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Advanced Neurology                                 BRRS: A screening and monitoring tool for better prognosis in AD



            improvement in the patient’s condition, for example, a   the  disease,  the compensatory  ability  deteriorates  and
            patient under 65 years old who scored in the weight item   eventually reaches a point of exhaustion due to extensive
            in S  but whose body mass index (BMI) has returned   neurodegeneration . Based on these findings, we suggest
                                                                              [32]
               0
            to normal at present, the improvement can only help to   scoring each brain region by assessing the functional
            potentially slow down the rate of disease deterioration,   connectivity, structural connectivity, and compensation
            making no difference to the reduction of the high AD   patterns as follows: (1) Functional damage (add 100
            risk level that has resulted from the former morbid state.   points); (2) structural damage of white matter (add 100
            Consequently, the S  assessment of the weight items in the   points); structural damage of gray matter (add 100 points);
                            n
            aforementioned case should be as follows: (1) If <65 years   (3) functional compensation (add 100 points); structural
            old but with normal BMI, no extra points will be added   compensation (add 100 points); and (4) decompensation
            or deducted; (2) if over 65 years old, the weight item will   or the disappearance of previously observed compensation
            be graded according to the over 65-year-old standard.   (add 100 points for each disappearance). The gray and
            As far as other items are concerned, for the same reason,   white matters are evaluated separately because there is
            once any item in O has scored points, there is no need to   no causal relationship in the damages between the two
            reappraise it at further tracing, that is, points should not   in AD. Meanwhile, white matter hyperintensity (WMH),
            be deducted, and the score should remain unchanged. Due   which represents vascular pathology and decreasing blood
            to the minimal change in the original score regardless of   flow and is considered a manifestation of cerebral small
            whether the patient’s condition becomes better or worse, it   vessel disease [33,34] , is associated with an increased risk of
            can be said to be a reliable index to assess the baseline risk   developing AD . Hence, if WMH is observed, add 100
                                                                           [35]
            level of AD patients.                              points. In every S  evaluation, score the changes as follows:
                                                                             n
              Part V consists of items related to the aberrant brain   (1) Grade all changes in each brain region based on the
            alterations of AD-spectrum patients who are detected   standard and (2) no extra points added or deducted with
            by neuroimaging techniques. As a brief scale for ease of   the disappearance of WMH that was previously observed.
            use and promotion, we choose MRI, the most commonly   It is known that the development of a disease is
            used imaging modality for AD patients in current clinical   influenced by  the interactions  among various factors
            practice, of difference sequences (i.e., sMRI, fMRI, and   and the modifiable network of interlocking feedback
            diffusion tensor imaging [DTI]) for evaluation at the   loops [12,36,37] .  However,  the  intention  of  introducing  the
            structural and functional levels. The evaluation standard   BRRS is to provide a preliminary screening and monitoring
            is based on the MRI features of AD that has been   tool that can be conveniently and effectively applied in
            comprehensively summarized from the previous studies   clinical settings with little additional burden added and
            (additional information can be found in Tables S1-S3). It   time consumed. Therefore, we propose a method with
            has been proven that different network types and functions   similar items but a larger value for each item to ensure
            may exist in the same region of the brain whose alterations   the ability to distinguish patients with a higher risk of
            are not linear across the AD continuum [5,20] . Besides, the   AD progression, thus serving as a replacement for the
            stimulation of non-invasive techniques, such as repetitive   extremely complex weighted coefficient in the interactions.
            transcranial magnetic stimulation and transcranial pulse
            stimulation (TPS), targets the surface area of the brain and   4. Discussion
            is unable to differentiate between gray and white matters   4.1. Advantages and characteristic of BRRS
            or  between  network  modules  or  types [13,26] .  Therefore,
            part V focuses on six brain regions, including the limbic,   The BRRS may be used as a supplementary method for
            frontal, parietal, temporal, and occipital regions as well   diagnosing AD with the following advantages: (1) Enabling
            as the cerebellum. Neural plasticity, which represents the   objective quantification of individual differences in terms
            adaptability and flexibility of the brain, contributes to a   of AD risk factors and neuroimaging abnormalities;
            compensatory phenomenon against impairment in the   (2) enabling early identification of patients at increased
            AD spectrum, including the abnormal hyperactivation   risk of rapid deterioration from those diagnosed in the
            or increased connectivity in multiple brain regions .   same stage; (3) enabling individually tailored intervention
                                                        [27]
            This compensatory phenomenon can be  viewed as a   based on individual’s respective scored items; (4) enabling
            process of brain  reconstruction or  function remodeling   convenient  monitoring  and  assessment  of  individual’s
            to sustain optimal network functioning [28,29] ; on the   trajectories of brain changes, disease development, and
            other hand, it can also be explained as a pathological   therapeutic effect at follow-up; (5) reducing the time
            state that may lead to further brain damage as a result   consumed and errors in calculation with the same but
            of neuronal excitotoxicity [30,31] . With the progression of   larger valued items, and enabling efficient judgment from


            Volume 1 Issue 3 (2022)                         6                       https://doi.org/10.36922/an.v1i3.208
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