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How Food Choices Impact on Male Fertility

Pecora, Giulia, Sciarra, Francesca, Gangitano, Elena, Venneri, Mary Anna·2023·Current Nutrition Reports

Abstract

Purpose of Review: Increasing evidence on the significance of nutrition in reproduction is emerging from both animal and human studies, suggesting an association between nutrition and male fertility. Here, we have highlighted the impact of the various food groups on reproductive hormones and on spermatogenesis, and the effects of classical and latest dietary patterns such as Mediterranean diet, Western diet, intermittent fasting, ketogenic diet, and vegan/vegetarian diet on male fertility. Recent Findings: Nutrients are the precursors of molecules involved in various body’s reactions; therefore, their balance is essential to ensure the correct regulation of different systems including the endocrine system. Hormones are strongly influenced by the nutritional status of the individual, and their alteration can lead to dysfunctions or diseases like infertility. In addition, nutrients affect sperm production and spermatogenesis, controlling sexual development, and maintaining secondary sexual characteristics and behaviors. Summary: The consumption of fruit, vegetables, fish, processed meats, dairy products, sugars, alcohol, and caffeine importantly impact on male fertility. Among dietary patterns, the Mediterranean diet and the Western diet are most strongly associated with the quality of semen. Nutrients, dietary patterns, and hormonal levels have an impact on male infertility. Therefore, understanding how these factors interact with each other is important for strategies to improve male fertility.

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Research works printed but not linked: 148

  1. Kamangar F, Karimi P. The state of nutritional epidemiology: why we are still unsure of what we should eat? Arch Iran Med. 2013;16(8):483–6.
  2. Aggerholm AS, et al. Is overweight a risk factor for reduced semen quality and altered serum sex hormone profile? Fertil Steril. 2008;90(3):619–26. · DOI
  3. Smith LB, Walker WH. The regulation of spermatogenesis by androgens. Semin Cell Dev Biol. 2014;30:2–13. · DOI
  4. Rosato E, et al. Revisiting the physiological role of androgens in women. Expert Rev Endocrinol Metab. 2022;17(6):547–61. · DOI
  5. Sciarra F, et al. Disruption of Circadian rhythms: a crucial factor in the etiology of infertility. Int J Mol Sci. 2020;21(11):3943. · DOI
  6. Belloc S, et al. High body mass index has a deleterious effect on semen parameters except morphology: results from a large cohort study. Fertil Steril. 2014;102(5):1268–73. · DOI
  7. Aitken RJ. Oxidative stress and the etiology of male infertility. J Assist Reprod Genet. 2016;33(12):1691–2. · DOI
  8. Björndahl L, Kirkman Brown J. The sixth edition of the WHO Laboratory Manual for the Examination and Processing of Human Semen: ensuring quality and standardization in basic examination of human ejaculates. Fertil Steril. 2022;117(2):246–251. · DOI · Paper page
  9. Hanis T, et al. Effects of dietary trans-fatty acids on reproductive performance of Wistar rats. Br J Nutr. 1989;61(3):519–29. · DOI
  10. Imoedemhe DA, et al. The effect of caffeine on the ability of spermatozoa to fertilize mature human oocytes. J Assist Reprod Genet. 1992;9(2):155–60. · DOI
  11. Salas-Huetos A, Bulló M, Salas-Salvadó J. Dietary patterns, foods and nutrients in male fertility parameters and fecundability: a systematic review of observational studies. Hum Reprod Update. 2017;23(4):371–89. · DOI · Paper page
  12. Ricci E, et al. Mediterranean diet and the risk of poor semen quality: cross-sectional analysis of men referring to an Italian Fertility Clinic. Andrology. 2019;7(2):156–62. · DOI
  13. Torres-Arce E, et al. Dietary Antioxidants in the Treatment of Male Infertility: Counteracting Oxidative Stress. Biology (Basel). 2021;10(3). · DOI
  14. Bakos HW, et al. The effect of paternal diet-induced obesity on sperm function and fertilization in a mouse model. Int J Androl. 2011;34(5 Pt 1):402–10. · DOI
  15. Dimofski P, et al. Consequences of paternal nutrition on offspring health and disease. Nutrients. 2021;13(8). · DOI
  16. Pipoyan D, et al. The effect of trans fatty acids on human health: regulation and consumption patterns. Foods. 2021;10(10). · DOI
  17. Attaman JA, et al. Dietary fat and semen quality among men attending a fertility clinic. Hum Reprod. 2012;27(5):1466–74. · DOI
  18. Jensen TK, et al. High dietary intake of saturated fat is associated with reduced semen quality among 701 young Danish men from the general population. Am J Clin Nutr. 2013;97(2):411–8. · DOI
  19. Afeiche MC, et al. Processed meat intake is unfavorably and fish intake favorably associated with semen quality indicators among men attending a fertility clinic. J Nutr. 2014;144(7):1091–8. · DOI
  20. Veaute C, et al. Effects of isomeric fatty acids on reproductive parameters in mice. Am J Reprod Immunol. 2007;58(6):487–96. · DOI
  21. Ye L, et al. Impacts of immunometabolism on male reproduction. Front Immunol. 2021;12:658432. · DOI
  22. Cocuzza M, et al. Clinical relevance of oxidative stress and sperm chromatin damage in male infertility: an evidence based analysis. Int Braz J Urol. 2007;33(5):603–21. · DOI
  23. Esmaeili V, et al. Saturated, omega-6 and omega-3 dietary fatty acid effects on the characteristics of fresh, frozen-thawed semen and blood parameters in rams. Andrologia. 2014;46(1):42–9. · DOI
  24. •• Liu YS, et al. Associations between meat and vegetable intake, cooking methods, and asthenozoospermia: a hospital-based case-control study in China. Nutrients. 2022;14(9). This article examines a case control study of patients with asthenozoospermia and healthy controls. The associations between meat, unprocessed meat, vegetable, and cooking methods are investigated. Results indicate a correlation between these foods and asthenozoospermia. · DOI
  25. Xia W, et al. Men’s meat intake and treatment outcomes among couples undergoing assisted reproduction. Fertil Steril. 2015;104(4):972–9. · DOI
  26. Braga DP, et al. Food intake and social habits in male patients and its relationship to intracytoplasmic sperm injection outcomes. Fertil Steril. 2012;97(1):53–9. · DOI
  27. Rozati R, et al. Role of environmental estrogens in the deterioration of male factor fertility. Fertil Steril. 2002;78(6):1187–94. · DOI
  28. Afeiche M, et al. Dairy food intake in relation to semen quality and reproductive hormone levels among physically active young men. Hum Reprod. 2013;28(8):2265–75. · DOI
  29. Wang XB, et al. Dairy product consumption and oligo-astheno-teratozoospermia risk: a hospital-based case-control study in China. Front Nutr. 2021;8:742375. · DOI
  30. Eslamian G, et al. Intake of food groups and idiopathic asthenozoospermia: a case-control study. Hum Reprod. 2012;27(11):3328–36. · DOI
  31. He H, et al. Lactoferrin alleviates spermatogenesis dysfunction caused by bisphenol A and cadmium via ameliorating disordered autophagy, apoptosis and oxidative stress. Int J Biol Macromol. 2022;222(Pt A):1048–62. · DOI
  32. Snoj T, Majdič G. Mechanisms in endocrinology: estrogens in consumer milk: is there a risk to human reproductive health? Eur J Endocrinol. 2018;179(6):R275-r286. · DOI
  33. Schaum J, et al. A national survey of persistent, bioaccumulative, and toxic (PBT) pollutants in the United States milk supply. J Expo Anal Environ Epidemiol. 2003;13(3):177–86. · DOI
  34. Meeker JD, Hauser R. Exposure to polychlorinated biphenyls (PCBs) and male reproduction. Syst Biol Reprod Med. 2010;56(2):122–31. · DOI
  35. Aguilar-Garduño C, et al. Changes in male hormone profile after occupational organophosphate exposure. A longitudinal study. Toxicology. 2013;307:55–65.
  36. Paradisi R, et al. Effects of high doses of recombinant human follicle-stimulating hormone in the treatment of male factor infertility: results of a pilot study. Fertil Steril. 2006;86(3):728–31. · DOI
  37. Akram M, et al. Dietary intake of probiotic fermented milk benefits the gut and reproductive health in mice fed with an obesogenic diet. Food Funct. 2022;13(2):737–52. · DOI
  38. Hammami I, et al. Kefir milk consumption decreases sperm alterations due to the high-fat diet in adult male rats. Andrologia. 2022;54(7):1631–42. · DOI
  39. Ricci E, et al. Dietary habits and semen parameters: a systematic narrative review. Andrology. 2018;6(1):104–16. · DOI
  40. •• Madej D, et al. Influence of fruit and vegetable consumption on antioxidant status and semen quality: a cross-sectional study in adult men. Front Nutr. 2021;8:753843.This article examines a cross-sectional study in adult men. The influence of fruit and vegetable consumption on semen quality by reducing oxidative stress was investigated. The results indicate a positive influence of high consumption of fruit and vegetables in sperm quality parameters. · DOI
  41. Tremellen K. Oxidative stress and male infertility—a clinical perspective. Hum Reprod Update. 2008;14(3):243–58. · DOI · Paper page
  42. Gharagozloo P, Aitken RJ. The role of sperm oxidative stress in male infertility and the significance of oral antioxidant therapy. Hum Reprod. 2011;26(7):1628–40. · DOI · Paper page
  43. Showell MG, et al. Antioxidants for male subfertility. Cochrane Database Syst Rev. 2014;12:Cd007411. · DOI · Paper page
  44. Yamamoto Y, et al. The effects of tomato juice on male infertility. Asia Pac J Clin Nutr. 2017;26(1):65–71.
  45. Erukainure OL, et al. Strawberry fruit (Fragaria x ananassa Romina) juice attenuates oxidative imbalance with concomitant modulation of metabolic indices linked to male infertility in testicular oxidative injury. Andrologia. 2021;53(9):e14175. · DOI
  46. Moghaddam MH, et al. Elderberry diet restores spermatogenesis in the transient scrotal hyperthermia-induced mice. Reprod Sci. 2022;29(12):3373–86. · DOI
  47. Beigi Boroujeni M, et al. Effects of pomegranate peel extract on histopathology, testosterone levels and sperm of testicular torsion-detorsion induced in adult Wistar rats. J Complement Integr Med. 2017;14(4). · DOI
  48. Amini N, et al. Protective effects of the fruit extract of raspberry (Rubus fruticosus L.) on pituitary-gonadal axis and testicular histopathology in streptozotocin induced diabetic male rats. Avicenna J Phytomed. 2021;11(2):199–209.
  49. Mongioì LM, et al. The role of resveratrol in human male fertility. Molecules. 2021;26(9). · DOI
  50. Robbins WA, et al. Walnuts improve semen quality in men consuming a Western-style diet: randomized control dietary intervention trial. Biol Reprod. 2012;87(4):101. · DOI
  51. Shehzad M, et al. Therapeutic potential of date palm against human infertility: a review. Metabolites. 2021;11(6). · DOI
  52. Salas-Huetos A, et al. Sperm DNA methylation changes after short-term nut supplementation in healthy men consuming a Western-style diet. Andrology. 2021;9(1):260–8. · DOI
  53. Sun ZY, et al. Correction: chestnut polysaccharides restore impaired spermatogenesis by adjusting gut microbiota and the intestinal structure. Food Funct. 2022;13(5):3077. · DOI
  54. Oresti GM, et al. Differentiation-related changes in lipid classes with long-chain and very long-chain polyenoic fatty acids in rat spermatogenic cells. J Lipid Res. 2010;51(10):2909–21. · DOI
  55. Wong WY, et al. Effects of folic acid and zinc sulfate on male factor subfertility: a double-blind, randomized, placebo-controlled trial. Fertil Steril. 2002;77(3):491–8. · DOI · Paper page
  56. Young SS, et al. The association of folate, zinc and antioxidant intake with sperm aneuploidy in healthy non-smoking men. Hum Reprod. 2008;23(5):1014–22. · DOI
  57. Goldin BR, et al. Estrogen excretion patterns and plasma levels in vegetarian and omnivorous women. N Engl J Med. 1982;307(25):1542–7. · DOI · Paper page
  58. Santti R, et al. Phytoestrogens: potential endocrine disruptors in males. Toxicol Ind Health. 1998;14(1–2):223–37. · DOI
  59. D’Adamo CR, Sahin A. Soy foods and supplementation: a review of commonly perceived health benefits and risks. Altern Ther Health Med. 2014;20(Suppl 1):39–51.
  60. Fielden MR, et al. Effect of human dietary exposure levels of genistein during gestation and lactation on long-term reproductive development and sperm quality in mice. Food Chem Toxicol. 2003;41(4):447–54. · DOI
  61. Kang KS, Che JH, Lee YS. Lack of adverse effects in the F1 offspring maternally exposed to genistein at human intake dose level. Food Chem Toxicol. 2002;40(1):43–51. · DOI
  62. Kang J, et al. Non-isoflavone phytochemicals in soy and their health effects. J Agric Food Chem. 2010;58(14):8119–33. · DOI
  63. Nagao T, et al. Reproductive effects in male and female rats of neonatal exposure to genistein. Reprod Toxicol. 2001;15(4):399–411. · DOI
  64. Atanassova N, et al. Comparative effects of neonatal exposure of male rats to potent and weak (environmental) estrogens on spermatogenesis at puberty and the relationship to adult testis size and fertility: evidence for stimulatory effects of low estrogen levels. Endocrinology. 2000;141(10):3898–907. · DOI · Paper page
  65. Beaton LK, et al. Soy protein isolates of varying isoflavone content do not adversely affect semen quality in healthy young men. Fertil Steril. 2010;94(5):1717–22. · DOI · Paper page
  66. Wisniewski AB, et al. Perinatal exposure to genistein alters reproductive development and aggressive behavior in male mice. Physiol Behav. 2005;84(2):327–34. · DOI
  67. Salas-Huetos A, et al. Women’s and men’s intake of omega-3 fatty acids and their food sources and assisted reproductive technology outcomes. Am J Obstet Gynecol. 2022;227(2):246.e1-246.e11. · DOI
  68. Lenzi A, et al. Fatty acid composition of spermatozoa and immature germ cells. Mol Hum Reprod. 2000;6(3):226–31. · DOI
  69. Lenzi A, et al. Polyunsaturated fatty acids of germ cell membranes, glutathione and blutathione-dependent enzyme-PHGPx: from basic to clinic. Contraception. 2002;65(4):301–4. · DOI
  70. Safarinejad MR. Effect of omega-3 polyunsaturated fatty acid supplementation on semen profile and enzymatic anti-oxidant capacity of seminal plasma in infertile men with idiopathic oligoasthenoteratospermia: a double-blind, placebo-controlled, randomised study. Andrologia. 2011;43(1):38–47. · DOI
  71. Axmon A, Rylander L, Rignell-Hydbom A. Reproductive toxicity of seafood contaminants: prospective comparisons of Swedish east and west coast fishermen’s families. Environ Health. 2008;7:20. · DOI
  72. Mocevic E, et al. Environmental mercury exposure, semen quality and reproductive hormones in Greenlandic Inuit and European men: a cross-sectional study. Asian J Androl. 2013;15(1):97–104. · DOI
  73. Ghiasvand R, et al. The association between animal flesh foods consumption and semen parameters among infertile Iranian men: a cross-sectional study. Nutr J. 2020;19(1):113. · DOI
  74. Miki K. Energy metabolism and sperm function. Soc Reprod Fertil Suppl. 2007;65:309–25.
  75. Ding GL, et al. The effects of diabetes on male fertility and epigenetic regulation during spermatogenesis. Asian J Androl. 2015;17(6):948–53. · DOI
  76. Meldgaard M, et al. Consumption of sugar-sweetened or artificially sweetened beverages and semen quality in young men: a cross-sectional study. Int J Environ Res Public Health. 2022;19(2). · DOI
  77. Nassan FL, et al. Association between intake of soft drinks and testicular function in young men. Hum Reprod. 2021;36(12):3036–48. · DOI
  78. • Kiwitt-Cárdenas J, et al. Sugar-sweetened beverage intake in relation to reproductive parameters in young men. Rev Int Androl. 2022;20(Suppl 1):S39–s47. This article examines a cross-sectional study in men evaluating SSB consumption, reproductive hormones, and seminal analysis. The results indicate an association with SSB intake and sperm morphology and estradiol levels. · DOI
  79. Hatch EE, et al. Intake of sugar-sweetened beverages and fecundability in a North American preconception cohort. Epidemiology. 2018;29(3):369–78. · DOI
  80. Jurewicz J, et al. Lifestyle and semen quality: role of modifiable risk factors. Syst Biol Reprod Med. 2014;60(1):43–51. · DOI
  81. Wesselink AK, et al. Caffeine and caffeinated beverage consumption and fecundability in a preconception cohort. Reprod Toxicol. 2016;62:39–45. · DOI
  82. Ricci E, et al. Maternal and paternal caffeine intake and ART outcomes in couples referring to an Italian fertility clinic: a prospective cohort. Nutrients. 2018;10(8). · DOI
  83. Jensen TK, et al. Caffeine intake and semen quality in a population of 2,554 young Danish men. Am J Epidemiol. 2010;171(8):883–91. · DOI
  84. Dias TR, et al. Dose-dependent effects of caffeine in human Sertoli cells metabolism and oxidative profile: relevance for male fertility. Toxicology. 2015;328:12–20. · DOI
  85. Nabavi N, Todehdehghan F, Shiravi A. Effect of caffeine on motility and vitality of sperm and in vitro fertilization of outbreed mouse in T6 and M16 media. Iran J Reprod Med. 2013;11(9):741–6.
  86. Yang H, et al. Lifestyles associated with human semen quality: results from MARHCS cohort study in Chongqing, China. Medicine (Baltimore). 2015;94(28):e1166. · DOI
  87. • Banihani SA, Khaled HJ. Caffeine increased progressive motility of human spermatozoa in normozoospermic and asthenozoospermic semen samples and enhanced activity of seminal creatine kinase. Andrologia. 2021;53(6):e14052. This article examinated the effect of caffeine on motility of human spermatozoa in normozoospermic and asthenozoospermic semen samples. The results indicate a correlation between progressive motility of human spermatozoa with higher concentration of caffeine. · DOI
  88. Akomolafe SF, et al. Caffeine improves sperm quality, modulates steroidogenic enzyme activities, restore testosterone levels and prevent oxidative damage in testicular and epididymal tissues of scopolamine-induced rat model of amnesia. J Pharm Pharmacol. 2019;71(10):1565–75. · DOI
  89. Kwak Y, Choi H, Roh J. The effects of caffeine on the long bones and testes in immature and young adult rats. Toxicol Res. 2017;33(2):157–64. · DOI
  90. Bae J, et al. Dose- and time-related effects of caffeine on the testis in immature male rats. Exp Anim. 2017;66(1):29–39. · DOI
  91. Parazzini F, et al. Risk factors for unexplained dyspermia in infertile men: a case-control study. Arch Androl. 1993;31(2):105–13. · DOI
  92. Muthusami KR, Chinnaswamy P. Effect of chronic alcoholism on male fertility hormones and semen quality. Fertil Steril. 2005;84(4):919–24. · DOI
  93. Silva JV, et al. Study on the short-term effects of increased alcohol and cigarette consumption in healthy young men’s seminal quality. Sci Rep. 2017;7:45457. · DOI
  94. Ricci E, et al. Alcohol intake and semen variables: cross-sectional analysis of a prospective cohort study of men referring to an Italian fertility clinic. Andrology. 2018;6(5):690–6. · DOI
  95. Lavranos G, et al. Investigating ROS sources in male infertility: a common end for numerous pathways. Reprod Toxicol. 2012;34(3):298–307. · DOI
  96. Dobrakowski M, et al. Oxidative stress and motility impairment in the semen of fertile males. Andrologia. 2017;49(10). · DOI
  97. Mendes LO, et al. Mast cells and ethanol consumption: interactions in the prostate, epididymis and testis of UChB rats. Am J Reprod Immunol. 2011;66(3):170–8. · DOI
  98. Finelli R, Mottola F, Agarwal A. Impact of alcohol consumption on male fertility potential: a narrative review. Int J Environ Res Public Health. 2021;19(1). · DOI
  99. La Vignera S, et al. Does alcohol have any effect on male reproductive function? A review of literature. Asian J Androl. 2013;15(2):221–5. · DOI
  100. Li H, et al. Chronic alcohol-induced dysbiosis of the gut microbiota and gut metabolites impairs sperm quality in mice. Front Microbiol. 2022;13:1042923. · DOI
  101. Adedara IA, et al. Interactive effects of ethanol on ulcerative colitis and its associated testicular dysfunction in pubertal BALB/c mice. Alcohol. 2017;64:65–75. · DOI
  102. Rao W, et al. The association between caffeine and alcohol consumption and IVF/ICSI outcomes: a systematic review and dose-response meta-analysis. Acta Obstet Gynecol Scand. 2022;101(12):1351–63. · DOI
  103. Karmon AE, et al. Male caffeine and alcohol intake in relation to semen parameters and in vitro fertilization outcomes among fertility patients. Andrology. 2017;5(2):354–61. · DOI
  104. Gaskins AJ, Chavarro JE. Diet and fertility: a review. Am J Obstet Gynecol. 2018;218(4):379–89. · DOI · Paper page
  105. Salas-Huetos A, et al. Adherence to the Mediterranean diet is positively associated with sperm motility: a cross-sectional analysis. Sci Rep. 2019;9(1):3389. · DOI
  106. Caruso P, et al. Effects of Mediterranean diet on semen parameters in healthy young adults: a randomized controlled trial. Minerva Endocrinol. 2020;45(4):280–7.
  107. Karayiannis D, et al. Association between adherence to the Mediterranean diet and semen quality parameters in male partners of couples attempting fertility. Hum Reprod. 2017;32(1):215–22.
  108. •• Montano L, et al. Effects of a lifestyle change intervention on semen quality in healthy young men living in highly polluted areas in Italy: the FASt randomized controlled trial. Eur Urol Focus. 2022;8(1):351–359. The study is a randomized controlled trial conducted in healthy young men. The effects of lifestyle were investigated. The results showed that an intervention based on Mediterranean diet and regular physical activity can determine an improvement of semen quality. · DOI
  109. Statovci D, et al. The impact of Western diet and nutrients on the microbiota and immune response at mucosal interfaces. Front Immunol. 2017;8:838. · DOI · Paper page
  110. Cheng L, et al. Abnormal lipid metabolism induced apoptosis of spermatogenic cells by increasing testicular HSP60 protein expression. Andrologia. 2020;52(11): e13781. · DOI
  111. Soubry A, et al. Opposing epigenetic signatures in human sperm by intake of fast food versus healthy food. Front Endocrinol (Lausanne). 2021;12: 625204. · DOI
  112. Sukur G, Uysal F, Cinar O. High-fat diet induced obesity alters Dnmt1 and Dnmt3a levels and global DNA methylation in mouse ovary and testis. Histochem Cell Biol. 2023;159(4):339–52. · DOI
  113. Luo D, et al. High fat diet impairs spermatogenesis by regulating glucose and lipid metabolism in Sertoli cells. Life Sci. 2020;257: 118028. · DOI
  114. Jarvis S, et al. High fat diet causes distinct aberrations in the testicular proteome. Int J Obes (Lond). 2020;44(9):1958–69. · DOI
  115. Cutillas-Tolín A, et al. Mediterranean and western dietary patterns are related to markers of testicular function among healthy men. Hum Reprod. 2015;30(12):2945–55.
  116. Domínguez-Vías G, et al. Influence of a virgin olive oil versus butter plus cholesterol-enriched diet on testicular enzymatic activities in adult male rats. Int J Mol Sci. 2017;18(8). · DOI
  117. Yörüsün T, et al. Nutritional factors related to male fertility: Turkish sample. Afr J Reprod Health. 2020;24(2):85–95.
  118. Gaskins AJ, et al. Dietary patterns and semen quality in young men. Hum Reprod. 2012;27(10):2899–907. · DOI
  119. Skoracka K, et al. Diet and nutritional factors in male (in)fertility-underestimated factors. J Clin Med. 2020;9(5). · DOI
  120. Cao LL, et al. The effect of healthy dietary patterns on male semen quality: a systematic review and meta-analysis. Asian J Androl. 2022;24(5):549–57. · DOI
  121. Haeri F, et al. The relationship between major dietary patterns and fertility status in iranian men: a case-control study. Sci Rep. 2021;11(1):18861. · DOI
  122. Vujkovic M, et al. Associations between dietary patterns and semen quality in men undergoing IVF/ICSI treatment. Hum Reprod. 2009;24(6):1304–12. · DOI
  123. Muffone A, de Oliveira Lübke PDP, Rabito EI. Mediterranean diet and infertility: a systematic review with meta-analysis of cohort studies. Nutr Rev. 2023;81(7):775–89. · DOI
  124. Appleby PN, Key TJ. The long-term health of vegetarians and vegans. Proc Nutr Soc. 2016;75(3):287–93. · DOI · Paper page
  125. Orlich MJ, et al. Vegetarian dietary patterns and mortality in Adventist Health Study 2. JAMA Intern Med. 2013;173(13):1230–8. · DOI · Paper page
  126. Caceres S, et al. Effects of soya milk on reproductive hormones during puberty in male Wistar rats. Reprod Domest Anim. 2019;54(6):855–63. · DOI
  127. Luo Q, et al. Soy isoflavones improve the spermatogenic defects in diet-induced obesity rats through Nrf2/HO-1 pathway. Molecules. 2019;24(16). · DOI
  128. Jeminiwa BO, et al. Regulation of the neuroendocrine axis in male rats by soy-based diets is independent of age and due specifically to isoflavone action. Biol Reprod. 2020;103(4):892–906. · DOI
  129. Povey AC, et al. Phytoestrogen intake and other dietary risk factors for low motile sperm count and poor sperm morphology. Andrology. 2020;8(6):1805–14. · DOI
  130. Orzylowska EM, et al. Food intake diet and sperm characteristics in a blue zone: a Loma Linda Study. Eur J Obstet Gynecol Reprod Biol. 2016;203:112–5. · DOI
  131. Franzago M, et al. Sperm DNA methylation at metabolism-related genes in vegan subjects. Front Endocrinol (Lausanne). 2021;12: 633943. · DOI
  132. Chamorro R, et al. Diet, plasma, erythrocytes, and spermatozoa fatty acid composition changes in young vegan men. Lipids. 2020;55(6):639–48. · DOI
  133. Kljajic M, et al. Impact of the vegan diet on sperm quality and sperm oxidative stress values: a preliminary study. J Hum Reprod Sci. 2021;14(4):365–71. · DOI
  134. Chiu YH, et al. Fruit and vegetable intake and their pesticide residues in relation to semen quality among men from a fertility clinic. Hum Reprod. 2015;30(6):1342–51. · DOI
  135. Chiminelli I, et al. Emerging mycotoxins and reproductive effects in animals: A short review. J Appl Toxicol. 2022;42(12):1901–9. · DOI
  136. Sinclair S. Male infertility: nutritional and environmental considerations. Altern Med Rev. 2000;5(1):28–38.
  137. Cienfuegos S, et al. Effect of intermittent fasting on reproductive hormone levels in females and males: a review of human trials. Nutrients. 2022;14(11). · DOI · Paper page
  138. Moro T, et al. Time-restricted eating effects on performance, immune function, and body composition in elite cyclists: a randomized controlled trial. J Int Soc Sports Nutr. 2020;17(1):65. · DOI
  139. Di Lorenzo C, et al. Applications of ketogenic diets in patients with headache: clinical recommendations. Nutrients. 2021;13(7). · DOI
  140. Gangitano E, et al. Ketogenic diet as a preventive and supportive care for COVID-19 patients. Nutrients. 2021;13(3). · DOI
  141. Gangitano E, et al. Ketogenic diet for obese COVID-19 patients: is respiratory disease a contraindication? A narrative review of the literature on ketogenic diet and respiratory function. Front Nutr. 2021;8: 771047. · DOI
  142. Liu CY, et al. Is a ketogenic diet superior to a high-fat, high-cholesterol diet regarding testicular function and spermatogenesis? Front Nutr. 2022;9: 805794. · DOI
  143. Kayode OT, et al. Monosodium glutamate (MSG)-induced male reproductive dysfunction: a mini review. Toxics. 2020;8(1). · DOI
  144. Tsao CW, et al. Curcumin remedies testicular function and spermatogenesis in male mice with low-carbohydrate-diet-induced metabolic dysfunction. Int J Mol Sci. 2022;23(17). · DOI
  145. Mendiola J, et al. Food intake and its relationship with semen quality: a case-control study. Fertil Steril. 2009;91(3):812–8. · DOI
  146. Türk G, et al. Effects of pomegranate juice consumption on sperm quality, spermatogenic cell density, antioxidant activity and testosterone level in male rats. Clin Nutr. 2008;27(2):289–96. · DOI
  147. Kara H, et al. Hazelnut consumption improves testicular antioxidant function and semen quality in young and old male rats. Food Chem. 2019;294:1–8. · DOI
  148. Chavarro JE, et al. Soy food and isoflavone intake in relation to semen quality parameters among men from an infertility clinic. Hum Reprod. 2008;23(11):2584–90. · DOI

Cited by

Metadata

Authors
Pecora, G., Sciarra, F., Gangitano, E., & Venneri, M. A.
Venue
Current Nutrition Reports
Published
2023-10-20
Volume
12
Issue
4
Pages
864-876
ISSN
2161-3311
Cited by
32
References
6
Language
en
Licence
Funders
Università degli Studi di Roma La Sapienza

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

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Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.