| Literature DB >> 33959846 |
Mariangela Rondanelli1,2, Milena Anna Faliva3, Alice Tartara3, Clara Gasparri4, Simone Perna5, Vittoria Infantino2, Antonella Riva6, Giovanna Petrangolini6, Gabriella Peroni3.
Abstract
In 2009 EFSA Panel concludes that a cause and effect relationship has been established between the dietary intake of magnesium (Mg) and maintenance of normal bone. After 2009, numerous studies have been published, but no reviews have made an update on this topic. So, the aim of this narrative review was to consider the state of the art since 2009 on relationship between Mg blood levels, Mg dietary intake and Mg dietary supplementation (alone or with other micronutrients; this last topic has been considered since 1990, because it is not included in the EFSA claims) and bone health in humans. This review included 28 eligible studies: nine studies concern Mg blood, 12 studies concern Mg intake and seven studies concern Mg supplementation, alone or in combination with other nutrients. From the various studies carried out on the serum concentration of Mg and its relationship with the bone, it has been shown that lower values are related to the presence of osteoporosis, and that about 30-40% of the subjects analyzed (mainly menopausal women) have hypomagnesaemia. Various dietetic investigations have shown that many people (about 20%) constantly consume lower quantities of Mg than recommended; moreover, in this category, a lower bone mineral density and a higher fracturing risk have been found. Considering the intervention studies published to date on supplementation with Mg, most have used this mineral in the form of citrate, carbonate or oxide, with a dosage varying between 250 and 1800 mg. In all studies there was a benefit both in terms of bone mineral density and fracture risk.Entities:
Keywords: Bone; Bone mineral density; Dietary supplementation; Magnesium; Nutrients
Mesh:
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Year: 2021 PMID: 33959846 PMCID: PMC8313472 DOI: 10.1007/s10534-021-00305-0
Source DB: PubMed Journal: Biometals ISSN: 0966-0844 Impact factor: 2.949
Fig. 1Flow chart of literature research
Studies that considered blood magnesium levels
| First author, year | Study design | Setting | Inclusion criteria | Exclusion criteria | Number of subjects (M-F) Mean age | Primary outcomes |
|---|---|---|---|---|---|---|
| Mederle et al. ( | Case–control study | Outpatient Department of Endocrinology of the CountyHospital,Timisoara | Women in the postmenopausal period, with lumbar or femoral neck BMD, expressed as T-score,2.5 standard deviation (SD). The control group included women in the postmenopausal period, with lumbar or femoral neck T-score. − 2 SD | Secondary causes of osteoporosis, other diseases that could influence the bone metabolism or electrolyte imbalance (especially Mg), fractures in the previous year, hormone replacement therapy, and any medication that could influence bone turnover | 213 F(132 cases–81 controls) | Determine the correlations between BMD and serum levels of bone resorption markers (TRAP-5b), bone formation markers (BSAP), estradiol (E2), and Mg(2 +) ion concentrations in postmenopausal osteoporotic women as compared to healthy postmenopausal subjects |
| Okyay et al. ( | Obesrvational study | Division of Reproductive Endocrinology and Infertility, Department of Obstetrics and Gynecology at DokuzEylulUniversitySchoolof Medicine,Izmir, Turkey | Postmenopausal women between age 45 and 80 y | History of drug abuse or alcohol consumption (to drink at least ≥ 2 days per week), and highly intake of caffeinated coffee (> 2 cups per day), laboratory tests or radiography of any bone metabolism disorder | 728 F | Determine the relationship between serum main minerals and postmenopausal osteoporosis |
| Mahdavi et al. ( | Observational study | Rheumatology clinic in Tabriz, Islamic Republic of Iran, | Women > 50 years old who had been no menstruation for ≥ 6 months prior to entry into the study, having no history of hormone replacement therapy, other bone disease, kidney stones, endocrine disorders or any medical conditions that could influence on the mineral status | Use of mineral supplements, having history of hormone replacement therapy, bone disease, kidney stones, endocrine disorders or any medical conditions that could influence on the mineral status | 51 F(23 had osteoporosis and 28 had osteopenia) | Investigate and compare the copper, magnesium, zinc and calcium status between osteopenic and osteoporotic postmenopausal women in Tabriz, Islamic Republic of Iran |
| Hayhoe et al. ( | Case Cohort Longitudinal Study | Norfolk, UK | Men and women aged 40–82 y living in the general community | – | 2328 ultrasound cohort group – 4713 fracture case-cohort group | The influence of dietary magnesium and potassium intakes, as well as circulating magnesium, on bone density status and fracture risk in an adult population in theUnited Kingdom |
| Sharma et al. ( | Observational study | TSMMedical College & Hospital, Lucknow,Uttar Pradesh, India | Postmenopausal women with 48 to 75 years | – | 68 F(33 with osteoporosis and 35 with osteopenia) | The role of magnesium in osteoporosis and in osteopenia |
| Kunutsor et al. ( | Prospective cohort study | Eastern Finland | Men aged 42–61 years (a cohort of the Kuopio Ischemic Heart Disease Prospective Study) living in the city of Kuopio and its neighbouring rural communities | – | 2245 M | Investigate the association of baseline serum magnesium concentrations with risk of incident fractures |
| Rai ( | Observational study | OPD Dept of Orthopedics, TSM Medical College & Hospital, Lucknow, India | Postmenopausal women 48–75 years | – | 68 F(33 with osteoporosis and 35 with osteopenia) | Evaluation of magnesium role in bone homeostasis, especially in postmenopausal women with osteopenia and osteoporosis |
| Huang et al. ( | Cross-sectional study | Hospital clinic of Central Taiwan | CKD patients not receiving dialysis | – | 56 (27 with Diabetes and 29 without Diabetes) | Investigate the impact of serum Mg on bone mineral metabolism in chronic kidney disease (CKD) patients with or without diabetes |
| Elshal et al. ( | Case–control study | Outpatient clinic of the university hospital of | Adults with an age range 20–40 years with sickle-cell anaemia in steady-state and race-matched healthy blood donors | Use of steroids, had anorexia nervosa, hyperthyroidism, chronic obstructive pulmonary disease, liver disease, inflammatory bowel disease, or had deranged renal functions (serum creatinine > 2.5 mg/dl) | 60 with sickle-cell anaemia (34 F – 26 M) and 40 healthy blood donors as controls (22 F – 18 M) | Investigate whether serum Mg levels may have an impact on bone mineral density in sickle-cell anaemia |
Studies that considered magnesium dietary intake
| First author, year | Study design | Setting | Inclusion criteria | Exclusion criteria | Number of subjects (M-F) mean age | Lowest quintile intake/RDA or EAR |
|---|---|---|---|---|---|---|
| Wright et al. ( | Prospective Cohort study | North-West University, Potchefstroom campus | Postmenopausal urban black South African women from PURE-SA-NWP, that underwent measurements of distal radius BMD, dual-energy X-ray absorptiometry (DXA), and had their blood profiles done in both 2010 and 2012 | – | 144 F | −/265 mg/d (EAR) |
| Onchard et al. ( | Prospective Cohort study | 40 clinical centers throughout theUnited States | Postmenopausal women enrolled in the Women’s Health Initiative Observational Study | Missing data on magnesium or other model covariates | 73,684 F | < 206.5 mg/d |
| Abrams et al. ( | Prospective study | GeneralClinical Research Center (GCRC) of Texas Children’s Hospital inHouston, TX, USA | Healthy subjects with 4.0 to 8.9 years of age at the time of starting the study not using any medications or multivitamins/multiminerals | Body mass index (BMI) Z‐score > 2.0 | 50 (28 F + 22 M) | −/110 mg/d (EAR) |
| Matias et al. ( | Prospective study | Faculty of Human Kinetics, Technical University ofLisbon | Elite swimmers, males and females, with minimum period of activity of approximately six years; > 10 h training per week; negative test outcomes for performance enhancing drugs; not taking any medications or dietary supplements | – | 17 (9 F + 8 M) | −/400 mg/d (RDA) |
| Esterle et al. ( | Prospective study | Junior high schools and at theUniversity of Caen | Healthy adolescent girls and young women (12 to 22 years old) | – | 192 F | −/360 mg/d (RDA) |
| Gunn et al. ( | Cross sectional study | Community dwelling from the Auckland, Hawke’s Bay and Manawatu regions in New Zealand | Healthy, postmenopausal women aged 50–70 years | Any known significant health condition or regular use of medication which could affect bone or inflammation including HRT, NSAID’s and proton pump inhibitors | 142 F | −/320 mg/d (RDA) |
| Kim et al. ( | Prospective study | Department of Food and Nutrition, Kangwon National University, Gangwon-do | Healthy females aged 19–25 years | Taken any medications or nutritional supplements | 484 F | −/280 mg/d (EAR) |
| Farrell et al. ( | Cross-sectional study | University of Arizona, Department of Nutritional Sciences | Cohorts (Fall 1995–Fall 1997) of postmenopausal women from the first year of the Bone Estrogen Strength Training (BEST), a blocked- randomized, clinical trial, with: 12-month measurements of BMD at the 5 sites of interest (lumbar spine L2–L4 (1.130.16 g/cm3), femur trochanter (0.75 ± 0.11 g/cm3), femur neck (0.88 ± 1.12 g/cm3), Ward’s triangle (0.76 ± 1.14 g/cm3), and total body (1.11 ± 0.08 g/cm3) | – | 244 F | −/320 mg/d (RDA) |
| Veronese et al. ( | Prospective study | Four clinical sites in the US (Baltimore, MD; Pittsburgh, PA; Pawtucket, RI; and Columbus, OH) | Subjects enrolled in the Osteoarthritis Initiative (OAI) database, at high risk of knee OA | – | 3765 (1577 M – 2071 F) | < 205 mg/d M—< 190 mg/d F |
| Welch et al. ( | Cross-sectional Cohort study | United Kingdom (UK) Biobank cohort | People aged 37–73 years | Subject without dietary or other relevant missing data, non-white ethnicity, pregnant women, those with a grip strength of zero, those with extremes of FFM, BMD, Mg, energy, protein, EI:EER, or BMI | 156,575 (36,118 M – 40,441 F in bone analysis) | 238 ± 37 mg/d M—217 ± 34 mg/d F |
| Hayhoe et al. ( | Case Cohort Longitudinal Study | Norfolk District (UK) | Men and women aged 40–82 y living in the general community | – | 2328 ultrasound cohort group – 4713 fracture case-cohort group | 218 ± 31 mg/d M—189 ± 26 mg/d F for ultrasound cohort group and 209 ± 31 mg/d M—175 ± 25 mg/d F for fracture case-cohort group |
| Mahdavi et al. ( | Observational study | Rheumatology clinic in Tabriz, Islamic Republic of Iran, | Women > 50 years old who had been no menstruation for ≥ 6 months prior to entry into the study, having no history of hormone replacement therapy, other bone disease, kidney stones, endocrine disorders or any medical conditions that could influence on the mineral status | Use of mineral supplements, having history of hormone replacement therapy, bone disease, kidney stones, endocrine disorders or any medical conditions that could influence on the mineral status | 51 F(23 had osteoporosis and 28 had osteopenia) | 325 mg/d |
Studies that considered Magnesium supplementation
| First author, year | Study design | Setting | Inclusion criteria | Exclusion criteria | Intervention | Parallel treatments |
|---|---|---|---|---|---|---|
| Elsinger et al. ( | Retrospective study | Osteoporotic women | ||||
| Stending-Lindberg et al. ( | Case- control | Back Rehabilitation Unit of Ichilov Hospital | Postmenopausal women with musculoskeletal pain of non-malignant origin and an initial bone density value below the reference range (≤ 1.19 g/cm3) | Diseases which preclude magnesium treatment (kidney disease, hypotension, A-V block or myasthenia gravis) | At beginning two Mg(OH)2 tablets (250 mg magnesium); The dosage was increased according to individual tolerance levels, to reach a maximum of two tablets three times daily (750 mg magnesium). The maximum dose was given for 6 months, followed by a maintenance dose of two tablets once daily (250 mg magnesium) for another 18 months | Assessment of bone density on two consecutive years during the period of the study, but no treatment |
| Carpenter et al. ( | Prospective, placebo-controlled, randomized, one-year double-blind trial | Clinical Research Centers at Yale University School of Medicine | Caucasian ethnicity, a ratio of weight-to-height between the third and 97th centiles, and the absence of bone disease | Scoliosis, onset of menses, use of chronic medications (retinoids, thyroid hormone, GH, glucocorticoids, oral contraceptives, anticonvulsants, diuretics, or supplements providing pharmacological dosages of vitamins A or D) | Twice daily in a capsule containing powdered magnesium oxide (300 mg of elemental Mg per day) | Encapsulatedmethylcellulose powder |
| Aydin et al. ( | Randomized controlled trial | Marmara University Medical School | Postmenopausal osteoporotic women with normal renal and hepatic function without use of drug that affect bone metabolism | Chronic systemic or bone disease or had a history of smoking, drug, or alcohol abuse | Daily oral dose of 1,830 mg magnesium citrate in the form of magnesium pastilles | Any treatment |
| Dimai et al. ( | Case- control study | University Hospital of Graz Medical School | Men, from 27–36 yr of age | Smokers, history of drug or alcohol abuse. Abnormal values of serum parameters of hepatic and renal functions or abnormal serum electrolytes and iPTH levels | Daily oral dose of 15 mmol Mg in the form of powder, containing 670 mg magnesium carbonate precipitate (equivalent to 169 mg Mg) and 342 mg magnesium oxide (equivalent to 196 mg), dissolved in 250 mL drinking water, taken in the early afternoon with a 2-h fasting period before and after the Mg intake | Glass of water daily in the afternoon with 2-h fasting |
| Abraham et al. ( | Case–control study | Menopause clinic | Postmenopausal women with hormonal replacement therapy | – | A complete supplement containing 500 mg of calcium as the citrate salt and 200 mg of magnesium as the oxide; six tablets/day | Dietary advice but chose not to take the supplement |
| Wood et al. ( | Double-blind, placebo-controlled trial | Center for Pediatric Nutrition Research, Department of Pediatrics, University of Utah, Salt Lake City, UT | Preadolescent girls (age 12, Tanner Stage 2) | – | Chewable vitamin/mineralsupplement: four tablets per day provided 800 mg/d elemental calcium (as calcium citrate and carbonate), 400 mg/d elemental magnesium (as magnesium citrate and oxide), and 400 IU/d vitamin D3 | Placebo supplement containing no vitamins or minerals |