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Article

Evaluation of chronotype and sleep quality in infertile population and comparison with fertile population: a cross-sectional study

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Article: 2148523 | Received 06 May 2022, Accepted 12 Nov 2022, Published online: 08 Dec 2022

Abstract

Purpose

Infertility is a stressful condition for couples and can affect patients’ circadian rhythm and sleep quality. The goal of this study is to assess differences in chronotype and sleep quality between infertile and fertile people.

Methods

A cross-sectional study was conducted. The infertile patient population consisted study group. Primiparous patients without any known gynecological disease who presented for routine cervical cancer screening follow-up were included in the control group. The Turkish version of the Morningness-Eveningness Questionnaire (MEQ) and Pittsburg Sleep Quality Index (PSQI) scores were evaluated between groups.

Results

A total of 227 patients were assessed. There were 110 patients in the study (infertile) group and 117 patients in the control (fertile) group. The evening chronotype proportion (23.6 vs. 0.9%, p < 0.001) was higher in the infertile group. The median of MEQ score was significantly higher in the fertile patients (50, IQR = 43 − 55 vs. 56, IQR = 51 − 59; p < 0.001), and the median of PSQI score was significantly higher in the infertile patients (5, IQR = 4 − 6, vs. 4, IQR = 3 − 5; p < 0.001).

Conclusions

In this study, we found significantly worse sleep quality, and more evening chronotype in the patients with infertility.

Introduction

Infertility is described as the inability to become pregnant after a year of frequent, unprotected sexual intercourse, and it is becoming more common every year [Citation1]. Quality of life, a complex state, is affected by individual’s biological, psychological and social conditions. The relationship between infertility and poor life quality is well known [Citation2]. There are known modifiable risk factors related to poor life quality for infertility, including obesity and smoking. Several determinants, such as physical and psychological status, desire and partnerships, may have an impact on sexual function.

Additionally, sleep is necessary for vital functions, and sleep characteristics might affect fertility. As a result, there has been a new trend toward evaluating the relationship between sleep quality and fertility. The ideal duration of sleep is defined as 7–9 h of sleep on a 24-h time span [Citation3], but in real life, one-third of premenopausal women sleep less than 7 h [Citation4]. Women not only have shorter sleep durations than men, but they also have higher sleep disruptions, which can be caused by fluctuations in reproductive hormone levels [Citation5].

Sleep falls under the control of endogenous circadian regulation [Citation6]. The secretion of reproductive hormones is also affected by the circadian cycle [Citation6]. Melatonin is the key regulatory hormone in the control mechanisms, and the suprachiasmatic nucleus is the primary control site on the brain for circadian regulation. These regulatory systems can operate in a variety of ways in different people, resulting in a variety of behavioral phenotypes known as chronotypes. Three sorts of chronotypes are defined as follows: morning-type, intermediate type and evening type. Morning people are more likely to get up early and stay active during the day. Evening people are the opposites of morning people, while intermediate-type people are those who are neither morning nor evening type. The degree and intensity of a person’s cognitive and physical activity throughout the day is influenced by their chronotype.

Several authors investigated the effects of sleep habits and chronotypes on reproductive health. In a systematic review which investigated the impact of sleep on female and male reproductive functions in 2021 [Citation7], they concluded that short sleep duration, evening chronotype or shift/night work schedules may affect female infertility, male fertility and in-vitro fertilization treatment (IVF) outcomes. Kloss et al. also showed that sleep disorders or changes in sleep habits directly or indirectly have an impact on reproductive health [Citation8]. Authors suggested three probable theoretic paths between sleep problems and infertility relation: the first one is that hypothalamic-pituitary-adrenal (HPA) axis diseases may cause sleep disturbances. The second one is that sleep disturbances cause HPA change and the last one is that circadian diseases may result in infertility independent of HPA [Citation8].

The association between chronotype and ovarian cycle, menstrual discomfort, menstrual duration, preeclampsia and premature birth has been studied in several research [Citation9–11]. However, there is a scarcity of data to measure the chronotype and sleep quality of infertile people and prospectively compare them to fertile cohorts. Toffol et al. evaluated 2672 patients retrospectively. Patients with intermediate chronotype had increased risk of infertility when compared to patients with morning chronotype (OR = 1.618, 95% CI = 1.090 to 2.402; p < 0.05) [Citation12]. Moreover, Huang et al. focused on in vitro fertilization (IVF) parameters instead of natural fertility and their results demonstrated that 43.3% of 97 IVF patients had poor sleep quality [Citation13]. On the other hand, Willis et al. did not find any association between shift work and fecundability [Citation14].

We hypothesized that the connection between infertility and sleep quality is a significant clinical issue. The quality of sleep could be a direct or indirect indicator of the reproductive health. There is a scarcity of evidence on the sleep quality of infertile women. As a result, we plan to use standardized questionnaires to evaluate the sleep quality and chronotype of infertile women and compare these parameters to those of fertile women.

Material and methods

A cross-sectional study was done between September 2020 and July 2021 at the Department of Obstetrics and Gynecology of Bezmialem University Hospital. Local ethical committee accepted the study protocol. All patients signed a written informed consent form. Throughout the investigation, the World Medical Association’s Code of Ethics (Declaration of Helsinki) was applied.

The research group consisted of women between the ages of 18 and 40 who had been diagnosed with either primary or secondary infertility and had failed to conceive after 12 months despite frequent and unprotected sexual intercourse. The women with at least one naturally conceived live birth occurred more than 2 years ago, who administered to gynecology department for cervical cancer screening were included in this study as control group. Patients with a history of mental, neurologic or sleep disorders, unwillingness to participate, women working night shifts, breastfeeding and patients taking medicines that alter the sleep–wake cycle were all ruled out.

Patients’ demographic parameters (age, smoking habits, gravida, parity, infertility length, type of infertility, occupation and BMI) were gathered, as well as Morningness-Eveningness Questionnaire (MEQ) groups and scores and Pittsburgh Sleep Quality Index (PSQI) groups and scores. One of the study authors (CO) applied PSQI and MEQ surveys before the administration of any treatment in infertile group. Both questionnaires were validated for Turkish-speaking people [Citation15,Citation16]. According to the survey results, sleep quality indices were calculated, and chronotypes were determined.

Pittsburgh sleep quality index (PSQI)

The PSQI, which is frequently used to assess sleep quality, has been demonstrated to be beneficial in the study of sleep disorders [Citation17]. In this study, the Pittsburg Sleep Quality Index (PSQI) was used to evaluate sleep quality. It has 19 self-report items composed of seven categories: subjective sleep quality, sleep latency, sleep duration, sleep efficiency, sleep disturbance, use of sleep medication and daytime dysfunction. The questions include sleep length, sleep latency, the regularity, and intensity of certain sleeping issues. This index has 24 questions, 19 of which are filled by the individual and five by the individual’s spouse or a person with whom they reside. There are seven modules to these 19 scored items: Some are made up of only one object, while others are made up of a number of them. A score of 0–3 is assigned to each module. These seven component ratings yield a total index score ranging from 0 to 21. Scores <5 were evaluated as good sleep quality, and scores >5 were set as poor sleep quality.

Morningness–Eveningness questionnaire (MEQ)

The MEQ scale is used to assess a person’s chronotype [Citation15]. We assessed chronotypes of patients with Morningness-Eveningness Questionnaire (MEQ), The questionnaire has 19 questions concerning an individual’s physical and psychological performance throughout a 24-h period, as well as their favorite periods for various activities. Scores range from 16 to 86, with scores between 16 and 41 indicating evening type, 42–58 indicating intermediate type and 59–86 indicating morning type.

Statistical analyses

Data analyses were performed using SPSS version 21.0 (IBM Corporation, Armonk, NY). Samples were tested with the Kolmogorov–Smirnov test to determine the normality of distributions. According to the results, non-parametric tests were preferred. Continuous variables were compared with Mann–Whitney U test. Categorical variables were compared with Fisher’s exact test. A p value of < 0.05 was considered statistically significant [Citation18]. An a priori power analysis was conducted using G*Power version 3.1.9.7 for sample size estimation, based on data from study of Kozak et al. [Citation18] (N = 112), which compared PSQI scores on patients with migraine (mean PSQI score: 52.80 ± 7.74) to controls (mean: 53.32 ± 9.75). With a significance criterion of α = 0.05 and power = 0.80, the minimum sample size needed in each group with this effect size is found as 103 patients.

Results

A total of 227 patients were included in the study. Flow chart of study population is shown in . There were 110 patients in the study (infertile) group and 117 patients in the control (fertile) group. summarizes the demographic and clinical features of the patients. The research and control groups had mean ages of 32 (24–36) and 32 (29–36), respectively. There were no statistically significant differences between groups in terms of age, BMI, smoking and profession (). Parity and gravida were significantly different between fertile and infertile groups (). The median of duration of infertility in the study group was 4 (3 − 7) and 68.2% (n = 75) of the study group had primary infertility and 31.8% (n = 35) of the study group had secondary infertility. Grouping participants compared MEQ and PSQI values according to fertility situations. An overview of our findings was presented below; PSQI and MEQ scores of the patients are shown in .

Figure 1. Flow chart of study population.

Figure 1. Flow chart of study population.

Table 1. Demographic characteristics of groups.

Table 2. Comparison of MEQ and PSQI scores of groups.

The median of MEQ scores in study and control groups was 50 (43 − 55) vs. 56 (51 − 59); respectively. It was significantly higher in the fertile group (U = 3775, p < 0.001). There was a significant difference between infertile and fertile groups in terms of chronotype (χ2 (2, N = 227) = 37.51, p < 0.001). The proportion of patients in study and control groups were 14.5 vs. 38.3% of morning type; 23.6 vs. 0.9% of evening type and 61.8 vs. 59.8% of intermediate type, respectively. In posthoc analysis the main contribution for MEQ group differences was from eveningness chronotype group. After exclusion of eveningness group difference of intermediate and morningness chronotypes was statistically important with Bonferroni correction (χ2(1, N = 200) = 9.67, p = 0.002). All group contributions for MEQ difference were statistically relevant.

The median of PSQI score was significantly higher in the infertility group (5, IQR= 4 − 6, vs. 4, IQR= 3 − 5; U = 3476, p < 0.001) (). In the infertile group, patients with PSQI-score > 5 were significantly more frequent (72.7 vs. 21.4%, χ2 (1, N = 227) = 227) = 60.15, p < 0.001) (). Domains of the PSQI were reviewed separately. Significant differences were on domains; sleep latency (median: 139.8 vs. 89.7, U = 3597, p < 0.001), sleep duration (median: 122.7 vs. 105.8, U = 5475, p = 0.005) and sleep efficiency (median: 117.7 vs. 110.5, U = 6025, p = 0.006).

In comparison of patients with primary and secondary infertility, no difference was found between these groups either on MEQ or PSQI scores (50.1±1.1 vs. 48.1±1.4, p = 0.288 and 5.2±0.2 vs. 5.3±0.3, p = 0.925).

Discussion

To the best of the authors’ knowledge, this is the first study to look at the quality of sleep in infertile women and compare the results to those of fertile women. Our findings revealed that the morning chronotype was proportionately more prevalent in the fertile group and the evening chronotype was more frequent in the infertile group. When compared to fertile women, our results show that infertile women have low sleep quality and high PSQI scores.

Short sleep duration and sleep disturbances have been linked to poor daily task performance, mental disorders, poorer memory, poor academic achievement, low motivation, obesity and heart morbidity [Citation19–21]. Our results might reflect the relationship between chronotype, sleep quality and the ovarian cycle. The reproduction cascade starts with ovulation and everything affecting the ovulation can also affect the fertility status of a person. Kang et al. and Xing et al. reported more menstrual irregularities in women with insomnia or poor sleep quality [Citation22,Citation23]. In addition, Toffol et al. reported an association between intermediate chronotype and higher risk of infertility than morning chronotype (OR 1.62, 95% CI 1.09–2.40; p < 0.05) [Citation12]. Similarly, we also found morning chronotype patients less in the infertile group; on the contrary, we found significantly higher evening chronotype patients in the infertile group. This difference might have originated from differences within study cohorts. Toffol et al. conducted a study on the Finnish population, and the mean age of the cohort was 54; in contrast, our study was conducted on the Turkish population with a mean age of 32. Furthermore, Sk Willis et al. reported no significant association between sleep duration and fecundability and no significant association between work schedules and fecundability [Citation14]. However, we found evening chronotype more in the infertile group. They did not use a MEQ questionnaire for the determination of chronotypes; the shift work status determined groups. Study was performed with 6873 American participants from couples attempting pregnancy more than 6 months. Moreover, their time criterion was six months for fecundability; our time criterion for infertility was one year.

Consequently, all of these differences between populations and methods might be the reason for the conflicting results. Lastly, Goksu et al. a group of investigators from Turkey investigated the improvement of the PSQI scores in grade 4 endometriosis patients after surgery, and they found that the proportion of those with bad sleep quality was more in the infertile population [Citation24]. That was similar to our results. Taken together, our findings and the findings of previous studies point toward there being differences in terms of sleep quality and chronotype status between fertile and infertile patients. This should not be forgotten in the assessment of infertile women.

Due to the cross-sectional design of our study, exact interaction between sleep, circadian rhythm and infertility is not clarified. On the other hand, there is not one mechanism between sleep and infertility. Molecular, genetic and hormonal pathways are taking role in this interaction [Citation25]. Infertility can cause stress in couples, and disrupt their sleep pattern. However, blood levels of hormones acting in reproduction vary according to sleep patterns [Citation26]. As a result of this complexity, does sleep disturbance lead to infertility or vice versa is true? Stays in mind as a question with no answer.

The main strength of this study is, we investigated the sleep quality and chronotype differences between fertile and infertile populations with a statistically significant number of patients. There were also limitations of our study. Even though we included a statistically adequate number of patients, our sample size was less than that of other research that looked into sleep quality and its impact on natural fertility, but those studies were retrospective. On the fertile group, patients had a child at home. We did not know the age distribution of children in control group but an infant at home can affect the sleep quality negatively in control group [Citation27]. Researchers can compare infertile group with a fertile group with no infant at home on future studies and difference between chronotypes and sleep quality in infertile vs. fertile populations will be determined with less confounding factors.

In conclusion, in this article, we concluded infertile patients had a worse sleep quality, and evening chronotype was significantly more common in the infertile group. Although we found worse sleep quality and eveningness chronotype more common in infertile population, effect of change in these variables on infertility treatment outcomes need to be evaluated with future prospective studies.

Disclosure statement

The authors report there are no competing interests to declare.

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