Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_2745_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
29 Мб
Скачать
modifying therapies. There are some smaller studies that suggest that breastfeeding may reduce the risk of MS in offspring.
81,82
Overall, the literature suggests that those
patients with mild disease are more likely to breastfeed, whereas those with active or severe disease cannot afford to forego treatment and often defer breastfeeding. 83 In general, because breastfeeding has both maternal and neonatal health benefits, women with MS should not be discouraged from breastfeeding, although they should be supported if they chose not to.
Postpartum Relapse
Several studies have shown that there is a reduced rate of relapse frequency during pregnancy, especially in the last trimester, and an increase in the rate of relapse in the postpartum period. The rates of relapse seem to return to baseline starting at about 3 months postpartum. 3 Studies have also shown that women with higher rates of relapse in the year before pregnancy, as well as a higher disease activity, have increased rates of postpartum relapse. 84 Therapies that have been shown to somewhat reduce the risk of postpartum relapse include high-dose glucocorticoids and intravenous immunoglobulins.
3,84
Studies have shown that exclusive
breastfeeding can have a modestly protective effect against MS relapse, but this must be weighed against the risk of not reinstituting medications that may be contraindicated in breastfeeding.
85
There is also an increased rate of relapse after pregnancy termination or spontaneous miscarriage. Studies have shown that abortion induces reactivation of inflammation in relapse­remitting MS, which may be due to dysregulated inflammatory processes that occur in the early stages of pregnancy and then are acutely changed when the pregnancy abruptly ends. 86 The increase in MS symptoms may occur as long as 12 months after miscarriage or termination.
12,86
Postpartum Depression
https://t.me/medicina_free
There are many psychosocial and physical issues that patients with MS face that can become exponentially increased in the postpartum period. The hormonal shifts accompanying delivery, as well as having to endure childbirth and then care for a newborn infant, can cause distress, fatigue, anxiety, and sometimes depressive symptoms in all postpartum women.
87
This is exacerbated in women with MS, who may be dealing with relapse, have underlying depression, or be on medications causing side effects such as lethargy and mood changes. Not surprisingly, peripartum depression has been found to be significantly more common among patients with MS than patients without MS. Interestingly, some studies have shown an increased rate of psychiatric disorders in the children of parents with MS.
88
Increased social support and
psychotherapy, as well as antidepressant and anxiolytic medications, can be used to treat postpartum depression in patients with MS; however, treatment of relapse symptoms should also be used to help decrease both physical and neurocognitive symptoms.
MS During Menopause and Beyond
Menopause
Menopause is defined as the permanent cessation of ovarian functioning, and the average age for this to occur in the United States is 51 years. 89 During the onset of puberty, hormonal shifts occur and the pattern of this shift is associated with an increased risk of MS. However, the hormonal shifts that occur in pregnancy, as previously discussed, typically cause a decrease in MS symptoms. Studies on patient-reported outcomes have been limited. Two small studies have shown that menopause is associated with worsening of MS symptoms in 40% to 54% of women, but these studies differed in how beneficial hormone replacement therapy (HRT) was at relieving these symptoms.
90,91
The symptoms commonly experienced in menopause include malaise, headache, fatigue, poor sleep, as well as cognitive, emotional, visual, and urogenital symptoms. These symptoms
https://t.me/medicina_free
significantly overlap with symptoms of MS and may therefore be very difficult to differentiate. Menopause symptoms may therefore go unrecognized in patients with MS. “Hot flashes” may trigger pseudorelapses in patients with MS, which can be differentiated on physical examination and MRI.
7
Nonpharmacologic interventions for menopausal and perimenopausal symptoms include psychotherapy, changes in diet or clothing, bladder training and biofeedback for urinary symptoms, and lifestyle changes, such as smoking cessation and decrease in alcohol intake. Pharmacologic interventions can include hormone replacement, antispasmodics, tricyclic antidepressants, selective serotonin or norepinephrine reuptake inhibitors, gabapentin, anticonvulsants, benzodiazepines, and sleep aids. 92 An integrated approach to perimenopausal symptom management is recommended.
Hormone Replacement
HRT may be used in postmenopausal women with MS. Studies have shown that symptom severity was improved in postmenopausal patients with MS on HRT therapy. 90 There are risks associated with HRT, such as the increased risk of endometrial cancer with unopposed estrogen in women with an intact uterus. Studies have also implicated some forms of HRT in increasing the risk of breast cancer recurrence, thrombosis, and coronary heart disease. 92 Studies in patients with MS on HRT have shown that it can be neuroprotective; however, it alters immune regulation and can increase the risk of osteoporosis, which is more common in patients with MS in than healthy women. Therefore, the ratio of risks to benefits for HRT in patients with MS may be different than reported for patients without MS, and a multidisciplinary approach is needed in treating patients with MS with HRT. Of concern is that premature ovarian failure is increased in patients with MS because of exposure to medications such as cyclophosphamide and Novantrone (which are now rarely used), and therefore, HRT may be used for longer periods in these patients. Studies analyzing the risks and benefits of long-term HRT use in patients with MS who are taking more commonly used medications, such as monoclonal antibody therapies, are
https://t.me/medicina_free
lacking. Owing to the various risks associated with HRT, it is recommended that HRT be used for the shortest possible duration and with the lowest possible dose, in patients with and without MS.
7
Osteoporosis and Its Treatment
Postmenopausal patients are at increased risk for osteoporosis, which is a condition associated with increased fractures and subsequently increased morbidity and mortality. Patients with MS are at high risk for osteoporosis because they are more likely to have had long-term exposure to steroids and deconditioning from being less physically active. The neurocognitive effects of MS can lead to issues with balance, gait, and impaired cognition, which can predispose these patients to falling and suffering from fractures.
Lifestyle changes, such as increasing calcium and vitamin D intake, smoking cessation, decreasing alcohol intake, and performing aerobic exercise, can improve bone strength and are recommended for all patients at risk for osteoporosis. Physical therapy to improve gait and balance, as well as fall prevention precautions in the home, such as removing loose rugs and improving lighting, can also be implemented to decrease fall risk. Pharmacologic interventions are recommended for postmenopausal women with prior osteoporotic vertebral or hip fracture, postmenopausal women with bone mineral density values consistent with osteoporosis, postmenopausal women with abnormal bone mineral density scores and a 10-year fracture risk of at least 20% of major osteoporotic fracture or of hip fracture risk of at least 3%.
92
First-line therapies include calcium and vitamin D supplementation and bisphosphonates, and second-line therapies include parathyroid hormone, selective estrogen receptor modulators, the monoclonal antibody denosumab, as well as calcitonin. In women with premature ovarian failure and early menopause, hormonal therapy should be considered until they reach menopausal age, which is about 51 years.
93
Neurologists and other physicians caring for patients with MS should be cognizant of the increased risk of osteoporosis as the
https://t.me/medicina_free
woman ages. Early implantation of preventative strategies is recommended to decrease the risk of osteoporotic falls. These include making sure the patient with MS has a proper diet with adequate calcium and vitamin D, starting physical therapy and gait and balance training, encouraging aerobic exercise, and encouraging lifestyle modifications. At the time of this writing, pharmacologic interventions for osteoporosis in patients with MS have not been well studied, so recommendations for their implementation in patients with MS are not different from those in patients without MS.
7,93
Conclusion
Women affected by MS face a unique set of challenges as they progress through their reproductive years. When treating female patients with MS, medical providers must take into consideration how their disease and medications used to treat it interact with their menstrual cycle, sexual functioning, fertility concerns, pregnancy, and menopausal hormonal shifts. It is important for providers to both counsel female patients with MS thoroughly about the possible risks and side effects of recommended treatments and carefully listen to them when they discuss their concerns, their symptoms, and their reproductive goals and priorities. This often requires the care and treatment coordination of a multidisciplinary team of providers, with the patient being an integral part of this team, and part of their disease management.
References
Grinsted L, Heltberg A, Hagen C, Djursing H. Serum sex hormone and
gonadotropin concentrations in premenopausal women with multiple sclerosis. J Intern Med. 1989;226(4):241-244.
Lombardi G, Celso M, Bartelli M, Cilotti A, Del Popolo G. Female sexual
dysfunction and hormonal status in multiple sclerosis patients. J Sex Med. 2011;8(4):1138-1146.
Ghezzi A, Zaffaroni M. Female-specific issues in multiple sclerosis. Expert Rev
Neurother. 2008;8(6):969-977.
Deliconstantinos G. Effects of prostaglandin E2 and progesterone on rat brain
synaptosomal plasma membranes. Ciba Found Symp. 1990;153:190-199; discussion 9-205.
https://t.me/medicina_free
Elenkov IJ, Wilder RL, Bakalov VK, et al. IL-12, TNF-alpha, and hormonal
changes during late pregnancy and early postpartum: implications for autoimmune disease activity during these times. J Clin Endocrinol Metab. 2001;86(10):4933-4938.
Zorgdrager A, De Keyser J. The premenstrual period and exacerbations in multiple
sclerosis. Eur Neurol. 2002;48(4):204-206.
Bove R, Alwan S, Friedman JM, et al. Management of multiple sclerosis during
pregnancy and the reproductive years: a systematic review. Obstet Gynecol. 2014;124(6):1157-1168.
Demirkiran M, Sarica Y, Uguz S, Yerdelen D, Aslan K. Multiple sclerosis patients
with and without sexual dysfunction: are there any differences? Mult Scler. 2006;12(2):209-214.
Orasanu B, Frasure H, Wyman A, Mahajan ST. Sexual dysfunction in patients with
multiple sclerosis. Mult Scler Relat Disord. 2013;2(2):117-123.
Zavoreo I, Gržinčić T, Preksavec M, Madžar T, Bašić Kes V. Sexual dysfunction
and incidence of depression in multiple sclerosis patients. Acta Clin Croat. 2016;55(3):402-406.
Cavalla P, Rovei V, Masera S, et al. Fertility in patients with multiple sclerosis:
current knowledge and future perspectives. Neurol Sci. 2006;27(4):231-239. Hellwig K. Pregnancy in multiple sclerosis. Eur Neurol. 2014;72(suppl 1):39-42. Jalkanen A, Alanen A, Airas L. Finnish Multiple Sclerosis and Pregnancy Study
Group . Pregnancy outcome in women with multiple sclerosis: results from a
prospective nationwide study in Finland. Mult Scler. 2010;16(8):950-955. Hellwig K, Haghikia A, Rockhoff M, Gold R. Multiple sclerosis and pregnancy:
experience from a nationwide database in Germany. Ther Adv Neurol Disord.
2012;5(5):247-253. Niedziela N, Adamczyk-Sowa M, Pierzchała K. Epidemiology and clinical record
of multiple sclerosis in selected countries: a systematic review. Int J Neurosci.
2014;124(5):322-330. Sloka JS, Phillips PW, Stefanelli M, Joyce C. Co-occurrence of autoimmune
thyroid disease in a multiple sclerosis cohort. J Autoimmune Dis. 2005;2:9. Lublin FD, Reingold SC. Defining the clinical course of multiple sclerosis: results
of an international survey. National Multiple Sclerosis Society (USA) Advisory
Committee on Clinical Trials of New Agents in Multiple Sclerosis. Neurology.
1996;46(4):907-911. Lublin FD, Reingold SC, Cohen JA, et al. Defining the clinical course of multiple
sclerosis: the 2013 revisions. Neurology. 2014;83(3):278-286. Hellwig K, Correale J. Artificial reproductive techniques in multiple sclerosis. Clin
Immunol. 2013;149(2):219-224. Hellwig K, Beste C, Brune N, et al. Increased MS relapse rate during assisted
reproduction technique. J Neurol. 2008;255(4):592-593. Correale J, Farez MF, Ysrraelit MC. Increase in multiple sclerosis activity after
assisted reproduction technology. Ann Neurol. 2012;72(5):682-694. Hellwig K, Schimrigk S, Beste C, Muller T, Gold R. Increase in relapse rate during
assisted reproduction technique in patients with multiple sclerosis. Eur Neurol.
2009;61(2):65-68.
https://t.me/medicina_free
Michel L, Foucher Y, Vukusic S, et al. Increased risk of multiple sclerosis relapse
after in vitro fertilisation. J Neurol Neurosurg Psychiatry. 2012;83(8):796-802. Spence RD, Voskuhl RR. Neuroprotective effects of estrogens and androgens in
CNS inflammation and neurodegeneration. Front Neuroendocrinol.
2012;33(1):105-115. Voskuhl RR, Gold SM. Sex-related factors in multiple sclerosis susceptibility and
progression. Nat Rev Neurol. 2012;8(5):255-263. Bodhankar S, Offner H. GPR30 forms an integral part of e2-protective pathway in
experimental autoimmune encephalomyelitis. Immunol Endocr Metab Agents
Med Chem. 2011;11(4):262-274. Matejuk A, Hopke C, Vandenbark AA, Hurn PD, Offner H. Middle-age male mice
have increased severity of experimental autoimmune encephalomyelitis and are
unresponsive to testosterone therapy. J Immunol. 2005;174(4):2387-2395. Hussain R, Ghoumari AM, Bielecki B, et al. The neural androgen receptor: a
therapeutic target for myelin repair in chronic demyelination. Brain.
2013;136(Pt 1):132-146. Igra MS, Paling D, Wattjes MP, Connolly DJA, Hoggard N. Multiple sclerosis
update: use of MRI for early diagnosis, disease monitoring and assessment of
treatment related complications. Br J Radiol. 2017;90(1074):20160721. Kaunzner UW, Gauthier SA. MRI in the assessment and monitoring of multiple
sclerosis: an update on best practice. Ther Adv Neurol Disord. 2017;10(6):247-
261.
Wattjes MP, Steenwijk MD, Stangel M. MRI in the diagnosis and monitoring of
multiple sclerosis: an update. Clin Neuroradiol. 2015;25(suppl 2):157-165. Pakpoor J, Disanto G, Lacey MV, Hellwig K, Giovannoni G, Ramagopalan SV.
Breastfeeding and multiple sclerosis relapses: a meta-analysis. J Neurol.
2012;259(10):2246-2248. Munger KL, Åivo J, Hongell K, Soilu-Hänninen M, Surcel HM, Ascherio A.
Vitamin D status during pregnancy and risk of multiple sclerosis in offspring of
women in the Finnish maternity cohort. JAMA Neurol. 2016;73(5):515-519. Bove R, Chua AS, Xia Z, Chibnik L, De Jager PL, Chitnis T. Complex relation of
HLA-DRB1*1501, age at menarche, and age at multiple sclerosis onset. Neurol
Genet. 2016;2(4):e88. Kavak KS, Teter BE, Hagemeier J, Zakalik K, Weinstock-Guttman B; New York
State Multiple Sclerosis Consortium . Higher weight in adolescence and young
adulthood is associated with an earlier age at multiple sclerosis onset. Mult
Scler. 2015;21(7):858-865. Sloka JS, Pryse-Phillips WE, Stefanelli M. The relation between menarche and the
age of first symptoms in a multiple sclerosis cohort. Mult Scler. 2006;12(3):333-
339.
Juanatey A, Blanco-Garcia L, Tellez N. Ocrelizumab: its efficacy and safety in
multiple sclerosis. Rev Neurol. 2018;66(12):423-433. Coyle PK. Multiple sclerosis and pregnancy prescriptions. Expert Opin Drug Saf.
2014;13(12):1565-1568. Coyle PK. Disease-modifying agents in multiple sclerosis. Ann Indian Acad Neurol.
2009;12(4):273-282.
https://t.me/medicina_free
Ghezzi A, Annovazzi P, Portaccio E, Cesari E, Amato MP. Current
recommendations for multiple sclerosis treatment in pregnancy and puerperium.
Expert Rev Clin Immunol. 2013;9(7):683-691; quiz 92. Lu E, Wang BW, Guimond C, Synnes A, Sadovnick D, Tremlett H. Disease-
modifying drugs for multiple sclerosis in pregnancy: a systematic review.
Neurology. 2012;79(11):1130-1135. Brucker MC, King TL. The 2015 US Food and Drug Administration pregnancy and
lactation labeling rule. J Midwifery Womens Health. 2017;62(3):308-316. Center TRT. Available at https://reprotox.org/. Pritham UA, McKay L. Safe management of chronic pain in pregnancy in an era of
opioid misuse and abuse. J Obstet Gynecol Neonatal Nurs. 2014;43(5):554-567. Guille C, Barth KS, Mateus J, McCauley JL, Brady KT. Treatment of prescription
opioid use disorder in pregnant women. Am J Psychiatry. 2017;174(3):208-214. Guttuso T, Robinson LK, Amankwah KS. Gabapentin use in hyperemesis
gravidarum: a pilot study. Early Hum Dev. 2010;86(1):65-66. Guttuso T, Shaman M, Thornburg LL. Potential maternal symptomatic benefit of
gabapentin and review of its safety in pregnancy. Eur J Obstet Gynecol Reprod
Biol. 2014;181:280-283. Fromm GH, Terrence CF, Chattha AS. Baclofen in the treatment of trigeminal
neuralgia: double-blind study and long-term follow-up. Ann Neurol.
1984;15(3):240-244. Wang MJ, Kuper SG, Sims B, et al. Opioid detoxification in pregnancy: systematic
review and meta-analysis of perinatal outcomes. Am J Perinatol. 2018.
doi:10.1055/s-0038-1670680. Brar B, Jackson D, Nat M, Patil P, Iriye B, Planinic P. Antenatal interventions based
upon fetal surveillance of the daily opioid exposed fetus: a descriptive analysis.
J Matern Fetal Neonatal Med. 2018:1-11. Lacaze-Masmonteil T, O’Flaherty P. Managing infants born to mothers who have
used opioids during pregnancy. Paediatr Child Health. 2018;23(3):220-226. Johnson AJ, Jones CW. Opioid use disorders and pregnancy. Obstet Gynecol Clin
North Am. 2018;45(2):201-216. Weatherby SJM, Woolner P, Clarke CE. Pregnancy in stiff-limb syndrome. Mov
Disord. 2004;19(7):852-854. Goldkamp J, Blaskiewicz R, Myles T. Stiff person syndrome and pregnancy. Obstet
Gynecol. 2011;118(2 Pt 2):454-457. Moran LR, Almeida PG, Worden S, Huttner KM. Intrauterine baclofen exposure: a
multidisciplinary approach. Pediatrics. 2004;114(2):e267-e269. Dalton CM, Keenan E, Jarrett L, Buckley L, Stevenson VL. The safety of baclofen
in pregnancy: intrathecal therapy in multiple sclerosis. Mult Scler.
2008;14(4):571-572. Harden CL, Hopp J, Ting TY, Pennell PB, French JA, Hauser WA, et al. Practice
parameter update: management issues for women with epilepsy–focus on
pregnancy (an evidence-based review): obstetrical complications and change in
seizure frequency: report of the Quality Standards Subcommittee and
Therapeutics and Technology Assessment Subcommittee of the American
Academy of Neurology and American Epilepsy Society. Neurology.
2009;73(2):126-132.
https://t.me/medicina_free
Masarwa R, Bar-Oz B, Gorelik E, Reif S, Perlman A, Matok I. Prenatal exposure to
SSRIs and SNRIs and risk for persistent pulmonary hypertension of the
newborn: a systematic review, meta-analysis and network meta-analysis. Am J
Obstet Gynecol. 2019;220(1):57.e1-57.e13. Huybrechts KF, Hernández-Díaz S, Avorn J. Antidepressant use in pregnancy and
the risk of cardiac defects. N Engl J Med. 2014;371(12):1168-1169. Wegner I, Edelbroek P, de Haan GJ, Lindhout D, Sander JW. Drug monitoring of
lamotrigine and oxcarbazepine combination during pregnancy. Epilepsia.
2010;51(12):2500-2502. Voinescu PE, Park S, Chen LQ, et al. Antiepileptic drug clearances during
pregnancy and clinical implications for women with epilepsy. Neurology.
2018;91(13):e1228-e1236. Johnson EL, Stowe ZN, Ritchie JC, et al. Carbamazepine clearance and seizure
stability during pregnancy. Epilepsy Behav. 2014;33:49-53. Coyle PK, Sinclair SM, Scheuerle AE, Thorp JM, Albano JD, Rametta MJ. Final
results from the Betaseron (interferon β-1b) pregnancy registry: a prospective
observational study of birth defects and pregnancy-related adverse events. BMJ
Open. 2014;4(5):e004536. Fragoso YD, Boggild M, Macias-Islas MA, et al. The effects of long-term exposure
to disease-modifying drugs during pregnancy in multiple sclerosis. Clin Neurol
Neurosurg. 2013;115(2):154-159. Achiron A, Rotstein Z, Noy S, Mashiach S, Dulitzky M, Achiron R. Intravenous
immunoglobulin treatment in the prevention of childbirth-associated acute
exacerbations in multiple sclerosis: a pilot study. J Neurol. 1996;243(1):25-28. Kelly VM, Nelson LM, Chakravarty EF. Obstetric outcomes in women with
multiple sclerosis and epilepsy. Neurology. 2009;73(22):1831-1836. Mueller BA, Zhang J, Critchlow CW. Birth outcomes and need for hospitalization
after delivery among women with multiple sclerosis. Am J Obstet Gynecol.
2002;186(3):446-452. Chen YH, Lin HL, Lin HC. Does multiple sclerosis increase risk of adverse
pregnancy outcomes? A population-based study. Mult Scler. 2009;15(5):606-
612.
Bader AM, Hunt CO, Datta S, Naulty JS, Ostheimer GW. Anesthesia for the
obstetric patient with multiple sclerosis. J Clin Anesth. 1988;1(1):21-24. Hopkins AN, Alshaeri T, Akst SA, Berger JS. Neurologic disease with pregnancy
and considerations for the obstetric anesthesiologist. Semin Perinatol.
2014;38(6):359-369. Villard-Mackintosh L, Vessey MP. Oral contraceptives and reproductive factors in
multiple sclerosis incidence. Contraception. 1993;47(2):161-168. Thorogood M, Hannaford PC. The influence of oral contraceptives on the risk of
multiple sclerosis. Br J Obstet Gynaecol. 1998;105(12):1296-1299. Alonso A, Jick SS, Olek MJ, Ascherio A, Jick H, Hernán MA. Recent use of oral
contraceptives and the risk of multiple sclerosis. Arch Neurol. 2005;62(9):1362-
1365.
Robertson P, Hellriegel ET. Clinical pharmacokinetic profile of modafinil. Clin
Pharmacokinet. 2003;42(2):123-137.
https://t.me/medicina_free
Langer-Gould A, Hellwig K. One can prevent post-partum MS relapses by
exclusive breast feeding: yes. Mult Scler. 2013;19(12):1567-1568. Vukusic S, Confavreux C. One can prevent post-partum MS relapses by exclusive
breast feeding: no. Mult Scler. 2013;19(12):1565-1566. Hutchinson M. One can prevent post-partum MS relapses by exclusive breast
feeding: commentary. Mult Scler. 2013;19(12):1569-1570. Langer-Gould A, Huang S, Van Den Eeden SK, et al. Vitamin D, pregnancy,
breastfeeding, and postpartum multiple sclerosis relapses. Arch Neurol.
2011;68(3):310-313. Langer-Gould A, Beaber BE. Effects of pregnancy and breastfeeding on the
multiple sclerosis disease course. Clin Immunol. 2013;149(2):244-250. Coyle PK. Management of women with multiple sclerosis through pregnancy and
after childbirth. Ther Adv Neurol Disord. 2016;9(3):198-210. Conradi S, Malzahn U, Paul F, et al. Breastfeeding is associated with lower risk for
multiple sclerosis. Mult Scler. 2013;19(5):553-558. Ragnedda G, Leoni S, Parpinel M, et al. Reduced duration of breastfeeding is
associated with a higher risk of multiple sclerosis in both Italian and Norwegian
adult males: the EnvIMS study. J Neurol. 2015;262(5):1271-1277. Kieseier BC, Wiendl H. Postpartum disease activity and breastfeeding in multiple
sclerosis revisited. Neurology. 2010;75(5):392-393. Vukusic S, Hutchinson M, Hours M, et al. Pregnancy and multiple sclerosis (the
PRIMS study): clinical predictors of post-partum relapse. Brain. 2004;127(Pt
6):1353-1360.
Hellwig K, Rockhoff M, Herbstritt S, et al. Exclusive breastfeeding and the effect
on postpartum multiple sclerosis relapses. JAMA Neurol. 2015;72(10):1132-
1138.
Landi D, Ragonese P, Prosperini L, et al. Abortion induces reactivation of
inflammation in relapsing-remitting multiple sclerosis. J Neurol Neurosurg
Psychiatry. 2018;89(12):1272-1278. Airas L, Jalkanen A, Alanen A, Pirttilä T, Marttila RJ. Breast-feeding, postpartum
and prepregnancy disease activity in multiple sclerosis. Neurology.
2010;75(5):474-476. Razaz N, Tremlett H, Marrie RA, Joseph KS. Peripartum depression in parents with
multiple sclerosis and psychiatric disorders in children. Mult Scler.
2016;22(14):1830-1840. ACOG Practice Bulletin No. 141: management of menopausal symptoms. Obstet
Gynecol. 2014;123(1):202-216. Smith R, Studd JW. A pilot study of the effect upon multiple sclerosis of the
menopause, hormone replacement therapy and the menstrual cycle. J R Soc
Med. 1992;85(10):612-613. Holmqvist P, Wallberg M, Hammar M, Landtblom AM, Brynhildsen J. Symptoms
of multiple sclerosis in women in relation to sex steroid exposure. Maturitas.
2006;54(2):149-153. Practice bulletin No. 141: management of menopausal symptoms: Correction.
Obstet Gynecol. 2018;131(3):604.
https://t.me/medicina_free