What this is
- This research investigates the link between () and () in U.S. adults.
- Data from the National Health and Nutrition Examination Survey (NHANES) from 2005 to 2018 were analyzed.
- The study finds a positive association between and , particularly when six or more components are present.
Essence
- is positively associated with prevalence. A higher number of components correlates with increased risk.
Key takeaways
- is linked to a higher prevalence of , with an odds ratio (OR) of 1.238 in the fully-adjusted model. This indicates that individuals with are more likely to experience compared to those without.
- When the number of components reaches six or more, the prevalence of significantly increases, with an OR of 1.975. This suggests that the severity of may exacerbate symptoms.
- Age modifies the relationship between and , indicating that younger adults may exhibit a stronger association. However, the overall trend remains consistent across different age groups.
Caveats
- The study's cross-sectional design limits the ability to establish causal relationships between and . Longitudinal studies are needed for deeper insights.
- Diagnosis of relied on self-reported questionnaires, which may introduce recall bias and affect the accuracy of the findings.
- Although the study utilized a large and diverse population, factors such as lifestyle changes and environmental influences on were not fully explored.
Definitions
- Circadian Syndrome (CircS): A cluster of disorders including dyslipidemia, hypertension, obesity, diabetes, depression, and short sleep, resulting from disrupted circadian rhythms.
- Overactive Bladder (OAB): A condition characterized by an urgent need to urinate, often accompanied by urinary incontinence and nocturia.
Simplified
Introduction
Overactive bladder (OAB) is one of the common functional bladder disorders, and urinary urgency is defined as the core symptom. OAB is often accompanied by increased daytime frequency and/or nocturia, with urinary incontinence or without, in the absence of urinary tract infection or other detectable disease (1). With social stress increasing and lifestyle habits changing, the prevalence of OAB has risen in recent years (2). The five-country European Prospective Investigation into Cancer and Nutrition involving more than 19,000 adults demonstrates that the overall prevalence of OAB is 11.8% and is more common in women than in men (12.8 vs. 10.8%) (3). A study regarding OAB on physical occupational limitations shows the prevalence of OAB is around 30% in American women (4). In addition, the symptoms of OAB more easily occur, especially in a tense environment, which interferes with daily life and worsens the quality of life.
For OAB patients, the hallmark urodynamic feature is detrusor overactivity, and other forms of urethra–bladder dysfunction account for a small percentage. Although some theories are promoted to explain the pathophysiology of OAB, no identified doctrine has been established and universally accepted till now. Given the unclear etiology, long-term comprehensive treatment is proposed for most individuals, and life habit changes, regular local exercise, drugs (vaginal estrogen, anticholinergics, and β3 agonists), and invasive treatment (sacral neuromodulation, percutaneous tibial nerve stimulation, and surgery) are all considered (5). However, the treatments may only relieve the symptoms and are still substantially incapable of curing OAB.
With the awareness of internal biological rhythm raised, circadian syndrome (CircS) was proposed as a more reasonable cluster for metabolic syndrome (MetS) and its comorbidities (6). The CircS is present with any four of the following disorders, including dyslipidemia [triglycerides raising or high-density lipoprotein cholesterol decreased (HDL-C)], hypertension, central obesity, diabetes, depression, and short sleep. If a person is exposed to an unhealthy status in the long term, the circadian rhythm is vulnerable and more easily disturbed (7). Recent research has proposed that MetS and its comorbidities (sleep deprivation and depression) make a significant effect on the prevalence of OAB. In addition, mounting evidence shows that CircS is correlated with cardiovascular disease (CVD), lower urinary tract symptoms, and kidney stones (8–10). All of these factors mentioned above are not only closely related to internal biological clocks, but also are the risk factors for OAB (11, 12). Therefore, whether a relationship between the prevalence of CircS and OAB exists is worth exploring.
To the best of our knowledge, there is no study regarding the association between the prevalence of CircS and OAB. Thus, this cross-section study was established by analyzing the large population data from the National Health and Nutrition Examination Survey (NHANES). We hypothesize that CircS is positively associated with the prevalence of OAB.
Methods
Study design and population
All of the data analyzed here were cited from the NHANES 2005–2018 (seven cycles: 2005–2006, 2007–2008, 2009–2010, 2011–2012, 2013–2014, 2015–2016, and 2017–2018), which were conducted by the Center for Disease Control and Prevention (CDC). This database mainly consisted of a series of cross-sectional, nationally representative surveys involving civilian, non-institutionalized American adults, and was proposed to measure the health and nutritional status of American adults and children. In addition, NHANES was updated every 2 years as planned and designed to be accessible to researchers for free. There were 39,749 participants enrolled initially. First, we excluded 5,331 people without complete information about UUI, and 51 participants with absent information of nocturia frequency. Moreover, 18,269 people with missing data for CircS diagnosis were excluded. Finally, 16,098 participants were admitted (details in Figure 1).
All NHANES study protocols were approved by the Ethics Review Committee of the NCHS, and consent was obtained from all participants.
Flow diagram of obtaining the final inclusion in the population.
Diagnosis of overactive bladder
Overactive bladder was defined as an overactive micturition reflex, which was marked by urge urinary incontinence (UUI) and nocturia. All of the information acquired here was based on the questionnaires, which were completed by trained research staff through face-to-face interviews. UUI was obtained with the question “During the past 12 months, have you leaked or lost control of even a small amount of urine with an urge or pressure to urinate and you could not get to the toilet fast enough?,” and the severity was evaluated by the question “How frequently does this occur?.” Moreover, the gravity of nocturia was assessed with the question “During the past 30 days, how many times per night did you most typically get up to urinate, from the time you went to bed at night until the time you got up in the morning.” In addition, OAB was qualified with the aid of the overactive bladder symptom score (OABSS). The details were described in Figure 2. A participant with an overall OABSS ≥3 was considered to suffer from OAB.
Flow diagram of the overactive bladder diagnosis based on overactive bladder syndrome score.
Diagnosis of circadian syndrome
As the main exposure variable, CircS was diagnosed when a person had ≥4 of these components: (1) central obesity: women (men) with a waist circumference ≥ 88 cm (≥ 102 cm); (2) elevated triglycerides (≥150 mg/dL) or use of lipid-lowering medication; (3) decreased HDL-C (<40 mg/dL in men and < 50 mg/dL in women) or use of lipid-lowering medication; (4) elevated blood pressure (systolic ≥130 or diastolic ≥85 mmHg) or use of an antihypertensive drug; (5) elevated fasting glucose (≥100 mg/dL) or use of anti-diabetic medication; (6) reduced sleep duration (≤6 h/day); and (7) depression symptoms defined by patient health status questionnaire-9 (8).
Covariates
The information on covariates was collected through questionnaires, examinations, and laboratory tests. The continuous variables included age (≥20 years), poverty income ratio (PIR), body mass index (BMI), estimated glomerular filtration rate (eGFR), and healthy eating index-2015 (HEI-2015). The categorical variables were listed as gender, ethnicity (Mexican American, Non-Hispanic white, Non-Hispanic black, and Other ethnicity), education level (less than 9th grade, 9–11th grade, high school graduate, some college, college graduate, or above), marital status (married, widowed, divorced, separated, never married, and living with a partner), smoking (never, former, and now), and alcohol, cancer, stroke, CVD, moderate activity, and vigorous activity (all no/yes). Missing data were present in alcohol, moderate activity, and vigorous activity.
Statistical analysis
Proportions and mean ± standard errors (SE) were used to express the baseline characteristics. Chi-square analysis was used to adjust comparisons of categorical variables, while linear regression was used to correlate continuous variables. To avoid potential bias due to missing data in the covariates of alcohol, moderate and vigorous activity, the absent parts were established as dummy variables.
The participants were categorized into two groups by CircS diagnosis, and three multivariable logistic models were built to analyze the association between CircS and OAB. Additionally, the correlation between the number of CircS components and OAB was also analyzed. In the non-adjusted model, no factor was adjusted. In the minimally-adjusted model, age and ethnicity were adjusted. For the fully-adjusted model, age, ethnicity, gender, education, BMI, marital status, PIR, HEI-2015, smoking, vigorous activity, moderate activity, alcohol, stroke, CVD, eGFR, and cancer were all adjusted. To make a deep analysis of the association, stratified and interaction analyses were also performed regarding all potential confounding factors above.
For all analyses, the sample weights of the seven continuous cycles were combined according to the method recommended by the CDC.1 The essential work made the sample representative of the civilian population of the United States and produced an unbiased national estimate. Statistical analyses were all performed on R 4.0 (http://www.R-project.org↗; the R Foundation) and EmpowerStats (http://www.empowerstats.com↗; X&Y Solutions, Inc.). Differences were considered statistically significant when p was less than 0.05.
Results
Baseline characteristics of the population
From the seven cycles of NHANES (2005–2018), 16,098 participants were involved eventually. Then the participants were divided into two groups by CircS, including 5,943 people with CircS and 10,155 people without it. Significant differences were present in a majority of the baseline characteristics (Table 1). Females constituted most of the participants with OAB (61.46%, Supplementary Table S1). Compared to the non-CircS group, people with CircS were older (mean ± SE, 58.11 ± 0.31 years) and tended to have a higher BMI (33.07 ± 0.14 kg/m2). As expected, a larger proportion of the people with CircS had UUI (31.72%), nocturia (77.46%), and OAB (28.47%). Additionally, these people were more likely to have general education (less than college, 47.07%), solitary status (widowed, divorced, separated, and never married, 35.14%), cancer (16.42%), CVD (21.96%), stroke (6.67%), and smoking (52.86%). However, an opposite trend was seen in the lower PIR (2.86 ± 0.04), eGFR (84.51 ± 0.45 mL/min/1.73m2), proportions of moderate activity (34.99%), HEI-2015 (50.51 ± 0.27), vigorous activity (17.04%), and alcohol (59.42%). Moreover, each component of CircS appeared more frequently in the OAB group, such as central obesity (76.55%), elevated serum triglycerides (58.97%), reduced serum HDL-C (59.11%), hypertension (47.73%), elevated plasma glucose (69.37%), short sleep (16.18%), and depression (16.69%). Additionally, Table 2 presented the details of OABSS. Notably, people with CircS were linked with higher UUI scores (0.43 ± 0.01), nocturia scores (1.35 ± 0.02), and OABSS (1.78 ± 0.03).
| Variables | N | All (= 16,098)n | Groups | valuep | |
|---|---|---|---|---|---|
| Non-circadian syndrome (= 10,155)n | Circadian syndrome (= 5,943)n | ||||
| Age (years, mean ± SE) | 48.76 ± 0.26 | 44.17 ± 0.30 | 58.11 ± 0.31 | <0.001 | |
| 20–34 (%) | 3,664 | 24.81 | 33.67 | 6.75 | |
| 35–49 (%) | 3,735 | 26.56 | 29.61 | 20.35 | |
| 50–64 (%) | 4,477 | 28.1 | 23.79 | 36.87 | |
| ≥65 (%) | 4,222 | 20.53 | 12.93 | 36.03 | |
| PIR (mean ± SE) | 3.01 ± 0.04 | 3.09 ± 0.04 | 2.86 ± 0.04 | <0.001 | |
| ≤1.3 (%) | 4,602 | 20.72 | 19.65 | 22.9 | |
| >1.3 and ≤ 3.5 (%) | 5,697 | 36.73 | 35.51 | 39.21 | |
| >3.5 (%) | 4,473 | 42.56 | 44.83 | 64.65 | |
| BMI (kg/m, mean ± SE)2 | 29.32 ± 0.10 | 27.49 ± 0.11 | 33.07 ± 0.14 | <0.001 | |
| <25 (%) | 4,346 | 28.32 | 38.26 | 7.99 | |
| 25–30 (%) | 5,307 | 32.71 | 35.33 | 27.36 | |
| ≥30 (%) | 6,398 | 38.96 | 26.41 | 64.65 | |
| eGFR (mL/min/1.73m, mean ± SE)2 | 94.00 ± 0.33 | 98.58 ± 0.39 | 84.51 ± 0.45 | <0.001 | |
| HEI-2015 (mean ± SE) | 50.51 ± 0.23 | 50.75 ± 0.27 | 50.51 ± 0.27 | 0.022 | |
| Gender (%) | 0.301 | ||||
| Female | 8,033 | 49.8 | 50.18 | 49.04 | |
| Male | 8,065 | 50.2 | 49.82 | 50.96 | |
| Education (%) | <0.001 | ||||
| Less than 9th grade | 1,754 | 5.56 | 4.43 | 7.85 | |
| 9–11th grade | 2,324 | 10.71 | 9.85 | 12.47 | |
| High school graduate | 3,697 | 23.27 | 21.56 | 26.75 | |
| Some college | 4,696 | 31.33 | 31.04 | 31.93 | |
| College graduate or above | 3,616 | 29.13 | 33.12 | 20.99 | |
| Ethnicity (%) | <0.001 | ||||
| Mexican American | 2,588 | 8.51 | 8.91 | 7.69 | |
| Other Hispanic | 1,609 | 5.46 | 5.7 | 4.97 | |
| Non-Hispanic white | 6,927 | 68.52 | 67.43 | 70.74 | |
| Non-Hispanic black | 3,324 | 10.41 | 10.43 | 10.37 | |
| Other ethnicity | 1,650 | 7.1 | 7.52 | 6.23 | |
| Marital (%) | <0.001 | ||||
| Married | 8,492 | 56.61 | 55.3 | 59.28 | |
| Widowed | 1,337 | 5.95 | 3.76 | 10.42 | |
| Divorced | 1,782 | 10.48 | 9.18 | 13.14 | |
| Separated | 549 | 2.28 | 2.34 | 2.16 | |
| Never married | 2,665 | 16.62 | 20.15 | 9.42 | |
| Living with a partner | 1,268 | 8.06 | 9.27 | 5.58 | |
| Cancer (%) | <0.001 | ||||
| No | 14,502 | 89.55 | 92.48 | 83.58 | |
| Yes | 1,586 | 10.45 | 7.52 | 16.42 | |
| Smoking (%) | <0.001 | ||||
| Never | 8,652 | 53.47 | 56.57 | 47.14 | |
| Former | 4,228 | 26.89 | 23.16 | 34.49 | |
| Now | 3,208 | 19.65 | 20.28 | 18.37 | |
| Alcohol (%) | <0.001 | ||||
| No | 3,992 | 19.77 | 17.68 | 24.03 | |
| Yes | 9,892 | 65.04 | 67.8 | 59.42 | |
| Missing | 2,214 | 15.19 | 14.53 | 16.56 | |
| Stroke (%) | <0.001 | ||||
| No | 15,383 | 96.73 | 98.39 | 93.33 | |
| Yes | 697 | 3.27 | 1.61 | 6.67 | |
| Vigorous activity (%) | <0.001 | ||||
| No | 11,412 | 68.39 | 66.35 | 72.55 | |
| Yes | 2,766 | 18.75 | 19.59 | 17.04 | |
| Missing | 1,920 | 12.85 | 14.05 | 10.41 | |
| Moderate activity (%) | <0.001 | ||||
| No | 8,909 | 50.55 | 48.57 | 54.6 | |
| Yes | 5,267 | 36.85 | 37.37 | 34.99 | |
| Missing | 1,922 | 12.86 | 14.06 | 10.41 | |
| CVD (%) | <0.001 | ||||
| No | 14,056 | 89.75 | 95.49 | 78.04 | |
| Yes | 2,041 | 10.25 | 4.51 | 21.96 | |
| Central obesity (%) | <0.001 | ||||
| No | 6,479 | 41.02 | 56.18 | 10.11 | |
| Yes | 9,619 | 58.98 | 43.82 | 89.89 | |
| Elevated serum triglycerides (%) | <0.001 | ||||
| No | 8,652 | 56.46 | 79.13 | 10.22 | |
| Yes | 7,446 | 43.54 | 20.87 | 89.78 | |
| Reduced serum HDL-C (%) | <0.001 | ||||
| No | 8,613 | 56.25 | 77.86 | 12.21 | |
| Yes | 7,485 | 43.75 | 22.14 | 87.79 | |
| Hypertension (%) | <0.001 | ||||
| No | 9,514 | 64.48 | 78.44 | 36.01 | |
| Yes | 6,584 | 35.52 | 21.56 | 63.99 | |
| Elevated plasma glucose (%) | <0.001 | ||||
| No | 6,445 | 43.9 | 60.88 | 9.28 | |
| Yes | 9,653 | 56.1 | 39.12 | 90.72 | |
| Short sleep (%) | <0.001 | ||||
| No | 13,805 | 88.05 | 92.07 | 79.86 | |
| Yes | 2,293 | 11.95 | 7.93 | 20.14 | |
| Depression (%) | <0.001 | ||||
| No | 14,669 | 92.37 | 95.71 | 85.57 | |
| Yes | 1,429 | 7.63 | 4.29 | 14.43 | |
| UUI frequency (%) | <0.001 | ||||
| Never | 12,195 | 78.82 | 83.98 | 68.28 | |
| Less than once a month | 1,710 | 10.04 | 8.51 | 13.18 | |
| A few times a month | 1,258 | 6.59 | 4.74 | 10.38 | |
| A few times a week | 563 | 2.79 | 1.89 | 4.62 | |
| Every day and/or night | 363 | 1.76 | 0.88 | 3.54 | |
| Nocturia frequency (%) | <0.001 | ||||
| 0 | 4,673 | 33.24 | 38.46 | 22.54 | |
| 1 | 5,925 | 39.65 | 40.25 | 38.43 | |
| 2 | 3,173 | 17.42 | 14.52 | 23.38 | |
| 3 | 1,490 | 7.11 | 5.12 | 11.21 | |
| 4 | 490 | 2.04 | 1.37 | 3.42 | |
| 5 or more | 109 | 0.54 | 0.29 | 1.03 | |
| Overactive bladder (%) | <0.001 | ||||
| No | 12,460 | 82.45 | 87.81 | 71.53 | |
| Yes | 3,638 | 18.55 | 12.19 | 28.47 | |
| Variables | N | All (= 16,098)n | Groups | valuep | |
|---|---|---|---|---|---|
| Non-circadian syndrome (= 10,155)n | Circadian syndrome (= 5,943)n | ||||
| Urge urinary incontinence score (mean ± SE) | 0.27 ± 0.01 | 0.20 ± 0.01 | 0.43 ± 0.01 | <0.001 | |
| 0 (%) | 12,204 | 78.83 | 83.98 | 68.31 | |
| 1 (%) | 2,968 | 16.63 | 13.24 | 23.53 | |
| 2 (%) | 563 | 2.79 | 1.89 | 4.63 | |
| 3 (%) | 363 | 1.75 | 0.88 | 3.53 | |
| Nocturia score (mean ± SE) | 1.05 ± 0.01 | 0.91 ± 0.01 | 1.35 ± 0.02 | <0.001 | |
| 0 (%) | 4,673 | 32.94 | 38.21 | 22.21 | |
| 1 (%) | 5,925 | 39.29 | 39.99 | 37.87 | |
| 2 (%) | 3,173 | 17.26 | 14.42 | 23.04 | |
| 3 (%) | 2,327 | 10.51 | 7.38 | 16.88 | |
| Overactive bladder symptom score (mean ± SE) | 1.33 ± 0.02 | 1.11 ± 0.02 | 1.78 ± 0.03 | <0.001 | |
| 0 (%) | 4,069 | 29.14 | 34.6 | 17.99 | |
| 1 (%) | 5,183 | 34.85 | 36.64 | 31.22 | |
| 2 (%) | 3,208 | 18.46 | 16.57 | 22.32 | |
| 3 (%) | 2,338 | 11.75 | 9 | 17.37 | |
| 4 (%) | 856 | 3.9 | 2.32 | 7.11 | |
| 5 (%) | 266 | 1.2 | 0.62 | 2.41 | |
| 6 (%) | 178 | 0.69 | 0.25 | 1.59 | |
| Overactive bladder (%) | <0.001 | ||||
| No | 12,460 | 82.45 | 87.81 | 71.53 | |
| Yes | 3,638 | 17.55 | 12.19 | 28.47 | |
Multivariate regression analysis
We made a multivariate regression analysis and listed the effect sizes of association between CircS and OAB in Table 3. Results showed that the CircS group was associated with a higher prevalence of OAB in the non-adjusted model (OR = 2.868, 95%CI 2.582–3.185, p < 0.001). The same trend was seen both in the minimally-adjusted model (OR = 1.810, 95%CI 1.607–2.039, <0.001) and the fully-adjusted model (OR = 1.238, 95%CI 1.080–1.419, p = 0.003). Moreover, multivariate logistic regression analysis was conducted under stratified conditions, and a significant positive correlation between the number of CircS components and the prevalence of OAB was observed when the number of components was ≥6 (OR = 1.975, 95%CI 1.463–2.665, p ≤ 0.001).
| Variables | Non-adjusted model* | Minimally-adjusted model** | Fully-adjusted model*** | |||
|---|---|---|---|---|---|---|
| OR (95%CI) | p | OR (95%CI) | p | OR (95%CI) | p | |
| Circadian syndrome | ||||||
| No | Ref | Ref | Ref | |||
| Yes | 2.868 (2.582, 3.185) | <0.001 | 1.810 (1.607, 2.039) | <0.001 | 1.238 (1.080, 1.419) | 0.003 |
| Components of circadian syndrome | ||||||
| 4 | Ref | Ref | Ref | |||
| 5 | 1.218 (1.033, 1.437) | 0.021 | 1.077 (0.907, 1.280) | 0.399 | 0.972 (0.809 1.167) | 0.756 |
| ≥6 | 2.907 (2.288, 3.693) | <0.001 | 2.672 (2.068, 3.452) | <0.001 | 1.975 (1.463, 2.665) | <0.001 |
Stratified and interaction analyses
To further elucidate the association between the prevalence of CircS and OAB, we performed interaction analysis in the fully-adjusted model (Figure 3). We found that the association between the two was modified by age (p = 0.021) for interaction. In other words, when people were in the aged phase of 20–34, 35–49, 50–64, or ≥ 65 (OR: 1.607, 1.726, 1.289, 1.111), the positive association was more obvious. Nevertheless, the direction of effect values was consistent across subgroups. No more interaction was indicated among other factors.
Logistic regression analyses to identify variables that modify the correlation between circadian syndrome and overactive bladder.
Discussion
This study demonstrates a positive association between the prevalence of CircS and OAB, and the number of CircS components is also significantly related to a higher prevalence of OAB when the number is ≥6. Additionally, the positive association is modified by age, but the direction of effect values is consistent across subgroups.
Although numerous works have been done around the associations of OAB with MetS, depression, and sleep deprivation, these factors are always analyzed alone and never considered at the same time. Therefore, the first work to show the association between CircS and OAB was conducted here. With changes in life pace and lifestyle, the prevalence of CircS has increased annually (7). CircS depends primarily on the dysfunction of circadian rhythm, which is a set of biological variables (with about a 24-h period) produced by circadian clocks (13). Circadian rhythm can affect not only macroscopic organisms but also various organs and cells, making it one of the most important and fundamental features of biological activities (14). When the circadian rhythm in the body is abnormally altered, many problems are supposed to occur in the organism, including inflammatory, immune, and metabolic disorders. All of these changes contribute to OAB development. Moreover, recent evidence demonstrates that circadian clocks are governed by the suprachiasmatic nucleus in the hypothalamus regardless of peripheral clocks (15). The master body clock is accompanied by light intensity and duration, and the clock becomes unstable with the lifestyle change (16). Unfortunately, no prior research has yet focused on the association between light or shift work and the prevalence of OAB. Thus, this hypothesis still shall be elucidated with further evidence, which is what we plan to do in future studies to deeply explore the mechanism to support our results directly.
Furthermore, there is also some evidence to support our results indirectly. CircS is a cluster of diverse psychological and physiological impairments, including MetS (central obesity, elevated serum triglycerides, reduced serum HDL-C, elevated plasma glucose, and HBP), depression, and short sleep. Previous studies reveal that OAB is more prevalent in people with MetS than those without MetS (17). Moreover, higher risk and intensity of OAB were both observed in the population with psychological diseases, such as depression and anxiety (18). On the flip side, incontinence in public makes people fear, so they always avoid social interaction, which further exacerbates the severity of depression. Thus, a vicious circle is formed. Additionally, insomnia increases the odds of nocturia in some ways. First, most of these patients develop bad habits, such as drinking a large quantity of water before bedtime or drinking stimulating drinks at night including tea, coffee, and alcohol (19, 20). Second, people with insomnia are often accompanied by anxiety, which is worsened upon waking at night and causes reflex hyperactivity of the detrusor, leading to the appearance of OAB (21). For those patients with severe insomnia, who often feel difficultly falling asleep within a short time after waking up at night, they make a habit of urination, whether or not they have symptoms of urinary urgency. Jooyeon et al. revealed that urinary symptoms were improved significantly with great sleep efficiency via a biofeedback-based sleep improvement program (22).
In recent studies, several potential mechanisms were also proposed to explain the association between CircS and the prevalence of OAB. Autonomic hyperactivity plays an essential role. Compared to people without it, overactivated sympathetic activity and decreased vagal activity are more likely to be seen in people with MetS and depression (18, 23). In a long-term fructose-induced metabolic syndrome model, the expressions of acetylcholine and muscarinic cholinergic receptors were upregulated (24, 25). Additionally, the risk of atherosclerosis and CVD was raised when people suffered from CircS (8). The vascular alternation led to less blood supply to the bladder and bladder ischemia, which contributed to the occurrence of OAB. Apart from that, endoplasmic reticulum stress, autophagy, and apoptosis of the bladder were enhanced in the rat model of pelvis ischemia (26). For men with benign prostate enlargement, intravesical pressure increased due to enhanced contraction of the detrusor muscle as a result of bladder outlet obstruction, making bladder ischemia more pronounced (27). In addition to the gut microbiota, evidence supported that urine microbiota also affected urinary diseases, including OAB, kidney stones, and bladder cancer (28, 29). When circadian rhythms were disturbed, the microbiota in the urine was altered and its decreased abundance resulted in dysbiosis of the urinary flora. This impaired the beneficial effects of urinary microbiota on the bladder regulation and protection (30, 31). Moreover, the bladder-gut-brain axis (BGBA) might play an indispensable role in the pathophysiology of OAB (32). In addition to frequent co-occurrence and the symptom overlap with intestinal disorders, the functional urological disorder was also related to neuroticism (33). Central sensitization was induced by some negative affectivity, such as depression, and anxiety. The exact mechanism of BGBA is complex and remains elusive, but the following factor may be involved. An increase in membrane excitability and synaptic efficacy resulted in central sensitization, leading to automatic nervous system imbalance (34). Ovarian hormone deficiency was more likely to attack people with CircS, which contributed to the development of OAB (35). In a rat animal experiment, the ovariectomized rats mimicking the physiological condition of menopause were subjected to OAB, and low-intensity extracorporeal shock wave therapy attenuated inflammatory response and inhibited interstitial fibrosis (36). Therefore, although many efforts have been made, more trials and experiments are still needed to draw some convening pathological and psychological explanations.
This study also reveals that age modifies the positive association between the prevalence of CircS and OAB, but the direction of effect values is consistent across subgroups. Previous studies reported that aging people were more prone to a higher prevalence of OAB, which disagrees with our results. The disrupted circadian rhythm made aging accelerate, and the aging process was also associated with the frailty of the circadian rhythm (37, 38). Moreover, previous studies certificated that the incidence of OAB increased with age. A clinical trial showed that the nocturnal polyuria index was upregulated significantly with age, but no difference existed in genders (39). Based on a rat study, it was reported that aging bladders exhibited an elevated release of intrinsic ATP, resulting in heightened stimulation of downstream targets (40). Despite the complexity of the mechanisms behind the phenomenon, the spontaneous rise of intracellular Ca2+ may serve as an underlying mechanism (41). However, contrary to expectations, no significant interaction was found in gender in the study. Therefore, prospective and comprehensive studies with larger populations are required to elaborate on the conflicting phenomenon, and this is our further work.
This study has both pros and cons. First, the national multi-ethnic survey based on NHANES in a large number of populations makes the study representative and applicable. Second, CircS is a new concept combined with biological rhythms that are more consistent with the majority of physiological processes. No study has focused on the association between the prevalence of CircS and OAB. However, some limitations still need to be mentioned. Owing to the cross-section analyses, the causal relationship between the prevalence of CircS and OAB cannot be elucidated. In addition, although the diagnosis of OAB was governed by the synthesized OABSS in our study, laboratory diagnostic tests were absent in NHANES. Third, the symptoms of nocturia and urinary incontinence were collected via questionnaires, recall bias was probable.
Conclusion
There is a positive association between the prevalence of CircS and OAB. Notably, CircS is positively correlated with a higher prevalence of OAB. Furthermore, individuals with six or more CircS components have a strong correlation with an increased likelihood of experiencing OAB. However, to gain a deeper understanding, it is necessary to conduct more comprehensive and prospective cohort studies due to the cross-sectional design.
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found at: https://www.cdc.gov/nchs/nhanes/index.htm↗, National Center for Health Statistics.
Ethics statement
This study was performed using public data from the National Center for Health Statistics (NCHS) program and the National Health and Nutrition Examination Survey (NHANES). The data have been de-identified and not merged or augmented in a way that has compromised the privacy of the participants. Therefore, the study requires no further approval and follows ethical guidelines. Participant data were obtained from the publicly available NHANES, so no additional consent was obtained.
Author contributions
YFX and SY: conception and design. JW and YJB: administrative support and supervision. YFX, JHW, JWC, and ZZY: collection and assembly of data. SY and JHW: data analysis and interpretation. YFX: manuscript writing. YFX, SY, JHW, JWC, ZZY, JW, and YJB: final approval of manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the Key Research and Development Projects of Sichuan Science and Technology Department (grant number: 2020YFS0189 and 2022YFS0306), and the Project of Sichuan Provincial Health and Health Commission (grant number: 20PJ064).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Footnotes
Supplementary material
The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpubh.2023.1137191/full#supplementary-material↗
References
Associated Data
Supplementary Materials
Data Availability Statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found at: https://www.cdc.gov/nchs/nhanes/index.htm↗, National Center for Health Statistics.