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1.
Zhong Nan Da Xue Xue Bao Yi Xue Ban ; 49(4): 508-515, 2024 Apr 28.
Article in English, Chinese | MEDLINE | ID: mdl-39019779

ABSTRACT

Gut microbiota refers to the vast and diverse community of microorganisms residing in the intestines. Factors such as genetics, environmental influences (e.g., exercise, diet), and early life experiences (e.g., infant feeding methods) can all affect the ecological balance of gut microbiota within the body. Dysbiosis of the gut microbiota is associated with extra-intestinal diseases such as Parkinson's syndrome, osteoporosis, and autoimmune diseases, suggesting that disturbances in gut microbiota may be one of the causes of these diseases. Exercise benefits various diseases, with gut microbiota playing a role in regulating the nervous, musculoskeletal, and immune systems. Gut microbiota can impact the body's health status through the gut-brain axis, gut-muscle axis, and immune pathways. Moderate-intensity aerobic exercise can increase the quantity of gut microbiota and change microbial abundance, although short-term exercise does not significantly affect the alpha diversity of the microbiota. Resistance exercise also does not have a significant regulatory effect on gut microbiota.


Subject(s)
Exercise , Gastrointestinal Microbiome , Humans , Gastrointestinal Microbiome/physiology , Exercise/physiology , Dysbiosis/microbiology , Brain-Gut Axis/physiology , Parkinson Disease/microbiology , Osteoporosis/microbiology , Osteoporosis/prevention & control
2.
Medicine (Baltimore) ; 103(29): e38861, 2024 Jul 19.
Article in English | MEDLINE | ID: mdl-39029026

ABSTRACT

Osteoporosis (OP) constitutes a notable public health concern that significantly impacts the skeletal health of the global aging population. Its prevalence is steadily escalating, yet the intricacies of its diagnosis and treatment remain challenging. Recent investigations have illuminated a profound interlink between gut microbiota (GM) and bone metabolism, thereby opening new avenues for probing the causal relationship between GM and OP. Employing Mendelian randomization (MR) as the investigative tool, this study delves into the causal rapport between 211 varieties of GM and OP. The data are culled from genome-wide association studies (GWAS) conducted by the MiBioGen consortium, in tandem with OP genetic data gleaned from the UK Biobank, BioBank Japan Project, and the FinnGen database. A comprehensive repertoire of statistical methodologies, encompassing inverse-variance weighting, weighted median, Simple mode, Weighted mode, and MR-Egger regression techniques, was adroitly harnessed for meticulous analysis. The discernment emerged that the genus Coprococcus3 is inversely associated with OP, potentially serving as a deterrent against its onset. Additionally, 21 other gut microbial species exhibited a positive correlation with OP, potentially accentuating its proclivity and progression. Subsequent to rigorous scrutiny via heterogeneity and sensitivity analyses, these findings corroborate the causal nexus between GM and OP. Facilitated by MR, this study successfully elucidates the causal underpinning binding GM and OP, thereby endowing invaluable insights for deeper exploration into the pivotal role of GM in the pathogenesis of OP.


Subject(s)
Gastrointestinal Microbiome , Genome-Wide Association Study , Mendelian Randomization Analysis , Osteoporosis , Humans , Mendelian Randomization Analysis/methods , Osteoporosis/prevention & control , Osteoporosis/genetics , Bone and Bones/metabolism
3.
Science ; 385(6707): 359-361, 2024 Jul 26.
Article in English | MEDLINE | ID: mdl-39052796

ABSTRACT

There's growing evidence that breathing polluted air increases the risk of osteoporosis.


Subject(s)
Bone and Bones , Osteoporosis , Humans , Osteoporosis/prevention & control , Air Pollutants/adverse effects , Air Pollution/adverse effects , Animals , Particulate Matter/adverse effects , Bone Density/drug effects , Female
4.
Front Endocrinol (Lausanne) ; 15: 1417191, 2024.
Article in English | MEDLINE | ID: mdl-38974581

ABSTRACT

Osteoporosis and osteoarthritis continue to pose significant challenges to the aging population, with limited preventive options and pharmacological treatments often accompanied by side effects. Amidst ongoing efforts to discover new therapeutic agents, tocotrienols (TTs) have emerged as potential candidates. Derived from annatto bean and palm oil, TTs have demonstrated efficacy in improving skeletal and joint health in numerous animal models of bone loss and osteoarthritis. Mechanistic studies suggest that TTs exert their effects through antioxidant, anti-inflammatory, Wnt-suppressive, and mevalonate-modulating mechanisms in bone, as well as through self-repair mechanisms in chondrocytes. However, human clinical trials in this field remain scarce. In conclusion, TTs hold promise as agents for preventing osteoporosis and osteoarthritis, pending further evidence from human clinical trials.


Subject(s)
Osteoarthritis , Osteoporosis , Tocotrienols , Tocotrienols/therapeutic use , Tocotrienols/pharmacology , Humans , Animals , Osteoarthritis/drug therapy , Osteoarthritis/prevention & control , Osteoporosis/drug therapy , Osteoporosis/prevention & control , Bone and Bones/drug effects , Bone and Bones/metabolism
5.
Nitric Oxide ; 149: 32-40, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38830571

ABSTRACT

Endogenous hydrogen sulfide (H2S) plays an important role in bone metabolism. However, the exact role of H2S in intestinal calcium and phosphorus absorption and its potential in preventing and treating primary osteoporosis remains unknown. Therefore, this study aimed to investigate the potential of H2S in promoting intestinal calcium and phosphorus absorption and alleviating primary osteoporosis. We measured the apparent absorptivity of calcium, femoral bone density, expression and sulfhydration of the duodenal endoplasmic reticulum protein of 57 kDa (ERp57), duodenal cystathionine γ-lyase (CSE) expression, and serum H2S content in adult and old CSE-knockout and wild-type mice. We also assessed intracellular reactive oxygen species (ROS) and Ca2+ content in CSE-overexpressing or knockout intestinal epithelial cell (IEC)-6 cells. In senile mice, CSE knockout decreased endogenous H2S, ERp57 sulfhydration, and intestinal calcium absorption and worsened osteoporosis, which were partially reversed by GYY4137, an H2S donor. CSE overexpression in IEC-6 cells increased ERp57 sulfhydration, protein kinase A and C activity, and intracellular Ca2+, whereas CSE knockout exerted the opposite effects. Furthermore, hydrogen peroxide (H2O2) stimulation had similar effects as in CSE knockout, which were reversed by pretreatment with sodium hydrosulfide before H2O2 stimulation and restored by DL-dithiothreitol. These findings suggest that H2S attenuates primary osteoporosis by preventing ROS-induced ERp57 damage in intestinal epithelial cells by enhancing ERp57 activity and promoting intestinal calcium absorption, thereby aiding in developing therapeutic interventions to prevent osteoporosis.


Subject(s)
Calcium , Hydrogen Sulfide , Osteoporosis , Protein Disulfide-Isomerases , Animals , Male , Mice , Calcium/metabolism , Cell Line , Cystathionine gamma-Lyase/metabolism , Hydrogen Sulfide/metabolism , Hydrogen Sulfide/pharmacology , Intestinal Absorption/drug effects , Mice, Inbred C57BL , Mice, Knockout , Osteoporosis/metabolism , Osteoporosis/prevention & control , Protein Disulfide-Isomerases/metabolism , Reactive Oxygen Species/metabolism
6.
Nihon Ronen Igakkai Zasshi ; 61(2): 93-102, 2024.
Article in Japanese | MEDLINE | ID: mdl-38839326

ABSTRACT

Fracture prevention in the elderly is an urgent issue at all levels: individual, family, and societal. Osteoporosis is the underlying cause of fractures in the elderly, and it is important to understand its pathogenesis and treatment. Diet, exercise, and pharmacotherapy are all important for fracture prevention. Particularly with regard to pharmacotherapy, it is important to understand the mechanism of action of each drug and its characteristics and problems from a clinical point of view. Appropriate treatment of osteoporosis has been proven to reduce fractures in the elderly, and its widespread implementation is desirable.


Subject(s)
Osteoporosis , Humans , Aged , Osteoporosis/drug therapy , Osteoporosis/complications , Osteoporosis/prevention & control , Fractures, Bone/prevention & control , Fractures, Bone/etiology , Osteoporotic Fractures/prevention & control , Aged, 80 and over
7.
Arch Osteoporos ; 19(1): 46, 2024 Jun 08.
Article in English | MEDLINE | ID: mdl-38850469

ABSTRACT

INTRODUCTION: These guidelines aim to provide evidence-based recommendations for the supplementation of Vitamin D in maintaining bone health. An unmet need persists in Latin American regarding the availability of clinical and real-world data for rationalizing the use of vitamin D supplementation. The objective of these guidelines is to establish clear and practical recommendations for healthcare practitioners from Latin American countries to address Vitamin D insufficiency in clinical practice. METHODS: The guidelines were developed according to the GRADE-ADOLOPMENT methodology for the adaptation or adoption of CPGs or evidence-based recommendations. A search for high quality CPGs was complemented through a comprehensive review of recent literature, including randomized controlled trials, observational studies, and systematic reviews evaluating the effects of Vitamin D supplementation on bone health. The evidence to decision framework proposed by the GRADE Working Group was implemented by a panel of experts in endocrinology, bone health, and clinical research. RESULTS: The guidelines recommend Vitamin D supplementation for individuals aged 18 and above, considering various populations, including healthy adults, individuals with osteopenia, osteoporosis patients, and institutionalized older adults. These recommendations offer dosing regimens depending on an individualized treatment plan, and monitoring intervals of serum 25-hydroxyvitamin D levels and adjustments based on individual results. DISCUSSION: The guidelines highlight the role of Vitamin D in bone health and propose a standardized approach for healthcare practitioners to address Vitamin D insufficiency across Latin America. The panel underscored the necessity for generating local data and stressed the importance of considering regional geography, social dynamics, and cultural specificities when implementing these guidelines.


Subject(s)
Dietary Supplements , Osteoporosis , Vitamin D Deficiency , Vitamin D , Humans , Vitamin D/therapeutic use , Vitamin D/administration & dosage , Latin America , Vitamin D Deficiency/drug therapy , Vitamin D Deficiency/prevention & control , Osteoporosis/drug therapy , Osteoporosis/prevention & control , Adult , Aged , Female , Male
8.
ACS Nano ; 18(27): 17630-17641, 2024 Jul 09.
Article in English | MEDLINE | ID: mdl-38924391

ABSTRACT

Osteoporosis disrupts the fine-tuned balance between bone formation and resorption, leading to reductions in bone quantity and quality and ultimately increasing fracture risk. Prevention and treatment of osteoporotic fractures is essential for reductions in mortality, morbidity, and the economic burden, particularly considering the aging global population. Extreme bone loss that mimics time-accelerated osteoporosis develops in the paralyzed limbs following complete spinal cord injury (SCI). In vitro nanoscale vibration (1 kHz, 30 or 90 nm amplitude) has been shown to drive differentiation of mesenchymal stem cells toward osteoblast-like phenotypes, enhancing osteogenesis and inhibiting osteoclastogenesis simultaneously. Here, we develop and characterize a wearable device designed to deliver and monitor continuous nanoamplitude vibration to the hindlimb long bones of rats with complete SCI. We investigate whether a clinically feasible dose of nanovibration (two 2 h/day, 5 days/week for 6 weeks) is effective at reversing the established SCI-induced osteoporosis. Laser interferometry and finite element analysis confirmed transmission of nanovibration into the bone, and microcomputed tomography and serum bone formation and resorption markers assessed effectiveness. The intervention did not reverse SCI-induced osteoporosis. However, serum analysis indicated an elevated concentration of the bone formation marker procollagen type 1 N-terminal propeptide (P1NP) in rats receiving 40 nm amplitude nanovibration, suggesting increased synthesis of type 1 collagen, the major organic component of bone. Therefore, enhanced doses of nanovibrational stimulus may yet prove beneficial in attenuating/reversing osteoporosis, particularly in less severe forms of osteoporosis.


Subject(s)
Osteoporosis , Spinal Cord Injuries , Vibration , Animals , Rats , Osteoporosis/pathology , Osteoporosis/prevention & control , Rats, Sprague-Dawley , X-Ray Microtomography , Osteogenesis/drug effects , Female , Wearable Electronic Devices , Nanotechnology
9.
Pharmazie ; 79(6): 124-128, 2024 Jun 01.
Article in English | MEDLINE | ID: mdl-38877679

ABSTRACT

Fragility fractures associated with glucocorticoid-induced osteoporosis (GIO) can markedly impair quality of life. However, only 20% of patients are treated in compliance with the relevant management guidelines, and bone mineral density analysis with dual-energy X-ray absorptiometry (DXA) is only rarely performed. We report the intervention methods suggested by pharmacists and describe their efficacy. Patients who visited the outpatient clinic of the General Medicine Department of Ogaki Municipal Hospital and received steroids were enrolled. The rates of DXA implementation and compliance with GIO pharmacotherapy guidelines before and after pharmacist to physician-suggested interventions were compared. Guideline compliance was defined as prescription of osteoporosis drugs to patients with a score of ≥3. Administered prophylaxes and bone mineral density were subsequently assessed. The before and after intervention DXA rates were 1% (1/100 patients) and 96.0% (96/100 patients; P<0.01), respectively. Overall, 96.9% (93/96) of the patients met the GIO criteria for pharmacotherapy initiation (score ≥3), and the guideline compliance rates before and after the intervention were 39.8% (37/93) and 93.5% (87/93; P<0.01), respectively. Of the 56 patients who did not receive prophylaxis, 52 were recommended treatment, yielding an acceptance rate of 82.7% (43/52). Among the 37 patients receiving prophylaxis, 20 (54.1%) had a DXA-related young adult mean of ≤70%, of whom 11 (55.0%) agreed to drug therapy. The acceptance rate of pharmacotherapy recommendations for patients not receiving prophylaxis was higher than that for those receiving prophylaxis (P=0.03). Pharmacist-initiated interventions for GIO facilitates the administration of appropriate pharmacotherapy.


Subject(s)
Absorptiometry, Photon , Bone Density Conservation Agents , Bone Density , Glucocorticoids , Guideline Adherence , Osteoporosis , Pharmacists , Humans , Bone Density/drug effects , Osteoporosis/drug therapy , Osteoporosis/prevention & control , Female , Male , Aged , Glucocorticoids/administration & dosage , Glucocorticoids/adverse effects , Middle Aged , Bone Density Conservation Agents/administration & dosage , Aged, 80 and over , Adult
10.
Int J Mol Sci ; 25(11)2024 May 28.
Article in English | MEDLINE | ID: mdl-38892062

ABSTRACT

Bone health is the result of a tightly regulated balance between bone modeling and bone remodeling, and alterations of these processes have been observed in several diseases both in adult and pediatric populations. The imbalance in bone remodeling can ultimately lead to osteoporosis, which is most often associated with aging, but contributing factors can already act during the developmental age, when over a third of bone mass is accumulated. The maintenance of an adequate bone mass is influenced by genetic and environmental factors, such as physical activity and diet, and particularly by an adequate intake of calcium and vitamin D. In addition, it has been claimed that the integration of specific nutraceuticals such as resveratrol, anthocyanins, isoflavones, lycopene, curcumin, lutein, and ß-carotene and the intake of bioactive compounds from the diet such as honey, tea, dried plums, blueberry, and olive oil can be efficient strategies for bone loss prevention. Nutraceuticals and functional foods are largely used to provide medical or health benefits, but there is an urge to determine which products have adequate clinical evidence and a strong safety profile. The aim of this review is to explore the scientific and clinical evidence of the positive role of nutraceuticals and functional food in bone health, focusing both on molecular mechanisms and on real-world studies.


Subject(s)
Bone and Bones , Dietary Supplements , Functional Food , Humans , Bone and Bones/metabolism , Bone and Bones/physiology , Bone and Bones/drug effects , Osteoporosis/prevention & control , Animals , Bone Remodeling/drug effects , Bone Density/drug effects
11.
Nutrients ; 16(11)2024 May 27.
Article in English | MEDLINE | ID: mdl-38892573

ABSTRACT

With the global aging population, addressing prevalent age-related conditions such as osteoporosis and sarcopenia is crucial. Traditional nutritional strategies focusing on single nutrients like calcium, vitamin D, or protein have limitations, prompting a nuanced exploration of the relationship between aging, nutrition, and musculoskeletal health. This cross-sectional study examines the complex interplay between dietary intake of macronutrients, common micronutrients, and water, as well as their association with musculoskeletal health in adults aged 50 to 80 years, using U.S. National Health and Nutrition Examination Survey data (NHANES). Employing multiple linear regression, restricted cubic splines, weighted quantile sum (WQS), and quantile-based g-computation (QGC) regression models, our initial analysis using the WQS model revealed that a one-quartile increase in mixed macronutrient intake was associated with a significant 0.009 unit increase in bone mineral density (BMD) and a 0.670 unit increase in grip strength, while a similar increase in mixed micronutrient intake showed a 0.007 unit increase in BMD and a 0.442 unit increase in grip strength. Our findings highlight the importance of a balanced dietary approach in promoting musculoskeletal health in the elderly, offering holistic strategies for overall well-being.


Subject(s)
Bone Density , Micronutrients , Nutrients , Nutrition Surveys , Humans , Aged , Micronutrients/administration & dosage , Male , Female , Nutrients/administration & dosage , Middle Aged , Cross-Sectional Studies , Aged, 80 and over , Bone Density/drug effects , Nutritional Status , Aging/physiology , Diet/methods , Hand Strength , Osteoporosis/prevention & control
12.
Rev Med Liege ; 79(5-6): 429-435, 2024 Jun.
Article in French | MEDLINE | ID: mdl-38869135

ABSTRACT

Osteoporosis is a skeletal disease characterized by low bone density and altered microarchitecture, exposing to bone fragility and an increased risk of fracture. Several therapeutic modalities can effectively reduce the risk of fractures both vertebral and non-vertebral. While a significant part of bone strength and structure is genetically determined, it should be recalled that the environment also plays a significant role in these parameters and the risk of fracture, thus offering preventive opportunities thanks to lifestyle. In this article, we review the common misconceptions and myths about the influence of diet and physical activity on bone mineral density and fracture risk.


L'ostéoporose est une maladie du squelette caractérisée par une densité osseuse basse et une microarchitecture altérée, exposant à une fragilité osseuse et à un risque accru de fracture. Plusieurs classes thérapeutiques existent, capables de réduire efficacement le risque de fracture à la fois vertébrale et non vertébrale. Si une partie importante de la force et de la structure osseuse est déterminée génétiquement, il faut garder en mémoire que l'environnement joue aussi un rôle non négligeable sur ces paramètres et le risque de fracture, offrant donc des opportunités de prévention grâce au style de vie. Dans cet article, nous passons en revue les idées préconçues et les mythes qui circulent à propos de l'influence de l'alimentation et de l'activité physique sur la densité minérale osseuse et le risque de fracture.


Subject(s)
Bone Density , Osteoporosis , Humans , Osteoporosis/prevention & control , Exercise , Diet , Osteoporotic Fractures/prevention & control , Osteoporotic Fractures/etiology , Life Style , Risk Factors
13.
Microb Biotechnol ; 17(6): e14485, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38850270

ABSTRACT

Proanthocyanidin-rich grape seed extract (GSE) has been shown to have the potential to protect bones, although the underlying mechanism remains unknown. The current study aims to explore GSE's preventive and therapeutic impact on bone loss induced by oestrogen deficiency and the underlying mechanism through the gut microbiota (GM) and metabolomic responses. In oestrogen-deficient ovariectomized (OVX) mice, GSE ameliorated bone loss by inhibiting the expansion of bone marrow adipose tissue (BMAT), restoring BMAT lipolysis and promoting bone formation. GSE regulated OVX-induced GM dysbiosis by reducing the abundance of opportunistic pathogenic bacteria, such as Alistipes, Turicibacter and Romboutsia, while elevating the abundance of beneficial bacteria, such as Bifidobacterium. The modified GM primarily impacted lipid and amino acid metabolism. Furthermore, the serum metabolites of GSE exhibited a significant enrichment in lipid metabolism. In summary, GSE shows potential as a functional food for preventing oestrogen deficiency-induced bone loss by modulating GM and metabolite-mediated lipid metabolism.


Subject(s)
Estrogens , Gastrointestinal Microbiome , Grape Seed Extract , Gastrointestinal Microbiome/drug effects , Animals , Grape Seed Extract/pharmacology , Mice , Female , Estrogens/deficiency , Estrogens/metabolism , Lipid Metabolism/drug effects , Dysbiosis/prevention & control , Mice, Inbred C57BL , Bacteria/metabolism , Bacteria/classification , Bacteria/drug effects , Bacteria/genetics , Osteoporosis/prevention & control , Disease Models, Animal , Adipose Tissue/metabolism , Ovariectomy
14.
BMC Musculoskelet Disord ; 25(1): 487, 2024 Jun 22.
Article in English | MEDLINE | ID: mdl-38909178

ABSTRACT

BACKGROUND: Increased intake of specific vitamins has been linked to a decreased prevalence of osteoporosis. However, the association between dietary folate intake and the risk of osteoporosis in the general population remains incompletely understood. Therefore, we aimed to determine the association between dietary folate intake and the risk of osteoporosis in the general population of the USA. METHODS: In this cross-sectional study, data from the National Health and Nutrition Examination Survey (2017-2020) were collected. Osteoporosis was considered to be indicated by a bone mineral density greater than 2.5 standard deviations below the mean of the young adult reference group. Dietary folate intake was measured by a 24-hour dietary recall. Multivariate logistic regression models and restricted cubic spline models were used. RESULTS: The study included 2297 participants (mean age: 63.69 ± 0.35 years), 49.92% of whom were female. In the general population, increased dietary folate intake was directly associated with a decreased risk of osteoporosis (P for trend = 0.005). In the age > 60 years and female subgroups, folate intake was inversely associated with the risk of osteoporosis (P for trend < 0.001). The dose‒response curve suggested that this association was nonlinear (P for nonlinearity = 0.015). CONCLUSIONS: Our cross-sectional study provides initial insights into the inverse association between dietary folate intake and the risk of osteoporosis in the general U.S. POPULATION: Further research is needed to confirm these associations.


Subject(s)
Folic Acid , Nutrition Surveys , Osteoporosis , Humans , Female , Cross-Sectional Studies , Male , Middle Aged , Osteoporosis/epidemiology , Osteoporosis/prevention & control , Folic Acid/administration & dosage , Risk Factors , Bone Density/drug effects , United States/epidemiology , Aged , Diet/adverse effects , Adult
17.
J Nutr Sci Vitaminol (Tokyo) ; 70(3): 262-272, 2024.
Article in English | MEDLINE | ID: mdl-38945892

ABSTRACT

Osteoporosis is characterized by bone loss and deterioration in bone microstructure, leading to bone fragility. It is strongly correlated with menopause in women. Previously, we reported that diets supplemented with a kudzu (Pueraria lobata) vine extract suppressed bone resorption in ovariectomized (OVX) mice, a postmenopausal model. The main isoflavone in kudzu is puerarin (daidzein-8-C-glycoside). Puerarin (daidzein-8-C-glycoside), which is main isoflavone of kudzu, probably contributes to the beneficial effect. However, the underlying mechanism is unclear. Therefore, the nutrikinetics of puerarin and the comparison with the suppressive effects of kudzu isoflavones on osteoclast differentiation was examined in this study. We demonstrated that orally administered puerarin was absorbed from the gut and entered the circulation in an intact form. In addition, puerarin accumulated in RAW264.7 pre-osteoclast cells in a time-dependent manner. Tartrate-resistant acid phosphatase activity was decreased by puerarin treatment in a concentration-dependent manner in RAW264.7 cells stimulated with the receptor activator of nuclear factor kappa-B ligand. Ovariectomy-induced elevated bone resorption was suppressed, and the fragile bone strength was improved by puerarin ingestion in the diet. These findings suggested that orally administered puerarin was localized in bone tissue and suppressed bone resorption and osteoclastogenesis in ovariectomized mice.


Subject(s)
Cell Differentiation , Femur , Isoflavones , Osteoclasts , Ovariectomy , Pueraria , Animals , Isoflavones/pharmacology , Isoflavones/administration & dosage , Osteoclasts/drug effects , Female , Mice , Femur/drug effects , Femur/metabolism , Pueraria/chemistry , Cell Differentiation/drug effects , RAW 264.7 Cells , Bone Resorption/prevention & control , Plant Extracts/pharmacology , Plant Extracts/administration & dosage , Osteoporosis/prevention & control , Osteoporosis/drug therapy , Tartrate-Resistant Acid Phosphatase/metabolism
18.
Compr Rev Food Sci Food Saf ; 23(4): e13374, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38847750

ABSTRACT

Dairy is recognized as a good source of calcium, which is important for preventing osteoporosis. However, the relationship between milk and bone health is more complex than just calcium supplementation. It is unwise to focus solely on observing the effects of a single nutrient. Lactose, proteins, and vitamins in milk, as well as fatty acids, oligosaccharides, and exosomes, all work together with calcium to enhance its bioavailability and utilization efficiency through various mechanisms. We evaluate the roles of dairy nutrients and active ingredients in maintaining bone homeostasis from the perspective of the dairy matrix effects. Special attention is given to threshold effects, synergistic effects, and associations with the gut-bone axis. We also summarize the associations between probiotic/prebiotic milk, low-fat/high-fat milk, lactose-free milk, and fortified milk with a reduced risk of osteoporosis and discuss the potential benefits and controversies of these dairy products. Moreover, we examine the role of dairy products in increasing peak bone mass during adolescence and reducing bone loss in old age. It provides a theoretical reference for the use of dairy products in the accurate prevention and management of osteoporosis and related chronic diseases and offers personalized dietary recommendations for bone health in different populations.


Subject(s)
Dairy Products , Milk , Osteoporosis , Osteoporosis/prevention & control , Humans , Animals , Milk/chemistry , Calcium, Dietary , Bone Density/drug effects , Nutrients
19.
Health Educ Behav ; 51(3): 446-456, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38741366

ABSTRACT

Narratives have been widely acknowledged as a powerful persuasion tool in health promotion and education. Recently, great efforts have been devoted to identifying message components and causal pathways that maximize a narrative's persuasion power. Specifically, we investigated how narrator point of view and readers' subjective relative risk moderate the effects of protagonist competence on intentions to adopt osteoporosis-prevention behaviors, and proposed identification with the protagonist, self-referencing, and fear arousal as three mediators explaining the effect. Women aged 35 to 55, still young enough to reduce osteoporosis risk, read a narrative in which the 60-year-old female character reflects on either taking actions to prevent osteoporosis (competent protagonist) or failing to do so, resulting in osteoporosis (incompetent protagonist) (N = 563). The narratives were told from either the first- or third-person point of view. We found that women who perceived themselves to be at lower risk for developing osteoporosis relative to their peers identified more with the competent protagonist. For women at higher perceived risk, the competent and incompetent protagonists elicited similar levels of identification. Identification was higher when the protagonist's story was told from the first-person perspective, but only for the incompetent protagonist narrative. Identification, self-referencing, and fear arousal played important mediating roles. Implications for theory development and practice are examined.


Subject(s)
Narration , Osteoporosis , Persuasive Communication , Humans , Female , Middle Aged , Osteoporosis/prevention & control , Adult , Fear , Intention
20.
PLoS One ; 19(5): e0304358, 2024.
Article in English | MEDLINE | ID: mdl-38820403

ABSTRACT

Osteoporosis is an important health problem that occurs due to an imbalance between bone formation and resorption. Hormonal deficiency post-menopause is a significant risk factor. The probiotic Limosilactobacillus reuteri has been reported to prevent ovariectomy (Ovx)-induced bone loss in mice and reduce bone loss in postmenopausal women. Despite the numerous health benefits of probiotics, as they are live bacteria, the administration is not risk-free for certain groups (e.g., neonates and immunosuppressed patients). We evaluated the effects of L. reuteri (ATCC PTA 6475) and its heat-killed (postbiotic) form on Ovx-induced bone loss. Adult female mice (BALB/c) were randomly divided into four groups: group C-control (sham); group OVX-C-Ovx; group OVX-POS-Ovx + heat-killed probiotic; group OVX-PRO-Ovx + probiotic. L. reuteri or the postbiotic was administered to the groups (1.3x109 CFU/day) by gavage. Bacterial morphology after heat treatment was accessed by scanning electron microscopy (SEM). The treatment started one week after Ovx and lasted 28 days (4 weeks). The animals were euthanized at the end of the treatment period. Bone microarchitecture and ileum Occludin and pro-inflammatory cytokines gene expression were evaluated by computed microtomography and qPCR techniques, respectively. The Ovx groups had lower percentage of bone volume (BV/TV) and number of bone trabeculae as well as greater total porosity compared to the control group. Treatment with live and heat-killed L. reuteri resulted in higher BV/TV and trabecular thickness than the Ovx group. The heat treatment caused some cell surface disruptions, but its structure resembled that of the live probiotic in SEM analysis. There were no statistical differences in Occludin, Il-6 and Tnf-α gene expression. Both viable and heat-killed L. reuteri prevented bone loss on ovariectomized mice, independently of gut Occludin and intestinal Il-6 and Tnf-α gene expression.


Subject(s)
Limosilactobacillus reuteri , Osteoporosis , Ovariectomy , Probiotics , Animals , Female , Limosilactobacillus reuteri/physiology , Probiotics/administration & dosage , Probiotics/pharmacology , Mice , Osteoporosis/prevention & control , Mice, Inbred BALB C , Hot Temperature
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