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1.
Sci Rep ; 11(1): 20485, 2021 10 14.
Article in English | MEDLINE | ID: mdl-34650186

ABSTRACT

Sarcopenia is an age-related disease with an increased risk of mortality. It is emerging that low serum 25-hydroxyvitamin D [25(OH)D] affects the sarcopenic state in general, but in rheumatoid arthritis (RA), these associations are not understood although the prevalence of vitamin D insufficiency is high in RA. We conducted a cross-sectional study of older female outpatients from our cohort (KURAMA) database. We measured skeletal muscle mass, handgrip strength, and gait-speed to diagnose severe sarcopenia. The serum 25(OH)D concentration was measured using electrochemiluminescence immunoassay. A total of 156 female patients with RA (sarcopenia:44.9%, severe sarcopenia: 29.5%, and without sarcopenia: 25.6%) were enrolled. Classification of vitamin D status at a cutoff point of median 25(OH)D concentration revealed that low 25(OH)D status was associated with a high prevalence of severe sarcopenia and with low measured values of muscle mass, handgrip, and gait speed. Furthermore, multivariable logistic regression analysis identified that low 25(OH)D status was associated with a high prevalence of severe sarcopenia (OR 6.00; 95% CI 1.99-18.08).The same association was observed when the cut-off value was set at 20 ng/ml. In components of sarcopenia, both low physical performance and muscle mass were associated with low 25(OH)D status. In conclusion, vitamin D status was inversely associated with severe sarcopenia, low physical performance, and low skeletal muscle mass. Modification of vitamin D status including vitamin D supplementation should be investigated as a therapeutic strategy for sarcopenic patients with RA.


Subject(s)
Arthritis, Rheumatoid/epidemiology , Sarcopenia/epidemiology , Vitamin D/analogs & derivatives , Aged , Cross-Sectional Studies , Female , Humans , Japan , Middle Aged , Sarcopenia/blood , Vitamin D/blood , Vitamin D Deficiency/epidemiology
2.
Nutrients ; 13(4)2021 Apr 10.
Article in English | MEDLINE | ID: mdl-33920130

ABSTRACT

Vitamin D deficiency frequently occurs in older people, especially in individuals with comorbidity and polypharmacotherapy. In this group, low vitamin D plasma concentration is related to osteoporosis, osteomalacia, sarcopenia and myalgia. Vitamin D levels in humans is an effect of the joint interaction of all vitamin D metabolic pathways. Therefore, all factors interfering with individual metabolic stages may affect 25-hydroxyvitamin D plasma concentration. The known factors affecting vitamin D metabolism interfere with cytochrome CYP3A4 activity. There is another group of factors that impairs intestinal vitamin D absorption. The phenomenon of drugs and vitamin D interactions is observed first and foremost in patients with comorbidity. This is a typical situation, where the absence of "hard evidence" is not synonymous with the possible lack of adverse effects. Osteoporosis and sarcopenia (generalized and progressive decrease of skeletal muscle mass and strength) are some of the musculoskeletal consequences of hypovitaminosis D. These consequences are related to an increased risk of adverse outcomes, including bone fractures, physical disabilities, and a lower quality of life. This can lead not only to an increased risk of falls and fractures but is also one of the main causes of frailty syndrome in the aging population. Generally, Vitamin D plasma concentration is significantly lower in subjects with osteoporosis and muscle deterioration. In some observational and uncontrolled treatment studies, vitamin D supplementation resulted in a reduction of proximal myopathy and muscle pain. The most conclusive results were found in subjects with severe vitamin D deficiency and in patients avoiding large doses of vitamin D. However, the role of vitamin D in muscle pathologies is not clear and research has provided conflicting results. This is plausibly due to the heterogeneity of the subjects, vitamin D doses and environmental factors. This report presents data on some problems with vitamin D deficiency in the elderly population and the management of vitamin D deficiency D in successful or unsuccessful aging.


Subject(s)
Dietary Supplements , Osteoporosis/epidemiology , Sarcopenia/epidemiology , Vitamin D Deficiency/complications , Vitamin D/analogs & derivatives , Aged , Aged, 80 and over , Comorbidity , Drug Interactions , Frail Elderly , Humans , Osteoporosis/blood , Osteoporosis/etiology , Osteoporosis/prevention & control , Polypharmacy , Quality of Life , Sarcopenia/blood , Sarcopenia/etiology , Sarcopenia/prevention & control , Vitamin D/administration & dosage , Vitamin D/blood , Vitamin D/metabolism , Vitamin D Deficiency/blood , Vitamin D Deficiency/drug therapy , Vitamin D Deficiency/epidemiology
3.
Pharm Res ; 37(12): 235, 2020 Nov 02.
Article in English | MEDLINE | ID: mdl-33140122

ABSTRACT

PURPOSE: The pharmacokinetic properties of plasma NO3- and its reduced metabolite, NO2-, have been separately described, but there has been no reported attempt to simultaneously model their pharmacokinetics following NO3- ingestion. This report describes development of such a model from retrospective analyses of concentrations largely obtained from primary endpoint efficacy trials. METHODS: Linear and non-linear mixed effects analyses were used to statistically define concentration dependency on time, dose, as well as patient and study variables, and to integrate NO3- and NO2- concentrations from studies conducted at different times, locations, patient groups, and several studies in which sample range was limited to a few hours. Published pharmacokinetic studies for both substances were used to supplement model development. RESULTS: A population pharmacokinetic model relating NO3- and NO2- concentrations was developed. The model incorporated endogenous levels of the two entities, and determined these were not influenced by exogenous NO3- delivery. Covariate analysis revealed intersubject variability in NO3- exposure was partially described by body weight differences influencing volume of distribution. The model was applied to visualize exposure versus response (muscle contraction performance) in individual patients. CONCLUSIONS: Extension of the present first-generation model, to ultimately optimize NO3- dose versus pharmacological effects, is warranted.


Subject(s)
Dietary Supplements , Models, Biological , Nitrates/pharmacokinetics , Nitrites/pharmacokinetics , Administration, Oral , Aged , Aging/metabolism , Biological Availability , Body Weight , Cross-Over Studies , Female , Heart Failure/blood , Heart Failure/diet therapy , Heart Failure/metabolism , Humans , Male , Nitrates/administration & dosage , Nitrates/metabolism , Nitrites/metabolism , Retrospective Studies , Sarcopenia/blood , Sarcopenia/diet therapy , Sarcopenia/metabolism
4.
Clin Nutr ESPEN ; 32: 88-95, 2019 08.
Article in English | MEDLINE | ID: mdl-31221297

ABSTRACT

BACKGROUNDS & AIMS: Obesity and sarcopenia are independent illnesses associated with contemporary dietary and physical activity behaviors, aggravated by aging. Their coexistence is termed sarcopenic obesity (SO). Hence, increasing protein intake and resistance training (RT) are interventions that could counteract these illnesses. The objective of this investigation was to analyze the effects of whey protein (WP) supplementation associated with RT on body composition, muscular strength, functional capacity, and plasma-metabolism biomarkers in older women with SO. METHODS: Twenty six sarcopenic (appendicular lean soft tissue ALST < 15.02 kg) obese (body fat mass ≥ 35%) older women were randomly assigned to receive daily, either 35 g of WP (WP group) or placebo (PLA group), combined with supervised RT (8 exercises, 3 × 8-12 rep, 3 times a week), during a 12-week protocol. Blood samples, blood pressure, dietary intake, functional capacity tests, the one repetition maximum (1RM) test, and body composition were assessed before and after the intervention period. Two-way analysis of variance for repeated measures was applied for comparisons. RESULTS: The WP group presented greater (P < 0.05) increases in ALST (WP = 6.0% vs. PLA = 2.5%) and decreases in (P < 0.05) total (-3.3% vs. -0.3%) and trunk fat mass (WP = -5.1% vs. PLA = -1.1) and IL-6 (WP = -34.6% vs. PLA = 9.3%) compared with the PLA group. Both groups demonstrated improved (P < 0.05) scores for muscular strength, waist-hip ratio, functional capacity, and other plasma-metabolism biomarkers without significant differences between conditions. CONCLUSION: Whey protein combined with RT increased ALST, and decreased total and trunk fat mass, improving sarcopenia and decreasing SO in older women, with a limited impact on inflammation. Registered under ClinicalTrials.gov Identifier n° NCT03752359.


Subject(s)
Obesity , Sarcopenia/therapy , Whey Proteins/administration & dosage , Aged , Biomarkers/metabolism , Body Composition , Dietary Supplements , Double-Blind Method , Female , Humans , Middle Aged , Muscle Strength , Resistance Training , Sarcopenia/blood , Treatment Outcome
5.
Aging Clin Exp Res ; 31(6): 845-854, 2019 Jun.
Article in English | MEDLINE | ID: mdl-31049877

ABSTRACT

BACKGROUND: A chronic low-grade inflammatory profile (CLIP) is associated with sarcopenia in older adults. Protein and Vitamin (Vit)D have immune-modulatory potential, but evidence for effects of nutritional supplementation on CLIP is limited. AIM: To investigate whether 13 weeks of nutritional supplementation of VitD and leucine-enriched whey protein affected CLIP in subjects enrolled in the PROVIDE-study, as a secondary analysis. METHODS: Sarcopenic adults (low skeletal muscle mass) aged ≥ 65 years with mobility limitations (Short Physical Performance Battery 4-9) and a body mass index of 20-30 kg/m2 were randomly allocated to two daily servings of active (n = 137, including 20 g of whey protein, 3 g of leucine and 800 IU VitD) or isocaloric control product (n = 151) for a double-blind period of 13 weeks. At baseline and after 13 weeks, circulating interleukin (IL)-8, IL-1 receptor antagonist (RA), soluble tumor-necrosis-factor receptor (sTNFR)1, IL-6, high-sensitivity C-reactive protein, pre-albumin and 25-hydroxyvitamin(OH)D were measured. Data-analysis included repeated measures analysis of covariance (corrected for dietary VitD intake) and linear regression. RESULTS: IL-6 and IL-1Ra serum levels showed overall increases after 13 weeks (p = 0.006 and p < 0.001, respectively). For IL-6 a significant time × treatment interaction (p = 0.046) was observed, with no significant change over time in the active group (p = 0.155) compared to control (significant increase p = 0.012). IL-8 showed an overall significant decrease (p = 0.03). The change in pre-albumin was a significant predictor for changes in IL-6 after 13 weeks. CONCLUSIONS: We conclude that 13 weeks of nutritional supplementation with VitD and leucine-enriched whey protein may attenuate the progression of CLIP in older sarcopenic persons with mobility limitations.


Subject(s)
Leucine/therapeutic use , Sarcopenia/drug therapy , Vitamin D/therapeutic use , Whey Proteins/therapeutic use , Aged , Aged, 80 and over , Dietary Supplements , Double-Blind Method , Female , Humans , Interleukin 1 Receptor Antagonist Protein/blood , Interleukin-6/blood , Leucine/pharmacology , Male , Middle Aged , Mobility Limitation , Muscle, Skeletal/drug effects , Sarcopenia/blood , Vitamin D/pharmacology , Whey Proteins/pharmacology
6.
J Aging Phys Act ; 27(3): 384-391, 2019 06 01.
Article in English | MEDLINE | ID: mdl-30299198

ABSTRACT

To investigate the effects of resistance training and epicatechin supplementation on muscle strength, follistatin, and myostatin in older adults with sarcopenia, a total of 62 males with sarcopenia (68.63 ± 2.86 years) underwent a supervised 8-week randomized controlled trial. Participants were divided into resistance training (RT), epicatechin (EP), resistance training+epicatechin (RT+EP), and placebo (PL) in a double-blind method. A pretest and posttest measurement was conducted. One-way analysis of variance was used to analyze between-group differences. The significantly greatest increase was observed in follistatin, follistatin/myostatin ratio, leg press, and chest press in RT+EP comparing RT, EP, and PL groups, whereas myostatin decreased significantly only in RT+EP and RT groups. However, appendicular muscle mass index and timed up and go test were enhanced significantly in all experimental groups than the PL group (p ≤ .05). Consequently, by comparing the results between three experimental groups, the greatest improvement was detected in the RT+EP group. Therefore, using two interventions simultaneously seems to have a better impact on improving muscle growth factors and preventing the progression of sarcopenia.


Subject(s)
Catechin/administration & dosage , Follistatin/blood , Muscle, Skeletal/drug effects , Myostatin/blood , Resistance Training/methods , Sarcopenia/prevention & control , Aged , Biomarkers/blood , Catechin/pharmacology , Dietary Supplements , Female , Humans , Male , Muscle Strength/physiology , Muscle, Skeletal/physiology , Sarcopenia/blood , TGF-beta Superfamily Proteins/blood , Treatment Outcome
7.
Br J Nutr ; 120(4): 445-453, 2018 08.
Article in English | MEDLINE | ID: mdl-29909813

ABSTRACT

Branched-chain amino acids (BCAA) are essential amino acids that are necessary for muscle mass maintenance. Little is known about the plasma concentrations of BCAA and the protein intake in relation to sarcopenia. We aimed to compare the non-fasting plasma concentrations of the BCAA and the dietary protein intake between sarcopenic and non-sarcopenic older adults. Norwegian older home-dwelling adults (≥70 years) were invited to a cross-sectional study with no other exclusion criteria than age. Sarcopenic subjects were defined by the diagnostic criteria by the European Working Group on Sarcopenia in Older People. Non-fasting plasma concentrations of eight amino acids were quantified using NMR spectroscopy. Protein intake was assessed using 2×24-h dietary recalls. In this study, ninety out of 417 subjects (22 %) were sarcopenic, and more women (32 %) than men (11 %) were sarcopenic (P<0·0001). Sex-adjusted non-fasting plasma concentrations of leucine and isoleucine, and the absolute intake of protein (g/d), were significantly lower among the sarcopenic subjects, when compared with non-sarcopenic subjects (P=0·003, P=0·026 and P=0·003, respectively). A similar protein intake was observed in the two groups when adjusted for body weight (BW) and sex (1·1 g protein/kg BW per d; P=0·50). We show that sarcopenia is associated with reduced non-fasting plasma concentration of the BCAA leucine and isoleucine, and lower absolute intake of protein. More studies are needed to clarify the clinical relevance of these findings, related to maintenance of muscle mass and prevention of sarcopenia.


Subject(s)
Amino Acids, Branched-Chain/blood , Sarcopenia/blood , Aged , Aged, 80 and over , Amino Acids/blood , Amino Acids, Essential/blood , Anthropometry , Body Weight , Cognition , Cross-Sectional Studies , Diet , Dietary Supplements , Female , Glycolysis , Humans , Male , Malnutrition , Muscles/metabolism , Norway , Nutritional Status , Quality of Life , Randomized Controlled Trials as Topic
8.
J Steroid Biochem Mol Biol ; 175: 60-81, 2018 01.
Article in English | MEDLINE | ID: mdl-27662817

ABSTRACT

The aim of this study is to determine and critically evaluate the plausible relationships of vitamin D with extra-skeletal tissues in humans. Severe vitamin D deficiency results in rickets in children and osteomalacia in adults; these beneficial effects in the musculoskeletal system and certain physiological functions are well understood. Nevertheless, mounting reports support additional beneficial effects of vitamin D, outside the musculoskeletal system. This review explores the recent advances in knowledge about the non-skeletal effects of vitamin D. Peer-reviewed papers were extracted from research databases using key words, to assess correlations between vitamin D and extra-skeletal diseases and conditions. As per the guidelines of the Preferred Reporting Items for Systematic Reviews (PRISMA); general interpretations of results are included; taking into consideration the broader evidence and implications. This review summarizes current knowledge of the effects of vitamin D status on extra-skeletal tissues with special attention given to relationships between vitamin D status and various diseases commonly affecting adults; the effects of intervention with vitamin D and exposure to sunlight. Evidence suggests that vitamin D facilitates the regulation of blood pressure; and cardiac; endothelial; and smooth muscle cell functions; playing an important role in cardiovascular protection. In addition; 1,25(OH)2D improves immunity; subdues inflammation; and reduces the incidence and severity of common cancers; autoimmune diseases and infectious diseases. Almost all adequately powered; epidemiological and biological studies that use; adequate doses of vitamin D supplementation in D-deficient populations have reported favorable outcomes. These studies have concluded that optimizing 25(OH)D status improves the functionality of bodily systems; reduces comorbidities; improves the quality of life; and increases survival. Although accumulating evidence supports biological associations of vitamin D sufficiency with improved physical and mental functions; no definitive evidence exists from well-designed; statistically powered; randomized controlled clinical trials. Nevertheless, most studies point to significant protective effects of vitamin D in humans when the minimum 25(OH)D serum level exceeds 30ng/mL and is maintained throughout the year.


Subject(s)
Autoimmune Diseases/blood , Cardiovascular Diseases/blood , Diabetes Mellitus/blood , Neurodegenerative Diseases/blood , Vitamin D Deficiency/blood , Vitamin D/analogs & derivatives , Autoimmune Diseases/complications , Autoimmune Diseases/ethnology , Autoimmune Diseases/mortality , Cardiovascular Diseases/complications , Cardiovascular Diseases/ethnology , Cardiovascular Diseases/mortality , Diabetes Complications , Diabetes Mellitus/ethnology , Diabetes Mellitus/mortality , Humans , Incidence , Neurodegenerative Diseases/complications , Neurodegenerative Diseases/ethnology , Neurodegenerative Diseases/mortality , Osteoporosis/blood , Osteoporosis/complications , Osteoporosis/ethnology , Osteoporosis/mortality , Racial Groups , Sarcopenia/blood , Sarcopenia/complications , Sarcopenia/ethnology , Sarcopenia/mortality , Survival Analysis , Vitamin D/blood , Vitamin D Deficiency/complications , Vitamin D Deficiency/ethnology , Vitamin D Deficiency/mortality
9.
Metabolism ; 78: 167-178, 2018 01.
Article in English | MEDLINE | ID: mdl-28986165

ABSTRACT

BACKGROUND: The aging process is often associated with the presence of sarcopenia. Although changes in the plasma concentration of several amino acids have been observed in older adults, it remains unclear whether these changes are related to disturbances in whole body production and/or interconversions. METHODS: We studied 10 healthy young (~22.7y) and 17 older adults (~64.8y) by administering a mixture of stable amino acid tracers in a pulse and in a primed constant infusion. We calculated whole body production (WBP) and metabolite to metabolite interconversions. In addition, we measured body composition, muscle function, and provided questionnaires to assess daily dietary intake, physical activity, mood (anxiety, depression) and markers of cognitive function. Plasma enrichments and metabolite concentrations were measured by GC- and LC-MS/MS and statistics were performed by student t-test. RESULTS: Older adults had a 11% higher body mass index (p=0.04) and 27% reduced peak leg extension force (p=0.02) than the younger group, but comparable values for muscle mass, mood and cognitive function. Although small differences in several plasma amino acid concentrations were observed, we found older adults had about 40% higher values of WBP for glutamine (221±27 vs. 305±21µmol/kgffm/h, p=0.03) and tau-methylhistidine (0.15±0.01 vs. 0.21±0.02µmol/kgffm/h, p=0.04), 26% lower WBP value for arginine (59±4 vs. 44±4µmol/kgffm/h, p=0.02) and a reduction in WBP (50%; 1.23±0.15 vs. 0.69±0.06µmol/kgffm/h, p=0.001) and concentration (25%; 3.5±0.3µmol/l vs. 2.6±0.2µmol/l, p=0.01) for ß-Hydroxy ß-Methylbutyrate. No differences were observed in protein catabolism. Clearance of arginine was decreased (27%, p=0.03) and clearance of glutamine (58%, p=0.01), leucine (67%, p=0.001) and KIC (76%, p=0.004) were increased in older adults. CONCLUSIONS: Specific differences exist between young and older adults in amino acid metabolism.


Subject(s)
Aging/metabolism , Amino Acids/blood , Adult , Affect/physiology , Aging/blood , Body Composition/physiology , Body Mass Index , Cognition/physiology , Dietary Supplements , Exercise/physiology , Female , Humans , Kinetics , Male , Middle Aged , Muscle, Skeletal/metabolism , Sarcopenia/blood , Sarcopenia/metabolism , Young Adult
10.
Eur J Gastroenterol Hepatol ; 29(12): 1416-1423, 2017 Dec.
Article in English | MEDLINE | ID: mdl-29016470

ABSTRACT

BACKGROUND/AIM: Sarcopenia is recognized as a condition related to quality of life and prognosis in patients with chronic liver disease, although no useful strategy for improving muscle volume and strength has been established. Here, we evaluated the efficacy of supplementation with branched-chain amino acid (BCAA) administration and walking exercise. PATIENTS AND METHODS: From December 2015 to July 2016, 33 Japanese outpatients with liver cirrhosis were enrolled (median: 67 years, HCV : HBV : alcohol : others=26 : 2 : 2 : 3, male : female=13 : 20, Child-Pugh A : B=30 : 3). None had a history of BCAA supplementation. After calculating the average number of daily steps using a pedometer for a 2-3-week period, BCAA supplementation (protein 13.5 g, 210 kcal/day) as a late evening snack and walking exercise (additional 2000 steps/day prescribed) were started. Body composition including muscle volume was analyzed using a bioelectrical impedance analysis method, and serological data and muscle strength (leg, handgrip) were evaluated at enrollment, and then 1, 2, and 3 months after starting the protocol. RESULTS: The median average number of daily steps was 3791 (interquartile range: 2238-5484). The average period of BCAA supplementation was 2.7±0.7 months. During the period from enrollment to 3 months after starting the protocol, HbA1c and NH3 were not significantly changed, whereas the BCAA/tyrosine ratio improved (4.3±1.35 to 5.24±2.04, P=0.001). In addition, the ratios for average daily steps (1.595, P=0.02) as well as muscle volume, leg strength, and handgrip strength (1.013, 1.110, and 1.056, respectively; all P<0.01) were increased at 3 months. CONCLUSION: BCAA supplementation and walking exercise were found to be effective and easily implemented for improving muscle volume and strength in liver cirrhosis patients.


Subject(s)
Amino Acids, Branched-Chain/therapeutic use , Dietary Supplements , Liver Cirrhosis/complications , Muscle, Skeletal/pathology , Sarcopenia/prevention & control , Walking/physiology , Aged , Amino Acids, Branched-Chain/blood , Ammonia/blood , Body Composition , Exercise Test , Exercise Therapy , Female , Glycated Hemoglobin/metabolism , Hand Strength , Humans , Liver Cirrhosis/blood , Lower Extremity/physiopathology , Male , Middle Aged , Organ Size , Sarcopenia/blood , Sarcopenia/etiology , Tyrosine/blood
11.
Curr Opin Clin Nutr Metab Care ; 20(6): 498-503, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28806178

ABSTRACT

PURPOSE OF REVIEW: The review summarizes recent epidemiological studies that examined the relationship between osteoporosis and sarcopenia to assess the impact of vitamin D status or supplementation on health outcomes related to these two medical conditions. RECENT FINDINGS: Osteoporosis and sarcopenia are major public health problems, but whether these two diseases should be considered alone or combined into a single condition is not clear. No consensual definition of osteosarcopenia is largely accepted. Most observational studies demonstrate some relationship between muscle and bone health. Vitamin D status is generally lower in study participants with bone or muscle wasting. Studies on the effects of vitamin D supplementation on muscle or bone health have provided conflicting results, likely because of the heterogeneity between studies. However, the most positive results were observed in study participants with low vitamin D status and in studies that avoided massive boluses of vitamin D. SUMMARY: More observational and interventional studies are needed to confirm the exact role of vitamin D in the pathophysiology and treatment of osteosarcopenia.


Subject(s)
Osteoporosis/epidemiology , Sarcopenia/epidemiology , Vitamin D Deficiency/epidemiology , Vitamin D/blood , Bone Density/drug effects , Bone and Bones/drug effects , Bone and Bones/metabolism , Dietary Supplements , Epidemiologic Studies , Humans , Meta-Analysis as Topic , Muscle, Skeletal/drug effects , Muscle, Skeletal/metabolism , Observational Studies as Topic , Osteoporosis/blood , Osteoporosis/diagnosis , Prevalence , Randomized Controlled Trials as Topic , Sarcopenia/blood , Sarcopenia/diagnosis , Vitamin D/administration & dosage , Vitamin D Deficiency/blood
12.
J Gerontol A Biol Sci Med Sci ; 73(1): 131-138, 2017 Dec 12.
Article in English | MEDLINE | ID: mdl-28549108

ABSTRACT

BACKGROUND: To explore the associations between serum 25-hydroxyvitamin D (25D) and 1,25-dihydroxyvitamin D (1,25D) levels at baseline and incidence of sarcopenia over time in older Australian community-dwelling older men. METHODS: Of the 1,705 men aged ≥70 years (2005-2007) participating in the Concord Health and Ageing in Men Project, those without sarcopenia at baseline (n = 1,312 for 25D and n = 1,231 for 1,25D), 2 years (n = 1,024 for 25D and n = 956 for 1,25D), and 5-year follow-up (n = 709 for 25D and n = 663 for 1,25D) were included in the study. The main outcome measurement was the incidence of sarcopenia defined as appendicular lean mass adjusted for body mass index <0.789 and grip strength <26.0 kg. Serum 25D and 1,25D levels were measured at baseline by radioimmunoassay (Diasorin, Stillwater, MN) and categorized into quartiles as predictor variables. Covariates included age, income, season of blood collection, physical activity, vitamin D supplement and medication use, measures of health, serum parathyroid hormone (PTH), estimated glomerular filtration rate (eGFR), albumin, and white blood cell count. RESULTS: In this study, incidence of sarcopenia was 3.9% in men at the 2-year follow-up and 8.6% at the 5-year follow-up. In adjusted analysis, men with vitamin D levels in the lowest quartiles (25D <40nmol/L; 1,25D <62 pmol/L) showed significant associations with increased odds of incident sarcopenia compared to those with vitamin D levels in the highest quartiles over 5 years. [25D: odds ratio (OR) 2.53 (95% confidence interval (CI) 1.14, 5.64) p = .02; 1,25D: OR 2.67 (95% CI 1.28, 5.60) p = .01]. After further adjustments for the respective other serum vitamin D measure, (either 25D or 1,25D), the association remained significant [25D: OR 2.40 (95% CI 1.02, 5.64) p = .04; 1,25D: OR 2.23 (95% CI 1.04, 4.80) p = .04]. CONCLUSION: Low serum 1,25D and 25D concentrations at baseline are independently associated with the incidence of sarcopenia over the subsequent 5 years. Although our data do not prove any causal relationship, it is conceivable that maintaining vitamin D sufficiency may reduce the incidence of sarcopenia in ageing men.


Subject(s)
Aging/blood , Motor Activity/physiology , Muscle, Skeletal/physiopathology , Parathyroid Hormone/blood , Sarcopenia/blood , Vitamin D/analogs & derivatives , Aged , Australia/epidemiology , Biomarkers/blood , Body Mass Index , Cross-Sectional Studies , Dietary Supplements , Follow-Up Studies , Humans , Incidence , Male , Muscle Strength/physiology , Prognosis , Radioimmunoassay , Retrospective Studies , Sarcopenia/epidemiology , Sarcopenia/physiopathology , Time Factors , Vitamin D/blood
13.
Clin Nutr ESPEN ; 21: 31-39, 2017 10.
Article in English | MEDLINE | ID: mdl-30014867

ABSTRACT

This article aims to provide an overview of the prevalence, causes and risk factors associated with malnutrition in the elderly. It includes the clinical consequences and economic impact of malnutrition in the elderly and in particular the osteoporotic population. It encompasses the significance of dietary protein and its effects on bone health.


Subject(s)
Bone Density , Frailty/epidemiology , Malnutrition/epidemiology , Sarcopenia/epidemiology , Vitamin D Deficiency/epidemiology , Aged , Calcium/administration & dosage , Calcium/blood , Dietary Proteins/administration & dosage , Dietary Supplements , Frailty/blood , Humans , Milk Proteins/administration & dosage , Nutritional Requirements , Prevalence , Randomized Controlled Trials as Topic , Sarcopenia/blood , Vitamin D/administration & dosage , Vitamin D/blood , Vitamin D Deficiency/blood
14.
Curr Opin Clin Nutr Metab Care ; 20(1): 26-29, 2017 01.
Article in English | MEDLINE | ID: mdl-27749712

ABSTRACT

PURPOSE OF REVIEW: This article reviews recently published evidence regarding the role of vitamin D in the physiopathology of physical frailty in elderly populations and its role in the management of this geriatric condition. RECENT FINDINGS: Some recent studies have found a low level of 25-hydroxyvitamin D, considered the best marker of vitamin D status, in frail individuals. All prospective studies consistently report that low vitamin D status is associated with an increased risk of becoming frail. Recent studies also suggest that the relationship between vitamin D status and frailty is largely mediated by the development of sarcopenia. Very few well designed randomized controlled trials are available that assess the effectiveness of vitamin D supplementation in the prevention or management of frailty. In the absence of specific guidelines, a minimal serum 25-hydroxyvitamin D level of 75 nmol/l is proposed for frail elderly patients by some scientific societies. The doses necessary to reach this target are between 800 and 2000 IU/day. SUMMARY: Several studies suggest a potential effect of vitamin D on physical frailty but large clinical trials are lacking at this time to provide solid evidence of clinical benefit.


Subject(s)
Dietary Supplements , Frailty/blood , Vitamin D/analogs & derivatives , Vitamin D/therapeutic use , Vitamins/therapeutic use , Aged , Aged, 80 and over , Female , Frail Elderly , Frailty/etiology , Frailty/therapy , Humans , Male , Nutritional Status , Sarcopenia/blood , Sarcopenia/complications , Vitamin D/blood , Vitamin D Deficiency/blood , Vitamin D Deficiency/complications
15.
Br J Nutr ; 115(12): 2181-8, 2016 06.
Article in English | MEDLINE | ID: mdl-27079329

ABSTRACT

Previous studies have demonstrated that betaine supplements increase lean body mass in livestock and improve muscle performance in human beings, but evidence for its effect on human lean mass is limited. Our study assessed the association of circulating betaine with lean mass and its composition in Chinese adults. A community-based study was conducted on 1996 Guangzhou residents (weight/mass: 1381/615) aged 50-75 years between 2008 and 2010. An interviewer-administered questionnaire was used to collect general baseline information. Fasting serum betaine was assessed using HPLC-MS. A total of 1590 participants completed the body composition analysis performed using dual-energy X-ray absorptiometry during a mean of 3·2 years of follow-up. After adjustment for age, regression analyses demonstrated a positive association of serum betaine with percentage of lean mass (LM%) of the entire body, trunk and limbs in men (all P<0·05) and LM% of the trunk in women (P=0·016). Each sd increase in serum betaine was associated with increases in LM% of 0·609 (whole body), 0·811 (trunk), 0·422 (limbs), 0·632 (arms) and 0·346 (legs) in men and 0·350 (trunk) in women. Multiple logistic regression analysis revealed that the prevalence of lower LM% decreased by 17 % (whole body) and 14 % (trunk) in women and 23 % (whole body), 28 % (trunk), 22 % (arms) and 26 % (percentage skeletal muscle index) in men with each sd increment in serum betaine. Elevated circulating betaine was associated with a higher LM% and lower prevalence of lower LM% in middle-aged and elderly Chinese adults, particularly men.


Subject(s)
Betaine/blood , Body Composition , Body Fluid Compartments/metabolism , Muscle, Skeletal/metabolism , Sarcopenia/blood , Absorptiometry, Photon , Aged , Asian People , Betaine/pharmacology , Body Composition/drug effects , China , Dietary Supplements , Female , Humans , Logistic Models , Male , Middle Aged , Sex Factors
16.
Hormones (Athens) ; 15(4): 471-488, 2016 Oct.
Article in English | MEDLINE | ID: mdl-28222403

ABSTRACT

Muscles are major targets of vitamin D. Exposure of skeletal muscles to vitamin D induces the expression of multiple myogenic transcription factors enhancing muscle cell proliferation and differentiation. At the same time vitamin D suppresses the expression of myostatin, a negative regulator of muscle mass. Moreover, vitamin D increases the number of type II or fast twitch muscle cells and in particular that of type IIA cells, while its deficiency causes type IIA cell atrophy. Furthermore, vitamin D supplementation in young males with low vitamin D levels increases the percentage of type IIA fibers in muscles, causing an increase in muscular high power output. Vitamin D levels are strongly associated with exercise performance in athletes and physically active individuals. In the elderly and in adults below the age of 65, several studies have established a close association between vitamin D levels and neuromuscular coordination. The aim of this review is to appraise our current understanding of the significance of vitamin D on muscular performance in both older and frail individuals as well as in younger adults, athletes or non-athletes with regard to both ordinary everyday musculoskeletal tasks and peak athletic performance.


Subject(s)
Aging/metabolism , Athletic Performance/physiology , Motor Activity/physiology , Muscle, Skeletal/metabolism , Sarcopenia/blood , Vitamin D/pharmacology , Vitamin D/physiology , Adult , Aged , Animals , Humans , Male , Mice , Middle Aged , Young Adult
17.
Int J Mol Sci ; 16(10): 23227-49, 2015 Sep 25.
Article in English | MEDLINE | ID: mdl-26404241

ABSTRACT

Numerous specific age-related morbidities have been correlated with low intake and serum levels of tocopherols and tocotrienols. We performed a review in order to evaluate the extant evidence regarding: (1) the association between intake and serum levels of tocopherols and tocotrienols and age-related pathologies (osteoporosis, sarcopenia and cognitive impairment); and (2) the optimum diet therapy or supplementation with tocopherols and tocotrienols for the treatment of these abnormalities. This review included 51 eligible studies. The recent literature underlines that, given the detrimental effect of low intake and serum levels of tocopherols and tocotrienols on bone, muscle mass, and cognitive function, a change in the lifestyle must be the cornerstone in the prevention of these specific age-related pathologies related to vitamin E-deficient status. The optimum diet therapy in the elderly for avoiding vitamin E deficiency and its negative correlates, such as high inflammation and oxidation, must aim at achieving specific nutritional goals. These goals must be reached through: accession of the elderly subjects to specific personalized dietary programs aimed at achieving and/or maintaining body weight (avoid malnutrition); increase their intake of food rich in vitamin E, such as derivatives of oily seeds (in particular wheat germ oil), olive oil, hazelnuts, walnuts, almonds, and cereals rich in vitamin E (such as specific rice cultivar rich in tocotrienols) or take vitamin E supplements. In this case, vitamin E can be correctly used in a personalized way either for the outcome from the pathology or to achieve healthy aging and longevity without any adverse effects.


Subject(s)
Aging/blood , Diet , Dietary Supplements , Tocopherols/blood , Tocotrienols/blood , Adult , Aged , Aged, 80 and over , Cognition Disorders/blood , Cognition Disorders/diet therapy , Female , Humans , Male , Middle Aged , Osteoporosis/blood , Osteoporosis/diet therapy , Sarcopenia/blood , Sarcopenia/diet therapy , Tocopherols/therapeutic use , Tocotrienols/therapeutic use , Young Adult
18.
Maturitas ; 82(1): 56-64, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25882761

ABSTRACT

BACKGROUND: Recently, special attention has been given to the role of vitamin D on the pathogenesis and therapy of sarcopenia in postmenopausal women. AIMS: To elucidate the role of vitamin D with respect to sarcopenia in postmenopausal women, providing current evidence from both molecular and clinical studies. MATERIALS AND METHODS: Systematic search to PubMed and Medline databases for publications reporting data on the role of vitamin D in sarcopenia. RESULTS: Sarcopenia has a high prevalence in postmenopausal women, leading to mobility restriction, functional impairment, physical disability and fractures. Accumulating evidence from molecular and clinical studies suggest that vitamin D deficiency is associated with sarcopenic status in elderly women independent of body composition, diet and hormonal status. Current data, but not in a uniform way, provide evidence about the beneficial effect of vitamin D supplementation on muscle strength, physical performance and prevention of falls and fractures in elderly female populations. It is still unclear if and to what extent treatment modalities, such as dose, mode of administration and duration of supplementation, could influence treatment outcome. CONCLUSIONS: Studies with superior methodological characteristics are needed in order to establish a role for vitamin D on the treatment of sarcopenia in postmenopausal women.


Subject(s)
Dietary Supplements , Postmenopause/blood , Sarcopenia/drug therapy , Vitamin D Deficiency/drug therapy , Vitamin D/therapeutic use , Vitamins/therapeutic use , Accidental Falls , Aged , Body Composition , Diet , Female , Fractures, Bone/etiology , Fractures, Bone/prevention & control , Humans , Middle Aged , Sarcopenia/blood , Sarcopenia/complications , Treatment Outcome , Vitamin D/blood , Vitamin D Deficiency/blood , Vitamin D Deficiency/complications
19.
Am J Clin Nutr ; 99(4): 899-910, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24477043

ABSTRACT

BACKGROUND: Physical inactivity, inadequate dietary protein, and low-grade systemic inflammation contribute to age-related muscle loss, impaired function, and disability. OBJECTIVE: We assessed the effects of progressive resistance training (PRT) combined with a protein-enriched diet facilitated through lean red meat on lean tissue mass (LTM), muscle size, strength and function, circulating inflammatory markers, blood pressure, and lipids in elderly women. DESIGN: In a 4-mo cluster randomized controlled trial, 100 women aged 60-90 y who were residing in 15 retirement villages were allocated to receive PRT with lean red meat (∼160 g cooked) to be consumed 6 d/wk [resistance training plus lean red meat (RT+Meat) group; n = 53] or control PRT [1 serving pasta or rice/d; control resistance training (CRT) group; n = 47)]. All women undertook PRT 2 times/wk and received 1000 IU vitamin D3/d. RESULTS: The mean (± SD) protein intake was greater in the RT+Meat group than in the CRT group throughout the study (1.3 ± 0.3 compared with 1.1 ± 0.3 g · kg⁻¹ · d⁻¹, respectively; P < 0.05). The RT+Meat group experienced greater gains in total body LTM (0.45 kg; 95% CI: 0.07, 0.84 kg), leg LTM (0.22 kg; 95% CI: 0.02, 0.42 kg), and muscle strength (18%; 95% CI: 0.03, 0.34) than did the CRT group (all P < 0.05). The RT+Meat group also experienced a 10% greater increase in serum insulin-like growth factor I (P < 0.05) and a 16% greater reduction in the proinflammatory marker interleukin-6 (IL-6) (P < 0.05) after 4 mo. There were no between-group differences for the change in blood lipids or blood pressure. CONCLUSION: A protein-enriched diet equivalent to ∼1.3 g · kg⁻¹ · d⁻¹ achieved through lean red meat is safe and effective for enhancing the effects of PRT on LTM and muscle strength and reducing circulating IL-6 concentrations in elderly women. This trial was registered at the Australian Clinical Trials Registry as ACTRN12609000223235.


Subject(s)
Dietary Proteins/therapeutic use , Down-Regulation , Interleukin-6/blood , Meat , Muscle, Skeletal/metabolism , Resistance Training , Sarcopenia/prevention & control , Aged , Aged, 80 and over , Animals , Body Composition , Cholecalciferol/therapeutic use , Cohort Studies , Combined Modality Therapy , Dietary Proteins/adverse effects , Dietary Supplements , Female , Follow-Up Studies , Housing for the Elderly , Humans , Meat/adverse effects , Middle Aged , Muscle Strength , Muscle, Skeletal/immunology , Muscle, Skeletal/pathology , Sarcopenia/blood , Sarcopenia/immunology , Sarcopenia/pathology , Victoria
20.
Eur J Clin Nutr ; 67(10): 1050-5, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23942175

ABSTRACT

BACKGROUND/OBJECTIVES: Serum 25-hydroxyvitamin D (25(OH)D) status has been associated with muscle mass, strength and physical performance in healthy elderly people. Yet, in pre-frail and frail elderly people this association has not been studied. The objective of this study was to explore the association between vitamin D intake and serum 25(OH)D status with muscle mass, strength and physical performance in a pre-frail and frail elderly population. SUBJECTS/METHODS: This cross-sectional study included 127 pre-frail and frail elderly people in The Netherlands. Whole body and appendicular lean mass (ALM) (dual energy X-ray absorptiometry), leg strength (one repetition maximum), handgrip strength and physical performance (short physical performance battery) were measured, and blood samples were collected for the assessment of serum 25(OH)D status (liquid chromatography-tandem mass spectrometry). In addition, habitual dietary intake (3-day food records) and physical activity data (accelerometers) were collected. RESULTS: In total, 53% of the participants had a serum 25(OH)D level below 50 nmol/l. After adjustment for confounding factors, 25(OH)D status was associated with ALM (ß=0.012, P=0.05) and with physical performance (ß=0.020, P<0.05). Vitamin D intake was associated with physical performance (ß=0.18, P<0.05) but not with ALM (P>0.05). CONCLUSION: In this frail elderly population, 25(OH)D status is low and suggests a modest association with reduced ALM and impaired physical performance. In addition, vitamin D intake tended to be associated with impaired physical performance. Our findings highlight the need for well-designed intervention trials to assess the impact of vitamin D supplementation on 25(OH)D status, muscle mass and physical performance in pre-frail and frail elderly people.


Subject(s)
Body Composition , Frail Elderly , Muscle Strength , Muscle, Skeletal , Physical Fitness , Sarcopenia/etiology , Vitamin D Deficiency/complications , Aged , Aged, 80 and over , Cross-Sectional Studies , Female , Humans , Male , Netherlands , Sarcopenia/blood , Vitamin D/analogs & derivatives , Vitamin D/blood , Vitamin D Deficiency/blood
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