jennifer L GraefHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Stephen L ClarkeHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Elizabeth Rendina-RuedyHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Edralin A LucasHS 420, Department of Nutritional Sciences, Oklahoma State University, Stillwater, OK, 74078, USA.
Oklahoma State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAge-related bone loss is a consequence of endocrine and immune changes that disrupt bone remodeling. Functional foods (e.g., tart cherries) with antioxidant, anti-inflammatory and prebiotic activity can potentially counter this age-related phenomenon. The aim of this study was to determine if Montmorency tart cherry protects against early age-related bone loss and the culpable alterations in bone metabolism.

methodsFemale, 5-month-old, C57BL/6 mice were assigned to baseline or treatment groups: AIN-93M diet supplemented with 0, 1, 5, or 10% tart cherry for 90 days. Bone mineral density (BMD) and trabecular and cortical bone microarchitecture were assessed. Treatment effects on bone metabolism and regulators of bone formation, resorption and mineralization were determined.

resultsMice consuming the 5% and 10% doses had higher vertebral and tibial BMD (p < 0.05) compared to controls. The age-related decrease in trabecular bone volume (BV/TV) of the distal femur was prevented with these doses. Vertebral trabecular BV/TV and cortical bone thickness of the femur mid-diaphysis were greater (p < 0.05) in the groups receiving the 5% and 10% cherry than the control diet. Notably, these improvements were significantly greater than the baseline controls, consistent with an anabolic response. Although no differences in systemic biomarkers of bone formation or resorption were detected at 90 days, local increases in Phex and decreases in Ppar-γ suggest a bone environment that supports increased mineralization.

conclusionsThese findings demonstrate that cherry supplementation (5% and 10%) improves BMD and some indices of trabecular and cortical bone microarchitecture; these effects are likely attributed to increased bone mineralization.

Indexed as

Prunus aviumAnabolic AgentsAnimalsDisease Models, AnimalFemaleMiceMice, Inbred C57BLOsteoporosisPlant ExtractsAnabolic AgentsPlant ExtractsAgingAntioxidantsBoneOsteoporosisPolyphenols

Identifiers

PMID30377814
OpenAlexW2899018877

What OpenQuestion holds

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Registered trials

None linked

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.