Dietary fat and fatty acid consumptions and the odds of asthenozoospermia: a case-control study in China.

China asthenozoospermia case–control study diet fat fatty acid

Journal

Human reproduction open
ISSN: 2399-3529
Titre abrégé: Hum Reprod Open
Pays: England
ID NLM: 101722764

Informations de publication

Date de publication:
2023
Historique:
received: 15 05 2023
revised: 09 07 2023
medline: 7 8 2023
pubmed: 7 8 2023
entrez: 7 8 2023
Statut: epublish

Résumé

Are dietary fat and fatty acid (FA) intakes related to the odds of asthenozoospermia? Plant-based fat consumption was associated with decreased asthenozoospermia odds, while the consumption of animal-based monounsaturated fatty acid (MUFA) was positively related to asthenozoospermia odds. Dietary fat and FA are significant ingredients of a daily diet, which have been demonstrated to be correlated to the reproductive health of men. However, to date, evidence on fat and FA associations with the odds of asthenozoospermia is unclear. The hospital-based case-control study was performed in an infertility clinic from June 2020 to December 2020. Briefly, 549 asthenozoospermia cases and 581 controls with normozoospermia were available for final analyses. We collected dietary data through a verified food frequency questionnaire of 110 food items. Asthenozoospermia cases were ascertained according to the World Health Organization guidelines. To investigate the correlations of dietary fat and FA consumptions with the odds of asthenozoospermia, we calculated the odds ratios (ORs) and corresponding 95% CIs through unconditional logistic regression models. Relative to the lowest tertile of consumption, the highest tertile of plant-based fat intake was inversely correlated to the odds of asthenozoospermia (OR = 0.68, 95% CI = 0.50-0.91), with a significant dose-response relation (OR = 0.85, 95% CI = 0.75-0.97, per standard deviation increment). Inversely, animal-based MUFA intake (OR = 1.49, 95% CI = 1.04-2.14) was significantly correlated to increased odds of asthenozoospermia, and an evident dose-response relation was also detected (OR = 1.24, 95% CI = 1.05-1.45, per standard deviation increment). Subgroup analyses showed similar patterns of associations to those of the primary results. Moreover, we observed significant interactions on both multiplicative and additive scales between animal-based MUFA and cigarette smoking. Selection bias and recall bias were unavoidable in any of the observational studies. As we failed to obtain the information of trans-fatty acid (TFA) consumption, the relation of TFA intake and asthenozoospermia odds was unclear. This study indicated that different sources of fat and FAs might exert different effects on the etiology of asthenozoospermia, and cigarette smoking could exacerbate the adverse effect of high animal-based MUFA intake on asthenozoospermia. Our findings provide novel evidence pertaining to the fields of prevention of asthenozoospermia through decreasing animal-derived fat and FA consumptions and smoking cessation. This work was supported by the JieBangGuaShuai Project of Liaoning Province, Natural Science Foundation of Liaoning Province, Clinical Research Cultivation Project of Shengjing Hospital, and Outstanding Scientific Fund of Shengjing Hospital. All authors have no conflict of interest to declare. N/A.

Identifiants

pubmed: 37547665
doi: 10.1093/hropen/hoad030
pii: hoad030
pmc: PMC10403433
doi:

Types de publication

Journal Article

Langues

eng

Pagination

hoad030

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology.

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest regarding the publication of this article.

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Auteurs

Jun-Qi Zhao (JQ)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.

Xiao-Bin Wang (XB)

Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.

Xu Leng (X)

Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.

Yi-Fan Wei (YF)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.

Dong-Hui Huang (DH)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.

Jia-Le Lv (JL)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.

Qiang Du (Q)

Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.

Ren-Hao Guo (RH)

Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.

Bo-Chen Pan (BC)

Center of Reproductive Medicine, Shengjing Hospital of China Medical University, Shenyang, China.

Qi-Jun Wu (QJ)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.
Department of Obstetrics and Gynecology, Shengjing Hospital of China Medical University, Shenyang, China.
NHC Key Laboratory of Advanced Reproductive Medicine and Fertility (China Medical University), National Health Commission, Shenyang, China.

Yu-Hong Zhao (YH)

Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, Shenyang, China.
Clinical Research Center, Shengjing Hospital of China Medical University, Shenyang, China.

Classifications MeSH