Accessing spinal networks to address sexual dysfunction
View Patent ↗In various embodiments methods and devices are provided for facilitating sexual function in a subject with a neuromotor disorder. In certain embodiments the methods involve providing magnetic stimulation of the spinal cord at a location, frequency and intensity sufficient to facilitate sexual function.
1. A method of improving or restoring sexual function in a subject with impaired sexual function, said method comprising:
determining a first frequency of a magnetic stimulation based on a plurality of bulbocavernosus reflex (BCR) measurements corresponding to an application of one or more frequency values;
applying the magnetic stimulation to the cervical and/or thoracic, and/or lumbosacral spinal cord wherein the magnetic stimulation is at the first frequency, the first frequency ranging from about 0.5 Hz up to about 100 Hz, and wherein the magnetic stimulation is sufficient to and effective to improve or restore a volitional control of sexual function in said subject;
repeatedly applying the magnetic stimulation at the first frequency after a first interval of time has passed, the first interval of time comprising one or more days until the volitional control of sexual function is achieved;
applying the magnetic stimulation to the cervical and/or thoracic, and/or lumbosacral spinal cord at a second frequency once the volitional control of sexual function is achieved, wherein the second frequency is less than the first frequency; and
repeatedly applying the magnetic stimulation at the second frequency at a second interval of time to maintain the volitional control of sexual function, wherein the second interval of time is longer than the first interval of time.
2. The method of claim 1 , wherein:
said subject is a subject without a neuromotor disorder but having impaired sexual function; or
said subject is a subject with erectile dysfunction (ED), but who is otherwise healthy; or
said subject is a subject with erectile dysfunction (ED), who is diagnosed with a pathology associated with said ED, other than a neuromotor disorder; or
said subject is a subject with erectile dysfunction (ED), who is diagnosed with a pathology selected from the group consisting of heart disease, atherosclerosis, high cholesterol, high blood pressure, diabetes, obesity, metabolic syndrome, Parkinson's disease, multiple sclerosis, prostate cancer or enlarged prostate; or
said subject is a subject with erectile dysfunction after prostate biopsy; or
said subject is a subject with a neuromotor disorder.
3. The method of claim 1 , wherein:
the magnetic stimulation initiates or increases/improves erectile function in a male; and/or
said method mitigates erectile dysfunction; and/or
said method improves a sexual health inventory for men (SHIM) score of said subject.
4. The method of claim 1 , wherein:
at least one of the first frequency or the second frequency ranges from about 1 Hz, or from about 5 Hz, or from about 10 Hz up to about 100 Hz, or up to about 80 Hz, or up to about 60 Hz, or up to about 50 Hz, or up to about 40 Hz, or up to about 20.
5. The method of claim 1 , wherein:
said method comprises a single period of continuous stimulation, or 2, or 3, or 4, or 5, or 6, or 7, or 8, or 9, or 10 or more periods of continuous stimulation wherein said single period of continuous stimulation or said 2, or 3, or 4, or 5, or 6, or 7, or 8, or 9, or 10 or more periods of continuous stimulation each range in duration from about 10 sec, or from about 20 sec, or from about 3 sec or from about 40 sec, or from about 50 sec, or from about 1 min, or from about 2 minutes up to about 30 minutes, or up to about 15 minutes, or up to about 10 minutes, or up to about 8 minutes, or up to about 6 minutes.
6. The method of claim 5 , wherein:
a delay between said 2, or 3, or 4, or 5, or 6, or 7, or 8, or 9, or 10 or more periods of continuous stimulation ranges from about 5 sec, or from about 10 sec, or from about 15 sec, or from about 20 sec up to about 5 minutes, or up to about 4 minutes, or up to about 3 minutes, or up to about 2 minutes, or up to about 1 min, or up to about 45 sec, or up to about 30 sec; or
a delay between said 2, or 3, or 4, or 5, or 6, or 7, or 8, or 9, or 10 or more periods of continuous stimulation is about 30 sec.
7. The method of claim 1 , wherein the magnetic stimulation is stopped and said improving or restoring of sexual function persists in the absence of the magnetic stimulation.
8. The method of claim 1 , wherein the second interval of time is every three days, or a weekly treatment, or about every 10 days, or about every 2 weeks.
9. The method of claim 1 , wherein:
the magnetic stimulation is applied over one or more regions straddling or spanning a region selected from the group consisting of T1-T1, T1-T2, T1-T3, T1-T4, T1-T5, T1-T6, T1-T7, T1-T8, T1-T9, T1-T10, T1-T11, T1-T12, T2-T2, T2-T3, T2-T4, T2-T5, T2-T6, T2-T7, T2-T8, T2-T9, T2-T10, T2-T11, T2-T12, T3-T3, T3-T4, T3-T5, T3-T6, T3-T7, T3-T8, T3-T9, T3-T10, T3-T11, T3-T12, T4-T4, T4-T5, T4-T6, T4-T7, T4-T8, T4-T9, T4-T10, T4-T11, T4-T12, T5-T5, T5-T6, T5-T7, T5-T8, T5-T9, T5-T10, T5-T11, T5-T12, T6-T6, T6-T7, T6-T8, T6-T9, T6-T10, T6-T11, T6-T12, T7-T7, T7-T8, T7-T9, T7-T10, T7-T11, T7-T12, T8-T8, T8-T9, T8-T10, T8-T11, T8-T12, T9-T9, T9-T10, T9-T11, T9-T12, T10-T10, T10-T11, T10-T12, T11-T11, T11-T12, T12-T12; or
the magnetic stimulation is applied over one or more regions straddling or spanning a region selected from the group consisting of L1-L1, L1-L2, L1-L3, L1-L4, L1-L5, L1-S1, L1-S2, L1-S3, L1-S4, L1-S5, L2-L2, L2-L3, L2-L4, L2-L5, L2-S1, L2-S2, L2-S3, L2-S4, L2-S5, L3-L3, L3-L4, L3-L5, L3-S1, L3-S2, L3-S3, L3-S4, L3-S5, L4-L4, L4-L5, L4-S1, L4-S2, L4-S3, L4-S4, L4-S5, L5-L5, L5-S1, L5-S2, L5-S3, L5-S4, L5-S5, S1-S1, S1-S2, S1-S3, S1-S4, S1-S5, S2-S2, S2-S3, S2-S4, S2-S5, S3-S3, S3-S4, S3-S5, S4-S4, S4-S5, and S5-S6; or
the magnetic stimulation is applied over one or more regions straddling or spanning a region selected from the group consisting of C0-C1, C0-C2, C0-C3, C0-C4, C0-C5, C0-C6, C0-C7, C0-T1, C1-C1, C1-C2, C1-C3, C1-C4, C1-C7, C1-C6, C1-C7, C1-T1, C2-C2, C2-C3, C2-C4, C2-C5, C2-C6, C2-C7, C2-T1, C3-C3, C3-C4, C3-C5, C3-C6, C3-C7, C3-T1, C4-C4, C4-C5, C4-C6, C4-C7, C4-T1, C5-C5, C5-C6, C5-C7, C5-T1, C6-C6, C6-C7, C6-T1, C7-C7, and C7-T1; or
the magnetic stimulation is applied over a region between T11 and L4; or
the magnetic stimulation is applied over one or more regions selected from the group consisting of T11-T12, L1-L2, and L2-L3; or wherein said magnetic stimulation is applied over L1-L2 and/or over T11-T12; or
the magnetic stimulation is applied over L1.
10. The method of claim 1 , wherein said subject is administered one or more drugs for an erectile dysfunction.
11. The method of claim 2 , wherein said subject has a spinal cord injury.
12. The method of claim 1 , wherein the magnetic stimulation is applied by a magnetic stimulator disposed over the cervical and/or thoracic, and/or lumbosacral spinal cord.
13. The method of claim 1 , wherein:
the magnetic stimulation comprises magnetic pulses ranging in duration from about 5 μs, or from about 10 μs, or from about 15 μs, or from about 20 μs up to about 500 μs, or up to about 400 μs, or up to about 300 μs, or up to about 200 μs, or up to about 100 μs, or up to about 50 μs; or
the magnetic pulses are about 25 μs in duration.
14. The method of claim 10 , wherein said one or more drugs comprises:
a drug selected from the group consisting of tadalafil, sildenafil, vardenafil, and alprostadil; or
a monoaminergic agonist selected from the group consisting 8-hydroxy-2-(di-n-propylamino) tetralin, 4-(benzodioxan-5-yl) 1-(indan-2-yl) piperazine (S15535), N-{2-[4-(2-methoxyphenyl)-1-piperazinyl] ethyl}-N-(2-pyridinyl) cyclo-hexanecarboxamide, Quipazine, Ketanserin, 4-amino-(6-chloro-2-pyridyl)-1 piperidine hydrochloride, Ondanesetron, Buspirone, Methoxamine, Prazosin, Clonidine, Yohimbine, 6-chloro-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol, 7-chloro-3-methyl-1-phenyl-1,2,4,5-tetrahydro-3-benzazepin-8-ol, Quinpirole, and Eticlopride.