Recent Advances in the Pathophysiology of Fatty Acid Oxidation Defects: Secondary Alterations of Bioenergetics and Mitochondrial Calcium Homeostasis Caused by the Accumulating Fatty Acids

Deficiencies of medium-chain acyl-CoA dehydrogenase, mitochondrial trifunctional protein, isolated long-chain 3-hydroxyacyl-CoA dehydrogenase, and very long-chain acyl-CoA dehydrogenase activities are considered the most frequent fatty acid oxidation defects (FAOD). They are biochemically characterized by the accumulation of medium-chain, long-chain hydroxyl, and long-chain fatty acids and derivatives, respectively, in tissues and biological fluids of the affected patients. Clinical manifestations commonly include hypoglycemia, cardiomyopathy, and recurrent rhabdomyolysis. Although the pathogenesis of these diseases is still poorly understood, energy deprivation secondary to blockage of fatty acid degradation seems to play an important role. However, recent evidence indicates that the predominant fatty acids accumulating in these disorders disrupt mitochondrial functions and are involved in their pathophysiology, possibly explaining the lactic acidosis, mitochondrial morphological alterations, and altered mitochondrial biochemical parameters found in tissues and cultured fibroblasts from some affected patients and also in animal models of these diseases. In this review, we will update the present knowledge on disturbances of mitochondrial bioenergetics, calcium homeostasis, uncoupling of oxidative phosphorylation, and mitochondrial permeability transition induction provoked by the major fatty acids accumulating in prevalent FAOD. It is emphasized that further in vivo studies carried out in tissues from affected patients and from animal genetic models of these disorders are necessary to confirm the present evidence mostly achieved from in vitro experiments.

Mitochondrial trifunctional protein comprises three enzyme activities that catalyze the second, third, and fourth step of mitochondrial fatty acid oxidation cycle, namely, longchain enoyl-CoA hydratase, LCHAD, and long-chain ketoacyl-CoA thiolase. Two inherited diseases are caused by defects of this complex protein, the isolated LCHAD deficiency and MTP deficiency. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency is caused by a common mutation (c.1528 G > C) in the HADHA gene, whereas all other HADHA and HADHB mutations in this complex enzyme lead to MTP deficiency (De Biase et al., 2017).
Very long-chain acyl-CoA dehydrogenase is the first and ratelimiting intramitochondrial step in the mitochondrial oxidation of LCFA. The deficiency of this enzyme activity causes the most prevalent defect of LCFA β-oxidation. The affected patients commonly manifest hypoglycemia, cardiomyopathy, and recurrent rhabdomyolysis. Hypoglycemia usually occurs during 2-4 years of life, whereas rhabdomyolysis is manifested later, and cardiomyopathy can occur at any age. Patients may present three different clinical phenotypes: (a) a severe early onset manifestation with life-threatening cardiomyopathy associated with arrhythmias, hypotonia, hepatomegaly, and intermittent hypoglycemia, (b) an early childhood presentation with hypoketotic hypoglycemia associated with liver alterations and hepatomegaly, or (c) a late-onset myopathic form with recurrent episodes of rhabdomyolysis and muscle pain usually induced by exercise (Spiekerkoetter, 2010;Diekman et al., 2014;Katz et al., 2017;Leslie et al., 2019;Rovelli et al., 2019). Recurrent rhabdomyolysis is a common and acute complication of this disease and should be treated with hydration and alkalization of the urine to prevent acute renal failure secondary to myoglobinuria. Elevated levels of myristic (Myr) and cis-5-tetradecenoic (Cis-5) acids, as well as their acylcarnitine derivatives tetradecenoyl-L-carnitine (C14:1), tetradecadienyl-L-carnitine (C14:2), tetradecanoyl-L-carnitine (C14), and dodecanoyl-L-carnitine (C12), are commonly found in blood (McHugh et al., 2011).
The diagnosis of MCAD, LCHAD/MTP, and VLCAD deficiencies is mainly performed by the detection of high concentrations of characteristic acylcarnitines in blood. The determination of enzyme activities in lymphocytes and/or fibroblasts and molecular analyses of mutations may be necessary for diagnosis confirmation. Since early diagnosis and prompt treatment are available in MCAD, LCHAD/MTP, and VLCAD deficiencies, these diseases have been included in the expanded newborn screening programs, allowing a much better outcome for the affected patients by significantly reducing morbidity and mortality (Wilcken et al., 2007;Maguolo et al., 2020).
The current treatments for these diseases include frequent meals and avoidance of catabolic stress situations caused by prolonged fasting or infectious illness. Fatty acid restriction, allied to medium-chain triglycerides (MCT) formulas and essential fatty acids to LCHAD/MTP and VLCAD deficiencies, as well as high oral or intravenous glucose administration to sustain anabolism is also critical in these disorders. The objective is therefore preventing hypoketotic hypoglycemia and metabolite accumulation. L-Carnitine supplementation should be used mainly to correct L-carnitine deficiency, but its beneficial effect to significantly increase the urinary excretion of potentially toxic fatty acids has still to be demonstrated (Spiekerkoetter et al., 2009. More recently, clinical trials have shown that bezafibrate, an agonist of peroxisome-proliferating activator receptor that increases mitochondrial biogenesis and the gene expression of mitochondrial fatty acid oxidation enzymes, may be useful in VLCAD (Yamada et al., 2018;Shiraishi et al., 2019) and MTP (Suyama et al., 2020) deficiencies. However, the clinical efficacy of bezafibrate is still disputed and needs to be further confirmed (Ørngreen et al., 2014, 2015). Furthermore, replacement of longchain triglycerides by MCT and replenishment of citric acid cycle (CAC) intermediates by the seven-carbon fatty acid triglyceride (C7) triheptanoin to support ATP production have been recently demonstrated to improve the clinical outcome of these patients (Gillingham et al., 2017;Vockley et al., 2017Vockley et al., , 2019.
Treatment is effective to decrease mortality and morbidity for most FAOD, although it does not completely prevent longterm systemic and neurological complications. It is therefore expected that elucidation of the exact underlying mechanisms of pathogenesis of these disorders will potentially help in the development of novel treatments to improve the quality of life of the affected patients. In particular, observations of mitochondrial biochemical and morphological abnormalities in highly mitochondria-enriched tissues of MCAD-, LCHAD/ MTP-, and VLCAD-deficient patients, such as the heart, liver, and skeletal muscle, indicate that disturbances of mitochondrial functions are probably involved in their pathophysiology. The present review will mainly focus on recent evidence indicating secondary alterations of important mitochondrial properties caused by major fatty acids accumulating in these disorders.

MITOCHONDRIAL FUNCTIONS: BIOENERGETICS AND CALCIUM HOMEOSTASIS
The mitochondria are dynamic organelles with essential roles in cellular physiology, particularly in tissues with high energy demand and oxidative metabolism, such as the heart, skeletal muscle, liver, and brain. The mitochondria regulate ATP production, redox status, cytosolic calcium concentrations, and apoptosis-induced cell death. These mitochondrial functions are closely associated with efficient dynamic processes, such as mitochondrial fission and fusion, biogenesis, and mitophagy.
Mitochondrial fatty acid oxidation is the main source of ATP generation in the heart, skeletal muscle, and liver. Acetyl-CoA originated from fatty acid degradation is oxidized in the CAC, providing the electrons to form NADH and FADH 2 , which are transferred through the respiratory chain complexes in the electron transfer system. Protons are pumped into the mitochondrial intermembrane space, generating an electrochemical gradient (mitochondrial membrane potential, m). The energy of the electrochemical gradient is used by ATP synthase to support ATP production, and the whole process is called oxidative phosphorylation (OXPHOS; Nicholls and Ferguson, 2013).
Calcium regulates a significant number of critical intracellular events necessary to cell survival, particularly in the heart, skeletal muscle, and liver . The mitochondria continuously promote calcium influx down the electrochemical gradient through the mitochondrial calcium uniporter (MCU) and efflux by the Na + /Ca 2+ and H + /Ca 2+ exchangers, contributing together with the endoplasmic reticulum to maintain the cytosolic concentrations of this ion that would be adequate for cell functioning (De Stefani et al., 2016). At physiological or pathological situations of calcium overload, the capacity of the mitochondria to retain calcium is particularly important (Williams et al., 2013;Granatiero et al., 2017;Nicholls, 2017).
Mitochondrial permeability transition (mPT) pore opening in the inner mitochondrial membrane occurs when the threshold of mitochondrial calcium retention capacity is exceeded. Mitochondrial permeability transition pore opening is deleterious to cell functioning and survival mainly due to non-selective mitochondrial permeabilization that leads to significant calcium, glutathione, and NADH and NAD(P)H release, inducing mitochondrial swelling, m dissipation, disruption of ATP synthesis, and finally apoptotic cell death (Rasola and Bernardi, 2011;Bernardi and von Stockum, 2012;Giorgio et al., 2018).
Mitochondrial calcium homeostasis represents an important regulatory mechanism in muscular tissue physiology, being extremely important for normal cardiomyocyte (Drago et al., 2012;Eisner, 2014;Kohlhaas et al., 2017) and myocyte (Yi et al., 2011;Eisner, 2014) functioning. Dysregulation of intracellular calcium concentration due to mitochondrial dysfunction associated with mPT induction has been related to cardiac diseases (Gordan et al., 2016;Bravo-Sagua et al., 2017) and suggested as a pathophysiologic event leading to rhabdomyolysis (Hamel et al., 2015). Disturbance of mitochondrial calcium homeostasis and mPT pore opening has also been demonstrated to be involved in liver diseases (Ferreira et al., 2003;Brenner et al., 2013;Go et al., 2015).
On the other hand, balanced mitochondrial fusion (elongation) and fission (fragmentation) is essential for normal mitochondrial morphology, distribution, and function, being also necessary in response to the variable physiological demands of the cell (El-Hattab et al., 2018). These processes can restore or remove defective mitochondria and are mainly coordinated by the pro-fusion mitochondrial proteins optic atrophy 1 (OPA1), mitofusin 1 (MFN1), and mitofusin 2 (MFN2), as well as by the cytosolic pro-fission dynamin-related protein 1 (DRP1; Burté et al., 2015). The quantity and the quality of the mitochondria are regulated by the equilibrium between their formation (biogenesis) and removal (mitophagy). Upregulation of biogenesis improves mitochondrial function and has been related to various proteins, such as the peroxisome proliferator-activated receptor gamma coactivator 1-alpha (PGC-1α) and sirtuin 1 (SIRT1), whereas mitophagy is dependent on the PTEN-induced putative kinase 1 (PINK1; Ploumi et al., 2017). PTEN-induced putative kinase 1 is highly expressed in injured mitochondria with collapsed m, recruiting and activating mitophagy-related proteins, particularly ubiquitin ligase parkin. It is noteworthy that the defects in mitochondrial dynamics result in the impairment of mitochondrial bioenergetics and calcium homeostasis, potentially leading to cell death (Pernas and Scorrano, 2016;Kowaltowski et al., 2019). Furthermore, failure in mitochondrial dynamics has been related to various pathological processes, including myopathies, cardiomyopathy, hepatopathy, neurodegeneration, diabetes, and cancer (Archer, 2013;Vásquez-Trincado et al., 2016;Bartsakoulia et al., 2018;Mansouri et al., 2018;Ji and Yeo, 2019). Table 1 summarizes the biochemical and morphological evidence of mitochondrial abnormalities in patients, genetic knockout mice, and cultured cell models of MCAD, LCHAD/MTP, and VLCAD deficiencies.

FATTY ACID OXIDATION DEFECTS AND MITOCHONDRIAL ABNORMALITIES
Increased lactate formation commonly results from the impairment of mitochondrial bioenergetics, with lactic acidosis being therefore considered a biochemical hallmark of mitochondrial disorders (Kerr, 1991;Zeviani and Di Donato, 2004). However, it should be noted that, apart from being indicative of altered mitochondrial functions, lactic acidemia may be also a consequence of decreased lactate utilization due to liver dysfunction as found in some FAOD, particularly during episodes of metabolic decompensation. Patients with these diseases also present episodes of rhabdomyolysis that signalize severe disturbance of mitochondrial functions (Nance and Mammen, 2015). Oxidative stress has been also associated with mitochondrial dysfunction (Wang et al., 2014;Kudryavtseva et al., 2016;Rose et al., 2018) due to impairment of the mitochondrial electron flow through the respiratory chain, resulting in increased electron loss and subsequent reactive oxygen species (ROS) generation (Lambert and Brand, 2009;Nickel et al., 2014).
Although uncommon, lactic acidosis (Feillet et al., 2003), oxidative stress (Derks et al., 2014;Najdekr et al., 2015), and rhabdomyolysis (Ruitenbeek et al., 1995;Schatz and Ensenauer, 2010) have been observed in some patients with MCAD deficiency, particularly during episodes of metabolic decompensation. Reduced mitochondrial oxygen consumption, decreased respiratory chain complex protein levels, and increased ROS production were also found in fibroblasts from MCADdeficient patients and in MCAD knockout 143B osteosarcoma cells (Lim et al., 2018), supporting a role for the disruption of bioenergetics and of redox homeostasis in the pathogenesis and progression of this disorder.
On the other hand, abnormal mitochondrial morphology and altered biochemical markers of mitochondrial functions, reflecting an impairment of bioenergetics, were commonly reported in isolated LCHAD and MTP deficiencies. In this scenario, lactic acidemia (Tyni et al., 1996;Ventura et al., 1998;Das et al., 2000;Enns et al., 2000), as well as rhabdomyolysis (Olpin, 2005;Diekman et al., 2014), mitochondrial morphological abnormalities, and inhibition of the respiratory chain electron flow (Tyni et al., 1996;Das et al., 2000;Enns et al., 2000;Hintz et al., 2002), was observed in skeletal muscle and cultured fibroblasts from patients with these diseases. Decreased mitochondrial oxygen consumption and reduced ATP synthesis were also detected in the fibroblasts of MTP-deficient patients (Lefort et al., 2017). Furthermore, an interesting study utilizing LCHAD-deficient fibroblasts demonstrated a dysregulation of the mitochondrial fusion/fission machinery as revealed by a decreased MFN2/DRP1 ratio, leading to the accumulation of fragmented mitochondria due to increased fission (Hagenbuchner et al., 2018). Mitochondrial swelling and distortion , as well as induction of oxidative stress, have been also reported in the liver of LCHAD-deficient mice (Ibdah et al., 2005).
As regards to VLCAD deficiency, lactic acidosis (Ventura et al., 1998) and rhabdomyolysis (Roe et al., 2002;Engbers et al., 2005;Diekman et al., 2014) were found in a considerable number of patients with this disorder. Decreased mitochondrial respiration associated with low ATP levels, as well as increased Frontiers in Genetics | www.frontiersin.org ROS generation, was verified in the fibroblasts of VLCADdeficient patients (Seminotti et al., 2019). These fibroblasts revealed elevated mitochondrial mass and fusion, as well as an increased expression of MFN1, indicating alterations of mitochondrial dynamics besides the disruption of the endoplasmic reticulum-mitochondria crosstalk that is involved in cytosolic calcium homeostasis (Seminotti et al., 2019). This is in line with the observations of increased intracellular calcium concentrations that were correlated with fatty acid intermediate accumulation in fibroblasts from VLCAD-deficient patients differentiated into cardiomyocytes (Knottnerus et al., 2020). Furthermore, results obtained in the genetic mice model of VLCAD deficiency showed bioenergetics disruption. Thus, increased resting respiration suggesting uncoupling of OXPHOS was found in brown adipose tissue (Exil et al., 2006), and decreased phosphocreatine/ATP ratio (Tucci et al., 2014), ATP production (Xiong et al., 2014), and CAC intermediate pools (Bakermans et al., 2013;Gaston et al., 2020) were demonstrated in the heart of these animals.

DISTURBANCE OF MITOCHONDRIAL BIOENERGETICS AND CALCIUM HOMEOSTASIS CAUSED BY THE MAJOR FATTY ACIDS ACCUMULATING IN FATTY ACID OXIDATION DEFECTS
The pathophysiology of tissue damage in patients with MCAD, LCHAD/MTP, and VLCAD deficiencies has not yet been well established, although energy deprivation caused by fatty acid oxidation blockage, leading to hypoketotic hypoglycemia and sequestration of CoA and L-carnitine, was presumed to be mainly involved in the pathogenesis of these disorders (Spiekerkoetter and Wood, 2010;Olpin, 2013). More recently, alternative pathogenetic mechanisms have been hypothesized to contribute to their symptomatology, more particularly the toxicity of the accumulating metabolites. This is in accordance with the observations that clinical worsening occurs during stress catabolic situations characterized by intense lipolysis leading to the massive production of these compounds (Gregersen and Olsen, 2010;Olpin, 2013;Tein, 2013;Knottnerus et al., 2018). In particular, there is mounting evidence of bioenergetics impairment in tissues that primarily consume fatty acids for their energy needs in patients and in the genetic models of MCAD, LCHAD/MTP, and VLCAD deficiencies ( Table 1). Tables 2-4 summarize the updated data showing that the major metabolites, particularly MCFA, LCHFA, and LCFA, accumulating in these disorders provoke alterations of mitochondrial functions in the heart, liver and skeletal muscle of rats and also in cultured cell lines, mainly impairing mitochondrial bioenergetics and calcium homeostasis by distinct mechanisms. It is emphasized that, overall, the doses of the accumulating metabolites used in most of these studies were similar to the levels described in the blood of affected patients during metabolic decompensation. However, a significant impairment of mitochondrial functions was also achieved with lower concentrations of these compounds in LCHAD/MTP and VLCAD deficiencies that better approach the levels found in blood during periods of stable disease, therefore suggesting the chronic toxicity of these compounds in these inherited deficiencies.
Thus, OA, DA, and cDA, the MCFA that most commonly accumulate in MCAD deficiency, were shown to provoke mitochondrial dysfunction in the liver and skeletal muscle of rats. OA and DA were shown to inhibit the activities of the respiratory chain complexes I-III and II-III in rat liver, as well as of complex IV in the liver and skeletal muscle, besides inducing oxidative stress in these tissues (Scaini et al., 2012). In addition, DA and cDA severely inhibited ATP-linked (ADPstimulated) and maximal (CCCP-stimulated) mitochondrial oxygen consumption, increased resting respiration (induced by the ATP synthase inhibitor oligomycin), and inhibited complexes II-III and IV activities, indicating metabolic inhibition and uncoupling of OXPHOS that lead to energy deficiency besides provoking a disruption of redox homeostasis in isolated liver mitochondria . It is noteworthy that, in the same study, it was shown that DA and cDA decreased m and matrix NAD(P)H content and stimulated the opening of cyclosporin A-sensitive mPT pore. Calcium retention capacity was also decreased by DA and cDA, probably as a result of mPT induction in the liver mitochondria . Other studies reported that OA and DA caused m dissipation in hepatocytes (Rial et al., 2018) and induced apoptosis in adipocytes (Yang et al., 2009), whereas OA was demonstrated to decrease the ATP/O ratio in perfused liver, indicating OXPHOS impairment (Gallis et al., 2007). In contrast, the carnitine derivatives of the corresponding MCFA tested, OC and DC, caused no changes in the mitochondrial parameters evaluated, implying that medium-chain acylcarnitine derivatives do not disturb these mitochondrial functions. This is consistent with a recent study showing no alterations of OC and DC on mitochondrial respiration in fibroblasts (Lefort et al., 2017).
As regards to LCHFA, it was demonstrated that 3HTA and 3HPA, which mostly accumulate in tissues and biological fluids of patients affected by LCHAD or MTP deficiencies, decrease m, matrix NAD(P)H content, calcium retention capacity, and ATP synthesis besides inducing mitochondrial swelling in calcium-loaded liver and heart mitochondria Hickmann et al., 2015). It was proposed that these effects were due to the induction of cyclosporin A-sensitive mPT pore opening as well as due to uncoupling and to the metabolic inhibition caused by these fatty acids Hickmann et al., 2015). Similar results were achieved in cultured cell lines from the heart and liver (Cecatto et al., 2018b), as well as in skeletal muscle mitochondria and permeabilized muscle fibers . Altered mitochondrial membrane fluidity caused by the LCHFA was also shown in the skeletal muscle . However, the corresponding dicarboxylic 3HTDA caused no effect on these parameters, implying a selective toxicity of monocarboxylic LCHFA Hickmann et al., 2015).
Frontiers in Genetics | www.frontiersin.org TABLE 3 | Major metabolites accumulating in LCHAD/MTP deficiencies disturb mitochondrial bioenergetics and calcium homeostasis in heart, liver and skeletal muscle of rats, as well as in cultured cell lines.
concentrations of Myr and Cis-5, which mostly accumulate in this disorder, were shown to be toxic to mitochondrial functions by impairing bioenergetics and calcium homeostasis. In particular, previous works performed in isolated liver mitochondria showed that Myr uncouples OXPHOS through the involvement of the dicarboxylate carrier (Wieckowski and Wojtczak, 1998) and of the ANT (Bodrova et al., 2000). Induction of mPT pore opening was also demonstrated to be caused by Myr (Bodrova et al., 2003). Recent studies demonstrated that, apart from Myr, pathological concentrations of Cis-5 disturb mitochondrial bioenergetics and calcium homeostasis in the heart, liver, and skeletal muscle (Cecatto et al., 2018a(Cecatto et al., , 2019(Cecatto et al., , 2020. These results were obtained in different tissue preparations, such as isolated mitochondria, permeabilized cardiomyocytes and hepatocytes, and heart fibers. Myr and Cis-5 also inhibited complex I-III and α-ketoglutarate dehydrogenase activities and altered mitochondrial respiration, behaving as metabolic inhibitors and uncouplers of OXPHOS, leading to ATP depletion besides reducing m and matrix NAD(P)H content. These LCFA also induced cyclosporin A-sensitive mPT in the presence of calcium, causing mitochondrial m dissipation, reduction of calcium retention capacity, swelling, and cytochrome c release. These observations are in accordance with a previous study showing that monounsaturated LCFA (C14:1 and C16:1) accumulating in VLCAD deficiency decrease m and induce apoptosis and necrosis in cardiomyocytes (Hoffmann et al., 2014). On the other hand, the toxicity of long-chain acylcarnitines (LCAC) was reported to be involved in long-chain FAOD pathogenesis (McCoin et al., 2015a(McCoin et al., , 2019. In particular, it was demonstrated that LCAC disturb cell calcium homeostasis in myocytes (McCoin et al., 2015b), cardiomyocytes (Berezhnov et al., 2008), and heart sarcoplasmic reticulum (Yamada et al., 2000) besides decreasing resting respiration (Lefort et al., 2017) and provoking m dissipation (Nguyen et al., 2017) in fibroblasts. LCAC were also shown to reduce calcium retention capacity (De Villiers and Lochner, 1986;Baydoun et al., 1988), inhibit ATP-linked respiration, and generate ROS in the heart mitochondria (Liepinsh et al., 2016). Figure 1 illustrates the main mechanisms of mitochondrial dysfunction caused by major fatty acids that accumulate in MCAD, LCHAD/MTP, and VLCAD deficiencies.

CONCLUDING REMARKS
Mounting evidence of altered mitochondrial morphology, functions, and dynamics has been recently described in various tissues of patients with MCAD, LCHAD/MTP, and VLCAD deficiencies and in the genetic models of these diseases, suggesting that impairment of mitochondrial homeostasis may play a relevant role in the pathogenesis of these disorders. In particular, the major accumulating MCFA, LCHFA, and LCFA were demonstrated to severely disturb mitochondrial bioenergetics and calcium homeostasis in vitro in highly oxidative mitochondria-enriched tissues, such as the heart, liver, and skeletal muscle. These fatty acids behaved as metabolic inhibitors, uncouplers of OXPHOS, and inductors of mPT pore opening. It is therefore presumed that these pathomechanisms probably contribute to the mitochondrial alterations observed in patients and animal models with these pathological conditions. Interestingly, severe cardiomyopathy, hepatopathy, and skeletal muscle alterations are mainly manifested during catabolic stress situations in which the concentrations of the characteristic fatty acids dramatically increase in tissues and biological fluids, therefore supporting an acute toxicity for these endogenous compounds. However, the present evidence of bioenergetics disruption caused by the accumulating metabolites must be interpreted with caution since most available data were achieved by in vitro assays. Further studies performed preferentially in vivo in animal models and in patients affected by FAOD are therefore necessary to further clarify the underlying mechanisms of tissue damage in these disorders. Finally, it is expected that, besides restricting fat dietary intake and avoiding fasting, drugs that stimulate mitochondrial function such as bezafibrate and the anaplerotic compound triheptanoin may hopefully improve the clinical outcome of the affected patients (Gillingham et al., 2017;Vockley et al., 2017Vockley et al., , 2019Yamada et al., 2018;Shiraishi et al., 2019;Suyama et al., 2020).

AUTHOR CONTRIBUTIONS
Both authors planned and wrote the review article.