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Dietary tryptophan and bone health: a cross-sectional, population-based study

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Abstract

Summary

Tryptophan metabolites influence bone. We aimed to investigate the relationship between dietary tryptophan and bone health in a population-based sample of men and women. Following adjustment for age, dietary tryptophan was not associated with bone quantity or quality, suggesting a non-critical role of superfluous tryptophan on the skeleton.

Purpose

Tryptophan metabolites, such as serotonin, influence bone. We sought to determine the relationship between dietary intake of tryptophan and bone health in a population-based study of men and women.

Methods

Participants (1033 women and 900 men, aged 20–98 years) enrolled in the Geelong Osteoporosis Study (GOS) were investigated. Dietary information was collected using a validated questionnaire. Tryptophan levels were calculated (mg/day) in accordance with Food Standards Australia and New Zealand and dichotomised according to the median. Bone mineral density (BMD; g/cm2) was measured at the spine (postero-anterior projection) and total hip using dual-energy X-ray absorptiometry. Stiffness index (SI), broadband ultrasound attenuation (BUA) and speed of sound (SOS) were derived from quantitative heel ultrasound. Linear regression models were used to test associations between dietary tryptophan and bone health, after adjustment for potential confounders.

Results

Tryptophan intakes ranged from 112 to 3796 mg/day (median 1035) in men and 115–2869 mg/day (median 885) in women. In men older than 45 years and women, a high tryptophan intake was associated with greater hip BMD compared to participants with a low tryptophan intake (p = 0.002 and p = 0.04, respectively); however, these relationships were attenuated by age (all p > 0.05). Participants with high tryptophan intake had greater BUA and SI compared to participants with low tryptophan intake (men; BUA, p = 0.02 and SI, p = 0.02, and women; BUA, p = 0.03 and SI, p = 0.08), yet also attenuated by age (all p > 0.05).

Conclusion

No association was found between tryptophan intake and bone health in this population, which suggests a non-critical role of superfluous tryptophan consumption on the skeleton.

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Data Availability

Data available on reasonable request.

References

  1. Michalowska M, Znorko B, Kaminski T, Oksztulska-Kolanek E, Pawlak D (2015) New insights into tryptophan and its metabolites in the regulation of bone metabolism. J Physiol Pharmacol 66(6):779–791

    CAS  PubMed  Google Scholar 

  2. Alkhalaf Lona M, Ryan KS (2015) Biosynthetic manipulation of tryptophan in bacteria: pathways and mechanisms. Chem Biol 22(3):317–328

    Article  CAS  Google Scholar 

  3. National Research Council (1989) Recommended Dietary Allowances: 10th Edition. Food and Nutrition Board CoLS, National Research Council, editor. National Academy Press (US), Washington, DC

  4. Food and Agriculture Organization/World Health Organization (1973) Energy and protein requirements. World Health Organization, Geneva

    Google Scholar 

  5. World Health Organization TFaAOotUN (2007) The United Nations University (Joint WHO, FAO, UNU). Protein and amino acid requirements in human nutrition: report of a Joint FAO/WHO/UNU expert consultation. United Nations University, Geneva

    Google Scholar 

  6. Institute of Medicine (2005) Dietary reference intakes for energy, carbohydrate, fiber, fat, fatty acids, cholesterol, protein, and amino acids. The National Academies Press, Washington, DC, p 1358

    Google Scholar 

  7. Jenkins TA, Nguyen JCD, Polglaze KE, Bertrand PP (2016) Influence of tryptophan and serotonin on mood and cognition with a possible role of the gut-brain axis. Nutrients. 8(1):56

    Article  Google Scholar 

  8. Al Saedi A, Sharma S, Summers MA, Nurgali K, Duque G (2020) The multiple faces of tryptophan in bone biology. Exp Gerontol 129:110778

    Article  Google Scholar 

  9. Bihuniak JD, Insogna KL (2015) The effects of dietary protein and amino acids on skeletal metabolism. Mol Cell Endocrinol 410:78–86

    Article  CAS  Google Scholar 

  10. Sibilia V, Pagani F, Dieci E, Mrak E, Marchese M, Zarattini G, Guidobono F (2013) Dietary tryptophan manipulation reveals a central role for serotonin in the anabolic response of appendicular skeleton to physical activity in rats. Endocrine. 44(3):790–802

    Article  CAS  Google Scholar 

  11. Sibilia V, Pagani F, Lattuada N, Greco A, Guidobono F (2009) Linking chronic tryptophan deficiency with impaired bone metabolism and reduced bone accrual in growing rats. J Cell Biochem 107(5):890–898

    Article  CAS  Google Scholar 

  12. Refaey ME, Zhong Q, Ding K-H, Shi X-m, Xu J, Bollag WB et al (2014) Impact of dietary aromatic amino acids on osteoclastic activity. Calcif Tissue Int 95(2):174–182

    Article  CAS  Google Scholar 

  13. El Refaey M, Zhong Q, Hill WD, Shi X-M, Hamrick MW, Bailey L et al (2014) Aromatic amino acid activation of signaling pathways in bone marrow mesenchymal stem cells depends on oxygen tension. PLoS ONE 9(4):e91108

    Article  Google Scholar 

  14. Ammann P, Laib A, Bonjour JP, Meyer JM, Rüegsegger P, Rizzoli R (2002) Dietary essential amino acid supplements increase bone strength by influencing bone mass and bone microarchitecture in ovariectomized adult rats fed an isocaloric low-protein diet. J Bone Miner Res 17(7):1264–1272

    Article  CAS  Google Scholar 

  15. Pernow Y, Thorén M, Sääf M, Fernholm R, Anderstam B, Hauge EM, Hall K (2010) Associations between amino acids and bone mineral density in men with idiopathic osteoporosis. Bone. 47(5):959–965

    Article  CAS  Google Scholar 

  16. Sabour H, Latifi S, Soltani Z, Ghodsi S-M, Razavi S-HE, Nazari M et al (2016) The relationship between dietary intakes of amino acids and bone mineral density among individuals with spinal cord injury. Oman Med J 31(1):22–28

    Article  CAS  Google Scholar 

  17. Pasco JA, Nicholson GC, Kotowicz MA (2012) Cohort profile: Geelong Osteoporosis Study. Int J Epidemiol 41(6):1565–1575

    Article  Google Scholar 

  18. Gould H, Brennan SL, Nicholson GC, Kotowicz MA, Henry MJ, Pasco JA (2013) Calcaneal ultrasound reference ranges for Australian men and women: the Geelong Osteoporosis Study. Osteoporos Int 24(4):1369–1377

    Article  CAS  Google Scholar 

  19. Giles GG, Ireland PD (1996) Dietary questionnaire for epidemiological studies (version 2). Melbourne, The Cancer Council Victoria

    Google Scholar 

  20. Food Standards Australia New Zealand (2010) Nutrient tables for use in Australia (NUTTAB) Australia: Food Standards Australia New Zealand. [Available from: www.foodstandards.gov.au]

  21. Monthly Index of Medical Specialties (MIMS) Online (2004) MIMS Annual: June 2004. Medi Media, St Leonards, NSW, Australia. [Available from: http://www.mims.com.au/index.php/about-mims/about-mims-overview]

  22. Le B, Bůžková P, Robbins JA, Fink HA, Raiford M, Isales CM et al (2019) The association of aromatic amino acids with incident hip fracture, aBMD, and body composition from the cardiovascular health study. Calcif Tissue Int 105(2):161–172

    Article  CAS  Google Scholar 

  23. United States Department of Agriculture (1987) Nationwide Food Consumption Survey. U.S. Department of Agriculture, Nutrition Monitoring Division HNIS, Hyattsville

    Google Scholar 

  24. Yadav VK, Ryu J-H, Suda N, Tanaka KF, Gingrich JA, Schütz G, Glorieux FH, Chiang CY, Zajac JD, Insogna KL, Mann JJ, Hen R, Ducy P, Karsenty G (2008) Lrp5 controls bone formation by inhibiting serotonin synthesis in the duodenum. Cell. 135(5):825–837

    Article  CAS  Google Scholar 

  25. Yadav VK, Oury F, Suda N, Liu Z-W, Gao X-B, Confavreux C, Klemenhagen KC, Tanaka KF, Gingrich JA, Guo XE, Tecott LH, Mann JJ, Hen R, Horvath TL, Karsenty G (2009) Leptin regulation of bone mass, appetite and energy expenditure relies on its ability to inhibit serotonin synthesis in the brainstem. Cell. 138(5):976–989

    Article  CAS  Google Scholar 

  26. Yadav VK, Oury F, Suda N, Liu Z-W, Gao X-B, Confavreux C, Klemenhagen KC, Tanaka KF, Gingrich JA, Guo XE, Tecott LH, Mann JJ, Hen R, Horvath TL, Karsenty G (2009) A serotonin-dependent mechanism explains the leptin regulation of bone mass, appetite, and energy expenditure. Cell. 138(5):976–989

    Article  CAS  Google Scholar 

  27. Karsenty G, Yadav VK (2011) Regulation of bone mass by serotonin: molecular biology and therapeutic implications. Annu Rev Med 62:323–331

    Article  CAS  Google Scholar 

  28. Refaey ME, McGee-Lawrence ME, Fulzele S, Kennedy EJ, Bollag WB, Elsalanty M et al (2017) Kynurenine, a tryptophan metabolite that accumulates with age, induces bone loss. J Bone Miner Res 32(11):2182–2193

    Article  CAS  Google Scholar 

  29. Hebden L, Kostan E, O’Leary F, Hodge A, Allman-Farinelli M (2013) Validity and reproducibility of a food frequency questionnaire as a measure of recent dietary intake in young adults. PLoS One 8(9):e75156

    Article  CAS  Google Scholar 

  30. World Medical Association (2013) World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects World Medical Association Declaration of Helsinki Special Communication. JAMA. 310(20):2191–2194

    Article  Google Scholar 

  31. International Committee of Medical Journal Editors (2018) Recommendations for the Conduct, Reporting, Editing and Publication of Scholarly Work in Medical Journals. [Available from: http://www.ICMJE.org]

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Funding

The Geelong Osteoporosis Study was supported by the NHMRC, Australia (Projects 251638, 299831, 628582 and 1104438). JC is supported by a Deakin University Postgraduate Scholarship. MB is supported by a National Health and Medical Research Council (NHMRC) Senior Principal Research Fellowship (APP1059660 and APP1156072). LJW is supported by a NHMRC Career Development Fellowship (1064272). The funding providers played no role in the design or conduct of the study; collection, management, analysis and interpretation of the data; or in preparation, review or approval of the manuscript.

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Correspondence to Jasmine R. Cleminson.

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Conflict of interest

Authors JRC, ALS, JMH and RMS have no conflicts of interest to declare. JAP has recently received grant/research support from the National Health and Medical Research Council (NHMRC), Amgen, BUPA Foundation, Amgen/GlaxoSmithKline/Osteoporosis Australia/Australian and New Zealand Bone and Mineral Society, Western Alliance, Barwon Health, Deakin University and the Geelong Community Foundation.

MB has received grant/research support from the NIH, Cooperative Research Centre, Simons Autism Foundation, Cancer Council of Victoria, Stanley Medical Research Foundation, MBF, NHMRC, Beyond Blue, Rotary Health, Geelong Medical Research Foundation, Bristol Myers Squibb, Eli Lilly, Glaxo SmithKline, Meat and Livestock Board, Organon, Novartis, Mayne Pharma, Servier and Woolworths; has been a speaker for Astra Zeneca, Bristol Myers Squibb, Eli Lilly, Glaxo SmithKline, Janssen Cilag, Lundbeck, Merck, Pfizer, Sanofi Synthelabo, Servier, Solvay and Wyeth; and served as a consultant to Allergan, Astra Zeneca, Bioadvantex, Bionomics, Collaborative Medicinal Development, Eli Lilly, Glaxo SmithKline, Janssen Cilag, Lundbeck Merck, Pfizer and Servier.

LJW has received grant/research support from the National Health and Medical Research Council (NHMRC), Eli Lilly, Pfizer, the University of Melbourne and Deakin University.

Ethics approval

The study was approved through the Barwon Health Human Research Ethics Committee (ID 92/01 and ID 00/56), and all participants provided informed written consent.

Consent to participate

All procedures performed in the work described, involving human participants, were in accordance with the ethical standards of the institutional and/or national research committee and with the Code of Ethics of the World Medical Association (Declaration of Helsinki) [30], its later amendments or comparable ethical standards. Privacy rights were observed for all individual participants included in the study, as well as written informed consent. Further, the manuscript is in line with the Recommendations for the Conduct, Reporting, Editing and Publication of Scholarly Work in Medical Journals [31] and includes a representative human population (sex, age and ethnicity) as per the recommendations.

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Appendix

Appendix

Fig. 1
figure 1

Dietary tryptophan intake of participants. Values presented as median (interquartile range), boxplot width proportional to age stratified sample size

Table 1 Characteristics of men and women and according to high and low dietary tryptophan intake
Table 2 Unadjusted and adjusted linear regression analyses between tryptophan intake and bone health for men and women

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Cleminson, J.R., Stuart, A.L., Pasco, J.A. et al. Dietary tryptophan and bone health: a cross-sectional, population-based study. Arch Osteoporos 15, 167 (2020). https://doi.org/10.1007/s11657-020-00838-w

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