Volume 9, Issue 4 (Nov 2024)                   JNFS 2024, 9(4): 621-630 | Back to browse issues page


XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Beigrezaei S, Darabi Z, Babaie S, Hosseinzadeh M. The Adherence Mediterranean Diet and the Quality of Sperm Parameters in Men with Infertility: A Cross-Sectional Study. JNFS 2024; 9 (4) :621-630
URL: http://jnfs.ssu.ac.ir/article-1-872-en.html
Nutritional Health Research Center, School of Health and Nutrition, Lorestan University of Medical Sciences, Khorramabad
Full-Text [PDF 578 kb]   (120 Downloads)     |   Abstract (HTML)  (521 Views)
Full-Text:   (64 Views)
The Adherence Mediterranean Diet and the Quality of Sperm Parameters in Men with Infertility: A Cross-Sectional Study

Sara Beigrezaei; PhD1,2, Zahra Darabi; PhD1,2, Syavash Babaie; MSc1,2 & Mahdieh Hosseinzadeh; PhD*1,2

1 Julius Center for Health Sciences and Primary Care, University of Medical Center Utrecht, Utrecht University, Utrecht, the Netherland; 2 Nutritional Health Research Center, School of Health and Nutrition, Lorestan University of Medical Sciences, Khorramabad, Iran; 3 Department of Nutrition, School of Public Health, Shahid Sadughi University of Medical Sciences, Yazd, Iran; 4 Research Center for Food Hygiene and Safety, School of Public Health, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
ARTICLE INFO ABSTRACT
ORIGINAL ARTICLE Background: It is well known that dietary factors can affect male fertility. The aim of this study was investigating the effect of Mediterranean diet on sperm quality. Methods: This cross-sectional study was conducted on 218 men with infertility aged 20-50. A 168-item food frequency questionnaire (FFQ) was used to evaluate dietary intakes. Mediterranean diet scores were calculated based on the participant’s dietary intake. The evaluation of anthropometric and biochemical variables was performed through standard methods. To evaluate the relationship between Mediterranean dietary patterns and sperm parameters, the multivariate logistic regression controlled for potential confounders was used. Results: The prevalence of sperm’s low concentration in people with low, moderate, and high adherence to the Mediterranean diet was 43.4%, 34% and 25.9%, respectively. Participants in the highest tertile of adherence to the Mediterranean diet had lower odds of sperm low concentration (odds ratio: 0.37; 95% confidence interval: 0.15–0.91 P=0.02) compared with those in the lowest tertile after adjusting for potential confounders including energy intake, body mass index (BMI), smoking, age, level of education and physical activity. This association was observed between increasing trend adherence to the Mediterranean diet and decreasing the odds of sperm low concentration after full adjustments (odds ratio: 0.60; 95%, confidence interval: 0.98–0.94, Ptrend=0.02). Conclusion: In the present study, the authors observed a protective relation between Mediterranean diet and sperm’s low concentration. However, the association between adherence to this diet and other sperm parameters is unexplored. In future, more investigations are needed in this era.
Article history:
Received: 18 Aprc2023
Revised: 20 Jun 2023
Accepted: 28 Jun 2023
*Corresponding author:
hoseinzade.mahdie@gmail.com
Department of Nutrition, School of Public Health, Shahid Sadoughi University of Medical Sciences, Yazd.

Postal code: 8915173160
Tel: +98 35 38203232

Keywords:
Mediterranean diet; Sperm parameters; Male infertility.

Introduction
Infertility has been identified as a probably severe and costly problem for affected families (Vayena et al., 2002). Males are found to be entirely responsible for 20–30% of infertility cases overall (Vander Borght and Wyns, 2018). 90% of the couples with fertility problems have low quality and/or count sperm (Leaver, 2016). Lifestyle factors such as smoking, stress, and diet can play a role in infertility (Hart, 2016).
It is well acknowledged that diet and metabolic factors can affect male fertility (Nätt et al., 2019). Interestingly, some studies have shown that obesity may decline the quality of sperm (Ibañez-Perez et al., 2019, Liu and Ding, 2017, Salas-Huetos et al., 2017). High calorie diets, foods rich in trans-fatty acids, saturated fats, and cholesterol have been related to testicular interruption, involving damage in spermatogenesis, likely affecting male fertility (Morgan et al., 2014, Ng et al., 2010, Rato et al., 2014). Excessive energy intake may also cause mitochondrial dysfunction, which is closely related to reactive oxygen species (ROS). It easily targets spermatozoa DNA and lipids, which diminishes sperm quality (Rato et al., 2014).
However, epidemiological studies have shown that the use of dietary pattern can help better understand the correlation between dietary intake and chronic diseases such as infertility (Karayiannis et al., 2017, Salas-Huetos et al., 2017). The Mediterranean dietary pattern was proposed for the first time in 1995 to decrease cardiovascular risk factors in Mediterranean countries (Esposito and Giugliano, 2002).Vegetables, fruit, and olive oil are main components of Mediterranean diet. These compounds are rich in vitamins C and E, carotenoids, and polyphenols because they had antioxidant capacity (Lopes et al., 2003, Visioli, 2000). Antioxidants can play the role of scavenger ROS before they lead to damage to various biomolecules, or prohibit oxidative damage from spreading out by breaking down the radical chain reaction of lipid peroxidation (Frei, 1994).
Although some projects reported protective association of the Mediterranean diet on health (Guasch-Ferré and Willett, 2021, Schröder, 2007), the results of a review study reported that Mediterranean diet is associated with lower rates of incident diabetes, and has better glycemic control in diabetic patients compared to control diets (Guasch-Ferré and Willett, 2021). Some studies reported that high adherence to Mediterranean diet has a protective effect on sperm quality (Cutillas-Tolín et al., 2015a, Karayiannis et al., 2017). Considering the effects of Mediterranean diet on health, the limited number of studies on the effect of Mediterranean diet on infertility, the fact that most of the research has been done in western countries where the dietary habits and the prevalence and features of infertility are different, the aim of this study is to investigate the effect of following the Mediterranean diet on sperm quality.
Material and Methods
Study population
This cross-sectional study was conducted on aged 20-50 year infertile men attending the Yazd Research and Clinical Center for infertility. Eligible participants were infertile men (with any disorder in morphology, motility, and concentration of sperm). Exclusion criteria were chronic disease, azoospermia, genetic disorders, history of vasectomy, varicocele, macroorchidism, and cryptorchidism. In addition, the participants who did not answer more than 35 food items of the food frequency questionnaire items, and the participants that received calorie, 800-4200 kcal were excluded. 250 men were eligible after applying all inclusion and exclusion criteria, and finally, the study was conducted on 218 men.
Dietary intake and physical activity
Dietary intake data was collected by trained dietitians with face to face interviews and a validated semi-quantitative food frequency questionnaire (FFQ) including 168 food items (Mirmiran et al., 2010). The participants were asked about consumption frequency of each item in the questionnaire over the period of one year. The size of standard units and items reported based on household measures were converted to grams using instructions from nutritionist 4 scales (Afeiche et al., 2013). Then, the amount of food intake of each subject was reported based on their daily intake in gram. The responses of participants were transformed into grams per day. The authors used the information included in the food ingredients table adapted for Iranian food items to calculate energy, macronutrients, and micronutrients. Daily physical activity (MET h/week) was measured by a short International Physical Activity Questionnaire (IPAQ) (Chiu et al., 2014).
Mediterranean diet scale
The score of adherence to Mediterranean diet was calculated using the proposed method by Trichouplou et al. (Trichopoulou et al., 2003) . The scoring was based on 9 food items: vegetables, legumes, fruits and nuts, dairy products, cereals, red meat and meat products, fish, poultry, and the ratio of monounsaturated fatty aside (MUFA) to Poly Unsaturated Fatty Acids (PUFA). The median consumption of these food items was calculated for each of the 9 components. For red and processed meat consumption, poultry and dairy products of less than median were given a value of 1, and for their consumption at or higher than the median was a value of 0 was given. For beneficial components (vegetables, legumes, fruits and nuts, cereal, and fish) consumption of less than the median, a value of 0 was considered, and for their consumption at or higher than the median, a value of 1 was dedicated. Also, for fat intake, the ratio of MUFA to saturated fatty aside (SFA) was used.  The total Mediterranean-diet score ranged from 0 to 9.
Semen collection and analysis
Semen samples were taken by masturbation in the room near the laboratory and kept at 37 °C. Patients were asked not to ejaculate for at least 48 h before sampling. Semen analysis was conducted based on the WHO guidelines (Word Health Organization, 2010). Sperm parameters like sperm count (106/ml), motility, viability, and normal morphology were assessed on behalf of 200 spermatozoa for each sample. Sperm count and motility were evaluated by means of Makler chamber using light microscopy (Olympus Co., Tokyo, Japan). The viability and morphology were assessed by Eosin and Papanicolaou staining tests, respectively(Jörundsson et al., 1999).
General, medical, and anthropometric measurements
General information including education, economic, and employment status were collected by personal interview. Morphology, motility, concentration of sperm, and sperm volume examinations were recorded according to the individual tests (World Health Organisation, 1999). Anthropometric measurements were performed using the standard methods. Body weight was determined with 100 g accuracy using a Seca scale. Body height was measured with a tape meter in a standing position without shoes, while the shoulders were in normal position using a Seca scale. Body mass index (BMI) (kg/m2) was calculated by dividing weight in kilograms by the square of height in meters. Waist circumference (cm) was measured with the accuracy of 0.1 cm using a tape measure without any pressure on the body surface at the midpoint between the last rib and the upper part of the pelvis at the end of a normal exhalation. When it was hard to measure the narrowest area of the waist in individuals, waist circumstance was measured exactly under the last rib since in most subjects waist would be the narrowest area between the iliac crests and the lower ribs (Holm et al., 1991). Hip circumstance (cm) was measured by a tape measure with the accuracy of 0.1 cm in a standing position and without any extra cover in the head area of the biggest hip bone that is equal to the biggest circumstance of thigh bone.
Ethical considerations
The protocol of this study was approved by the ethics committee of Shahid Sadoughi University of Medical Sciences, Yazd, Iran (approval code: IR.SSU.SPH.HER.1399.193). Informed consent was obtained from each participant before enrollment.
Data analysis
To compare general characteristics across tertiles, one-way ANOVA test was used for continuous variables and chi-square test was conducted for categorical variables. Dietary intakes across tertiles were compared using ANOVA test. To evaluate the relation between Mediterranean dietary pattern and sperm parameters, the authors used multivariate logistic regression in crude and adjusted models; they fit a model adjusted for energy intake, BMI, and physical activity.
Results
Characteristics of the study population
Characteristics of the participants across tertiles score of Mediterranean diet participants are presented in Table1. The mean age of the participants was 33.7±5-79 year. There was no significant difference in age, BMI, fat mass, visceral fat, waist circumference, hip circumference, smoking, education level and physical activity between tertiles Mediterranean dietary pattern scores.
Table 1. Characteristics of the study participants across tertiles of Mediterranean diet scores.
Variables Mediterranean diet tertile P-valueb
T1 T2 T3
Quantitative variables
Age (year)

34.44±5.67a

33.60±5.91

33.40±5.76

0.61
Body mass index (kg/m2) 25.81±4.84 25.73±5.00 25.37±4.38 0.88
Fat mass (%) 23.25±7.84 23.21±12.65 22.31±8.61 0.81
Waist circumference (cm) 94.15±13.43 94.00±12.65 92.60±10.40 0.79
Hip circumference (cm) 99.94±8.04 99.65±8.56 95.04±21.85 0.10
Visceral fat (%) 8.76±4.56) 8.56±4.37) 7.91±4.07) 0.63
Qualitative variables
Low sperm concentration
23(43.6) 33(34.0) 14(25.9) 0.16
Low sperm volume 7(13.7) 5(5.7) 5(9.6) 0.27
Low sperm progressive motility 22(41.5) 33(34.4) 14(25.9) 0.68
Low morphology 43(86) 79(83.2) 73(81.5) 0.82
Smoking 22(38.6) 39(38.6) 21(35.0) 0.88
Education
   High school
   Diploma
   Bachelor’s degree
   Master’s degree and higher
0.40

16(29.6) 39(40.6) 22(37.3)
23(42.6) 36(37.5) 28(47.5)
7(13.0) 6(6.3) 2(3.4)
8(14.8) 15(15.6) 7(11.9)
Physical activity
   Low
   Moderate
   High
0.86
19(34.5) 25(26.6) 17(32.1)
30(54.5) 56(59.6) 30(6.6)
6(10.9) 13(13.8) 6(11.3)
a: Data are presented in quantitative variables as mean ±standard deviation (SD) and for qualitative variables as number (%); b: For qualitative and quantitative variables, Chi-square test and One-way ANOVA, were used respectively.

Dietary intakes of participants
Components of the Mediterranean diet across tertiles of Mediterranean diet scores are presented in Table2. Consumption of whole grain and dairy was not significantly different among tertiles of Mediterranean diet scores. However, intake of refined grain and poultry, fish, fruit, vegetable, legumes, nut, MUFA to SFA ratio, and meat significantly increased with increasing tertiles.

Table 2. Characteristics of the study participants based on tertiles of Mediterranean diet scores.
Variables Mediterranean diet tertile P-valueb
T1 T2 T3
Energy intake (kcal) 3113.08±653.15a 3106.08 ±653.15 3262.72±522.91 0.27
Whole grain (g) 91.44±112.40 106.08±104.04 110.63±89.31 0.56
Refine grain (g) 386.36±184.74 385.57±160.83 324.49±116.55 0.03
Fish (g) 14.45±20.17 25.61±33.20 39.23±35.49 <0.001
Meat (g) 57.88±56.67 41.05±37.66 35.25±38.27 0.01
Poultry (g) 100.48±77.89 72.27±76.37 69.19±59.02 0.03
Fruit (g) 417.42±290.93 440.76±284.94 767.99±591.88 <0.001
Vegetable (g) 87.57±45.81 111.83±125.53 187.14±132.85 <0.001
Legumes (g) 35.69±26.75 50.89±33.75 62.46±42.00 <0.001
Nut (g) 8.76±8.09 17.66±21.16 21.88±22.90 <0.01
Dairy (g) 359.17±355.71 313.76±231.48 434.46±667.30 0.22
MUFA/SFA 0.92±0.29 0.09±0.43 1.15±0.35 <0.01
MUFA: Monounsaturated fatty acid; SFA: Saturated fatty acid; a: Data reported on mean± SD; b: One-way ANOVA.

Association between Mediterranean diet and sperm quality
Crude and multivariate-adjusted odds ratios for decreased sperm quality based on tertiles of Mediterranean diet adherence are listed in Table 3. There was no significant association between adherence to Mediterranean diet and odds of low volume, low morphology, and low progressive motility in crude and adjusted models. Moreover, there was no significant association between odds of low concentration and score of Mediterranean diet in crude model (Odds Ratio (OR): 0.45; 95% confidence interval (CI): 0.20–1.03, P=0.06).
After adjusting for energy intake, BMI, age and physical activity, and smoking, significant protective association was observed between higher adherence to Mediterranean diet and odds of low concentration sperm. Men in the higher tertile of Mediterranean diet had 64% lower odds of sperm’s low concentration than the first tertile after full adjustment (OR=0.37, 95% CI: 0.15 to 0.91; P= 0.03).
Table 3. Odds ratio of the considered sperm disorder across tertiles of Mediterranean diet score
(Multivariable-adjusted odds ratios and 95% CI).
Ptrend P-valuea Mediterranean diet tertile Variables
T3 T2 T1
Low concentration
0.05 0.06 0.45 (0.20-1.03) 0.67(0.23-1.33) 1.00   Crude
0.02 0.03 0.37 (0.15-0.91) 0.58 (0.28-1.20) 1.00   Adjusted modela
Low progressive motility
0.72 0.72 0.87 (0.40-1.88) 0.73(0.37-1.47) 1.00   Crude
0.87 0.89 0.94 (0.40-2.17) 0.75(0.36-1.56) 1.00   Adjusted model
Low volume
0.47 0.51 0.66 (0.19-2.26) 0.37(0.11-1.26) 1.00   Crude
0.50 0.56 0.67 (0.17-2.64) 0.42 (0.12-1.50) 1.00   Adjusted model
Low morphology
0.53 0.53 0.71 (0.25-2.05) 0.80 (0.30-2.10) 1.00   Crude
0.39 0.40 0.62 (0.20-0.18) 0.87 (0.31-2.44) 1.00   Adjusted model
a: Adjusted model:  Adjusted for energy intake, BMI, physical activity, age, and smoking.

Discussion
This study was conducted to explore the association between adherence to Mediterranean diet and quality of sperm in Iranian adults as a Middle East country. The results showed that higher adherence to Mediterranean diet can reduce the odds of sperm’s low concentration but not sperm’s low volume and low progressive motility after full adjustment. Previous observational studies stated a positive relationship between the intake of individual components of a Mediterranean dietary pattern such as vegetables (Eslamian et al., 2012), fruits (Braga et al., 2012), fish (Afeiche et al., 2014b), poultry (Eslamian et al., 2012), whole grains (Braga et al., 2012), low-fat dairies (Afeiche et al., 2014a) and the improvement of some sperm quality parameters.
The findings regard a protective association between adherence to a Mediterranean dietary pattern and concentration of sperm, which was consistent with some studies. In a cross-sectional study of 225 men, Karayiannis et al. (Karayiannis et al., 2017) reported that men in the lowest tertile of the Mediterranean diet adherence  compared to the highest one, had a higher abnormal sperm concentration, total sperm count, and motility. Furthermore, in a study by Cutillas-Tolın et al. (Cutillas-Tolín et al., 2015b), the total sperm count of men in the higher quartile of Mediterranean diet consumption was 51.5% higher than those in the lower quartile adherence. In a study population of healthy men from the USA, higher adherence to a “prudent” dietary pattern, that was similar to the Mediterranean dietary pattern, was related to higher progressive motility (Gaskins et al., 2012). Hence, the findings confirmed some of the results but only in relation to the concentration of sperm as a key fertility-related parameter.
Regarding other dietary patterns assessing sperm parameters, in a study by Oostingh et al. (Oostingh et al., 2017) a positive relationship between higher adherence to a healthy dietary pattern and semen parameters in men with poor semen quality was found. On the other hand, Cutillas-Tolın et al  Observed an inverse relationship between adherence to Western diet and semen concentration among overweight or obese men (Cutillas-Tolín et al., 2015a). In addition, the findings of main components of western dietary patterns, including processed meat (Afeiche et al., 2014c), potatoes (Mendiola et al., 2009), full-fat dairy (Afeiche et al., 2013), sweets (Eslamian et al., 2012), sugar-sweetened beverages (Chiu et al., 2014), and alcohol (Anifandis et al., 2014) were adversely related to several quality parameters of semen.
Vegetables and fruits were two main food groups of the Mediterranean diet with high contents of micronutrients and antioxidants. The combination of losing cytoplasm, generating ROS by mitochondria, and accumulation of an oxidizable substrate in its cell membrane led to the susceptibility of sperm to oxidative damage (Nassan et al., 2018). Evidence from randomized trials demonstrated that antioxidant supplementation among men caused improving semen quality, particularly motility (Agarwal et al., 2004, Nassan et al., 2018).
This was while the intake of folic acid as affluent vitamins of fruit and vegetables in Mediterranean diet can affect sperm production. Folates may play a key role in spermatogenesis by acting as substrates or cofactors in the metabolism of one-carbon (Schröder, 2007). The metabolism of one-carbon occurs in testes (Chen et al., 2001, Holm et al., 1991, Holm et al., 1999). Generally, this pathway contains a series of related metabolic pathways that one-carbon moieties are transferred from donors to intermediate carriers and used in reactions of methylation or the synthesis of purines and thymidine; then, they are used in DNA synthesis (Eslamian et al., 2012, Lucock, 2000). In a randomized trial, the supplementation of folic acid led to an increase in sperm concentration (Bentivoglio et al., 1993). Additionally, in another randomized trial, sub fertile men who assigned to the folate and zinc arm showed a remarkable increase in total sperm count (Wong et al., 2002). The composition of fatty acids in sperm cell membrane is very important for proper function of sperms, and the sperm cell membrane have a main role in fertilization events (Flesch and Gadella, 2000). The PUFA content of sperm cell membrane, especially docosahexaenoic acid (DHA) increases as the sperm matures (Lenzi et al., 2000). Moreover, 20% of the fatty acid content in mature sperm is comprising of DHA (Lenzi et al., 2000). PUFAs must be obtained from consuming seafood, fish, nuts, seeds, and vegetable oils consumed highly in Mediterranean diet. It was demonstrated that intake of these food sources could alter the fatty acid composition of sperm quality (Nassan et al., 2018). In addition, evidence showed that supplementation with fish oil, as a rich source of DHA and eicosapentaenoic acid (EPA), could elevate the concentration of DHA in animals testicular and humans sperm membrane, resulting in higher sperm concentration, motility, and normal morphology (Conquer et al., 1999, Frei, 1994, Safarinejad, 2011, Schröder, 2007, Tavilani et al., 2006, Tavilani et al., 2007).
Low-fat dairy products as components of Mediterranean diet have been established with association between dairy products, and specifically, sperm parameters reference. In a longitudinal cohort study among men in the USA, the consumption of low-fat dairy products was related to a higher sperm concentration and progressive sperm motility (Afeiche et al., 2014a). Inversely, a cross-sectional investigation of a cohort of men found that the intake of full-fat dairy products was adversely associated with normal sperm morphology and better motility (Vujkovic et al., 2009). In another cross-sectional study of men in the Netherlands, dairy consumption was not associated with semen quality (Afeiche et al., 2013)
The strengths of the present study were the large study population, and using priori dietary patterns method due to the major advantage of method as a reference where data was achieved regarding adherence to healthy dietary habits. In addition, infertility clinic is referral in Middle East countries. Because of unique diet cultures and backgrounds, the findings of this study may identify novel insight into Mediterranean diet and infertility. One of the strengths of the study was that FFQ answering was not self-reported, and each item was explained for the participants, and then, marked the chosen option in the answer sheet by trained interviewer. Also, the other was controlled for a wide range of confounders such as energy intake, BMI and physical activity.
This study had several limitations as well. The cross-sectional nature of present study led to causal inference. Moreover, using one-year FFQ might have caused errors in measuring dietary intakes and patterns causing measurement error and misclassification of the study subjects and reporting bias. Therefore, generalizing the results should be done with caution.
Conclusion
Generally, the Mediterranean diet has consistently been related to improving sperm concentration. However, in the present study, the association between adherence to the Mediterranean diet and other sperm quality parameters is unexplored. In future, analytic studies such as clinical trials and cohorts are needed in this era for approve these results.
Acknowledgements
The authors would like to thank all the participants without whom this study was
impossible.

Funding
The present study was funded by Nutrition and Food Security Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Authors’ contributions
Hosseinzadeh M and Babaie S conceived the idea and supervised the study. Beigrezaei S and Darabi Z wrote the first draft. Darabi Z and Hosseinzadeh M were involved in study analysis. Hosseinzadeh M revised the manuscript. All the authors read and approved the final version of the manuscript. 
Conflict of interest
The authors declared no conflict of interests.
References
Afeiche M, et al. 2013. Dairy food intake in relation to semen quality and reproductive hormone levels among physically active young men. Human reproduction. 28 (8): 2265-2275.
Afeiche MC, et al. 2014a. Dairy intake and semen quality among men attending a fertility clinic. Fertility and sterility. 101 (5): 1280-1287.
Afeiche MC, et al. 2014b. Processed meat intake is unfavorably and fish intake favorably associated with semen quality indicators among men attending a fertility clinic. Journal of nutrition. 144 (7): 1091-1098.
Afeiche MC, et al. 2014c. Meat intake and reproductive parameters among young men. Epidemiology. 25 (3): 323.
Agarwal A, Nallella KP, Allamaneni SS & Said TM 2004. Role of antioxidants in treatment of male infertility: an overview of the literature. Reproductive biomedicine online. 8 (6): 616-627.
Anifandis G, et al. 2014. The impact of cigarette smoking and alcohol consumption on sperm parameters and sperm DNA fragmentation (SDF) measured by Halosperm®. Archives of gynecology and obstetrics. 290 (4): 777-782.
Bentivoglio G, Melica F & Cristoforoni P 1993. Folinic acid in the treatment of human male infertility. Fertility and sterility. 60 (4): 698-701.
Braga DPdAF, et al. 2012. Food intake and social habits in male patients and its relationship to intracytoplasmic sperm injection outcomes. Fertility and sterility. 97 (1): 53-59.
Chen Z, et al. 2001. Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Human molecular genetics. 10 (5): 433-444.
Chiu Y, et al. 2014. Sugar-sweetened beverage intake in relation to semen quality and reproductive hormone levels in young men. Human reproduction. 29 (7): 1575-1584.
Conquer JA, Martin JB, Tummon I, Watson L & Tekpetey F 1999. Fatty acid analysis of blood serum, seminal plasma, and spermatozoa of normozoospermic vs. Asthernozoospermic males. Lipids. 34 (8): 793-799.
Cutillas-Tolín A, et al. 2015a. Mediterranean and western dietary patterns are related to markers of testicular function among healthy men. Human reproduction. 30 (12): 2945-2955.
Cutillas-Tolín A, et al. 2015b. Mediterranean and western dietary patterns are related to markers of testicular function among healthy men. Human reproduction. 30 (12): 2945-2955.
Eslamian G, Amirjannati N, Rashidkhani B, Sadeghi M-R & Hekmatdoost A 2012. Intake of food groups and idiopathic asthenozoospermia: a case–control study. Human reproduction. 27 (11): 3328-3336.
Esposito K & Giugliano D 2002. Mediterranean diet and prevention of coronary heart disease. Journal of endocrinological investigation. 25 (3): 296-299.
Flesch FM & Gadella BM 2000. Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochimica et Biophysica Acta (BBA)-Reviews on Biomembranes. 1469 (3): 197-235.
Frei B 1994. Reactive oxygen species and antioxidant vitamins: mechanisms of action. American journal of medicine. 97 (3): S5-S13.
Gaskins AJ, Colaci DS, Mendiola J, Swan SH & Chavarro JE 2012. Dietary patterns and semen quality in young men. Human reproduction. 27 (10): 2899-2907.
Guasch-Ferré M & Willett W 2021. The Mediterranean diet and health: A comprehensive overview. Journal of internal medicine. 290 (3): 549-566.
Hart RJ 2016. Physiological aspects of female fertility: role of the environment, modern lifestyle, and genetics. Physiological reviews. 96 (3): 873-909.
Holm J, Hansen SI & Høier-Madsen M 1991. A high-affinity folate binding protein in human semen. Bioscience reports. 11 (5): 237-242.
Holm J, Hansen SI, Høier-Madsen M, Christensen TB & Nichols CW 1999. Characterization of a high-affinity folate receptor in normal and malignant human testicular tissue. Bioscience reports. 19 (6): 571-580.
Ibañez-Perez J, Santos-Zorrozua B, Lopez-Lopez E, Matorras R & Garcia-Orad A 2019. An update on the implication of physical activity on semen quality: a systematic review and meta-analysis. Archives of gynecology and obstetrics. 299 (4): 901-921.
Jörundsson E, Lumsden JH & Jacobs RM 1999. Rapid staining techniques in cytopathology: a review and comparison of modified protocols for hematoxylin and eosin, Papanicolaou and Romanowsky stains. Veterinary clinical pathology. 28 (3): 100-108.
Karayiannis D, et al. 2017. Association between adherence to the Mediterranean diet and semen quality parameters in male partners of couples attempting fertility. Human reproduction. 32 (1): 215-222.
Leaver RB 2016. Male infertility: an overview of causes and treatment options. British journal of nursing. 25 (18): S35-S40.
Lenzi A, et al. 2000. Fatty acid composition of spermatozoa and immature germ cells. Molecular human reproduction. 6 (3): 226-231.
Liu Y & Ding Z 2017. Obesity, a serious etiologic factor for male subfertility in modern society. Reproduction. 154 (4): R123-R131.
Lopes HF, et al. 2003. DASH diet lowers blood pressure and lipid-induced oxidative stress in obesity. Hypertension. 41 (3): 422-430.
Lucock M 2000. Folic acid: nutritional biochemistry, molecular biology, and role in disease processes. Molecular genetics and metabolism. 71 (1-2): 121-138.
Mendiola J, et al. 2009. Food intake and its relationship with semen quality: a case-control study. Fertility and sterility. 91 (3): 812-818.
Mirmiran P, Esfahani FH, Mehrabi Y, Hedayati M & Azizi F 2010. Reliability and relative validity of an FFQ for nutrients in the Tehran lipid and glucose study. Public health nutrition. 13 (5): 654-662.
Morgan DH, Ghribi O, Hui L, Geiger JD & Chen X 2014. Cholesterol-enriched diet disrupts the blood-testis barrier in rabbits. American journal of physiology-endocrinology and metabolism. 307 (12): E1125-E1130.
Nassan FL, Chavarro JE & Tanrikut C 2018. Diet and men's fertility: does diet affect sperm quality? Fertility and sterility. 110 (4): 570-577.
Nätt D, et al. 2019. Human sperm displays rapid responses to diet. PLoS biology. 17 (12): e3000559.
Ng S-F, et al. 2010. Chronic high-fat diet in fathers programs β-cell dysfunction in female rat offspring. Nature. 467 (7318): 963-966.
Oostingh EC, Steegers-Theunissen RP, de Vries JH, Laven JS & Koster MP 2017. Strong adherence to a healthy dietary pattern is associated with better semen quality, especially in men with poor semen quality. Fertility and sterility. 107 (4): 916-923. e912.
Rato L, Alves M, Cavaco J & Oliveira P 2014. High-energy diets: a threat for male fertility? Obesity reviews. 15 (12): 996-1007.
Safarinejad M 2011. Effect of omega3 polyunsaturated fatty acid supplementation on semen profile and enzymatic antioxidant capacity of seminal plasma in infertile men with idiopathic oligoasthenoteratospermia: a doubleblind, placebocontrolled, randomised study. Andrologia. 43 (1): 38-47.
Salas-Huetos A, Bulló M & Salas-Salvadó J 2017. Dietary patterns, foods and nutrients in male fertility parameters and fecundability: a systematic review of observational studies. Human reproduction update. 23 (4): 371-389.
Schröder H 2007. Protective mechanisms of the Mediterranean diet in obesity and type 2 diabetes. Journal of nutritional biochemistry. 18 (3): 149-160.
Tavilani H, Doosti M, Abdi K, Vaisiraygani A & Joshaghani H 2006. Decreased polyunsaturated and increased saturated fatty acid concentration in spermatozoa from asthenozoospermic males as compared with normozoospermic males. Andrologia. 38 (5): 173-178.
Tavilani H, et al. 2007. Lipid composition of spermatozoa in normozoospermic and asthenozoospermic males. Prostaglandins, leukotrienes and essential fatty acids. 77 (1): 45-50.
Trichopoulou A, Costacou T, Bamia C & Trichopoulos D 2003. Adherence to a Mediterranean diet and survival in a Greek population. New England Journal of Medicine. 348 (26): 2599-2608.
Vander Borght M & Wyns C 2018. Fertility and infertility: Definition and epidemiology. Clinical biochemistry. 62: 2-10.
Vayena E, Rowe PJ & Griffin PD 2002. Current practices and controversies in assisted reproduction: report of a meeting on medical, ethical and social aspects of assisted reproduction, held at WHO Headquarters in Geneva, Switzerland. World Health Organization.
Visioli F 2000. Antioxidants in Mediterranean diets. World review of nutrition and dietetics. 87: 43-55.
Vujkovic M, et al. 2009. Associations between dietary patterns and semen quality in men undergoing IVF/ICSI treatment. Human reproduction. 24 (6): 1304-1312.
Wong WY, et al. 2002. Effects of folic acid and zinc sulfate on male factor subfertility: a double-blind, randomized, placebo-controlled trial. Fertility and sterility. 77 (3): 491-498.
Word Health Organization 2010. WHO laboratory manual for the examination and processing of human semen.
World Health Organisation 1999. WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge university press.


 
Type of article: orginal article | Subject: public specific
Received: 2023/04/18 | Published: 2024/11/20 | ePublished: 2024/11/20

References
5. Afeiche M, et al. 2013. Dairy food intake in relation to semen quality and reproductive hormone levels among physically active young men. Human reproduction. 28 (8): 2265-2275.
6. Afeiche MC, et al. 2014a. Dairy intake and semen quality among men attending a fertility clinic. Fertility and sterility. 101 (5): 1280-1287.
7. Afeiche MC, et al. 2014b. Processed meat intake is unfavorably and fish intake favorably associated with semen quality indicators among men attending a fertility clinic. Journal of nutrition. 144 (7): 1091-1098.
8. Afeiche MC, et al. 2014c. Meat intake and reproductive parameters among young men. Epidemiology. 25 (3): 323.
9. Agarwal A, Nallella KP, Allamaneni SS & Said TM 2004. Role of antioxidants in treatment of male infertility: an overview of the literature. Reproductive biomedicine online. 8 (6): 616-627.
10. Anifandis G, et al. 2014. The impact of cigarette smoking and alcohol consumption on sperm parameters and sperm DNA fragmentation (SDF) measured by Halosperm®. Archives of gynecology and obstetrics. 290 (4): 777-782.
11. Bentivoglio G, Melica F & Cristoforoni P 1993. Folinic acid in the treatment of human male infertility. Fertility and sterility. 60 (4): 698-701.
12. Braga DPdAF, et al. 2012. Food intake and social habits in male patients and its relationship to intracytoplasmic sperm injection outcomes. Fertility and sterility. 97 (1): 53-59.
13. Chen Z, et al. 2001. Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Human molecular genetics. 10 (5): 433-444.
14. Chiu Y, et al. 2014. Sugar-sweetened beverage intake in relation to semen quality and reproductive hormone levels in young men. Human reproduction. 29 (7): 1575-1584.
15. Conquer JA, Martin JB, Tummon I, Watson L & Tekpetey F 1999. Fatty acid analysis of blood serum, seminal plasma, and spermatozoa of normozoospermic vs. Asthernozoospermic males. Lipids. 34 (8): 793-799.
16. Cutillas-Tolín A, et al. 2015a. Mediterranean and western dietary patterns are related to markers of testicular function among healthy men. Human reproduction. 30 (12): 2945-2955.
17. Cutillas-Tolín A, et al. 2015b. Mediterranean and western dietary patterns are related to markers of testicular function among healthy men. Human reproduction. 30 (12): 2945-2955.
18. Eslamian G, Amirjannati N, Rashidkhani B, Sadeghi M-R & Hekmatdoost A 2012. Intake of food groups and idiopathic asthenozoospermia: a case–control study. Human reproduction. 27 (11): 3328-3336.
19. Esposito K & Giugliano D 2002. Mediterranean diet and prevention of coronary heart disease. Journal of endocrinological investigation. 25 (3): 296-299.
20. Flesch FM & Gadella BM 2000. Dynamics of the mammalian sperm plasma membrane in the process of fertilization. Biochimica et Biophysica Acta (BBA)-Reviews on Biomembranes. 1469 (3): 197-235.
21. Frei B 1994. Reactive oxygen species and antioxidant vitamins: mechanisms of action. American journal of medicine. 97 (3): S5-S13.
22. Gaskins AJ, Colaci DS, Mendiola J, Swan SH & Chavarro JE 2012. Dietary patterns and semen quality in young men. Human reproduction. 27 (10): 2899-2907.
23. Guasch-Ferré M & Willett W 2021. The Mediterranean diet and health: A comprehensive overview. Journal of internal medicine. 290 (3): 549-566.
24. Hart RJ 2016. Physiological aspects of female fertility: role of the environment, modern lifestyle, and genetics. Physiological reviews. 96 (3): 873-909.
25. Holm J, Hansen SI & Høier-Madsen M 1991. A high-affinity folate binding protein in human semen. Bioscience reports. 11 (5): 237-242.
26. Holm J, Hansen SI, Høier-Madsen M, Christensen TB & Nichols CW 1999. Characterization of a high-affinity folate receptor in normal and malignant human testicular tissue. Bioscience reports. 19 (6): 571-580.
27. Ibañez-Perez J, Santos-Zorrozua B, Lopez-Lopez E, Matorras R & Garcia-Orad A 2019. An update on the implication of physical activity on semen quality: a systematic review and meta-analysis. Archives of gynecology and obstetrics. 299 (4): 901-921.
28. Jörundsson E, Lumsden JH & Jacobs RM 1999. Rapid staining techniques in cytopathology: a review and comparison of modified protocols for hematoxylin and eosin, Papanicolaou and Romanowsky stains. Veterinary clinical pathology. 28 (3): 100-108.
29. Karayiannis D, et al. 2017. Association between adherence to the Mediterranean diet and semen quality parameters in male partners of couples attempting fertility. Human reproduction. 32 (1): 215-222.
30. Leaver RB 2016. Male infertility: an overview of causes and treatment options. British journal of nursing. 25 (18): S35-S40.
31. Lenzi A, et al. 2000. Fatty acid composition of spermatozoa and immature germ cells. Molecular human reproduction. 6 (3): 226-231.
32. Liu Y & Ding Z 2017. Obesity, a serious etiologic factor for male subfertility in modern society. Reproduction. 154 (4): R123-R131.
33. Lopes HF, et al. 2003. DASH diet lowers blood pressure and lipid-induced oxidative stress in obesity. Hypertension. 41 (3): 422-430.
34. Lucock M 2000. Folic acid: nutritional biochemistry, molecular biology, and role in disease processes. Molecular genetics and metabolism. 71 (1-2): 121-138.
35. Mendiola J, et al. 2009. Food intake and its relationship with semen quality: a case-control study. Fertility and sterility. 91 (3): 812-818.
36. Mirmiran P, Esfahani FH, Mehrabi Y, Hedayati M & Azizi F 2010. Reliability and relative validity of an FFQ for nutrients in the Tehran lipid and glucose study. Public health nutrition. 13 (5): 654-662.
37. Morgan DH, Ghribi O, Hui L, Geiger JD & Chen X 2014. Cholesterol-enriched diet disrupts the blood-testis barrier in rabbits. American journal of physiology-endocrinology and metabolism. 307 (12): E1125-E1130.
38. Nassan FL, Chavarro JE & Tanrikut C 2018. Diet and men's fertility: does diet affect sperm quality? Fertility and sterility. 110 (4): 570-577.
39. Nätt D, et al. 2019. Human sperm displays rapid responses to diet. PLoS biology. 17 (12): e3000559.
40. Ng S-F, et al. 2010. Chronic high-fat diet in fathers programs β-cell dysfunction in female rat offspring. Nature. 467 (7318): 963-966.
41. Oostingh EC, Steegers-Theunissen RP, de Vries JH, Laven JS & Koster MP 2017. Strong adherence to a healthy dietary pattern is associated with better semen quality, especially in men with poor semen quality. Fertility and sterility. 107 (4): 916-923. e912.
42. Rato L, Alves M, Cavaco J & Oliveira P 2014. High-energy diets: a threat for male fertility? Obesity reviews. 15 (12): 996-1007.
43. Safarinejad M 2011. 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. 43 (1): 38-47.
44. Salas-Huetos A, Bulló M & Salas-Salvadó J 2017. Dietary patterns, foods and nutrients in male fertility parameters and fecundability: a systematic review of observational studies. Human reproduction update. 23 (4): 371-389.
45. Schröder H 2007. Protective mechanisms of the Mediterranean diet in obesity and type 2 diabetes. Journal of nutritional biochemistry. 18 (3): 149-160.
46. Tavilani H, Doosti M, Abdi K, Vaisiraygani A & Joshaghani H 2006. Decreased polyunsaturated and increased saturated fatty acid concentration in spermatozoa from asthenozoospermic males as compared with normozoospermic males. Andrologia. 38 (5): 173-178.
47. Tavilani H, et al. 2007. Lipid composition of spermatozoa in normozoospermic and asthenozoospermic males. Prostaglandins, leukotrienes and essential fatty acids. 77 (1): 45-50.
48. Trichopoulou A, Costacou T, Bamia C & Trichopoulos D 2003. Adherence to a Mediterranean diet and survival in a Greek population. New England Journal of Medicine. 348 (26): 2599-2608.
49. Vander Borght M & Wyns C 2018. Fertility and infertility: Definition and epidemiology. Clinical biochemistry. 62: 2-10.
50. Vayena E, Rowe PJ & Griffin PD 2002. Current practices and controversies in assisted reproduction: report of a meeting on medical, ethical and social aspects of assisted reproduction, held at WHO Headquarters in Geneva, Switzerland. World Health Organization.
51. Visioli F 2000. Antioxidants in Mediterranean diets. World review of nutrition and dietetics. 87: 43-55.
52. Vujkovic M, et al. 2009. Associations between dietary patterns and semen quality in men undergoing IVF/ICSI treatment. Human reproduction. 24 (6): 1304-1312.
53. Wong WY, et al. 2002. Effects of folic acid and zinc sulfate on male factor subfertility: a double-blind, randomized, placebo-controlled trial. Fertility and sterility. 77 (3): 491-498.
54. Word Health Organization 2010. WHO laboratory manual for the examination and processing of human semen.
55. World Health Organisation 1999. WHO laboratory manual for the examination of human semen and sperm-cervical mucus interaction. Cambridge university press.

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

© 2024 CC BY-NC 3.0 | Journal of Nutrition and Food Security

Designed & Developed by : Yektaweb