Practical Approaches to Treat ED in PDE5i Nonresponders

Abstract

Erectile dysfunction (ED) is a common sexual disorder in adult males and one of the most important factors affecting their quality of life and that of their partners. Although PDE5 inhibitors (PDE5is) are the first choice for improving erectile function, there is a substantial proportion of ED patients, termed PDE5i nonresponders, who do not respond to PDE5is. Because of the lack of effective therapies, these patients always have serious social and psychological problems due to ED, which should be addressed. Here, we review the available literature about ED and PDE5is and propose several strategies for mitigating ED in PDE5i nonresponders.

1. Introduction

Erectile dysfunction (ED) is a common sexual disorder in adult males and has significant biological, psychological and social effects on the quality of life (QOL) of men with ED and their sexual partners or spouses [1-2]. Indeed, the high prevalence of ED has become a global health concern [3]. The percentages of men affected by ED are as follows: 14.3-70% of men aged ≥60 years, 6.7-48% of men aged ≥70 years, and 38% of men aged ≥80 years [4]. Many treatments are available for ED, including psychotherapy, oral medication, vacuum constriction devices (VCDs), intraurethral drugs, intracavernous drugs, and implantable prosthetics. Among them, phosphodiesterase type 5 inhibitors (PDE5is), as a first-line treatment, are recognized as the most satisfying and effective drugs for ED [5-6]. However, with the increasing administration of PDE5is in clinical practice, it has found that approximately 30-35% of ED patients cannot respond to PDE5is [7]. Although the unreasonable use of PDE5is, including the use of inadequate dosages, administration of a single dose, and lack of dosage regulation, is considered the main reason for the lack of a response to PDE5is [8], 50-70% of ED patients still do not respond to PDE5is after restoring rational PDE5i use [9]. In general, the detailed mechanisms of the lack of a response to PDE5is in ED remain to be clarified, and treating these patients is a challenge that urgently needs to be addressed.

ED is closely related to aging. Penile erection is a complex physiological activity involving the neuroendocrine vascular tissue system [10], and aging can not only cause tissue dysfunction related to this physiological activity, including dysfunction involving the nerves, blood vessels, cavernous tissue and reproductive hormones, but also increase the risk of penile ED [11]. Aging also increases the risk of various chronic diseases in the elderly, such as cardiovascular diseases, diabetes, metabolic syndrome, late-onset hypogonadism (LOH), and lower urinary tract symptoms (LUTSs) [11]. These chronic diseases have been recognized as risk factors for ED and can cause and/or aggravate ED [12]. It has been shown that the prevalence of ED ranges from 1-10% for men aged under 40 years, 2-15% for men aged 40-49 years, 22-31% for men aged 50-69 years, 20-40% for men aged 60-69 years, and 50-100% for men over 70 years old [13]. Therefore, aging is an important risk factor for ED development. At the same time, the changes caused by aging will also increase the difficulty of ED treatment, which is an important factor of the lack of a response to PDE5i treatment. It is worth noting that according to previous reports, approximately 15% of the global population will be over 65 years old by the year 2025 due to the increase in life expectancy [11, 14]. Therefore, sexual dysfunction, especially ED, in elderly men is a problem that cannot be ignored. Moreover, PDE5i nonresponsiveness in older men as a result of age is a major challenge that urgently needs to be addressed. Here, we propose several strategies for treating ED in PDE5i nonresponders and present a summary of the direct evidence of rescue treatment in PDE5i responders in Table 1.

Table 1.

Direct evidence of rescue treatment in PDE5i nonresponders.

Approaches for rescue treatment in PDE5i nonresponders	PDE5i nonresponse				Rescue therapy with/without PDE5is				Ref.
	PDE5i	Dosage	Dosing regimen	PDE5i	Dosage	Dosing regimen	Other therapeutic approaches	Salvage success rate
Increased PDE5i doses	Sildenafil	100 mg	On demand	Sildenafil	150 or 200 mg	On demand	NA	24.1%	38
Different dosing regimens	Tadalafil	20 mg	On demand	Tadalafil	Flexible doses of 10 and 20 mg	Once daily	NA	58.0%	46
Different dosing regimens	Vardenafil	20 mg	On demand	Vardenafil	10 mg	Once daily	NA	38.8%	47
Different PDE5is	Sildenafil	100 mg	On demand	Vardenafil	Flexible doses of 10 and 20 mg	On demand	NA	12.0%	48
Different PDE5is	Sildenafil	≤100 mg	On demand	Vardenafil	Flexible doses of 5, 10 and 20 mg	On demand	NA	53.0%	49
Non-drug therapeutic approaches with or without PDE5is	At least one PDE5i (20 mg for tadalafil or vardenafil hydrochloride, 100 mg for sildenafil)			Taking the same PDE5i as PDE5i nonresponse			VED	70.0%	59
Non-drug therapeutic approaches with or without PDE5is	Tadalafil	5?mg	Once daily	NA	NA	NA	LiSWT	41.7%	62
Non-drug therapeutic approaches with or without PDE5is	PDE5is (unclear in detail)			NA	NA	NA	LiSWT	60.0%	63
Non-drug therapeutic approaches with or without PDE5is	Sildenafil (100 mg), tadalafil (20 mg), and vardenafil (20 mg) as needed or tadalafil (5 mg) daily			Taking the same PDE5i as PDE5i nonresponse			LiSWT	67.3%	64
Attention to psychological factors	Sildenafil	100 mg	On demand	Sildenafil	100 mg	On demand	Trazodone (50 or 100 mg, once daily)	66.7%	68
PDE5is combined with other non-PDE5i drugs	Highest available dosage of sildenafil, tadalafil, or vardenafil therapy			Tadalafil	10 mg	Once daily	Testogel (5 g up to 10 g, once daily)	33.1%	110
PDE5is combined with other non-PDE5i drugs	Sildenafil	100 mg	On demand	Sildenafil	100 mg	On demand	Oral testosterone undecanoate (Restandol, 80 mg, bid or tid)	34.3% after testosterone replacement only, 37.5% more after combined therapy	111
PDE5is combined with other non-PDE5i drugs	Tadalafil	20 mg	On demand	Tadalafil	20 mg	Twice a week	Testogel (5 g, once daily)	NA (improvement in IIEF-EF)	113
PDE5is combined with other non-PDE5i drugs	Sildenafil	100 mg	On demand	Sildenafil	100 mg	On demand	Atorvastatin (40 mg, once daily)	NA (significant improvements in all IIEF-5 questions and GEQ)	117

Salvage success is defined as being able to successfully complete sexual intercourse. NA, not applicable; VED, vacuum erectile device; LiSWT, low-intensity shockwave therapy; IIEF, international index of erectile function; EF, erectile function; GEQ, global efficacy question.

2. Possible causes for ED in PDE5i nonresponders

PDE5i-nonresponsive ED patients always have comorbidities, including diabetes, cardiovascular disease, and metabolic syndrome, among others [15-16]. The nerves, blood vessels, and cavernous tissues in the penis can be injured as a result of these comorbidities, which is the basis of ED development [17-18]. Although PDE5is can improve erectile function through the cGMP-PKG and cAMP-PKA signaling pathways, among others, the therapeutic effect of PDE5is depends on the proper function of tissue effectors, such as nerves, blood vessels and cavernous tissues. Therefore, the above comorbidities affect the therapeutic efficacy of PDE5is in ED by damaging these tissues in the penis. As diabetes can disrupt the balance of sex hormones, such as by lowering testosterone levels to affect erection function [19-20], the presence of such comorbidities may be an important cause of PDE5i nonresponsiveness. In addition, the side effects of some drugs used for comorbidities, such as selective serotonin-reuptake inhibitors, thiazides, and β-blockers, affect erectile function and thereby weaken the effect of PDE5is on ED [21-22]. Interestingly, unhealthy behaviors, such as excessive drinking, smoking, and a high-fat diet, can also promote the development and progression of these comorbidities in men, in turn affecting the efficacy of PDE5is in the treatment of ED [23-25]. Hence, lifestyle factors should be emphasized in ED treatment when there is the lack of a response to PDE5is.

In addition to comorbidities, complications from treatments for diseases are common reasons for ED. For example, radical prostatectomy (RP) can cause cavernous nerve injury and vascular damage, and pelvic radiation therapy for prostate cancer can result in the death or fibrosis of cavernosal smooth muscle cells, nerve cells, and vascular smooth muscle cells, among others [26-27]. These complications destroy the tissues that are the basis for the therapeutic efficacy of PDE5is in ED, thus reducing the efficacy of the drug. If the damage is significant enough, the ED patient will not respond to PDE5i therapy. Furthermore, spinal cord injury can directly damage nerves, resulting in damage to or the attenuation of sexual activity-related nerve reflex arcs, e.g., nerves and blood vessels in the penis, by altering neuroendocrine reflexes [21, 28]. Such traumas involving injury to nerves, blood vessels, and cavernous tissues related to erectile function can cause the abovementioned adverse events.

It has been found that nonresponsiveness to sildenafil for ED is related to incorrect administration factors, such as taking the medication after heavy meals, a lack of sexual stimulation, administration timing, too few attempts and other reasons [22, 29]. Additional mechanisms are unknown. However, correcting PDE5i administration or replacing the PDE5i regimen according to the metabolic and distribution characteristics of different PDE5i drugs can attenuate the abovementioned problems associated with incorrect drug administration.

Male erectile function is closely related to psychological factors [30]. Mental disorders can cause or aggravate ED, and such disorders can be derived from society, family, spouse, and self [30-31]. During PDE5i treatment for ED, the sexual psychological disorders of ED patients will directly influence the effects of PDE5i treatment for ED and could even lead to the lack of a response to the treatment [31-32]. Fortunately, psychological interventions, such as cognitive behavioral therapy and sexual counseling, can improve the patient’s erectile function or enhance the efficacy of PDE5is in the treatment of ED [31-32]. Therefore, psychological factors may be another cause of PDE5i nonresponsiveness.

3. Approaches to improve ED in PDE5i nonresponders

3.1 Improved pharmacotherapy with PDE5is

3.1.1 Sufficient medication attempts

During treatment with an on-demand regimen, insufficient medication attempts is a common reason for patients not achieving a response to PDE5is [29], and the reason may be associated with an insufficient blood concentration. It has been shown that the coital success rate was elevated with increased sildenafil frequency but remained stable after eight doses (with a success rate of up to 86%) [33]. For vardenafil, another short-acting drug, research has also indicated that the likelihood of successful penetration and intercourse increases with additional medication attempts, with the effect of vardenafil on ED reaching a plateau at approximately the fourth dose [34]. Therefore, it has been suggested that patients who fail to achieve treatment success initially should continue treatment with increased doses [34]. Interestingly, for the long-acting PDE5i drug tadalafil (as needed), a substantial proportion of ED patients who fail on the first attempt will achieve success provided the treatment is maintained [35]. Moreover, approximately 80% of patients achieved successful sexual intercourse within eight attempts at 10 mg and within four attempts at 20 mg, which also indicates that fewer attempts are required with a greater dose; these findings reflect the importance of an adequate PDE5i blood level in the treatment of ED [35]. Overall, to ensure efficacy, ED patients should be given regular and sufficient PDE5i doses. Indeed, sufficient medication attempts is an important strategy for improving the therapeutic efficacy of PDE5is in nonresponders.

3.1.2 Increased PDE5i doses

The therapeutic efficacy of PDE5is in ED increases with increasing dose. ED patients treated with 50 mg of sildenafil on demand achieved 1.4 sexual intercourse attempts per week, with a success rate of 82% [36]. However, with 100 mg of sildenafil as needed, the number of sexual intercourses attempts per week increased to 1.7, with a 91% success rate, indicating that increasing the dose of sildenafil can increase both the number of sexual intercourse attempts and the sexual success rate [36]. Early sildenafil treatment failure does not necessarily mean that there will be no effect in the future, and on-demand administration can be increased to 100 mg to increase the success rate of treatment, further demonstrating that increasing the dose can improve the effect of sildenafil on ED [37]. Additionally, the dose of sildenafil can be increased to 200 mg, which can render 24.1% of sildenafil nonresponders responsive to the drug [38]. Although 200 mg of sildenafil on demand has a higher incidence of adverse effects, increasing the administered dose within a safe range is a viable treatment strategy in PDE5i nonresponders. Vardenafil has a similar dose-effect trend as sildenafil. Clinical studies on vardenafil have indicated that regarding indexes of the therapeutic efficacy of PDE5is in ED, such as the Sexual Encounter Profile question 2 (SEP-2) (penetration) and SEP-3 (maintenance) scores, and overall satisfaction with the sexual experience, first-attempt and subsequent success rates increase with increasing dose [39-40]. For long-acting PDE5is, such as tadalafil, increasing clinical studies have also demonstrated gradual increases in indexes of erectile function, such as the International Index of Erectile Function (IIEF)-EF, SEP-2, SEP-3, and Global Assessment Question (GAQ) scores, with increasing dose, regardless of the dosing regimens, e.g., as needed or daily [41-43]. Additionally, no association with the severity of ED has been observed in the gradually enhanced therapeutic effect with increasing dose [44], suggesting that an increased PDE5i dose may be key for improving efficacy in ED treatment. Furthermore, during early treatment, PDE5i nonresponders may not actually be nonresponders, and it is recommended to use PDE5is starting from the highest label-approved dose followed by down-titration to minimize the frustration caused by inadequate response due to inadequate drug dosage, thereby reducing the impact of psychological factors on the treatment [12, 45]. Thus, increased doses may be an important strategy in PDE5i nonresponders.

3.1.3 Different dosing regimens

The use of PDE5is for ED has two dosing regimens, i.e., on demand and daily. In ED patients who were previously unresponsive to on-demand tadalafil, daily flexible tadalafil (10/20 mg) significantly improved the IIEF-EF and SEP-3 scores compared to baseline and on-demand tadalafil, and more patients had achieved an erection at the end point [46]. Thus, tadalafil with a daily dosing regimen (10/20 mg) is considered an effective salvage treatment in previous on-demand tadalafil nonresponders [46]. Regarding the short-acting PDE5i vardenafil, one study on daily dosing for on-demand nonresponders has shown that according to the SEP-3 score, 38.8% of patients with ED who previously did not respond to the as-needed regimen became responders; the study suggests that daily vardenafil can be applied as a salvage strategy in ED patients with no response to the on-demand regimen [47]. In summary, regardless of whether a PDE5i is short acting or long acting, the daily dosing regimen allows ED patients who do not respond to the on-demand dosing regimen to achieve appropriate blood levels for improved therapeutic efficacy and is thus expected to be an important strategy for treating on-demand regimen nonresponders.

3.1.4 Different PDE5is

Because of the heterogeneity among individuals, each ED patient’s response to PDE5is differs. The advantage of individual responsiveness to different PDE5is may be an important strategy for improving the efficacy of PDE5is in nonresponders.

Vardenafil can be used for salvage treatment in a small proportion of sildenafil (100 mg) nonresponders [48], and flexible-dose vardenafil (5-20 mg) for moderate to severe ED in sildenafil nonresponders achieved high insertion and sexual success rates [39, 49]. Most patients receiving vardenafil reported improved erections and the achievement of normal erections [42,49]. Therefore, vardenafil can be used to treat ED patients who do not respond to sildenafil. As a long-acting PDE5i, tadalafil has been shown in several studies to change the dosing and sexual attempt behavior of ED patients, reflecting the extended period of efficacy of tadalafil [50]. Compared to sildenafil, as-needed tadalafil has several advantages, including a broader window of opportunity available for sexual activity, decreased time concerns, reduced IIEF-EF scores, reduced side-effect severity scores, more satisfying erection hardness and more sexual attempts [51-52]. Therefore, more patients prefer on-demand tadalafil [52]. In conclusion, changes in the dosing and sexual attempt behavior in patients taking tadalafil on demand and patient preferences for tadalafil suggest that on-demand tadalafil may be superior to sildenafil and an important strategy for treating PDE5i nonresponders. Unfortunately, in ED patients who do not respond to the maximum dose of sildenafil or vardenafil, the recommended maximum dose of tadalafil (20 mg) did not significantly improve the IIEF-5, SEP-2, SEP-3, or GAQ score by the end point [53]. However, it has been shown that daily tadalafil can serve as a rescue therapy in previous on-demand tadalafil nonresponders [46]. Daily tadalafil may have potential as a salvage treatment in ED patients nonresponsive to sildenafil or vardenafil, but more studies are needed to demonstrate this hypothesis. It is worth mentioning that first-generation PDE5is had a high discontinuation rate due to side effects. According to the results of a meta-analysis, avanafil, a new PDE5i, showed efficacy comparable to that of first-generation PDE5is but a lower incidence of side effects and thus a reduced discontinuation rate [54]. By increasing compliance, reducing the discontinuation rate is beneficial to ensure the smooth implementation of related treatment approaches in PDE5i nonresponders. Nonetheless, research to date on avanafil for the treatment of PDE5i nonresponders is insufficient, and further studies are needed. Overall, other PDE5is can be used in ED patients who do not respond to a given PDE5i.

3.1.5 Combined use of long-acting and short-acting PDE5is

PDE5i nonresponders always suffer from pathological changes in penile vascular tissue. Most ED patients with no response to 100 mg of sildenafil have been found to also have vascular diseases, such as arterial insufficiency, mixed vascular insufficiency, and cavernous venous occlusive disease [48]. The chronic use of low-dose, long-acting PDE5is, such as tadalafil, contributes to repair of the injury to penile vascular endothelial cells, and short-acting PDE5i administration on demand has an instantaneous effect on improving erection [55]. Thus, the combination of long-acting and short-acting PDE5is may be an important direction for treating PDE5i non-responders. Compared with 5 mg of tadalafil daily alone, 5 mg of tadalafil daily combined with sildenafil on demand resulted in higher IIEF-5 scores and percentages of 'yes' responses to SEP-4 and SEP-5 at the end of a 12-week follow-up period. Interestingly, in the combination group, the IIEF-5 scores of severe ED patients were significantly higher [56]. The side effects were similar in the two groups. Overall, the long-term, low-dose administration of long-acting PDE5is combined with short-acting PDE5is on demand is an important strategy in those who do not respond to PDE5i treatment.

3.2 Non-drug therapeutic approaches with or without PDE5is

Vacuum erectile devices are a noninvasive treatment for ED, and their first treatment efficiency can reach 90% [57]. For ED patients who are not satisfied with the therapeutic effect of PDE5is, the combination of a PDE5i and a vacuum erectile device can improve the IIEF-EF score, with a good therapeutic effect [58]. For example, a PDE5i combined with a vacuum erectile device significantly improved the SEP-2, SEP-3, and global patient assessment scale (GPAS) scores in PDE5i nonresponders. The IIEF-5 score increased from 9 to 17.6, and there were no obvious side effects [59]. Accordingly, a PDE5i combined with a vacuum erectile device can be considered an important strategy for treating PDE5i nonresponders.

Low-intensity shock-wave therapy (LISWT) is a new treatment method for ED. The low-intensity shock wave can release endogenous media and nitric oxide (NO) to promote the regeneration of neovascularization and improve both the blood supply to the cavernous artery and vasodilation [60]. A meta-analysis of LISWT for ED has shown that the effect of LISWT on improving ED can last for 6 and 12 months [61]. For example, LISWT was effective for 41.7% of ED patients who did not respond to PDE5is, resulting in satisfactory erectile function [62]. Similarly, in a study on LISWT for PDE5i nonresponders, it was confirmed that LISWT was effective for approximately 60%, and the therapeutic effect continued until the end of the 12-month follow-up period [63]. A PDE5i [sildenafil (100 mg), tadalafil (20 mg), or vardenafil (20 mg) with a trial of at least four attempts, or tadalafil (5 mg) with a trial of at least 28 days] combined with LISWT (twice a week for 12 weeks) also resulted in 67.3% of PDE5i nonresponders achieving successful sexual intercourse [64]. In summary, the administration of LISWT with or without a PDE5i is an important direction in treating PDE5i nonresponders.

3.3 Attention to psychological factors

ED is a complex disease, and minimal organic ED can induce psychogenic components. The incidence of psychological distress, including anxiety, depression and stress, is also closely related to the severity of ED [65-66]. Therefore, psychological distress is a crucial factor affecting the therapeutic effect on ED. It has been shown that psychological intervention combined with PDE5is could restore erectile function more effectively than psychological intervention alone, as based on the IIEF score [67]. Drugs are considered an adjunct to the treatment of psychosocial disorders, and sildenafil combined with trazodone, an antidepressant, was effective for men with ED who initially failed to respond to oral sildenafil and allowed them to achieve satisfactory sexual activity [68].

As one type of psychological intervention, sexual counseling can not only improve erectile function and sexual satisfaction but also increase treatment compliance in patients with ED caused by RP and penile prosthesis implantation, extended device application or hypospadias repair performed in childhood [69-73]. A meta-analysis has demonstrated that taking PDE5is to improve erectile function requires other comprehensive management, including sexual counseling, exercise and lifestyle changes [74]. While an ED patient is using a PDE5i, the addition of counseling therapy can more effectively improve sexual function and sexual satisfaction, even in the elderly male population [74].

Cognitive behavioral therapy is another psychotherapeutic approach that can be applied to treat psychogenic ED. Compared to sildenafil or cognitive behavioral therapy alone, the combination of cognitive behavioral therapy and sildenafil significantly improved the IIEF-EF score, with a higher success rate for treating ED within the first 4 weeks of therapy [75]. At the same time, PDE5is combined with cognitive behavioral therapy can both effectively improve ED and alleviate anxiety, depression and other mental problems, and the effect can be maintained for 15-18 months compared with PDE5is alone [31, 76].

Increased satisfaction is related to increased therapeutic efficacy, partner support, and the number of sexual attempts [77]. In fact, the partner’s role in ED treatment is an important influential and psychological factor that can be presented in many different ways, such as partner-initiated communication to relieve the anxiety and stress of ED patients, partner-facilitated activities to improve intimacy, partner-facilitated adaptation of sexual techniques and lifestyle changes, and partner-encouraged professional counseling and follow-up of medical treatment [3]. Thirty-four percent of ED patients express willingness to visit a doctor if their sexual partners asked them to do so [3], and 10.7% of ED patients cited their partner’s preference as an influential factor of their treatment choice [78]. Partner negativity is also an important factor that affects the responsiveness of ED patients to PDE5is [29]. Therefore, the roles of partners should be considered when treating PDE5i nonresponders. In summary, paying attention to psychological factors is important for enhancing the effects of PDE5is on ED, even in nonresponders.

3.4 Focus on the comorbidities of ED

3.4.1 Selection of PDE5is with greater effects on ED

Many diseases are likely associated with ED, causing refractory ED and a poor prognosis. Males who have metabolic syndrome, diabetes, hypertension, coronary heart disease, and hypogonadism, among other conditions, are particularly susceptible to ED [79]. Moreover, the comorbidities of ED are reasons why patients with ED might not respond to PDE5is, although the potential mechanisms differ. Thus, the selection of a PDE5i that is suitable or more suitable for the treatment of ED along with any comorbidities is a key strategy for improving the therapeutic efficacy in patients with a poor or no response to some PDE5is.

3.4.1.1 PDE5is, ED and premature ejaculation

In some ED patients, premature ejaculation is associated with ED, forming a vicious cycle [80]. It has been reported that 29.5% and 52.4% of patients with mild and severe ED, respectively, experience premature ejaculation [81]. To conceal the decrease in hardness during sexual intercourse, some ED patients often subjectively and consciously hope to end sexual intercourse as soon as possible (ejaculation is an important sign of the end of sexual intercourse), resulting in premature ejaculation [82]. The poor sexual performance caused by premature ejaculation will further aggravate the anxiety and pain of patients and lead to reactive ED, thus weakening the therapeutic effect, including the response to PDE5i treatment [82]. In addition, the treatment of premature ejaculation, whether psychologically or medically, aims to reduce the intensity of local stimulation and sexual excitation to delay ejaculation, and a reduction in stimulation intensity and sexual excitation leads to or aggravates ED, further the weakening therapeutic effect [83]. Hence, premature ejaculation is an important comorbidity of ED, and ED along with premature ejaculation is a reason for the lack of a response to PDE5i treatment. Interestingly, PDE5is can reduce sympathetic nerve tension in the vas deferens and seminal vesicles through the NO/cGMP signaling pathway and relax smooth muscle to achieve the dual goals of treating ED and delaying ejaculation [84]. Several studies have confirmed that regardless of whether they are combined with drugs for treating premature ejaculation, such as paroxetine (20 mg daily) and fluoxetine (90 mg once a week), PDE5is, including sildenafil (25-100 mg on demand), vardenafil (10 mg on demand) and tadalafil (20 mg on demand), can enhance ejaculation control, effectively prolonging the ejaculation time, improving anxiety and overall satisfaction and reducing the recovery time after orgasm to achieve a second erection [85-89]. Although a few studies have indicated that PDE5is cannot prolong the ejaculation time, PDE5is can help improve anxiety and overall satisfaction, which can partly alleviate the vicious cycle of ED and premature ejaculation from a therapeutic perspective [90]. Furthermore, the emotional outcomes of the loss of erectile function are more painful than those of premature ejaculation. Although PDE5is improve erectile function and enhance erectile confidence, patients with ED and premature ejaculation can achieve delayed ejaculation without the fear of losing erectile stiffness, but the ability to delay ejaculation often does not exceed that before ED [82]. Therefore, drugs for premature ejaculation, as well as psychosocial and behavioral therapy, are needed to increase the ejaculation threshold from a biological point of view and enable patients to achieve the physical and psychological changes necessary for delayed ejaculation [82, 91]. Premature ejaculation will aggravate the difficulty using PDE5is for the treatment of ED. PDE5is, including sildenafil, tadalafil and vardenafil, can be used to treat ED; however, both drugs for treating premature ejaculation and psychosocial behavioral therapy should be implemented to break the vicious cycle of ED and premature ejaculation, restore responsiveness to PDE5is and improve overall life satisfaction in the treatment of ED.

3.4.1.2 PDE5is, ED and diabetes

The presence of diabetes increases the difficulty of treating ED. In patients with type 1/2 diabetes and ED, as-needed tadalafil remarkably improved the IIEF-EF, SEP-2 and SEP-3 scores; thus, it is believed that tadalafil (10 mg or 20 mg as needed or 20 mg three times per week) can enhance erectile function in men with diabetes and ED [92-94]. Additionally, flexible-dose vardenafil (5-20 mg) in men with type 1 diabetes and ED significantly improved the mean success rate according to the SEP-2 and SEP-3 scores [95]. Nonetheless, the effect of sildenafil on ED in patients with diabetes was moderate, and the response rate was relatively low [93]. Accordingly, tadalafil or vardenafil may be a suitable PDE5i for ED patients with diabetes.

3.4.1.3 PDE5is, ED and spinal injury

Spinal injuries are closely related to the therapeutic efficacy of PDE5is in secondary ED. Sildenafil, tadalafil, and vardenafil are effective for ED secondary to spinal injury, at a rate of 85%, 72% and 74%, respectively [96-97]. Interestingly, upper motor neuron (UMN) lesions are associated with PDE5i treatment success, and poorer responses to PDE5is are observed in patients with lower motor neuron lesions and horsetail injuries [97]. The efficacy of sildenafil in ED patients with UMN lesions was significantly higher than that of the placebo (85% vs 25%, P<0.05) [98]; only 28% of patients with non-UMN lesions showed a response to sildenafil, although the difference was not significant [98]. Furthermore, research has shown that compared to sildenafil, tadalafil allowed significantly more ED patients to achieve normal sexual function up to 24 h postdosing, as well as a more satisfying sex life [99]. In other words, the effect of PDE5is on ED secondary to spinal injury is limited to the spinal injury site. Although sildenafil, tadalafil, and vardenafil are effective for ED secondary to UMN lesions, their suitability is not clear and requires further study.

3.4.1.4 PDE5is, ED and RP

One common complication after RP is ED. The therapeutic effect of PDE5is on ED is closely associated with the degree of neurovascular sparing. In one study, 76% of patients with bilateral nerve-sparing treatment and 53.5% of patients with unilateral nerve-sparing treatment responded to sildenafil, whereas only 14.2% of patients with non-nerve-sparing treatment responded to sildenafil [100]. Similar to sildenafil, 10 mg and 20 mg of vardenafil as needed for ED secondary to nerve-sparing RP improved erectile function according to the IIEF domains and allowed patients to have more satisfying sexual experiences [100]. Interestingly, a systematic review has shown that after bilateral nerve-sparing RP, avanafil on demand was the most effective PDE5i for the recovery of drug-assisted erectile function; tadalafil was equally effective when used on demand and daily, although vardenafil significantly improved drug-assisted erectile function recovery only when used on demand [101]. In addition to the degree of neurovascular bundle preservation, the effect of sildenafil on ED has been shown to correlate with age, the preoperative erectile function status, and the interval before starting treatment [102-103]. Therefore, when PDE5is are used to treat ED after RP, the therapeutic effect depends on more than the PDE5i, and avanafil, tadalafil, sildenafil and vardenafil are all candidates for treating ED after RP with neurovascular bundle preservation.

3.4.1.5 PDE5is, ED and other comorbidities

Dyslipidemia is a common etiological or causative factor of ED. The effectiveness of vardenafil was not affected by the TC/HDL-C ratio, the LDL-C level, or the presence of metabolic syndrome, and it has been recommended for treating ED in patients with dyslipidemia [104]. ED patients with comorbid benign prostate hyperplasia/lower urinary tract symptoms (BPH/LUTSs) can benefit from the long-term use of long-acting tadalafil [105]. Therefore, it is necessary to consider the characteristics of the comorbidities during ED treatment with PDE5is, and more suitable PDE5is should be selected for treating ED. Fortunately, an integrated analysis of 11 double-blind, placebo-controlled studies showed that on-demand tadalafil (10 mg or 20 mg) significantly improved the IIEF-EF, SEP-3 and GAQ scores of ED patients with different comorbidities, such as diabetes mellitus, hypertension, cardiovascular disease, hyperlipidemia, depression, and BPH [79]. Therefore, it is believed that tadalafil, a long-acting PDE5i, can significantly improve the erectile function of patients with ED and different comorbidities. Tadalafil may be widely suitable for ED in most patients with comorbidities, but further research is needed.

3.4.2 Management of medications for comorbidities of ED

The comorbidities of ED include diabetes, cardiovascular diseases, sex hormone disorders, metabolic diseases, LUTSs, obstructive sleep apnea syndrome, and psychosocial diseases, among others, which are all important factors of the cause or aggravation of ED. At the same time, these comorbidities increase the difficulty of ED treatment and are important factors for the lack of a response to PDE5is. In the course of ED treatment, the treatment of comorbidities will improve the efficacy of the ED treatment. Nevertheless, the side effects of some drugs used to treat comorbidities can impair erectile function. Interestingly, some drugs combined with PDE5is have synergistic effects in treating ED. Overall, understanding the effects of drugs for comorbidities on ED will help in the development of therapeutic strategies for PDE5i nonresponders.

3.4.2.1 Associated medication modifications

It is worth noting that while treating primary diseases or comorbidities, the side effects of some drugs can impair male erectile function. Antidepressants, such as selective serotonin-reuptake inhibitors and tricyclic antidepressants, antipsychotic drugs, such as phenothiazines and butanones, antihypertensive drugs, such as thiazides and β-blockers, and lipid-lowering drugs, such as statins and antiandrogens, can lead to male ED [106-107]. In the course of ED treatment, the use of these drugs will aggravate the difficulty treating ED. The drugs taken by patients with ED should be considered, and associated medications should be modified to reduce the loss of therapeutic effects on ED.

3.4.2.2 PDE5is combined with other non-PDE5i drugs

For ED patients with other disorders, the therapeutic regimen focuses on the control or cure of the primary diseases, although the application of PDE5is at suitable doses for an adequate course of treatment, regardless of these diseases, is a definite factor related to the status of ED. Therefore, combining PDE5is with other drugs for comorbidities is an important strategy for improving ED or salvaging erectile function in PDE5i nonresponders.

In vitro studies have found that persistent low testosterone levels can lead to a decrease in the activity and expression of NO synthase (NOS), thereby damaging penile tissues [108]; normal testosterone levels result in PDE5i efficacy because PDE5 is under the control of testosterone [109]. Serum testosterone levels less than 300 ng/dl can hamper the response to PDE5is [110]. In patients with ED and hypogonadism, which leads to low testosterone levels, testosterone alone can enable 34.4% of patients to achieve satisfactory erection, with the combined use of testosterone and sildenafil allowing another 37.5% patients to achieve satisfactory erection. These results suggest that the combination of testosterone and sildenafil has synergism in ED [111]. Additionally, testosterone combined with 10 mg of tadalafil once a day or 20 mg twice a week can treat ED in patients with low testosterone levels (T ≤3 or 3.4 ng/ mL) who do not respond to tadalafil [110, 112-113]. Therefore, during treatment with PDE5is for ED along with hypogonadism, the addition of testosterone can rescue PDE5i nonresponsiveness. For routine treatment, testosterone alone can be used first in ED patients with hypogonadism. If this is not sufficient to restore erection, a short-acting PDE5i (sildenafil or vardenafil) can be added and, if necessary, combined with a long-acting PDE5i (tadalafil) [109] (Fig. 1). Middle-aged and elderly men commonly always suffer from BPH, which increases the risk of ED [114], and α-adrenergic antagonists are commonly used for treating BPH. Evidence-based studies have found that in patients with BPH and ED, the combination of a PDE5i and an α-adrenergic antagonist resulted in higher IIEF scores compared with the use of a PDE5i alone [115]; in particular, the long-term use of long-acting tadalafil was found to be remarkably beneficial for ED along with BPH/LUTSs [109]. Statins are important lipid-lowering drugs, and their side effects can cause male dysfunction. Interestingly, by activating endogenous NOS, atorvastatin significantly elevated the IIEF-5 score and improved erectile function in patients with ED who did not respond to sildenafil [116]. Two clinical studies have found that adding atorvastatin to sildenafil for ED significantly improved the response to sildenafil and enhanced erectile function in patients with hypercholesterolemia and no response to sildenafil [117-118]. In conclusion, combining non-PDE5i drugs with PDE5is to improve the therapeutic effect on ED in PDE5i nonresponders is an important strategy to consider. It is also worth noting that in studies of sildenafil nonresponders, some drugs, such as intraurethral alprostadil, cabergoline, and intracavernous PGE1 injections, were found to restore erectile function in patients who did not respond to sildenafil treatment [119-121]. Although there have been no studies to date on these drugs in combination with PDE5is for ED in PDE5i nonresponders, these drugs may also represent important future directions for ED treatment.

Figure 1.

Management of patients with ED and hypogonadism. In patients with ED, more attention should be paid to testosterone supplementation after hypogonadism is confirmed by the detection of testosterone. In patients with ED and hypogonadism, some will recover from ED after treatment with PDE5is, but others will show nonresponsiveness to PDE5is; in these cases, ED can be treated by adding testosterone to the PDE5i treatment. The reason for this lack of a response is that PDE5 is under the control of testosterone, and a normal testosterone level is the basis for the full effect of PDE5is. Therefore, in ED patients with hypogonadism, we recommend giving priority to testosterone supplementation to treat a portion of them and using a combination of testosterone supplementation and PDE5is for the remaining patients.

3.5 Lifestyle adjustments: a neglected issue

In the process of using PDE5is to treat ED, lifestyle adjustments, such as those involving smoking, drinking, low levels of physical activity, and obesity, are important factors affecting erectile function and the efficacy of these drugs. Smoking increases the risk for ED development, regardless of whether it is active or passive smoking [122]. Compared to a nonsmoking group, a (current and past) smoking group showed an odds ratio (OR) for ED of 1.51 (95% CI: 1.34-1.71), whereas the OR for ED in the group with a past smoking history was 1.29 (95% CI: 1.07-1.47) [123]. Indeed, the cessation of smoking is reported to enhance sexual health indexes in male smokers with a relatively long smoking history, and this effect was independent of the current ED status. Long-term and excessive drinking are also risk factors for sexual dysfunction [124]. For instance, it has been demonstrated that heavy drinking and nondrinking are associated with the ED risk and that moderate drinking actually protects males from developing ED and diabetes [125-126]. Alcohol consumption can also seriously affect the efficacy of sildenafil in the treatment of ED, which is related to the pharmacological characteristics of this drug. Overweight, obesity and metabolic syndrome are all associated with an increased risk of ED [127]. In one study, the risk of ED was increased to 40% in males with obesity [125], and sexual activity and behaviors improved in ED patients who participated in a weight-loss program [128]. Some studies have also reported that adherence to the Mediterranean diet could help patients with obesity and metabolic syndrome alleviate and resolve symptoms of ED in comparison with the controls [129]. Moreover, a high-fat meal slows the absorption of most PDE5is, except tadalafil and the orally disintegrating formulation of vardenafil, delaying the maximum blood concentration for up to approximately 1 h. Thus, some ED patients who have sex according to the drug instructions may inadvertently unconsciously and indirectly reduce the therapeutic effect due to an insufficient blood drug concentration [12]. It has been found that a low exercise level is an independent factor that correlates positively with the risk of ED [130-131]. A study on the mechanism involved found that with increasing exercise, markers of vascular endothelial dysfunction, such as serum endothelial progenitor cells and endothelial microparticles, decreased significantly, suggesting that exercise can improve erectile function by protecting vascular endothelial cells [67]. In short, ED patients treated with PDE5is should be advised to adopt a healthy lifestyle as part of their regimen. Although there have been no studies on the direct relationship between lifestyle adjustments and PDE5i nonresponsiveness, lifestyle adjustments may be a nonnegligible strategy in these patients.

3.6 Patient management

Counseling based on the needs of patients and their partners is an important part of ED management. The approach requires good communication between patients and doctors, which helps to resolve patients' concerns and facilitate implementation of the clinicians' recommendations [12]. Additionally, there are many factors affecting nonresponsiveness to PDE5is during ED treatment. For example, due to the pharmacokinetic characteristics of PDE5is, most should be taken 45-60 minutes before sexual intercourse, and premature sexual activity after taking a PDE5i will lead to a poor therapeutic effect due to an insufficient blood concentration [12]. A high-fat diet can also delay the maximum observed concentration of most PDE5is, except tadalafil and the orally disintegrating formulation of vardenafil, and thus affect the treatment outcome [132]. Furthermore, some patients also use herbal remedies or dietary supplements during ED treatment. Although some are effective, these medicines contain many unknown ingredients [12], and they may increase the difficulty of using PDE5is in nonresponders. Therefore, periodic follow-up visits with patients can help to reveal the use of such drugs, the psychological state and the medical status to determine whether the treatment is adequate, whether the medications are correct, whether poor lifestyle factors have been addressed, and whether there are other adverse factors affecting ED treatment to guide the correct management of ED [12, 22, 29].

4. Management of strategies for treating ED in PDE5i nonresponders

In the management of ED treatment, lifestyle factors, such as smoking, excessive drinking, high-fat diets, and low exercise levels are closely related to the treatment effect; thus, addressing the above unhealthy lifestyle factors is necessary in the treatment of PDE5i nonresponders. Accordingly, lifestyle adjustments combined with improved pharmacotherapy with PDE5is is the first choice. At the same time, for patients with definite mental issues, therapeutic strategies to improve the psychological status should be added. For ED patients with comorbidities, the treatment of these comorbidities is an important prerequisite to ensure and improve the therapeutic effects on ED. Therefore, on the basis of correcting unhealthy lifestyle factors and improving PDE5i treatment, cooperation with comorbidity-related treatment strategies should be instilled. Of course, disease characteristics vary among ED patients, and individualized treatment should be emphasized. In particular, for the treatment of ED patients who are nonresponsive to PDE5is, the different treatment strategies mentioned above should be jointly adopted according to the characteristics of each patient (Fig. 2). It is noteworthy that there is a difference between the application of treatment approaches in young adults and elderly men. In young adults, psychological factors have a great impact on ED, and attention should be directed toward strengthening the treatment of these factors to quickly improve erectile function. In older men, the presence of comorbidities due to aging may be the main reason for the difficulty in treating ED, and attention should be directed toward overall health and the management of chronic diseases in these ED patients.

Figure 2.

Management of strategies to treat ED in PDE5i nonresponders. In the management of PDE5i nonresponders, the first-line strategies consist of lifestyle adjustments and improved pharmacotherapy with PDE5is, including sufficient medication attempts, increased PDE5i doses, different dosing regimens, different PDE5is and the combined use of long-acting and short-acting PDE5is. If the patient has an obvious mental disorder, we should focus on the patient’s psychology and give corresponding treatment, such as attaching importance to the partner’s role and providing psychological intervention, including drugs, sexual counseling and cognitive behavioral therapy. In addition, strategies of improved pharmacotherapy with PDE5is and lifestyle adjustments should be added. If ED patients have comorbidities, comorbidity-related strategies, such as the selection of PDE5is with greater effects on ED and the management of medications for comorbidities of ED, including associated medication modifications, and combining PDE5is with other non-PDE5i drugs, should be fully considered on the basis of the strategies of improved pharmacotherapy with PDE5is and lifestyle adjustments. If necessary, non-drug therapeutic approaches with or without PDE5is can be selected according to the actual treatment profile of each PDE5i nonresponder. It is worth noting that in process of treating every PDE5i nonresponder, patient management should be of great concern. Periodic follow-up visits should be carried out to find any deficiencies in the ED treatment process. Good communication should also be established through patient counseling to resolve patients' concerns and ensure the smooth implementation of treatment.

5. Conclusions

ED is a common sexual abnormality in adult men that measurably affects their psychological and physical QOL as well as that of their partners. The discovery and application of PDE5is has been revolutionary for the treatment of ED. With increasing clinical trials on PDE5is and ED, there are now many strategies for improving erectile function, as reviewed above. Regardless, ED is a very complex condition involving both psychological and physical factors. The treatment program for ED will vary among individuals, especially in patients with a poor response to PDE5is. Therefore, combinations of various strategies to enhance the response to PDE5is should be applied to improve the therapeutic efficacy according to the clinical characteristics of each patient. Additionally, PDE5i nonresponders are a unique group of ED patients, and the causes of the lack of a response to PDE5is remain to be clarified. Although some studies have suggested improved strategies for PDE5i nonresponders, these studies are limited, and more related basic and clinical research is needed to help PDE5i nonresponders achieve satisfactory sexual experiences.