This was a large, single-center, observational retrospective study that involved 665 patients with a clinical diagnosis of aSAH from April 2020 to January 2022. In addition, strict inclusion and exclusion criteria were established to ensure comparability of data and credibility of results. Women (424/665, 63.8%) were more vulnerable to have aSAH compared to men, and women were older. In our study, after adjusting for age, hypertension, diabetes, smoking, drinking, location and size of ruptured aneurysm, WFNS grade, Hunt Hess grade, mFS score, and treatment approach, the results showed that females were more likely to have DCI, with a higher incidence of poor prognosis at 3 months after discharge. In our study, females were approximately twice as likely as males to have a ruptured aneurysm, which is consistent with previous studies[5, 12].
In 665 patients with aSAH, our study found no significant difference in prognosis between male and female[7]. However, the age difference between female and male patients may lead to a comparison bias between the two groups. In addition, the different basic characteristics of aneurysms, comorbidities and treatment approaches in female and male patients may have an influence on the comparison between the two groups[13]. However, in our study, the ratio of female patients with mRS score ≥ 2 was significantly higher than that of male patients after adjusting for age, aneurysm characteristics, comorbidities, WNFS grade, Hunt Hess grade, mFisher score, and treatment approach.
It has been shown that DCI and hydrocephalus are two critical complications that affect the prognosis of aSAH[14]. After PSM, our study found that the incidence of DCI was significantly higher in female aSAH patients than in male patients, consistent with other studies[3, 15–17]. The poor prognosis of females with aSAH may be due to the fact that females are more prone to vasospasm[18]. Studies have shown that early vasospasm predicts a higher incidence of cerebral ischemia associated with subarachnoid hemorrhage and a poorer prognosis[19]. Women have been reported to be an independent risk factor for cerebral vasospasm after aSAH[20, 21]. In addition, catecholamine metabolites reflecting sympathetic excitation have been found to have higher levels in the cerebrospinal fluid of female patients with SAH, which also suggests that they are more prone to vasospasm[22]. Moreover, estrogen may play a protective role in vascular system mainly through its influence on the proliferation and migration of vascular smooth muscle cells[23]. Therefore, because of the decrease of estrogen in postmenopausal women, the role of vascular smooth muscle cells in the vascular system in the physiological and pathological process is affected to a certain extent. This may be a factor in the poor prognosis of some women with ruptured aneurysms, especially those near or past menopause. However, the role and mechanism of estrogen in subarachnoid hemorrhage diseases still need to be further studied.
Furthermore, sharp and abrupt decreases in estradiol concentrations during menopause, combined with genetic predisposition and environmental factors, may disrupt cerebrovascular homeostasis[24]. Increased hemodynamics and oxidative stress may trigger an inflammatory cascade response leading to macrophage, neutrophil, and chemotactic infiltrates that promote chronic inflammation in cerebral arteries. These changes lead to vessel wall degeneration, focal weakening, and cerebral arterial wall ectasia, ultimately leading to aneurysm formation and rupture, thus making postmenopausal women more susceptible to aneurysm rupture leading to aSAH[24].
In addition, after PSM, female patients with aSAH were more vulnerable to hydrocephalus than male patients in our study. Experimental studies in rats have shown that females have a higher risk of hydrocephalus after SAH[25]. In addition, clinical studies have found that females have a high risk of developing hydrocephalus after aSAH[26, 27]. This sex difference may be related to the role of estrogen in maintaining vascular integrity by reducing oxidative stress[24]. In addition, women have higher concentrations of norepinephrine and dopamine metabolites in the cerebrospinal fluid compared to men, therefore women are at a higher risk of developing hydrocephalus[22]. However, reports have shown no finding that female patients with aSAH are more vulnerable to hydrocephalus[17].
Besides confirming that female sex is independent risk factors for poor prognosis after ASAH, our results showed that age, smoking, high Hunt Hess grade, high mFisher score, DCI, and hydrocephalus are independent risk factors of poor prognosis[18]. We observed that high Hunt Hess grade, high mFisher score were more common in women whereas smoking was more frequent in men. In our study, older age was also an independent risk factor for poor prognosis, which is consistent with other studies[28, 29].
We reviewed clinical and imaging records and included only confirmed first-time ruptured intracranial aneurysm cases. Our study found that females were more likely to have aSAH and that females were an independent risk factor for poor prognosis, which may be related to the fact that females are more vulnerable to DCI and hydrocephalus. However, the reasons and mechanisms for this sex difference and whether it is related to estrogen remain unclear[30, 31]. Therefore, a rapid diagnosis and amelioration of DCI and hydrocephalus is important to improve the prognosis of patients with aSAH, especially in women, who have a higher morbidity.
Most studies show that the average size of a ruptured aneurysm is less than 7 mm[32]. Post-rupture thrombosis of the aneurysm lumen may explain why the diameter of many of the ruptured aneurysms in our series was relatively small. An additional factor that has biased our study cohort towards smaller ruptured aneurysms, is the fact that the higher cost of treating larger ruptured aneurysms led to earlier retrieval of care for many of the patients with larger aneurysms. We hope to address this bias in our future studies.
It’s worth mentioning that in our research, the proportion of patients with a history of alcohol consumption was high (134/665, 20.2%), and about 5:1 between men and women with a history of alcohol consumption, which may be related to the habits formed by the cold climate of the region. In this study, in order to exclude the influence of other factors and only consider the effect of gender on the prognosis of aSAH, we matched the propensity scores of hypertensions, diabetes, smoking and drinking in different genders, so we did not investigate the effect of drinking history on the prognosis of SAH. We did not have separate statistics on the effect of alcohol consumption on prognosis. However, it does not mean that alcohol consumption has no effect on aSAH prognosis. Some studies have shown that the patient proportion of alcohol consumption was dramatically greater in males than that in females[33]. Patients with alcohol consumption are at higher odds of angiographic vasospasm and delayed cerebral ischemia, which are related to poor prognosis following aSAH[33]. It remains to be further explored whether alcohol consumption has a significant impact on the prognosis of patients with aSAH by sex. In addition, the relationship between the location of the aneurysm and non-dominant hemispheres is crucial to the prognosis of the patient. Considering that the number of cases in this study is not enough, there are only 141 patients in each group after PSM. If divided according to the location of aneurysms and the non-dominant hemispheres, the number of patients who can be matched after PSM will be very small, which may affect the conclusion. In the next step, we will collect as many cases as possible, further classify the location of the aneurysm, and take into account the important factors such as the location of the aneurysm and the non-dominant hemisphere. In addition, smoking has a dose-dependent and cumulative association with SAH risk[34], whereas smoking was not quantified in our study.