Much of the epidemiologic research on intracerebral hemorrhage has concentrated on identifying risk factors for intracerebral hemorrhage. Not only do risk factors provide etiologic insights into disease, but in case of modifiable risk factors, these can also become targets for preventive or therapeutic strategies. Moreover, risk factors can be utilized for their predictive or diagnostic value. This latter notion also brings forth an important methodological consideration in epidemiologic studies on intracerebral hemorrhage. Clinically, intracerebral hemorrhage is usually subtyped according to location into lobar or deep intracerebral hemorrhage . This distinction is based on the presumed underlying etiology with lobar intracerebral hemorrhage thought to be caused primarily by cerebral amyloid angiopathy, and deep intracerebral hemorrhage more related to hypertensive vasculopathy. Similarly, another distinction of intracerebral hemorrhage is based on whether or not the intracerebral hemorrhage is related to warfarin use [7, 10, 14]. Whereas such distinctions may be useful in a clinical setting for prognostic and therapeutic stratification, for etiologic research it is important to note that intracerebral hemorrhage is a complex disease with multiple underlying etiologies and risk factors. An intracerebral hemorrhage is not caused by a single risk factor, but is more likely to be a result of a complex interplay of multiple risk factors—though a single or few risk factors may have a bigger role than others. Therefore, any distinction of intracerebral hemorrhage based on a single presumed underlying risk factor may preclude identification of additional risk factors. Nevertheless, having said this, we also note that such distinctions are useful if the aim is to identify risk factors that act in concert with either cerebral amyloid angiopathy or hypertension.
Abundant evidence, both from case–control studies and cohort studies, shows that hypertension is the single most important risk factor for intracerebral hemorrhage [15, 16••]. Most of the intracerebral hemorrhages due to hypertension are thought to occur deep in the brain parenchyma, although associations with lobar intracerebral hemorrhage have been reported . A meta-analysis across 11 case–control studies revealed that hypertensives had an almost 3.5-fold increased risk of intracerebral hemorrhage compared with normotensives . Another meta-analysis showed that self-reported hypertension or a measured blood pressure of >160/90 increased the risk of intracerebral hemorrhage more than ninefold [16••]. It should be noted that these risk estimates were not adjusted for potential confounding variables. Therefore, the true risk increase due to hypertension is likely to be smaller, but nevertheless still very substantial.
The increased risk associated with blood pressure does not seem to be restricted to clinical hypertension. Studies have shown that blood pressure increases within the normal range are also associated with a linear increase in the risk of intracerebral hemorrhage .
Given the strength of association, the high prevalence of hypertension, and the readily available treatment options, blood pressure control is considered the main option for prevention of intracerebral hemorrhage.
Studies have consistently shown tobacco use as a risk factor for intracerebral hemorrhage [19, 20], though the effect size is not as large as for hypertension. These studies almost exclusively focus on cigarette smoking, but there is no reason not to generalize these findings to other modes of tobacco use, such as pipes and cigars .
Studies have demonstrated a dose–response relationship with the number of cigarettes smoked and risk of intracerebral hemorrhage. Moreover, the effect of smoking extends to former smoking, albeit the risk is largest for current smokers. The reported relative risk of current smokers versus non-smokers lies between 1.3 and 1.5 [15, 16••].
Because the definition of high alcohol intake differs across various studies, it has been difficult to provide summary measures in meta-analyses. Nevertheless, there is compelling evidence relating high alcohol intake with a higher risk of intracerebral hemorrhage [15, 16••, 19]. Presumed pathways for this association include platelet dysfunction, coagulation disturbances, or endothelial damage. It is noteworthy that whereas for ischemic stroke moderate alcohol intake has been shown to be protective, the risk of intracerebral hemorrhage is increased suggesting a linear dose–response relationship between alcohol intake and intracerebral hemorrhage risk .
Cholesterol and Lipids
Increasing evidence from longitudinal studies suggests that hypercholesterolemia is associated with a lower risk of intracerebral hemorrhage [22, 23]. This is in contrast to earlier case–control studies that implicated high cholesterol as risk factor for intracerebral hemorrhage . The exact mechanism is still unclear but low cholesterol is thought to weaken the endothelial wall. More recent studies have investigated not only cholesterol, but several lipid fractions. These studies suggest that the associations with lipids are mainly driven by low triglyceride levels [25•]. How triglyceride levels lead to intracerebral hemorrhage still remains unclear.
Diabetes mellitus is of increasing interest as risk factor for intracerebral hemorrhage given the potential for relatively easy intervention and prevention strategies. A large meta-analysis of 102 prospective studies, including 698.782 participants, recently provided convincing evidence for diabetes as risk factor for intracerebral hemorrhage . The reported relative risk was 1.6 (95 % confidence interval from 1.2 to 2.1) for persons with diabetes compared to persons without diabetes. There is also evidence from other studies implicating diabetes mellitus as risk factor for intracerebral hemorrhage .
Cerebral Amyloid Angiopathy
After hypertension, the single most important risk factor for intracerebral hemorrhage is thought to be cerebral amyloid angiopathy. Cerebral amyloid angiopathy refers to the accumulation of β-amyloid in the media and adventitia of mostly cortical vessels, which can lead to leakage of blood through the vessel wall [27••]. Given the distribution of cerebral amyloid angiopathy, these intracerebral hemorrhage usually—though not exclusively—occur in the cortical brain regions, referred to as lobar intracerebral hemorrhage. The frequency of cerebral amyloid angiopathy is thought to increase with age, with almost half of all persons older than 90 showing some signs of cerebral amyloid angiopathy. Current estimates show that almost 50 % of intracerebral hemorrhages in a lobar region are related to amyloid angiopathy . Although this percentage is high for a single risk factor, it is important to keep in mind that the remaining 50 % are caused by other risk factors, many of which are still unidentified. Apart from intracerebral hemorrhage, cerebral amyloid angiopathy also increases the risk of Alzheimer’s disease, suggesting partly overlapping mechanisms between intracerebral hemorrhage and Alzheimer’s disease [27••].
Most research on cerebral amyloid angiopathy currently focuses on its early identification and risk stratification based on any such early markers (see section on pre-clinical imaging markers). However, the causes of cerebral amyloid angiopathy are still unknown. Apart from genetic influences no clear modifiable risk factors have been identified to date (see section on genetic risk factors). Therefore, primary prevention opportunities related to cerebral amyloid angiopathy as risk factor for intracerebral hemorrhage are limited.
Anticoagulant use, especially warfarin, is considered a risk factor of intracerebral hemorrhage. Evidence for this association comes from various sources [7, 10]. It is important to note, however, that benefits of warfarin far outweigh the increased risk of intracerebral hemorrhage associated with it. Still, this demonstrates the urgent need for better risk stratification strategies in order to better balance the benefits and adverse events associated with warfarin use. Given that warfarin use has rapidly increased in the last decades, studies have also shown a drastic increase in intracerebral hemorrhage related to warfarin use , though this notion is contested by other studies . The increased risk of intracerebral hemorrhage related with anticoagulants also extends to other coumarin derivatives, such as acenocoumarol and fenprocoumon, which are more often used than warfarin in European settings . Data on other anticoagulants are scarce, though there is a suggestion of an increased risk of intracerebral hemorrhage related with direct thrombin inhibitors . However, more data are needed before a more conclusive judgement can be made.
Likewise, a large meta-analysis showed that aspirin use increases the risk of intracerebral hemorrhage , though here too the benefits of aspirin far outweigh the potential risks associated with its use.
Genetic Risk Factors
Evidence for a genetic predisposition for intracerebral hemorrhage comes from family studies. Several single-gene disorders leading to intracerebral hemorrhage have been identified, and include familial cerebral amyloid angiopathy due to mutations in the APP gene and cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) due to mutations in the NOTCH3 gene . However, these monogenetic disorders are rare and explain only a small proportion of the genetic predisposition of intracerebral hemorrhage.
Instead, the genetics of primary intracerebral hemorrhage are thought to be more complex with many other genes involved each with a small individual effect . Because of their modest effect sizes, many of such genes are still unidentified. So far, only the APOE gene has been identified as a robust genetic risk factor for intracerebral hemorrhage. APOE is considered a strong risk factor for cerebral amyloid angiopathy and it is for a large part via this underlying etiology that APOE relates with intracerebral hemorrhage [27••]. However, APOE has also been shown to affect blood vessels via other mechanisms.
Apart from APOE, many other candidate genes have been implicated, although evidence for such genes has been limited. These genes include ACE, APOH, Factor VII and Factor XIII, and IL-6 . The advent of genome-wide association studies, in which hundreds of thousands of genetic markers are tested concomitantly, provides a unique opportunity to identify additional genes with modest effects. The success and feasibility of genome-wide association studies has already been demonstrated in ischemic stroke and dementia [33, 34]. However, the necessity of having large sample sizes currently limits the full potential of genome-wide association studies for intracerebral hemorrhage. Nevertheless, CR1, a novel gene for Alzheimer’s disease identified using genome-wide association studies, has also been implicated in intracerebral hemorrhage .
Emerging Risk Factors
Apart from the aforementioned risk factors, for which associations are robust and have been established, there are several other putative risk factors for which a solid body of evidence is emerging.
Regular physical activity has been suggested to be protective of intracerebral hemorrhage, though studies have not shown conclusive evidence [16••, 36]. Dietary factors have been implicated in intracerebral hemorrhage, although it is still unclear which dietary constituents drive this association [19, 37].
Emerging evidence further shows that poor kidney function is a novel risk factor for stroke, including intracerebral hemorrhage . This risk is not only restricted to patients with overt kidney disease, but seemingly extends to the general population. However, it is worth noting that not all studies find associations between markers of kidney disease and intracerebral hemorrhage . This shows the need for further studies on this relationship.
There is also increasing interest in body-mass index as risk factor for intracerebral hemorrhage , though it is likely not a direct cause but rather an indicator of an underlying process. Interestingly, both low and high body mass index increase the risk of intracerebral hemorrhage .