Dear Dr. Finsterer,
It is challenging to answer point by point to your remarks in our article [1].
We clearly explained in our paper that we were investigating the use of microRNA (miRs). Our hypothesis is that microRNAs might be an interesting tool to study mitochondrial disorders and its multisystemic manifestations in Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) and we believe that researcher is fully aware of limitations mostly related to the use of preexisting data collected [2].
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We stated that additional clinical and experimental studies are necessary. Ideally, a clinical study should link the results of specific audiological and electrophysiological impairments with MELAS and, to the concentration of specific microRNAs. The necessity of prospective studies is clear due to the unspecificity of microRNAs [3], as you correctly underlined.
Our suggested microRNAs are the ones that have been identified in the human temporal bones of patients affected from MELAS [4]; thanks to the high quality of these studies the reported results are consistent and valid [5, 6].
We focused our attention on the variation of concentration of microRNAs only and not, on their multiple functions since this would need more experimental studies.
As far as the influence of aging, we reported that the temporal bones observed came from young subjects (“patients were under 30 years old”) and, in our opinion this is the strength of this research, in fact the “age” may be considered as a confounder if we consider the hearing impairment, that is a common finding in older age. Furthermore ROS that increase with age could be a common pathogenetic link to mitochondrial disorders, since mitochondrial deletions increase with age.
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We pointed out the heterogeneity of the human temporal bone and, we underlined different severities of hearing loss observed in MELAS patients are due to the stochastic segregation of mitochondria by determining changes of different entity and that involves different inner ear structures – spiral ganglion, vascular stria [5]. This is well documented by the fact that MELAS patient might have not only lactic acidosis but neurosensory hearing loss or the full MELAS syndrome.
I disagree with you, when you spoke about conductive form of hearing loss (HL) in patients with MELAS, your speculative statement is not correlated with that observed in human clinical observations, patients with MELAS are affected by a sensorineural form of hearing loss even if they present different severity of hearing impairment [1].
The central auditory pathways have been investigated from several authors in patient affected by MELAS [7, 8] by Auditory Brain Response (ABR) for evaluating the damage posterior to the cochlea and their results showed several discordant data [2], so we speculate to use miR-9/9*, that seems to be sensible to identify brain damage and that was validated by experimental data [9].
We included different type of studies in human temporal bones and clinical observations, that we analyzed for explaining that the biomarkers commonly observed in patients affected from MELAS (i.e. creatine kinase (CK), lactic acid) might add to the reported Magnetic Resonance Imaging (MRI) results in the temporal bone analysis.
We stated that hearing loss not only affects patients with MELAS, but also other mitochondrial disorders.
We think that microRNAs could be a valid biomarker for investigating the damage in hearing pathways, currently the method needs to be tested in prospective human clinical studies as first and, then if its accuracy will be confirmed microRNAs might be used in the screening of patients with sensory neural hearing loss.
Funding
supported by Telethon Grant GGP 14066 to C.A.
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Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.
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