Circadian dysfunction and Alzheimer's disease – An updated review

Abstract

Alzheimer's disease (AD) is considered to be the most typical form of dementia that provokes irreversible cognitive impairment. Along with cognitive impairment, circadian rhythm dysfunction is a fundamental factor in aggravating AD. A link among circadian rhythms, sleep, and AD has been well-documented. The etiopathogenesis of circadian system disruptions and AD serves some general characteristics that also open up the possibility of viewing them as a mutually reliant path. In this review, we have focused on different factors that are related to circadian rhythm dysfunction. The various pathogenic factors, such as amyloid-beta, neurofibrillary tangles, oxidative stress, neuroinflammation, and circadian rhythm dysfunction may all contribute to AD. In this review, we also tried to focus on melatonin which is produced from the pineal gland and can be used to treat circadian dysfunction in AD. Aside from amyloid beta, tau pathology may have a notable influence on sleep. Conclusively, the center of this review is primarily based on the principal mechanistic complexities associated with circadian rhythm disruption, sleep deprivation, and AD, and it also emphasizes the potential therapeutic strategies to treat and prevent the progression of AD.

INTRODUCTION

Alzheimer's disease (AD) is the most common type of neurodegenerative disorder, which largely causes dementia and mainly affects older aged people. By the year 2050, around 12 million cases will be reported.^1,2 In AD, accumulation of amyloid beta and hyperphosphorylated tau are microscopic pathologies, whereas reduction in hippocampal volume, frontotemporal, and associated cortical atrophy with ventricular enlargement are macroscopic findings.^3–5 To rule out AD, multiple biomarkers are available, like cerebrospinal fluid (CSF) molecules (for example, amyloid and tau), and to see atrophy in the brain, various neuroimaging techniques, such as computed tomography, magnetic resonance imaging, or positron emission tomography (PET). Current pharmacological treatments include donepezil, galantamine, and rivastigmine, which work as cholinesterase inhibitors. Memantine works as an N-methyl D-aspartate antagonist and Abun approved this in 2021.^6,7 Most current studies focus on the molecular aspect of AD, which mainly focuses on neuroinflammation, mitochondrial dysfunction, and glial cell activation.⁸ Currently, researchers focus on circadian rhythms, which help the researchers to understand AD pathophysiology in a relatively comprehensive and satisfactory way and also help to address or develop therapeutic targets of AD. Sleep disruptions and circadian disorders are quite common; around 45% of patients face problems with sleep.^9,10 These symptoms are present for several patients with AD even before the final medical diagnosis of AD. Based on multiple studies, it is seen that sleep disturbances can lead to neurodegeneration and even cognitive impairment. In the future, it can be utilized as a biomarker for neurodegeneration. In one study, it is seen that older women with diminished and irregular circadian rhythms have a higher risk of developing one of the types of impairments of AD, such as mild cognitive impairment and dementia. Various studies suggest that 25%–66% of patients with AD face sleep disruption, which can be easily noticeable.^11–17 Melatonin (N-acetyl 5–methoxytryptamine) is a hormone regulated by the circadian rhythms, and it plays a vital role in the neurodegenerative event of AD.¹⁸ The primary source of melatonin is the brain's pineal gland, but other organs like the retina, bone marrow, kidney, pancreas, skin, and glial cells are also involved. Melatonin is a multifunctional hormone that regulates circadian rhythm and shows anti-inflammatory, cytoprotective, and anti-oxidant properties. The circadian clock regulates melatonin and during a study in rat and mice models, melatonin shows the highest plasma melatonin level at midnight.^19,20 Melatonin production decreases with aging which can be considered a critical factor for the onset of AD. When impairment or disruption is seen in the suprachiasmatic nucleus (SCN), melatonin levels are reduced, resulting in circadian rhythm disruption.^21–23 Even reduction in CSF is linked with melatonin, and, finally, melatonin progresses AD by causing oxidative damage in the AD brain. Patients with AD have a low level of melatonin as compared with healthy patients. Melatonin can be a promising therapeutic approach to inhibit AD progression as it has free radical scavenging properties as well as anti-amyloidogenic properties. Melatonin also inhibits the secretion process of soluble amyloid precursor protein (APP) in various cell lines through APP maturation. Melatonin administration attenuates amyloid beta generation and deposition in vitro and in vivo models.^24–34 A sundowning phenomenon enhances mental health decline, confusion, and agitation in patients with AD, whereas melatonin reduces the symptoms of sundowning and enhances cognition. In this review, we discuss the association of circadian dysfunction with AD pathology as well as a few pharmacological and non-pharmacological interventions for sleep disruption in patients with AD.^35–39

CIRCADIAN BIOLOGICAL CLOCK MECHANISM IN THE BRAIN

A core gene of the circadian clock, the Period (PER) gene, was the first clock gene to be discovered by Jeffrey C. Hall and Michael Rosbach. The (PER protein is produced mainly at night and broken down during the day, and this whole cycle is regulated with the help of a negative feedback loop where PER protein blocks its production.^40,41 This protein is encoded by the PER gene. Recently, a new gene which is known as the double-time (DBT) gene, has been discovered to encode DBT protein. The DBT protein averts the PER accumulation, proving that rhythm can be flagged according to the 24 hour biological clock. Circadian rhythm regulation is observed both at the central and peripheral levels. In 2017, Jeffrey C. Hall, Michael Rosbash, and Michael Wyong uncovered the molecular mechanisms regulating circadian rhythm and received the Nobel Prize in physiology or medicine. This mechanism demonstrates that mammals have a central pacemaker called the SCN in the hypothalamus. When the retina gets photic input, it transmits information to the SCN. This central clock regulates the circadian rhythm throughout all body functions through the peripheral autonomic nervous system and hormonal factors. The circadian system is a web of interlinked feedback loops and oscillators across all organisms. The Period (PER 1–3), Cryptochrome (CRY1 and 2), and Reverb (NR1D1 and NR1D2) genes are negative feedback regulators which suppress the positive limb. The SCN helps in the synchronization of cellular oscillators across organs in humans. The retina sends light and dark signals to the SCN, which further regulates it. It synchronizes the core clock oscillations in neurons, ultimately translated into oscillatory synaptic output, which transfers the signals to the multiple nuclei in the hypothalamus. All these patterns in neuronal activity, and behavioral and physiological arrhythmicity can be lost post ablation of the SCN.^40–45 The circadian clock system is shown in Figure 1, and relationship between circadian rhythm and AD is shown in Figures 2 and 3.

FIGURE 1. Twenty-four hour biological clock in the human brain and its circadian disruption

FIGURE 2. Crosstalk between sleep deprivation and Alzheimer's disease. Aβ, amyloid beta

FIGURE 3. Linkage between circadian rhythm and Alzheimer's disease. Aβ, amyloid beta; EEG, electroencephalogram; nREM, non-rapid eye movement; SCN, suprachiasmatic nucleus

CHOLINERGIC DISTURBANCES AND CIRCADIAN DYSFUNCTION IN AD PATHOLOGY

Neurodegeneration can also be seen in the basal cholinergic forebrain. Disruption in circadian rhythm can also occur due to cells of the nucleus basalis magnocellularis, which projects to the SCN. Enrhardth reported that in rats, there are increased phase delays in response to lights when the cholinergic basal forebrain projects to the SCN. This study suggests a relationship between AD neurodegeneration and the circadian clock's signal entrainment ability.^46–48

NEURONAL LOSS IN THE SCN AND CIRCADIAN DYSFUNCTION IN AD

During the autopsy of patients with AD, it was seen that there is a neuronal loss in the SCN, which is related to loss of amplitude in the circadian rest-activity pattern. Apart from MT1, melatonin receptor expression was disturbed, which resulted in the SCN responding to the phase resetting signal and generating daily rhythms.^49,50

RETINAL GANGOLIAN CELL LOSS AND CIRCADIAN DYSFUNCTION IN AD

A particular type of subset of retinal ganglion cells (RGCs) known as Melanopsin expressing RGCs (mRGCs) was discovered in 2002. These cells are photoreceptors inside the retina, which help in the photoentrainment of circadian rhythms by projecting light to the SCN. Melanopsin expressing mRGCs constitutes 1%–2% of all RGCs, but they can direct signals to the SCN through the retinal hypothalamic tract. In patients with AD, mRGC loss can be seen, which can cause amyloid beta deposition, and lead to impairment of the entire RGCs even though there is a deposition of amyloid beta in mRGCs. The Toronto study shows interesting results involving retinal amyloid beta deposition in patients with AD. These findings will help better understand the pathology of retinal amyloid beta deposition in patients with AD. Amyloid beta deposition in mRGCs can lead to instability in transmitting the circadian signal of light from the retina to the SCN.^51–55

CIRCADIAN GENE DELETION AND CIRCADIAN DYSFUNCTION IN AD

Deletion mutations in the circadian clock gene cause neuronal injury. Core circadian clock disruption is directly linked to neurodegeneration in AD. BMAL1 is considered to be one of the core genes of the master clock, and a study conducted in mice has shown the deletion of BMAL1 in the hippocampus and cortex. In mice, we observe normal behavioral rhythms and normal sleep wake cycles assessed by wheel running actigraphy and electroencephalogram, respectively, in the presence of severe cortical astrogliosis, synaptic degeneration, and oxidative brain region damage in specific BMAL1 knockout mice. These mice are closely related to transcription multiple redox defenses linked with circadian impairment. Low levels of BMAL1 in the brain also lead to neurodegeneration caused by mitochondrial toxin B nitropropionic acid. The data suggest that decreased BMAL mediated transcriptional exacerbate neurodegeneration in AD. Clock-gene regulation and better insight into the linkage of clock genes and neurodegeneration require further research and a deeper understanding to examine such regulations.^56–59 The effect of different clock genes on animal models is shown in Table 1.

TABLE 1 Effect of different clock genes on different animal models

Subject no.	Different models	Effect of clock genes on different circadian models	References
1.	APP-PS1 mouse model	Casein kinase 1 isoforms ε and δ with inhibitor PF-670462 reduce amyloid and plaque size as well reduce Aβ signal in the prefrontal cortex and hippocampus, which proves chronotherapy as a promising tool to improve behavior in mice	103
2.	Two-month-old female APPSwe/PS1dE9 mice	Female APPSwe/PS1dE9 mice show abnormal locomotor activity in which clock gene expression of clock genes Per 1, Per 2, Cry 1, and Cry 2 was increased during night time compared to day type in wild type control mice as Cry 1 and Cry2 expression was low in APPSwe /PS1dE9 mice. This study proves APPSwe /PS1dE9 mice as a most promising AD model to test therapeutic agents related to behavioral and circadian rhythm changes.	104
3.	Cultured fibroblasts and brain samples	BMAL1 is a positive regulator of the circadian clock, and in cultured fibroblasts, DNA methylation regulates BMAL1 rhythms which is linked to circadian alteration in AD	105
4.	Tg 4510 mice	In Tg4510 mice, it is seen that there is tauopathy in SCN and even disruption in PER2 and BMAL1 in the hypothalamus of Tg4510 mice. This study proves that tauopathy can lead to normal circadian clock function disruption.	106
5.	AD brain	In this study, the glial fibrillary acid protein in human astrocytes is suppressed as there is an elevation in CLOCK and BMAL, which cause functional impairment by inhibition of aerobic glycolysis in AD	107
6.	5XFAD mouse model	Rev-erbα, a circadian repressor, decreases amyloid plaque number and size in the 5XFAD AD mouse model. Even Rev-erbα show a neuroinflammatory effect, which proves Rev-erbα as a novel therapeutic target.	108
7.	APP/PS1dE9 mice	In APP/PS1dE9 mice, there is an alteration of rhythmic expression patterns of BACE 1 and ApoE in the hippocampus, which is activated by E4BP4 and BMAL1, respectively. So, finally, study suggests that hippocampal clock and circadian oscillation of AD risk gene are regulated by orexin signaling.	109

Abbreviations: Aβ, amyloid beta; AD, Alzheimer's disease; SCN, suprachiasmatic nucleus.

MICROGLIA, ASTROCYTE, AND CIRCADIAN DYSFUNCTION IN AD

Activation of microglia and astrocyte leads to neuroinflammation, which ultimately causes neurodegeneration. Astrocyte activation can be observed to model clock gene deletion in the in vitro model. Even the inflammatory response of microglia leads to variation in the functional circadian clock. Rev-Erb alpha regulates pro-inflammatory cytokine production in macrophages. Finally, inflammation shows the effect of the circadian clock as both Rev-Erb alpha suppressing BMAL1 levels in macrophages in response to lipopolysaccharides. Therefore, the BMAL1 expression in the surrounding glia and neurons can be suppressed by cortex inflammation causing impairment of BMAL1-associated genes, ultimately leading to neurodegeneration.^56,60

OXIDATIVE STRESS AND CIRCADIAN DYSFUNCTION IN AD PATHOLOGY

Numerous studies support the presence of augmented oxidative stress in AD. Less concentration of glutathione and catalase with higher consumption of oxygen (20%–30%) and a higher amount of polyunsaturated fatty acids make the brain a highly vulnerable target for lipid peroxidation.^61–63 Lipids peroxidation interrupts cellular functions, followed by neuronal membrane destruction, and the production of highly reactive electrophilic aldehydes, including acrolein, malondialdehyde, and 4 hydroxy 2-nomial (elevated in AD brains).^64–66 Oxidative stress also damages nucleic acid and proteins. The role of oxidative stress etiology in AD pathogenesis is still unknown. In 1985, the activity of antioxidants, like superoxide dismutase and glutathione peroxidase with oxidative damage in the day-night cycle in the rat cerebral cortex, whereas in humans, anti-oxidants and circadian rhythmicity protect cells from oxidative damage.^67–70 The levels of glutathione reductase, glutathione peroxidase, superoxide dismutase, catalase, uric acid, and peroxiredoxin are high in the morning. In contrast, ascorbic melatonin and plasma level are high in the evening or night. This proves that oxidative stress leads to oxidative damage with the progression of AD, which is ultimately regulated by circadian dysregulation.⁷¹

ERK/MARK AND CIRCADIAN DYSFUNCTION IN AD

Cognitive impairment is the first symptom observed in AD. Impairment, such as memory, is enhanced by short-term stress and impaired by long-term stress, and the number of dendritic synapses decreases due to high cortisol levels during chronic stress.⁷² The pathway primarily revolves around memory consolidation, and the level of phosphor-ERK CAMP, phosphor CREB, and activity of PKA and MEK are associated with a circadian rhythm. Moreover, the SCN regulates the hippocampus' Camp/PKA/ERK/CREB signaling pathway.^73–75 The CREB/ERK/PKA/CAMP signaling pathway increases during rapid eye movement sleep. They are even ablating the BMAL1 gene results in reduced Per1 and PERK levels. A study reported that ERK appears overactivated and memory is improved by pharmacological inhibition of ERK in an AD mouse model, whereas memory impairment is seen due to reduction of pCREB level downstream of the ERK pathway.⁷⁶ ERK signaling pathway is disrupted in AD due to amyloid beta^1–42 bind injury. Finally, ERK/MAPK signaling pathway is a common pathway that causes stress as circadian rhythm even plays a role in memory consolidation.⁷⁷

HPA AXIS AND CIRCADIAN DYSFUNCTION IN AD

HPA axis activation promotes AD pathogenesis. Even reducing cortisol levels by taking dexamethasone does not show positive results in patients with AD; instead of cortisol levels, few approaches to decrease and modulate HPA axis activity can be a promising avenue for treating AD. Even amyloid beta promotes HPA axis activity and increases corticosterone. The HPA axis is one of the common pathways by which SCRD and stress increase amyloid beta production, leading to AD.⁷⁸

HIPPOCAMPAL VOLUME AND CIRCADIAN DYSFUNCTION IN AD

Reduced hippocampal volume was observed in AD and different neurodegenerative and psychiatric disorders. It is hypothesized that prolonged sleep restriction or sleep disruption can cause a decrease in hippocampal neuronal cell proliferation and neuronal cell survival. Few preliminary clinical trials and observational studies suggest that regular physical exercise, cognitive stimulation, and general medical conditions can reduce hippocampal volume or atrophy, reverse hippocampal atrophy, or even expand the hippocampal size.^79,80

GLYMPHATIC SYSTEM AND CIRCADIAN DYSFUNCTION IN AD

The glymphatic system was first described in 2012, which consists of intestinal fluid that regulates brain amyloid clearance by the perivascular space surrounding blood vessels. Glymphatic system dysfunction also plays a vital role in the severity of AD. To date, no clinically approved system has been developed to evaluate the functionality of the glymphatic system in humans. Recently, the glymphatic system has even played a role in glaucoma pathogenesis, characterized by progressive degeneration of RGCs and amyloid beta accumulation. This activity is higher during sleep and low during wakefulness. Even body posture during sleep, especially lateral body position, may increase the rat's glymphatic transport. Further studies need to be done to see the relation of the glymphatic system with patients with AD.^11,81,82

PROTEOSTATIS AND CIRCADIAN DYSFUNCTION IN AD

Amyloid beta and tau are specific protein hallmarks seen in AD. Heat shock factor 1 is a type of factor in which deletion alters circulation clock oscillation. Proteasomal degeneration of proteins display oscillations in circadian patterns and expected circadian clock timing requires an understanding of the proteasome function. It is still unknown how the circadian clock controls rhythmic protein degradation in the brain.⁸³

VASCULAR AND CIRCADIAN DYSFUNCTION IN AD

Microvascular change is considered an essential factor in the development of AD. Cerebral vascular perfusion is also under the control of the circadian system. According to PET scans and simple-photon emission computed tomography, people with moderate cognitive impairment and an increased risk of developing AD exhibit hypometabolism and cerebral hypoperfusion. Antihypertensive treatment has also been shown to reduce the risk of AD. Brain microvascular changes are critical to AD development, both pathologically and clinically. The circadian system regulates cerebral vascular circulation as well.^84–86 Conroy et al investigated the daily regularity of cerebral blood flow velocity (CBFV) across 30 hours of continuous awake time. The findings of this study suggested that human CBFV probably follows an endogenous circadian rhythm, which will be investigated further in the context of cerebrovascular/cardiovascular events and cognitive function deterioration.^87–89 Laser-Doppler flowmetry revealed similar results in rats. The cerebral blood flow has a diurnal periodicity independent of locomotor activity and blood pressure changes. The effect of the circadian rhythm on brain metabolism and perfusion should be carefully considered in future studies on the role of vascular function in AD etiopathogenesis.^90–92

METABOLIC CHANGES AND CIRCADIAN DYSFUNCTION IN AD

Circadian/sleep disruption may be mediated by metabolic changes in neurodegenerative disorders, particularly AD. Insulin resistance has been linked to an increased risk of AD in clinical studies, and childhood obesity can also cause cognitive impairment later in life apart from diabetes. Apolipoprotein E (APOE) is a key regulator of lipid metabolism found primarily in brain astrocytes. The APOE 4 allele can cause mitochondrial dysfunction, leading to insulin resistance and metabolic defects as a major risk factor for AD.^93–98 A recent study suggests that peripheral metabolic dysfunction plays a role in the development of AD-related neuropathology. The clock regulates the majority of metabolic activity, and the loss of circadian clocks has been linked to cellular and system-wide metabolic deficits. Sleep deprivation significantly impacts metabolism, including an increase in insulin resistance markers. Based on these findings, it is enticing to believe that sleep disruption increases the risk of AD by disrupting metabolism.^99–102

MELATONIN AS A PROMISING THERAPEUTIC TARGET FOR AD

In AD, melatonin has shown multiple beneficial effects, like prevention of mitochondrial dysfunction, inhibition of amyloid beta toxicity, free radical scavenging, and even circadian dysregulation like sundowning and sleep disturbances.¹¹⁰ Melatonin even has blood–brain barrier crossing capacity, anti-oxidant properties, as well as balanced amphiphilicity. Amyloid beta peptides are mainly produced with the help of amyloidogenic beta-amyloid precursor protein (beta APP). Amyloid beta 42 is the most neurotoxic form of amyloid beta. This beta pleated sheet peptide ultimately forms an aggregation of senile plaques in the brain in the form of amyloid fibrils that disrupts synaptic communications leading to abnormal function of neurons and neuronal death. As melatonin has anti-oxidant, neuroprotective, and anti-amyloidogenic properties, it might help in decreasing amyloid beta formation. Melatonin has shown effects on both in vivo and in vitro models.^111–115 Hyperphosphorylated tau plays a crucial role in dealing with memory and cognitive impairment in AD. Neurodegeneration happens due to tau hyperphosphorylation. This tau phosphorylation and protein kinase A (PKA) overactivation in the isopropanol-induced rat brain can be attenuated by melatonin. This process is followed in the neuroblastoma SHSY5Y cell line and N2a induced by calyculin A, okadaic acid, and wortmannin. Melatonin shows neuroprotective effects in the degeneration of the hippocampus and enhances cognitive effects. These effects are displayed through regulating GSK3 and CDK5 activities in hippocampal neurons. Melatonin inhibits the expression level of caspase 3, prostate apoptosis response 4 (Par4), and Bcl2 associated BAX, reducing neuronal death.^116–121 Melatonin has an anti-oxidant property that reduces oxidative stress. In an experimental study, it was observed that NF-KB commenced IL-6 in amyloid beta treated brain slices can be inhibited by melatonin in a concentration-dependent fashion. Melatonin injection (ie, 5 mg/kg, 0.1 to 10 mg/kg, and 10 mg/kg) in the rat in which melatonin shows anti-inflammatory effects and reduces neuroinflammation by increasing ATP production, stimulating GPX activities, and even enhances SOD activity.¹²² Therefore, this evidence shows the anti-neuroinflammatory effects of melatonin on AD.

RELATION AMONG EXERCISE, CIRCADIAN RHYTHM, AND AD

Various animal models show exercise chronobiotic properties. It is difficult to identify whether exercise has chronobiotic properties in humans because it is quite hard to differentiate the range of effects shown by exercise from multiple other factors, like food, social influences, and light.¹²³ Non-photic stimuli, on the other hand, appear to be capable of synchronizing circadian rhythms in people who are blind who lack sensitivity to light, and this helps them entrain to routine schedules without utilizing exogenous melatonin. A recent study related to circadian rhythms and AD has shown that when a person exercises just before habitual sleep, it accelerates circadian rhythm and if it is performed during habitual sleep time, it delays circadian rhythms.^124–126 Exercise also affects the hippocampus, which plays a role in affecting sleep quality. It has also been reported that people who do exercise regularly on a daily basis have better sleep quality as well as less daytime sleepiness when compared to people who are inactive and do not exercise. As a result, it is still possible that exercise has a greater impact on older adults who face difficulty in sleeping. Exercises also enhance the cognitive part and show neural plasticity which is effective in normal aging as well as a treatment for AD.^127–132 Sleep after exercise has a well-known effect on cognitive performance. According to the recent study findings, physical activity plays a huge role in diminishing the effects of poor sleep quality on cognitive functioning in older adult women. As a result, more research is needed to understand the mechanisms underlying exercise, sleep, and cognitive function that are linked in older adults.^133–138

CURRENT THERAPIES AND FUTURE IMPLICATIONS

Unfortunately, at present, we have limited pharmacological and non-pharmacological interventions to manage sleep disturbance in patients with AD. In AD, current behavioral practices include limited caffeine and alcohol intake, regular exercise, and maintaining regular bed and wake times with ample light exposure upon waking.⁶⁰ Sufficient daytime light exposure is crucial for patients with AD, mainly for institutionalized patients. Consistent light exposure may bring changes in dysfunctional circadian rhythms in AD and reduce the “sundowning.” Patients with moderate-to-severe AD were included in the melatonin and trazodone trials, but only patients with mild-to-moderate AD were included in the ramelteon study. Melatonin is considered a part of various clinical manifestations and treatment strategies of AD.^139–141 Actigraphy is used to measure all primary sleep outcomes. Despite the absence of severe side effects, we still have no evidence to suggest that melatonin and trazodone improve sleep quality. More comprehensive clinical trials are desperately needed in this area, particularly those focusing on sleep and cognitive or pathological outcomes in AD. Suvorexant is the first US Food and Drug Administration (FDA)-approved orexin receptor antagonist which can show effects on amyloid deposition and cognitive end points in early-stage or presymptomatic AD. Melatonin supplementation on a regular basis may help patients with mild cognitive impairment improve their cognitive performance slightly. However, there appears to be conflicting evidence in mice regarding the effectiveness of melatonin supplementation in reducing amyloid plaques and other AD correlates. Ramelteon has been approved for insomnia, whereas tasimelteon is for the treatment of non-24 hour sleep–wake disorder in the blind. Until now, these two drugs have not been tested for AD but can be more effective than melatonin. Researchers are trying to develop a drug that can directly target the circadian clock, although they are still in the early stages of development. Small molecules that can alter circadian oscillations' amplitude, frequency, and period have been discovered through high throughput screening. RevErb is a small molecule agonist of the nuclear receptor that can improve metabolic function in mice by directly affecting circadian rhythms. Finally, the right targeting of the circadian clock could be a promising remedial option for treating AD.^33,34

CONCLUSION

The pathology of AD (amyloid and tau) has been linked to circadian dysfunctions, and sleep disruptions are very common in patients with Alzheimer's disease that play an important role in disease succession and pathology. Moreover, circadian rhythms communicate with nearly all systems and risk factors involved in the growth and progression of AD. Recognizing early signs of AD, such as changes in sleep patterns and rest-activity rhythm anomalies, could be useful in identifying early biomarkers for interference to prevent the formation of amyloid-beta, neurofibrillary tangles and the succession of neurodegeneration. In patients with advanced AD, bright light therapy combined with chronobiotics is effective in treating sundowning characteristics and other cognitive symptoms. Future research into the function of circadian misalignment in the initial stages of AD could lead to new preventive and therapeutic approaches. As a result, circadian rhythms are an excellent target for combating pathology.

AUTHOR CONTRIBUTIONS

Manuscript writing and drawing figures: Faizan Ahmad. Manuscript writing, reviewing, and editing: Punya Sachdeva. Editing: Jasmine Sarkar. Reviewing: Rafiah Izhaar.

FUNDING INFORMATION

No funding was received for this study.

CONFLICT OF INTEREST

The authors declare they have no conflict of interest.