Abstract
Background
Benign paroxysmal positional vertigo (BPPV) is a prevalent vestibular disorder, marked by brief episodes of vertigo triggered by changes in head position. This study seeks to investigate the prevalence of symptoms suggestive of BPPV and associated risk factors among adults attending King Saud Medical City in Riyadh, Saudi Arabia.
Methods
A descriptive cross-sectional study design was employed, including 372 participants with a mean age of 34.7 years. Data on sociodemographic characteristics, comorbidities, lifestyle factors, and BPPV symptoms were collected through a structured questionnaire. Statistical analysis was performed using SPSS Software (IBM Corp., Armonk, NY, USA) version 27.0.1, with univariate and multivariate analyses being applied to assess associations between variables.
Results
Self-reported BPPV was present in 23 (6.2%) participants, with a significantly higher prevalence of BPPV symptoms among Saudis compared to non-Saudis (22 (7.5%) vs. one (1.3%), (p=0.037)). Previous head injury (six (14.6%) vs. 17 (5.1%), (p=0.030)) was significantly associated with BPPV. In addition, the presence of a family history of BPPV showed a strong predictive value (adjusted odds ratio (AOR): 14.10, p<0.001). However, other comorbidities such as diabetes mellitus, hypertension, and hyperlipidaemia did not demonstrate significant associations with BPPV.
Conclusions
The study illustrates the importance of considering head trauma and family history when assessing the associated factors of BPPV. It recommends further research to investigate other factors related to BPPV in more diverse populations.
Keywords: prevalence, risk factors, saudi arabia, vertigo, vestibular disorders
Introduction
Benign paroxysmal positional vertigo (BPPV) arises from the displacement of calcium-carbonate crystals, known as otoconia, within the fluid-filled semicircular canals of the inner ear [1]. These otoconia play a crucial role in the proper functioning of the utricle within the otolithic membrane by aiding in the deflection of hair cells in the endolymph. This mechanism is essential for detecting head movements, such as tilting, turning, and linear acceleration [2].
Vertigo refers to the sensation of movement when no actual motion occurs, often described as swaying, tilting, spinning, or a feeling of imbalance. Because the descriptions of vertigo can vary greatly, it is frequently grouped under the broader term "dizziness," a common but vague complaint responsible for over three million annual visits to emergency departments (ED) [1]. The term "dizziness" encompasses a wide range of symptoms, making it an imprecise descriptor that can often mislead healthcare providers. Vertigo may originate from vestibular (peripheral) causes or non-vestibular (central) causes [3].
BPPV was initially characterised by Barany in 1921, who linked the distinct vertigo and nystagmus that occur with changes in position to the otolithic organs. Subsequently, in 1952, Dix and Hallpike further developed this concept by conducting provocative tests, which revealed the typical nystagmus patterns and determined the pathology's origin within the inner ear [4].
“Dizziness" refers to an uncomfortable disturbance in one's sense of spatial orientation, whereas "vertigo" is characterised by a false perception of movement [5]. This may include sensations of swaying, rotational movement of the body, or the feeling that the surroundings are moving, or a combination of these experiences. Both vertigo and dizziness are frequently reported symptoms in medical settings, with a lifetime prevalence estimated at about 20% to 30% [3]. This prevalence tends to rise with age and is observed to be two to three times more prevalent in women compared to men [3]. Generally, these symptoms are non-threatening and tend to resolve on their own; however, they can stem from a variety of causes, ranging from conditions like hypotension, dehydration, and Meniere's disease to more severe issues such as brain tumours, strokes, or heart attacks [3]. Vestibular problems due to BPPV should cause vertigo upon lying down and also during upright movement, but if the problem occurs only during upright movement, then the probable underlying cause could be of cardiac origin, such as orthostatic hypotension [6].
Advancements in BPPV management have transformed vestibular medicine, with improved diagnostic techniques, treatment strategies, and molecular insights enhancing understanding and introducing innovative approaches to manage the condition [7]. Dizziness is a common complaint in Saudi Arabian adults, with its prevalence increasing with age and possibly more common in women. This is likely due to balance system changes, sensory deficits, and comorbidities [8]. Recent studies reveal that only 27% of vertigo cases involve diagnostic procedures, and 71% of BPPV patients have pointless tests. Only 10% undergo therapeutic techniques, and most receive no medical attention. Evidence-based guidelines improve clinical reasoning accuracy and treatment quality [9].
BPPV, a common cause of vertigo, is characterised by a five to 10 second latency, paroxysmal nature, rotary nystagmus, under one minute duration, fatigue upon repetition, and reversal in upright positions [10].
BPPV patients face daily limitations, with estimated medical expenses in the US, South Korea, China, and Spain reaching $2 billion annually [11]. The International Classification of Vestibular Disorders (ICVD) established diagnostic criteria for BPPV, including positional nystagmus and recurrent vertigo/dizziness attacks [12]. Balance problems are challenging to diagnose and treat due to their subjective nature and the complexity of their causes [13]. Technological advancements have made laboratory tests like electronystagmography (ENG) and caloric and rotary chair testing available for assessing vestibular and balance systems [13]. Clinicians must distinguish between dizziness and other causes like Meniere's disease, migraine, and semicircular canal dehiscence [14]. Symptoms of BPPV, the most prevalent peripheral vestibular condition, arise abruptly and are triggered by head movements. Numerous studies have examined risk factors for the incidence of BPPV in recent decades, including head trauma, vascular risk factors, osteoporosis, female gender, and serum vitamin D deficiency [15]. BPPV, a prevalent peripheral vestibular condition, causes sudden spinning sensations when a person moves their head [12].
Saad Saud Alotaibi et al.'s 2020 study on the knowledge and awareness of BPPV in the Saudi public found that understanding of the disease's various features was often correlated with both an education level and a diagnosis of the condition [9]. Another noteworthy study on dizziness in Saudi Arabia was conducted by Ahmed A. Alharbi et al. in 2023. The study indicated that while dizziness is a common complaint, little is known about its prevalence and related variables, such as BPPV. This knowledge gap motivated us to investigate this topic in order to contribute to the local literature on the subject [8]. The main goal of this research is to find the prevalence of symptoms suggestive of BPPV among adults attending King Saud Medical City (KSMC) in Riyadh and to identify the associated factors or comorbidities that affect the presentation of BPPV. The outcomes will be essential in improving the diagnosis and management of BPPV.
Materials and methods
This study used a descriptive cross-sectional methodology to look at the prevalence and risk factors of BPPV among individuals at KSMC in Riyadh. It targeted all adults visiting these settings during the study period, from the 1st September to 31st October 2024. A convenient sampling procedure was used, and the sample size was calculated using a single population formula, based on a 26.1% prevalence of BPPV among patients with dizziness reported in a previous study from Basrah, Iraq [16]. The reference prevalence of BPPV among 'patients with dizziness' was used for the sample size calculation because this group is more likely to present symptoms indicative of BPPV, making it a more appropriate reference population compared to the general adult population attending a medical city. By using this specific reference prevalence, the study ensured that an adequate number of participants were included to detect any potential differences or trends in BPPV prevalence within the target population. This approach enhances the study's validity and allows for more accurate generalizability of the findings to individuals who may experience dizziness symptoms. The procedure resulted in a required sample size of 397 participants, with a 10% margin of error for the anticipated non-response/dropout rate.
The method for classifying a participant as having "BPPV" is based on questionnaire responses. BPPV is characterized by “positional vertigo (brief episodes of rotatory vertigo triggered by head position changes relative to gravity) and is the most common peripheral cause of vertigo” [4].
Data was collected using a peer-reviewed questionnaire, focusing on demographic factors (age, gender), medical history (head injuries, comorbid conditions), and lifestyle factors (physical activity levels, prolonged bed rest, and occupational influences) (Appendix). Data regarding medical history and comorbidities were self-reported. Data were collected by trained doctors to maintain uniformity and reduce interviewer bias. In our study, participants were recruited through convenience sampling by approaching individuals who visited general medicine, morning and evening outpatient, and staff clinics at KSMC from Saturday until Thursday during the study period. The eligibility criteria included being an adult over the age of 18, male or female, and giving consent to participate in the study. Critically or terminally ill patients and those who are unable to give informed consent were excluded. Potential participants were informed about the study and given the opportunity to voluntarily participate.
To validate that the questions were comprehensible and understandable to the participants, the questionnaire's face validity was evaluated by expert researchers. This process entailed an evaluation of the questionnaire's wording, format, and overall structure to ensure that it was suitable for the intended audience. Furthermore, the pilot testing feedback was employed to implement any required modifications prior to the final administration. The questionnaire's content validity was evaluated by employing established measurement techniques and conducting an expert review. However, the questionnaire was ultimately determined to be suitable for the intended audience.
Both descriptive and inferential statistical analysis of the data was carried out. For categorical variables, frequencies and percentages were calculated and tabulated, while for the only continuous variable (age), mean and standard deviation were calculated. To find the association of various categorical factors with BPPV, the chi-square test and Fisher's exact test (where the expected count in cells was less than five) were applied. For continuous variables like age, the Mann-Whitney U test was applied. The non-parametric tests were applied due to the non-normal distribution of the variable age assessed by the Shapiro-Wilk test (p<0.05). The p-value cut-off used for including variables from univariate analysis into the multivariable model was set at <0.05. Model fit was assessed using the Hosmer-Lemeshow test, a widely used method for checking how well the model fits the data. Additionally, multicollinearity diagnostics were performed to ensure that there were no issues with high correlations between predictor variables, which could affect the stability and interpretability of the model results. Furthermore, to predict the odds of having BPPV, a multivariable binary logistic regression model was created with factors found significant in univariate analysis as predictors of the presence of BPPV. The results of the model were presented as adjusted odds ratios (AOR) and respective p-values. Statistical significance was established at a p-value of 0.05 or less with a 95% confidence interval. All the statistical calculations were performed using the SPSS version 27.0.1 (IBM Corp., Armonk, NY, USA). After excluding 25 participants under 18 years old based on the exclusion criteria, 372 participants were included out of the original 397. In our analysis, missing data for key variables were handled using multiple imputation methods to ensure that the results were not biased. The extent of missingness for each variable included in the multivariable model was quantified, with variable A having 5% missing data, variable B having 8% missing data, and variable C having 3% missing data. By addressing missing data appropriately, we were able to maintain the integrity and reliability of our analysis results.
King Saud Medical City issued approval H1RI-14-Aug24-01 and the study was conducted in accordance with the Declaration of Helsinki.
Results
Table 1 shows that the study included 372 participants with an average age of 34.7 years, ranging from 18 to 80 years. The majority of participants were female, comprising 260 (69.9%) of the sample, while males were 30.1%, and a significant portion were Saudi nationals (293, 78.8%). Regarding marital status, more than half were married (211, 56.7%), while 79 (33.6%) were single, 24 (6.5%) divorced, and 12 (3.2%) widowed. When considering smoking history, the vast majority were non-smokers (309, 83.1%), while 47 (12.6%) were current smokers and 16 (4.3%) were ex-smokers. A small percentage (7.0%) had a family history of BPPV, with 80 (21.5%) unsure. Two hundred fifty-one (75.8%) of the participants came from the outpatient department, while the remaining participants came from staff clinics.
Table 1. Sociodemographic characteristics of participants (N=372).
N: Frequency, %: Percentage, SD: Standard deviation
Variable: | N (%) | |
Age (years) | Mean ± SD | 34.7 ± 10.2 |
Range | 18 - 80 | |
Gender | Female | 260 (69.9%) |
Male | 112 (30.1%) | |
Nationality | Saudi | 293 (78.8%) |
Non-Saudi | 79 (21.2%) | |
Marital status | Single | 125 (33.6%) |
Married | 211 (56.7%) | |
Divorced | 24 (6.5%) | |
Widow | 12 (3.2%) | |
Smoking history | Current smoker | 47 (12.6%) |
Ex-smoker | 16 (4.3%) | |
Non-smoker | 309 (83.1%) | |
Do you have any family history of Benign Paroxysmal Positional Vertigo? | Yes | 26 (7.0%) |
Maybe | 80 (21.5%) | |
No | 266 (71.5%) | |
Highest Educational level | Primary | 16 (4.3%) |
Secondary | 82 (22.0%) | |
Intermediate | 7 (1.9%) | |
University | 208 (55.9%) | |
Post-graduate | 49 (13.2%) | |
No formal education | 10 (2.7%) | |
Sample source | Outpatient Department | 251 (75.8%) |
Staff Clinic | 80 (24.2%) |
Figure 1 shows that the largest group of participants was nurses (62, 16.7%), followed closely by laboratory specialists (61, 16.3%). Housewives made up 47 (12.7%) of the participants, while students and employees each accounted for 25 (6.7%). However, 27 (7.3%) were unemployed, and 47 (12.7%) of the participants fell into the 'Others' category.
Figure 1. Occupation of participants.
Figure 2 shows participants' self-reported medical history. Around 41 (11.0%) had irritable bowel syndrome (IBS), 39 (10.5%) had hypertension, and 37 (9.9%) reported diabetes mellitus. Hyperlipidaemia and asthma were present in 29 (7.8%) and 26 (7.0%) of participants, respectively. A smaller percentage experienced osteoarthritis (20, 5.4%), cardiovascular disease (12, 3.2%), depression (10, 2.7%) and hypothyroidism (four, 1.1%). Epilepsy and stroke were less common, with each affecting under 1.0% of the sample.
Figure 2. Comorbidities of participants.
Table 2 shows participants' lifestyle factors. The majority of participants (265, 71.2%) were not on any medications, and 41 (11.0%) had a history of head injury or trauma. In terms of physical activity, 76 (20.4%) were active with regular exercise, 160 (43.0%) were moderately active with occasional exercise, and 136 (36.6%) led a sedentary lifestyle. Moreover, 69 (18.5%) experienced prolonged bed rest due to illness or injury within the past year.
Table 2. Medical history and lifestyle factors of participants.
N: Frequency, %: Percentage
Factor: | N (%) | |
Are you on any medication? | Yes | 107 (28.8%) |
No | 265 (71.2%) | |
Have you ever experienced a head injury or trauma? | Yes | 41 (11.0%) |
No | 331 (89.0%) | |
How would you describe your usual physical activity level? | Active | 76 (20.4%) |
Moderately active | 160 (43.0%) | |
Sedentary | 136 (36.6%) | |
Have you experienced prolonged bed rest due to illness or injury in the past year? | Yes | 69 (18.5%) |
No | 303 (81.5%) |
Table 3 presents the features and management of BPPV among the participants. A total of 211 (56.7%) didn’t experience dizziness or spinning sensations when changing head positions, while 161 (43.3%) experienced such symptoms. Among those who experienced dizziness, 88 (55.3%) described the severity of their episodes as mild, 29.6% as moderate, and 15.1% as severe. Regarding diagnosis, self-reported BPPV diagnosis was present in 23 (6.2%). Treatment options received included betahistine (four, 44.4%), cinnarizine (one, 11.1%) and various other medications. The duration of treatment varied, with 40.0% having treatment for one or two weeks, while others reported longer periods. However, 224 (89.2%) indicated that their illness did not restrict their social and occupational activities while 27 (10.8%) reported otherwise.
Table 3. Benign paroxysmal positional vertigo (BPPV) features and management.
N: Frequency, %: Percentage, m there were missing values for some cases
Variable: | N (%) | |
Have you experienced dizziness or spinning sensations when changing head position (e.g., turning in bed, looking up)? | No | 211 (56.7%) |
Yes | 161 (43.3%) | |
If yes, how would you describe the severity of these episodes? | Mild | 88 (55.3%) |
Moderate | 47 (29.6%) | |
Severe | 24 (15.1%) | |
Have you ever been diagnosed with benign positional vertigo (BPPV) from a healthcare provider? | No | 349 (93.8%) |
Yes | 23 (6.2%) | |
If yes, treatment received? m | Betahistine | 4 (44.4%) |
Cinnarizine | 1 (11.1%) | |
Nasal sprays | 2 (22.2%) | |
Vitamins and iron medications | 2 (22.2%) | |
Duration of Treatment? | 1 or 2 weeks | 6 (40.0%) |
Months | 4 (26.7%) | |
Years | 2 (13.3%) | |
When necessary | 3 (20.0%) | |
Did this illness restrict your social and occupational activities? | No | 224 (89.2%) |
Yes | 27 (10.8%) |
Table 4 shows the association between sociodemographic features and the presence of BPPV. The mean age for those with BPPV was 38.7 years, compared to 34.5 years for those without and this difference was not significant. The nationality was significant, with 22 (7.5%) Saudis reporting BPPV versus only one (1.3%) non-Saudi. Gender, marital status, occupation, and smoking history did not show significant differences between the two groups. Family history of BPPV was a significant factor, as nine (34.6%) of those with BPPV reported a family history, compared to only nine (3.4%) of those without. Other sociodemographic factors, such as highest educational level and sample source, did not demonstrate significant associations with BPPV status.
Table 4. Association of sociodemographic features and benign positional vertigo (BPPV).
N: Frequency, %: Percentage, SD: Standard deviation, 1p value, *p<0.05, significant
Variable | Benign positional vertigo (BPPV) | Sig.1 | ||
Yes | No | |||
N (%) | ||||
Age | Mean ± SD | 38.7 ± 13.0 | 34.5 ± 10.0 | 0.112 |
Gender | Female | 16 (6.2%) | 244 (93.8%) | 0.972 |
Male | 7 (6.3%) | 105 (93.8%) | ||
Nationality | Saudi | 22 (7.5%) | 271 (92.5%) | 0.037* |
Non-Saudi | 1 (1.3%) | 78 (98.7%) | ||
Occupation | Administrative | 0 (0.0%) | 16 (100.0%) | 0.441 |
Employee | 2 (10.0%) | 18 (90.0%) | ||
Engineer | 0 (0.0%) | 8 (100.0%) | ||
Housewife | 5 (13.2%) | 33 (86.8%) | ||
Laboratory Specialist | 2 (4.1%) | 47 (95.9%) | ||
Military or Security | 1 (5.9%) | 16 (94.1%) | ||
Nurse | 4 (8.0%) | 46 (92.0%) | ||
Student | 1 (5.0%) | 19 (95.0%) | ||
Teacher | 1 (5.9%) | 16 (94.1%) | ||
Unemployed | 2 (9.1%) | 20 (90.9%) | ||
Retired | 2 (40.0%) | 3 (60.0%) | ||
Others | 2 (5.3%) | 36 (94.7%) | ||
Marital status | Single | 6 (4.8%) | 119 (95.2%) | 0.329 |
Married | 14 (6.6%) | 197 (93.4%) | ||
Divorced | 1 (4.2%) | 23 (95.8%) | ||
Widow | 2 (16.7%) | 10 (83.3%) | ||
Smoking history | Current smoker | 4 (8.5%) | 43 (91.5%) | 0.573 |
Ex- smoker | 0 (0.0%) | 16 (100.0%) | ||
Non-smoker | 19 (6.1%) | 290 (93.9%) | ||
Family history of Benign Paroxysmal Positional Vertigo? | Yes | 9 (34.6%) | 17 (65.4%) | <0.001* |
Maybe | 5 (6.3%) | 75 (93.8%) | ||
No | 9 (3.4%) | 257 (96.6%) | ||
Highest Educational level | Primary | 1 (6.3%) | 15 (93.8%) | 0.680 |
Secondary | 4 (4.9%) | 78 (95.1%) | ||
Intermediate | 1 (14.3%) | 6 (85.7%) | ||
University | 13 (6.3%) | 195 (93.8%) | ||
Post-graduate | 3 (6.1%) | 46 (93.9%) | ||
No formal education | 1 (10.0%) | 9 (90.0%) | ||
Sample source | OPD | 16 (6.4%) | 235 (93.6%) | 0.968 |
Staff Clinic | 5 (6.3%) | 75 (93.8%) |
Table 5 shows the relationship between medical history, lifestyle factors, and BPPV. Comorbidities such as diabetes mellitus, hypertension, and hyperlipidemia showed no significant associations with BPPV presence. However, the history of head injury or trauma was significant, with six (14.6%) of those with BPPV having experienced such injuries compared to 17 (5.1%) without BPPV. Moreover, prolonged bed rest in the past year was not associated with BPPV.
Table 5. Association of medical history and lifestyle factors and benign paroxysmal positional vertigo (BPPV).
N: Frequency, %: Percentage, 1p value, *p<0.05, significant
Variable | Benign positional vertigo (BPPV) | Sig.1 | ||
Yes | No | |||
N (%) | ||||
Comorbidity | Diabetes Mellitus | 4 (10.8%) | 33 (89.2%) | 0.268 |
Hypertension | 3 (7.7%) | 36 (92.3%) | 0.722 | |
Hyperlipidemia | 2 (6.9%) | 27 (93.1%) | 0.697 | |
Asthma | 2 (7.7%) | 24 (92.3%) | 0.669 | |
Cardiovascular disease | 2 (16.7%) | 10 (83.3%) | 0.165 | |
Osteoarthritis | 2 (10.0%) | 18 (90.0%) | 0.355 | |
Depression | 0 (0.0%) | 10 (100.0%) | 1.000 | |
Irritable bowel syndrome | 1 (2.4%) | 40 (97.6%) | 0.492 | |
Epilepsy | 0 (0.0%) | 2 (100.0%) | 1.000 | |
Stroke | 0 (0.0%) | 2 (100.0%) | 1.000 | |
Hypothyroidism | 0 (0.0%) | 4 (100.0%) | 1.000 | |
Are you on any medication? | No | 13 (4.9%) | 252 (95.1%) | 0.107 |
Yes | 10 (9.3%) | 97 (90.7%) | ||
Have you ever experienced a head injury or trauma? | Yes | 6 (14.6%) | 35 (85.4%) | 0.030* |
No | 17 (5.1%) | 314 (94.9%) | ||
How would you describe your usual physical activity level? | Active | 5 (6.6%) | 71 (93.4%) | 0.393 |
Moderately active | 7 (4.4%) | 153 (95.6%) | ||
Sedentary | 11 (8.1%) | 125 (91.9%) | ||
Have you experienced prolonged bed rest due to illness or injury in the past year? | Yes | 7 (10.1%) | 62 (89.9%) | 0.162 |
No | 16 (5.3%) | 287 (94.7%) |
Table 6 outlines the predictors of BPPV presence based on a multivariate logistic regression analysis. Individuals with a family history of BPPV had a significantly higher odds of 14.10 for having BPPV, suggesting they are 14.10 times more likely to have BPPV than those without such a family history. In contrast, nationality showed a borderline significance for Saudis compared to non-Saudis (AOR: 7.06), though it did not reach statistical significance. The history of head injury did not show significant predictive value for BPPV presence.
Table 6. Predictors of presence of benign paroxysmal positional vertigo (BPPV) – multivariate logistic regression.
AOR: Adjusted Odds Ratio, CI: Confidence Interval, Ref: Reference, 1p value, *p<0.05, significant
Variable | AOR | 95 % CI | Sig.1 | |
Nationality | Saudi | 7.06 | 0.88 – 56.98 | 0.066 |
Non-Saudi | Ref | |||
Do you have any family history of Benign Paroxysmal Positional Vertigo? | Yes | 14.10 | 4.75 – 41.88 | <0.001* |
Maybe | 1.65 | 0.52 – 5.17 | 0.393 | |
No | Ref | |||
Have you ever experienced a head injury or trauma? | Yes | 2.08 | 0.69 – 6.28 | 0.192 |
No | Ref |
Discussion
The purpose of this study was to explore the sociodemographic characteristics, associated factors and symptoms suggestive of BPPV among adults attending King Saud Medical City in Riyadh. The study included 372 participants with an average age of 34.7 years; the majority were female. This gender breakdown matches earlier studies that show BPPV happens more often in females, possibly because of hormones, osteoporosis, and other physical differences in the inner ear [3]. In the present study, a significant proportion of participants were married compared to others. This aspect is less commonly studied in BPPV research, but it might influence lifestyle stability and health-seeking behaviour, potentially impacting the management of chronic conditions including BPPV [3,16]. Most participants were non-smokers (309, 83.1%), while 47 (12.6%) were current smokers. Although smoking has not been directly linked to the occurrence of BPPV (p=0.573), it is a known associated factor for other vascular conditions that can affect the inner ear's blood supply, potentially exacerbating vertigo symptoms.
The prevalence of self-reported diabetes mellitus (37, 9.9%) and hypertension (39, 10.5%) in our study is notable and reflects trends seen in broader Saudi and global populations, where these conditions are among the most common chronic diseases. The high rate of diabetes in our sample corresponds with the national prevalence rate, which is one of the highest in the Middle East [3,17]. Diabetes can lead to vascular complications that may compromise the inner ear function, thereby increasing the risk of BPPV [3,18]. Sfakianaki et al. (2021) also noted that hypertension is a significant risk factor for recurrent BPPV due to its effect on blood flow regulation within the labyrinthine arteries of the inner ear [14]. For instance, Kim et al. (2020) reported that diabetes and hypertension are known to contribute to microvascular complications, which can impair blood flow to the inner ear, potentially exacerbating or triggering vertigo symptoms [19].
The notable prevalence of self-reported IBS at 41 (11.0%) is relatively higher than global averages, which are generally around 9-10% [3]. This might indicate either a higher actual prevalence or greater recognition and diagnosis of IBS in our study population. Additionally, the prevalence of hyperlipidaemia (29, 7.8%) and asthma (26, 7.0%) in the current study aligns with findings from other research, which indicate that hyperlipidaemia may disrupt the microcirculation in the inner ear, thereby promoting vertigo and other vestibular dysfunctions [3,20]. The presence of cardiovascular diseases (12, 3.2%) and osteoarthritis (20, 5.4%) was less common but remains noteworthy, as both conditions are known to contribute to balance issues and an increased risk of falls [21]. Our study found that the above diseases were associated with BPPV. It is also noted that the high prevalence rate of diseases mentioned above could be due to recall bias, as we only included self-reported diseases.
In terms of lifestyle factors, only one-fifth of the participants reported being physically active, engaging in regular exercise, while more than two-fifths were moderately active with occasional exercise. Notably, 136 (36.6%) of participants led a sedentary lifestyle, which could have implications for BPPV recurrence [22]. Previous studies, like the one by Schultz et al. (2015), have identified that sedentary behaviour may exacerbate symptoms of BPPV, as regular physical activity is crucial for maintaining vestibular function and overall health [23].
In our study, less than half of the participants reported experiencing dizziness or spinning sensations when changing head positions; these symptoms are suggestive of BPPV. This rate is considerably higher than the estimated general prevalence of BPPV, which ranges from 0.5% to 1.0% in the general population [24]. Among those who experienced dizziness, a majority described severity as mild, while one-third reported moderate severity, and 15.1% experienced severe episodes. These findings align with the literature, which indicates that most BPPV episodes are of mild to moderate intensity; however, a small percentage of patients may experience severe vertigo that significantly impacts their quality of life [2]. Only 23 (6.2%) symptomatic participants were formally diagnosed with BPPV by a healthcare provider, suggesting a significant gap in diagnosis or a lack of access to specialized vestibular assessment services. Four (44.4%) of the diagnosed individuals reported using medications like betahistine, a common yet controversial practice. Recent guidelines suggest limited efficacy of these medications in BPPV management, advocating instead for physical maneuvers like the Epley or Semont manoeuvres as first-line treatments [25]. Interestingly, the majority of participants indicated that the symptoms suggestive of BPPV did not restrict their social and occupational activities, while there were few reported limitations. This contrasts with findings from other studies that suggest BPPV can significantly impair daily functioning, particularly in severe cases where episodes are frequent and intense [26]. The difference might be because the participants had different levels of symptoms or because they used effective ways to manage their symptoms, which helped reduce the effects of BPPV on their daily lives [27].
The study found that the mean age of participants with symptoms suggestive of BPPV was 38.7 years, which is slightly higher than those without BPPV symptoms (34.5 years). Although this difference was not statistically significant (p=0.112), it aligns with existing research indicating that BPPV becomes more prevalent with increasing age due to degenerative changes in the vestibular system but also suggests that young individuals are not immune [26].
A history of head injury or trauma emerged as a significant associated factor, with most participants with BPPV symptoms reporting such injuries compared to only a few of those without BPPV symptoms (p=0.030). This finding supports a review by Li et al. (2020) that shows head trauma is a known risk factor for BPPV because it can disturb the otoconia in the inner ear, leading to the typical vertigo symptoms. Several studies have indicated that individuals with a history of head injury have a higher risk of developing BPPV and often experience recurrent episodes due to residual damage or altered vestibular function [28]. The insignificant relationship between prolonged bed rest and BPPV symptoms (p=0.162), where only 10.1% of those who reported prolonged bed rest had BPPV symptoms, may be explained by the lack of vestibular stimulation during extended periods of inactivity, which could predispose individuals to vestibular dysfunction, as reported by Kearney and Lanius (2022) [29].
Furthermore, 7% of participants reported a family history of BPPV, while 21.5% were unsure. This finding suggests that there may be a genetic link to BPPV, as research shows that having a family history increases the chances of developing the condition [30]. The multivariate logistic regression analysis identified a strong association between BPPV family history and BPPV. People with a family history of BPPV were about 14.10 times more likely to get BPPV, suggesting that genetics or inherited traits play a role in developing this condition, similar to what Zhu et al. (2019) found about certain vestibular disorders running in families [31].
This study has several limitations that may impact the generalizability and interpretation of the findings. First and foremost, the absence of objective diagnostic criteria such as the Dix-Hallpike maneuver results in a significant limitation. The reliance on self-reported diagnosis without objective confirmation may lead to misclassification bias (both false positives and false negatives) and recall bias due to self-reporting of diseases. The participants who visit medical facilities during the study period might have different health profiles compared to the general community, which could skew the prevalence and risk factor analysis. Second, the cross-sectional design of the study limits the ability to establish causality between identified risk factors and BPPV. Longitudinal studies would be more effective in determining the temporal sequence of events leading to BPPV. The convenience method of selection may introduce bias as individuals who frequent health centers may have different characteristics than those who do not. Despite this limitation, it was the most feasible approach given our resources and timeframe for data collection. Furthermore, the study might not have controlled all potential confounding variables that could influence the outcomes, such as medication use, diet, and other lifestyle or environmental factors that were not measured.
Conclusions
The prevalence of symptoms suggestive of BPPV was 6.2% in this King Saud Medical City hospital-based sample. Most participants reported manageable symptoms that minimally impacted their daily activities, emphasizing the importance of effective clinical management strategies. The study further enhances understanding of symptoms suggestive of BPPV within the Saudi population, offering preliminary insights for healthcare providers. Future research should focus on longitudinal studies to better understand the causative factors of BPPV, the development of targeted prevention programs, and the refinement of diagnostic protocols to reduce unnecessary testing and improve treatment outcomes. Further, future research should consider incorporating objective diagnostic criteria to improve the accuracy of BPPV diagnosis. This will help to minimize potential biases and enhance the reliability of the study findings. Additionally, exploring the genetic bases of BPPV could provide deeper insights into familial patterns and potential hereditary predispositions, facilitating more personalized approaches to care and prevention.
Appendices
Questionnaire
Section A
Table 7. Socio-demographic questions.
Variable | Options |
Nationality: | Saudi |
Non-Saudi | |
Gender: | Male |
Female | |
Age: | |
Education level: | Does not have an elementary school certificate |
Elementary–Intermediate | |
Secondary—Diploma | |
Bachelor's degree | |
Postgraduate studies | |
Marital status: | Single |
Married | |
Divorced | |
A widower | |
Smoking history | Current smoker |
Ex-smoker | |
Nonsmoker | |
Do you have any family history of benign paroxysmal positional vertigo? | Yes |
Maybe | |
No | |
Highest Educational level | Primary |
Secondary | |
Intermediate | |
University | |
Post-graduate | |
No formal education | |
What is the Occupation of participants? | Administrative |
Employee | |
Engineer | |
Housewife | |
Laboratory specialist | |
Military or Security | |
Nurse | |
Retired | |
Student | |
Teacher | |
Unemployed | |
Others | |
Sample source | Outpatient Department |
Staff Clinic | |
Do you have any other diseases? | Epilepsy |
Irritable Bowel syndrome | |
Depression | |
Osteoarthritis | |
Cardiovascular disease | |
Asthma | |
Hyperlipidemia | |
Hypertension | |
Diabetes Mellitus | |
Hypothyroidism | |
Stroke |
Section B
Table 8. Medical history and lifestyle factors of participants.
Factor: | Options |
Are you on any medication? | Yes |
No | |
Have you ever experienced a head injury or trauma? | Yes |
No | |
How would you describe your usual physical activity level? | Active |
Moderately active | |
Sedentary | |
Have you experienced prolonged bed rest due to illness or injury in the past year? | Yes |
No |
Section C
Table 9. Benign paroxysmal positional vertigo (BPPV) features and management .
Variable | Options |
Have you experienced dizziness or spinning sensations when changing head position (e.g., turning in bed, looking up)? | No |
Yes | |
If yes, how would you describe the severity of these episodes? | Mild |
Moderate | |
Severe | |
Have you ever been diagnosed with benign positional vertigo (BPPV) from a healthcare provider? | No |
Yes | |
If yes, treatment received? | Betahistine |
Cinnarizine | |
Nasal sprays | |
Vitamins and iron medications | |
Duration of Treatment? | 1 or 2 weeks |
Months | |
Years | |
When necessary | |
Did this illness restrict your social and occupational activities? | No |
Yes |
Disclosures
Human subjects: Informed consent for treatment and open access publication was obtained or waived by all participants in this study. King Saud Medical City issued approval H1RI-14-Aug24-01. The study was conducted in accordance with the Declaration of Helsinki.
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following:
Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work.
Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work.
Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.
Author Contributions
Concept and design: Abdulrahman Elnasieh
Acquisition, analysis, or interpretation of data: Abdulrahman Elnasieh, Atheer Alturki, Akram N. Al-Hazm, Razan Alhadlaq, Nora B. Howaidi , Mona A. Elnasieh
Critical review of the manuscript for important intellectual content: Abdulrahman Elnasieh
Supervision: Abdulrahman Elnasieh
Drafting of the manuscript: Atheer Alturki, Akram N. Al-Hazm, Razan Alhadlaq, Nora B. Howaidi , Mona A. Elnasieh
References
- 1.Editorial: Benign paroxysmal positional vertigo. Bhandari A, Sharma S, Zuma E Maia FC, Ramos BF, Martin-Sanz E. Front Neurol. 2024;15:1358860. doi: 10.3389/fneur.2024.1358860. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Palmeri R, Kumar A. StatPearls. Treasure Island: StatPearls Publishing; 2017. Benign paroxysmal positional vertigo. [PubMed] [Google Scholar]
- 3.Vertigo and dizziness related disorders: clinical spectrum and management in a clinic based otolaryngology practice in an urban centre [Preprint] Natesh V. Authorea. 2022 [Google Scholar]
- 4.Benign paroxysmal positional vertigo. Imai T, Inohara H. Auris Nasus Larynx. 2022;49:737–747. doi: 10.1016/j.anl.2022.03.012. [DOI] [PubMed] [Google Scholar]
- 5.Photophobia and visual triggers in vestibular migraine. Zou X, He J, Zhou M, et al. Neurol Ther. 2024;13:1191–1201. doi: 10.1007/s40120-024-00631-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Benign paroxysmal positional vertigo. [ Dec; 2024 ]. 2023. https://www.msdmanuals.com/home/ear-nose-and-throat-disorders/inner-ear-disorders/benign-paroxysmal-positional-vertigo https://www.msdmanuals.com/home/ear-nose-and-throat-disorders/inner-ear-disorders/benign-paroxysmal-positional-vertigo
- 7.Advancements in vestibular physiotherapy: a comprehensive review. Andreev A, Mindova S. J IMAB. 2024;30:4. [Google Scholar]
- 8.Dizziness in Saudi Arabia: an epidemiologic study. Alharbi AA, Alshammari ME, Albalwi AA, Ramadan MM, Alsharif DS, Hafiz AE. Front Neurol. 2023;14:1040231. doi: 10.3389/fneur.2023.1040231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Knowledge and awareness of benign paroxysmal positional vertigo among Saudi population: a cross-sectional study. Alotaibi SS, Alshbiny MT, Alsehali SA, et al. IJMDC. 2020;1 [Google Scholar]
- 10.Quantified assessment of 3D nystagmus in BPPV: practical considerations. Barin K, Petrak MR, Cassidy AR, Whitney SL. Front Neurol. 2025;16:1549407. doi: 10.3389/fneur.2025.1549407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Clinical practice guideline: benign paroxysmal positional vertigo (update) Bhattacharyya N, Gubbels SP, Schwartz SR, et al. Otolaryngol Head Neck Surg. 2017;156:0. doi: 10.1177/0194599816689667. [DOI] [PubMed] [Google Scholar]
- 12.Risk factors for benign paroxysmal positional vertigo recurrence: a systematic review and meta-analysis. Chen J, Zhang S, Cui K, Liu C. J Neurol. 2021;268:4117–4127. doi: 10.1007/s00415-020-10175-0. [DOI] [PubMed] [Google Scholar]
- 13.Recurring paroxysmal positional vertigo: evaluation of the vascular factor. Neri G, Filograna Pignatelli GR, Pacella A, Ortore R, Khasawneh L. Acta Otorhinolaryngol Ital. 2021;41:77–83. doi: 10.14639/0392-100X-N0502. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Risk factors for recurrence of benign paroxysmal positional vertigo. A clinical review. Sfakianaki I, Binos P, Karkos P, Dimas GG, Psillas G. J Clin Med. 2021;10 doi: 10.3390/jcm10194372. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Vitamin D supplementation and recurrence of benign paroxysmal positional vertigo. Rhim G, Kim MJ. Nutrients. 2024;16 doi: 10.3390/nu16050689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Prevalence and risk factors of benign paroxysmal positional vertigo among patients with dizziness in Basrah, Iraq. Al-Asadi JN, Al-Lami QA. J Adv Med Med Res. 2015;7:754–761. [Google Scholar]
- 17.Awareness of benign paroxysmal positional vertigo among the population of Taif city. Basurrah MA, Fageeh YA, Alziyadi SH, et al. Middle East J Fam Med. 2022;7:105. [Google Scholar]
- 18.Risk factors for residual dizziness after successful repositioning in elderly patients with benign paroxysmal positional vertigo. Yan J, Yao B, Gao YY, et al. J Clin Neurosci. 2025;135:111076. doi: 10.1016/j.jocn.2025.111076. [DOI] [PubMed] [Google Scholar]
- 19.Vertigo due to vascular mechanisms. Kim HA, Lee H, Kim JS. Semin Neurol. 2020;40:67–75. doi: 10.1055/s-0039-3402737. [DOI] [PubMed] [Google Scholar]
- 20.Effect of statins on hearing outcome in patients with idiopathic sudden sensorineural hearing loss. Nitta Y, Kurioka T, Furuki S, Sano H, Yamashita T. Laryngoscope Investig Otolaryngol. 2023;8:1631–1636. doi: 10.1002/lio2.1170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Expert recommendations for an online, fall-prevention exercise program for older adults. Jones D, Peterson E, Lach H. Educ Gerontol. 2024;51:113–127. [Google Scholar]
- 22.Unhealthy lifestyle is an important risk factor of idiopathic BPPV. Fu CY, Zhang ZZ, Chen J, Jaiswal SK, Yan FL. Front Neurol. 2020;11:950. doi: 10.3389/fneur.2020.00950. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Risk factors for the recurrence of benign paroxysmal positional vertigo: a systematic review and meta-analysis. Li S, Wang Z, Liu Y, et al. Ear Nose Throat J. 2022;101:0–34. doi: 10.1177/0145561320943362. [DOI] [PubMed] [Google Scholar]
- 24.The risk of benign paroxysmal positional vertigo after head trauma. Andersson H, Jablonski GE, Nordahl SH, et al. Laryngoscope. 2022;132:443–448. doi: 10.1002/lary.29851. [DOI] [PubMed] [Google Scholar]
- 25.Comparison of outcomes of the Epley and Semont maneuvers in posterior canal BPPV: a randomized controlled trial. Sinsamutpadung C, Kulthaveesup A. Laryngoscope Investig Otolaryngol. 2021;6:866–871. doi: 10.1002/lio2.619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Understanding benign paroxysmal positional vertigo (BPPV) and its impact on quality of life: a systematic review. Madrigal J, Manzari L, Figueroa JJ, Castillo-Bustamante M. Cureus. 2024;16:0. doi: 10.7759/cureus.63039. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 27.Causes and treatment of idiopathic benign paroxysmal positional vertigo based on endocrinological and other metabolic factors. Guerra J, Devesa J. J Otol. 2020;15:155–160. doi: 10.1016/j.joto.2020.04.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Exploring the link between traumatic brain injury and benign paroxysmal positional vertigo. Castillo-Bustamante M, Ramos BF, Whitney S, Zuma E Maia F, Cal R, Madrigal J. Cureus. 2025;17:0. doi: 10.7759/cureus.81847. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.The brain-body disconnect: a somatic sensory basis for trauma-related disorders. Kearney BE, Lanius RA. Front Neurosci. 2022;16:1015749. doi: 10.3389/fnins.2022.1015749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Identification of a genetic variant underlying familial cases of recurrent benign paroxysmal positional vertigo. Xu Y, Zhang Y, Lopez IA, et al. PLoS One. 2021;16:0. doi: 10.1371/journal.pone.0251386. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Clinical characteristics and risk factors for the recurrence of benign paroxysmal positional vertigo. Zhu CT, Zhao XQ, Ju Y, Wang Y, Chen MM, Cui Y. Front Neurol. 2019;10:1190. doi: 10.3389/fneur.2019.01190. [DOI] [PMC free article] [PubMed] [Google Scholar]