Association of Fatty Acid Synthase with Level of Fatty Acids in Osteoporosis Patients
DOI:
https://doi.org/10.30526/38.1.3625Keywords:
Osteoporosis, fatty acid, fatty acid synthase, lipid profile, total antioxidant status, total oxidant statusAbstract
Osteoporosis (OP) is a bone disease that makes bones more brittle and increases the risk of fractures. Osteoporosis, the most common type in postmenopausal women, is characterized by decreased bone mineral density, skeletal microstructure disintegration, and increased bone fragility. Osteoporotic fractures are more common in women than breast cancer, myocardial infarction, or stroke, and they also incur higher hospital treatment costs. This study aims to assess the connection between fatty acid and BMI, T-score, lipid profile(Triglyceride (TG), Total Cholesterol (TC), High-density lipoprotein (HDL), low-density lipoprotein(LDL), Very low-density lipoprotein(VLDL)), Total Antioxidant Status (TAS), Total Oxidant Status (TOS), Fatty acid synthase (FAS). The current study included 120 participants. Serum samples from postmenopausal women were collected and divided into three groups: 40 patients with OP (G2), 40 patients with osteopenia (G1), and 40 women as the control group. Gas chromatography (GC) to determine the levels of fatty acids (FAs). (ELIZA) was used to determine the levels of FAS, Whereas (TAS), (TOS), and (Triglyceride (TG), Total Cholesterol (TC), High-density lipoprotein (HDL)) were assayed using a spectrophotometer. The study's findings showed that OP (G2) had a significantly lower serum FAS level than osteopenia (G1) and control. The levels of palmitic, stearic, oleic, lenolinic, and linoleic (TC, LDL) in the G2 group were significantly higher than those in the G1 group and the control group. The HDL, VLDL, TG, TAS, and TOS levels in G2 were considerably lower than those in G1 and the control group. According to the Receiver Operating Characteristic (ROC) analysis, FAS showed high sensitivity and specificity. In conclusion, the parameters of FAS, HDL, VLDL, TG, TAS, and TOS were effective in monitoring the progression of osteoporosis, as well as fatty acid level.
References
1. Farhan LO, Taha EM, Farhan AM. A Case control study to determine macrophage migration inhibitor, and N-telopeptides of type I bone collagen levels in the sera of osteoporosis patients. Baghdad Sci J. 2022; 19(4):848. https://doi.org/10.21123/bsj.2022.19.4.0848.
2. Fadhil OH, Taha MM, Taha EM. Role of metalloproteinases-3 and sialidases in iraqi osteoporosis patients. Biochem Cell Arch. 2021; 21(1):939-943.
https://connectjournals.com/pages/articledetails/toc033365.
3. Farhan LO, Farhan AM, Obaidi SAl, Taha EM. A Case-control study to determine metalloproteinase-12 and lysyl oxidase levels in Iraqi women with osteoporosis. Res J Pharm Technol. 2022; 15(6):2655-0. https://doi.org/10.52711/0974-360X.2022.00444.
4. Shareef BH, Hasan BF. Status of zinc and selenium in Iraqi women with rheumatoid arthritis and secondary osteoporosis. Biochem Cell Arch. 2021; 21(1):1185-1194.
https://connectjournals.com/03896.2021.21.1185.
5. Al-Toma A, Herman A, Lems WF, Mulder CJJ. The dietary and non-dietary management of osteoporosis in adult-onset celiac disease: Current status and practical guidance. Nutrients. 2022; 14(21):4554. https://doi.org/10.3390/nu14214554.
6. Pennington Z, Ehresman J, Lubelski D, Cottrill E, Schilling A, Ahmed AK, Feghali J, Witham TF, Sciubba MD. Assessing underlying bone quality in spine surgery patients: a narrative review of dual-energy X-ray absorptiometry (DXA) and alternatives. Spine J. 2021; 21(2):321–331.
https://doi.org/ 10.1016/j.spinee.2020.08.020.
7. Lund J, Rustan AC. Fatty acids: Structures and properties. Encycl Life Sci. 2020: 283-292. https://doi.org/10.1038/npg.els.0003894.
8. Duwaerts CC, Maher JJ. Macronutrients and the adipose-liver axis in obesity and fatty liver. Cell Mol Gastroenterol Hepatol. 2019; 7(4):749–761. https://doi.org/10.1016/j.jcmgh.2019.02.001.
9. Koundouros N, Poulogiannis G. Reprogramming of fatty acid metabolism in cancer. Br J Cancer. 2020; 122(1):4–22. https://www.nature.com/articles/s41416-019-0650-z.
10. Huyben D, Roehe BK, Bekaert M, Ruyter B, Glencross B. Dietary lipid: protein ratio and n-3 long-chain polyunsaturated fatty acids alters the gut microbiome of Atlantic salmon under hypoxic and normoxic conditions. Front Microbiol. 2020; 11:589898. https://doi.org/10.3389/fmicb.2020.589898.
11. Gammone MA, Riccioni G, Parrinello GD, Orazio N. Omega-3 polyunsaturated fatty acids: Benefits and endpoints in sport. Nutrients. 2019; 11(1):46. https://doi.org/10.3390/nu11010046.
12. Waktola HD, Zeng AX, Chin ST, Marriott PJ. Advanced gas chromatography and mass spectrometry technologies for fatty acids and triacylglycerols analysis. TrAC Trends Anal Chem. 2020; 129:115957. https://doi.org/10.1016/j.trac.2020.115957.
13. Qiu X, Xie X, Meesapyodsuk D. Molecular mechanisms for biosynthesis and assembly of nutritionally important very long chain polyunsaturated fatty acids in microorganisms. Prog Lipid Res. 2020 ;79:101047. https://doi.org/10.1016/j.plipres.2020.101047.
14. Yki-Järvinen H, Luukkonen PK, Hodson L, Moore JB. Dietary carbohydrates and fats in nonalcoholic fatty liver disease. Nat Rev Gastroenterol Hepatol. 2021;18(11):770–786. https://doi.org/10.1038/s41575-021-00472-y.
15. Xu Z, Feng W, Shen Q, Yu N, Yu K, Wang S, Chen Z, Shioda S, Guo Y. Rhizoma coptidis and berberine as a natural drug to combat aging and aging-related diseases via anti-oxidation and AMPK activation. Aging Dis. 2017; 8(6):760-777. https://doi.org/10.14336/AD.2016.0620.
16. Jiang Y, Zhang P, Zhang X, Lv L, Zhou Y. Advances in mesenchymal stem cell transplantation for the treatment of osteoporosis. Cell Prolif. 2021; 54(1):e12956. https://doi.org/10.1111/cpr.12956.
17. Ascar IF, Khaleel FM, Hameed AS, Alabboodi MK. Evaluation of some antioxidants and oxidative stress tests in Iraqi lung cancer patients. Baghdad Sci J. 2022; 19(6 (Suppl.)):1466.
http://dx.doi.org/10.21123/bsj.2022.7597.
18. Khaleel FM, Oda NN, Abed BA. Disturbance of arginase activity and nitric oxide levels in Iraqi type 2 diabetes mellitus. Baghdad Sci J. 2018; 15(2):0189. https://doi.org/10.21123/bsj.2018.15.2.0189.
19. Baral P, Shrestha R, Shrestha RN, Banstola D, Prajapati R. A study of height, weight and body mass index in Nepalese. J Gandaki Med Coll. 2021; 14(2):88–92. https://doi.org/10.3126/jgmcn.v14i2.40021.
20. Kuno T, Tanimoto E, Morita S, Shimada YJ. Effects of bariatric surgery on cardiovascular disease: a concise update of recent advances. Front Cardiovasc Med. 2019; 6:94.
https://doi.org/10.3389/fcvm.2019.00094.
21. Ferraz-Amaro I, Delgado-Frías E, Hernández-Hernández V, Sánchez-Pérez H, de Armas-Rillo L, Armas-González E, David Machado J, Diaz-González F. HDL cholesterol efflux capacity and lipid profile in patients with systemic sclerosis. Arthritis Res Ther. 2021; 23(1):1–11.
https://doi.org/10.1186/s13075-021-02443-9.
22. Sabry M, Mostafa S, Rashed L, Abdelgwad M, Kamar S, Estaphan S. Matrix metalloproteinase 9 a potential major player connecting atherosclerosis and osteoporosis in high fat diet fed rats. PLOS One. 2021; 16(2):e0244650. https://doi.org/10.1371/journal.pone.0244650.
23. Shen C-L, Mo H, Dunn DM, Watkins BA. Tocotrienol supplementation led to higher serum levels of lysophospholipids but lower acylcarnitines in postmenopausal women: A randomized double-blinded placebo-controlled clinical trial. Front Nutr. 2021; 8: 766711. https://doi.org/10.3389/fnut.2021.766711.
24. Berland C, Small DM, Luquet S, Gangarossa G. Dietary lipids as regulators of reward processes: multimodal integration matters. Trends Endocrinol Metab. 2021; 32(9):693–705.
https://doi.org/10.1016/j.tem.2021.05.008.
25. Zhang M, Xie Z, Long H, Ren K, Hou L, Wang Y, Xuf X, Leig W, Yanga Z, Ahmed S, Zhangi H, Zhao G. Current advances in the imaging of atherosclerotic vulnerable plaque using nanoparticles. Mater Today Bio. 2022; 14: 100236. https://doi.org/10.1016/j.mtbio.2022.100236.
26. Paiva P, Medina FE, Viegas M, Ferreira P, Neves RPP, Sousa JPM. Animal fatty acid synthase: A chemical nanofactory. Chem Rev. 2021; 121(15):9502–9553.
https://doi.org/10.1021/acs.chemrev.1c00147.
27. Fhu CW, Ali A. Fatty acid synthase: an emerging target in cancer. Molecules. 2020; 25(17):3935.
https://doi.org/10.3390/molecules25173935.
28. Azizgolshani H, Coppeta JR, Vedula EM, Marr EE, Cain BP, Luu RJ, Lech b, Kann SH, Mulhern TJ, Tandon V, Tan K, Haroutunian NG, Keegan P, Rogers M, Gard AL, Baldwin KB, de Souza JC, Hoefler BC, Bale SS, Kratchman LB, Zorn A, Patterson A, Kim ES, Petrie AT, Wiellette EL, Williams C, Isenberg BC, Charest JL. High-throughput organ-on-chip platform with integrated programmable fluid flow and real-time sensing for complex tissue models in drug development workflows. Lab Chip. 2021; 21(8):1454–1474. https://doi.org/10.1039/D1LC00067E.
29. Pino AM, Rodríguez JP. Is fatty acid composition of human bone marrow significant to bone health? Bone. 2019; 118:53–61. https://doi.org/10.1016/j.bone.2017.12.014.
30. Das S, Juliana N, Yazit NAA, Azmani S, Abu IF. Multiple myeloma: challenges encountered and future options for better treatment. Int J Mol Sci. 2022; 23(3):1649.
https://doi.org/10.3390/ijms23031649.
31. Abshirini M, Ilesanmi-Oyelere BL, Kruger MC. Potential modulatory mechanisms of action by long-chain polyunsaturated fatty acids on bone cell and chondrocyte metabolism. Prog Lipid Res. 2021; 83: 101113. https://doi.org/10.1016/j.plipres.2021.101113.
32. Lucas S, Omata Y, Hofmann J, Böttcher M, Iljazovic A, Sarter K, Albrecht O, Schulz O, Krishnacoumar B, Krönke G, Herrmann M, Mougiakakos D, Strowig T, Schett G, Zaiss M. Short-chain fatty acids regulate systemic bone mass and protect from pathological bone loss. Nat Commun. 2018; 9(1):55. https://doi.org/10.1038/s41467-017-02490-4.
Downloads
Published
Issue
Section
License
Copyright (c) 2025 Ibn AL-Haitham Journal For Pure and Applied Sciences
This work is licensed under a Creative Commons Attribution 4.0 International License.
licenseTerms