Paternal therapy with disease modifying drugs in multiple sclerosis and pregnancy outcomes: a prospective observational multicentric study

被引:30
作者
Pecori, Chiara [1 ,13 ]
Giannini, Marta [1 ]
Portaccio, Emilio [1 ]
Ghezzi, Angelo [2 ]
Hakiki, Bahia [1 ]
Pasto, Luisa [1 ]
Razzolini, Lorenzo [1 ]
Sturchio, Andrea [1 ]
De Giglio, Laura [3 ]
Pozzilli, Carlo [3 ]
Paolicelli, Damiano [4 ]
Trojano, Maria [4 ]
Marrosu, Maria Giovanna [5 ]
Patti, Francesco [6 ]
Mancardi, Gian Luigi [7 ]
Solaro, Claudio [8 ]
Totaro, Rocco [9 ]
Tola, Maria Rosaria [10 ]
De Luca, Giovanna [11 ]
Lugaresi, Alessandra [11 ]
Moiola, Lucia [12 ]
Martinelli, Vittorio [12 ]
Comi, Giancarlo [12 ]
Amato, Maria Pia [1 ]
机构
[1] Univ Florence, Sect Neurosci, Dept NEUROFARBA, I-50134 Florence, Italy
[2] S Antonio Abate Hosp, Multiple Sclerosis Ctr, Gallarate, Italy
[3] Univ Roma La Sapienza, S Andrea Hosp, Multiple Sclerosis Ctr, Rome, Italy
[4] Univ Bari, Dept Neurol, Bari, Italy
[5] Univ Cagliari, Dept Neurol, Multiple Sclerosis Ctr, Cagliari, Italy
[6] Univ Catania, Multiple Sclerosis Ctr, Catania, Italy
[7] Univ Genoa, Dept Neurol, Genoa, Italy
[8] ASL3 Genovese, Dept Neurol, Genoa, Italy
[9] Univ Aquila, Dept Neurol, I-67100 Laquila, Italy
[10] Univ Ferrara, Dept Neurosci, I-44100 Ferrara, Italy
[11] Univ G DAnnunzio, Neurol Sect, Dept Oncol & Neurosci, Chieti, Italy
[12] Univ Milan, Sci Inst H San Raffaele, Dept Neurol, Milan, Italy
[13] Univ Pisa, Dept Clin & Expt Med, Neurol Unit, Pisa, Italy
关键词
Multiple sclerosis; Paternity; Pregnancy; Interferon beta; Glatiramer acetate; FETAL OUTCOMES; EXPOSURE;
D O I
10.1186/1471-2377-14-114
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Most of Multiple Sclerosis (MS) patients undergo disease modifying drug (DMD) therapy at childbearing age. The objective of this prospective, collaborative study, was to assess outcomes of pregnancies fathered by MS patients undergoing DMD. Methods: Structured interviews on pregnancies fathered by MS patients gathered in the Italian Pregnancy Dataset were collected; pregnancies were divided according to father exposure or unexposure to DMD at time of procreation. Treatment were compared with multivariable logistic and linear models. Results: Seventy-eight pregnancies fathered by MS patients were tracked. Forty-five patients were taking DMD at time of conception (39 beta-interferons, 6 glatiramer acetate), while 33 pregnancies were unexposed to DMD. Seventy-five pregnancies ended in live-births, 44 in the exposed and 31 in the unexposed group. No significant differences between the two groups were found in the risk of spontaneous abortion or malformations (p > 0.454), mean gestational age (p = 0.513), frequency of cesarean delivery (p = 0.644), birth weight (p = 0.821) and birth length (p = 0.649). In comparison with data of the Italian general population, the proportion of spontaneous abortion and caesarean delivery in exposed pregnancies fell within the estimates, while the proportion of pre-term delivery in the exposed group was higher than expected. Conclusions: Our data indicate no association between paternal DMD exposure at time of conception and risk of spontaneous abortion, adverse fetal outcomes and congenital malformations. Further studies clarifying the role of DMD fathers intake prior and during pregnancy are desirable, to supply guidelines for clinical practice.
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