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Review

The Risk of Using Cosmetics and Cosmetic Procedures During Pregnancy

by
Foteini Biskanaki
*,
Niki Tertipi
,
Eleni Andreou
,
Eleni Sfyri
,
Vasiliki Kefala
and
Efstathios Rallis
*
Department of Biomedical Sciences, School of Health Sciences and Welfare, University of West Attica, 12243 Athens, Greece
*
Authors to whom correspondence should be addressed.
Appl. Sci. 2024, 14(21), 9885; https://doi.org/10.3390/app14219885
Submission received: 20 September 2024 / Revised: 21 October 2024 / Accepted: 22 October 2024 / Published: 29 October 2024
(This article belongs to the Special Issue Cosmetics Ingredients Research - 2nd Edition)

Abstract

:
This review aimed to identify the risks of cosmetics during the sensitive period of pregnancy. Pregnancy causes many hormonal changes and skin issues, such as red stretch marks, cellulite, and more. These aesthetic concerns can impact both the appearance and health of the pregnant woman. Cosmetics and aesthetic treatments can help improve these problems and positively affect the mental well-being of these women. However, the lack of clinical trials regarding the safety of such treatments during pregnancy has led to the recommendation of only the mildest aesthetic applications. Additionally, professional aestheticians and dermatologists who provide cosmetics and other aesthetic treatments (e.g., laser, radiofrequency (RF), ultrasound) during pregnancy face challenging and sometimes adverse working conditions. They should be treated with respect for their situation, with careful consideration of all the peculiarities associated with pregnancy. Further research and additional recorded data are crucial for better understanding the use of cosmetics and aesthetic treatments during pregnancy.

1. Introduction

Pregnancy is a period during which more than 90% of women experience changes in their skin, which can lead to negative emotions and impact a woman’s self-confidence. Pregnancy-related skin conditions can be categorized into three groups: normal skin changes during pregnancy, pre-existing skin conditions affected by pregnancy, and pregnancy-specific skin diseases [1]. Although most of these conditions are benign and subside after childbirth, some may pose a risk to the fetus and require prenatal monitoring. The prenatal period is a critical phase for the fetal development and is divided into two stages. The first stage lasts 56 days from fertilization, during which many organ systems grow rapidly. At this time, the sexual glands also differentiate into either testes or ovaries. During this stage, the developing fetus is particularly vulnerable, and malformations can occur during this “vulnerability window”. The second stage, known as the fetal period, begins in the 9th week and continues until birth. During this period, the development and differentiation of organs formed in the earlier stage take place [2].

2. Pregnancy and Skin Changes

During pregnancy, a woman’s body undergoes several modifications, including an increase in uterine volume, which shifts the center of gravity forward. The chest doubles in size, stretch marks may appear, and the venous network becomes more prominent. While stretch marks are common on the chest, they can also develop on other parts of the body (Figure 1).
Stretch marks are influenced by various risk factors, such as:
  • A pre-conception Body Mass Index (BMI) of greater than 26;
  • Young age, especially in teenage pregnancies;
  • Weight gain during pregnancy exceeding 15 kg;
  • Baby birth weight of greater than 3.5 kg.
Other factors, such as carbohydrate intolerance and the pregnant woman’s medical history, may also affect the development of stretch marks. Additionally, the breasts may undergo hyperpigmentation around the nipple, affecting 40 to 100% of pregnant women, which typically resolves completely after childbirth [3]. Apart from hormonal changes, pregnancy, childbirth, and lactation can cause alterations in the skin, nails, and hair, which are briefly summarized in the table below (Table 1):

3. Cosmetics and Pregnancy

The term “cosmetic” originates from the ancient Greek word “cosmetikos”, which is derived from “kosmos”, referring to beauty, ornament, and appearance [10]. Cosmetics are used to alter the body’s appearance, not its actual structure or function. There are distinctions between substances that only alter bodily appearance or aesthetics and medicinal compounds that affect the body’s structure or health (e.g., the prevention of gingivitis). Paracelsus, the 16th-century Swiss physician and philosopher, observed that any substance applied to or in the body can cause harm, given the right circumstances [11].
However, after the Morhange talc scandal—in which several talc products, contaminated with high concentrations of hexachlorophene, resulted in 36 deaths in 1972—cosmetics became subject to regulations encoded in the French Public Health Code (Code de la Santé Publique—CSP). Among these regulations is a fundamental principle: “The cosmetic product must not harm human health under normal or reasonably foreseeable conditions of use”. Despite this, many cosmetic products still contain chemicals that are potentially harmful or dangerous to the body [12].
Given the widespread use of these substances, special attention must be paid to pregnant women and their fetuses. During pregnancy, consumers should be vigilant, as certain changes they notice can indicate various risks. Preserving maternal immunity is crucial, and beauty products known to be harmful remain prohibited. The use of cosmetic products during pregnancy requires careful recommendations due to substances that may be harmful to the fetus. Intrauterine exposure to certain chemicals can have irreversible effects on the developing child, particularly if exposure occurs during the first 8 weeks of development [3,11].
Pregnant women may be inclined to overuse cosmetic products due to the extensive physical changes associated with pregnancy (e.g., stretch marks) [10]. The concerns of aestheticians and dermatologists have drawn the attention of legislators to the real dangers posed by cosmetology. The perception of risks associated with cosmetic use during pregnancy, both for the health of the woman and her future child, is closely linked to the crucial contributions of cosmetovigilance [13].

Cosmetovigilance

Cosmetovigilance is “a system for monitoring and recording adverse reactions associated with the use of cosmetics in humans”. It applies to cosmetic products once they are available on the market through its assessments, expertise, and surveillance policies, that those health products available are safe, effective, accessible, and used correctly [14]. Under Article 23 of the European Union (EU) Cosmetics Product Regulation (CPR) and the United Kingdom (UK) Cosmetics Regulation (UKCR), the Responsible Person (RP) and distributors have obligations to review reports and act on undesirable effects and serious undesirable effects. The cosmetovigilance system is very similar between both legislations [14].
Cosmetovigilance is based on the following principles:
  • Reporting adverse effects and collecting all relevant information concerning them.
  • Recording, evaluating, and using information related to these effects for prevention purposes.
  • Conducting studies and research concerning the safety of cosmetic use.
  • Implementing and monitoring corrective actions if necessary [15].
Cosmetovigilance covers any adverse reaction, serious or not, that occurs during the use of a cosmetic product under normal or reasonably foreseeable conditions or as a result of misuse. A side-effect is an unwanted reaction caused by a cosmetic, though it is not necessarily harmful. In contrast, an adverse reaction is characterized as harmful to human health and is attributable to the normal or reasonably foreseeable use of a cosmetic product [15]. A serious adverse event is defined as a reaction that leads to temporary or permanent functional incapacity, disability, hospitalization, congenital anomalies, immediate threat to life, or death [16].

4. The Risks of Cosmetics and Cosmetic Procedures

Humans are exposed daily to pollution from the ground, air, and water, and anything that enters the body can trigger inflammation. Chronic inflammation can affect the immune system and the body’s defenses, potentially leading to allergies and neoplasms. Fetal life is particularly vulnerable to external pollutants, including cosmetics [17]. However, confirming this observation is challenging, as research on the effects of cosmetics during the prenatal period is limited [3].
There is significant concern about the ingredients (raw materials) in cosmetic products and the treatments that women undergo during this critical period. Safety guidelines prioritize the well-being of the mother and her unborn child, resulting in heightened attention to the potential negative effects of these products. The safety of cosmetics and aesthetic applications for women during pregnancy or breastfeeding remains a complex clinical issue surrounded by uncertainty [18].

4.1. Dermatosurgical Procedures

The most common minor surgeries include the removal of benign skin lesions, such as seborrheic keratosis, nevi, and hemangiomas, through methods like shave excision, cryotherapy, electrocautery, or radiation. These procedures have been used safely by doctors for many years in pregnant women [19]. Electrocautery is considered harmless to the fetus when used on the mother. However, precautions should be taken to reduce exposure to the smoke plume, which can be mutagenic and carcinogenic. This risk applies to both pregnant and non-pregnant patients, and, by extension, to the fetus. Masks are considered inadequate barriers against the plume; therefore, using a smoke evacuator is preferred to minimize smoke exposure [19].
Sclerotherapy may be safe during pregnancy but should be avoided in the first trimester and after the 36th week of pregnancy. Sclerotherapy and laser-assisted liposuction are not recommended for breastfeeding women. CO2 lasers have shown good efficacy and a low complication rate in the treatment of human papillomavirus (HPV) genital warts and laryngeal verrucous carcinoma in pregnant women due to their coagulating properties, with no reported adverse effects on the fetus [20]. However, there are concerns regarding maternal exposure to potentially mutagenic airborne particles generated during laser vaporization. This risk can be mitigated using aspirators, fume extraction devices, and masks for both the patient and physician. Several studies support the safety of carbon dioxide lasers in treating genital warts in pregnant patients [21,22]. Additionally, Nd:YAG lasers have also been used safely to treat genital warts during pregnancy [23].
Laser lithotripsy during pregnancy has been shown to be safe. Another study reported the successful and safe use of a pulse dye laser to treat symptomatic urolithiasis in a woman who was 20 weeks pregnant [24].
Botulinum toxin type A (BTX) has both cosmetic and medical applications [25]. Current studies suggest, though they do not fully confirm, that the toxin does not reach significant systemic concentrations when properly administered intramuscularly or intradermal. Additionally, the size of the BTX molecule makes it unlikely to cross the placental barrier [26]. There are no clinical studies on the cosmetic use of Botulinum toxin type A during pregnancy. However, two cases were reported by De Oliveira Monteiro (2006), in which BTX was used cosmetically during the 6th and 5th weeks of pregnancy without adverse effects on the fetus [27]. Two studies have shown the safety of botulinum toxin A for the treatment of achalasia in women who were pregnant. The first study reported the administration of an intradose injection of BTX during the 14th week of pregnancy without negative effects on fetal health and a successful childbirth outcome. The second study described a similar case in which BTX was administered during the 33rd week of pregnancy to treat persistent esophageal spasms and subsequent malnutrition, with no adverse effects observed at five days postpartum [28]. Robinson and Grogan also reported the safe use of BTX in the 18th week of pregnancy to treat migraines, with no issues noted in the infant for 6.5 years following birth [29].
A study of 900 doctors revealed that only 12 had performed accidental BTX injections in 16 patients during pregnancy. Only one of these patients experienced a miscarriage after the injection [30]. Concerns have been raised that high doses of BTX are associated with cases of systemic weakness. However, the doses used in cosmetic procedures for pregnant women are typically much lower. If pregnant women choose to undergo BTX treatment, they should provide informed consent before the procedure. Procedures that are absolutely contraindicated during pregnancy include fillers, sclera therapy, and liposuction [19].

4.2. Aesthetics and Biomedical Technology

Endermology was developed in France by Louis Paul Guitay in the 1970s after he sustained soft tissue injuries in a car accident. The resulting scars were treated using hand massage, which inspired Guitay to develop a device that mimics this technique. The device was initially used for scars caused by trauma and burns. However, researchers observed that it also improved the appearance of cellulite and the distribution of fat. The most recent versions of this device are the Integral and Endermolab (LPG Systems). The mechanism of action involves negative pressure suction combined with a roller that passes over areas with fat deposits [31]. Medical LPG is also suitable for pregnant women, providing relief to the legs from swelling caused by increased weight. Additionally, it can alleviate lower back pain by facilitating lymphatic system mobility. The treatment is painless and non-invasive, and for pregnant women, it is conducted with great care, with the patient lying on their side rather than on the abdomen [32].
Massage is the oldest method of pain management and is integral to many facial and body aesthetic treatments. It involves a variety of techniques with numerous benefits at the organic level. Massage requires special attention during pregnancy, and the therapist must be knowledgeable about the anatomy and physiology of the female body. Stimulating massage is contraindicated during this sensitive period as it can cause contractions and potentially lead to premature birth [31]. The massage should be gentle and is not recommended if there are pregnancy complications. The primary goal is to relax and relieve the muscles bearing the extra weight, improve blood and lymph circulation, and reduce stress. It also helps alleviate fatigue, muscle cramps, headaches, back pain, and leg swelling [33]. Studies conducted over the past decade on pregnant women have shown a significant reduction in stress hormones such as cortisol, while dopamine and serotonin levels increased in women who received massage twice a week for five consecutive weeks. Low levels of dopamine and serotonin are associated with depression, so these hormonal changes can contribute to a reduction in pregnancy and childbirth complications. During the first trimester, when fetal organ formation occurs and the risk of miscarriage is high, it is recommended to avoid massage to prevent any association between massage and potential pregnancy failure. Almond oil is considered an ideal product for massage application, as strong-smelling oils may cause discomfort and nausea [31].
Radiofrequency (RF) applications have been used since 2002 to improve cellulite, skin laxity, and wrinkles, and more recently to reduce fat. The mechanism of action is based on volumetric heating of the skin and subcutaneous tissues. Unipolar RF devices can reduce fat circumference in about 60–80% of individuals. However, there are no studies examining the use of RF during pregnancy [34,35].
During pregnancy and breastfeeding, laser hair removal, intense pulse light (IPL), or electrolysis is generally not recommended due to a lack of data and clinical studies on their safety and efficacy. There is a theoretical concern about electrolysis, as amniotic fluid is a conductor of galvanic current. For hair removal during pregnancy, shaving and depilatory creams are recommended. The use of lasers for aesthetic treatments has not been studied in pregnant women [36].
Repeated and prolonged exposure to ultraviolet radiation (UVA, UVB, and UVC) increases the risk of skin cancer due to DNA damage and impaired repair mechanisms. While the lamps used in IPL hair removal devices are capable of emitting UV radiation, these devices are designed to include cut-off filters that allow only wavelengths above 400 nm to pass through, preventing UV exposure. However, if these filters become damaged, UV emission could occur. The potential effects of IPL devices, based on their operating principles, have not been conclusively reported in recent studies. Only long-term epidemiological studies that analyze IPL exposure as a specific variable could confirm or refute the associated risks [37]. There is a potential risk of developing basal cell and squamous cell carcinomas in keratinocytes and melanomas in melanocytes. However, this risk is primarily linked to severe damage to the cut-off filter within the IPL device. No publications have yet identified cancers caused by the thermal effects associated with IPL. The limited follow-up of IPL use, the short duration of follow-up in existing studies, and the small number of subjects included do not provide sufficient information on these potential long-term effects (which may be observable 5 to 15 years later).
The safety of using laser and IPL for hair removal depends on the energy absorbed by the epidermis, hair follicle, and adjacent tissues, which varies with the emission characteristics of the devices and the individual characteristics of the users. Key factors for safe exposure include:
  • The nominal operating characteristics of the device defined during its design.
  • The stability of the device’s operating characteristics, which depend on design and maintenance.
  • Correct device usage, which is linked to the training and skill of operators, proper user information for household devices, and adherence to best practices.
  • The characteristics of the pregnant woman at the time of hair removal, including phototype, skin color, hair color, and individual response.
  • Possible contraindications, such as pre-existing diseases, photosensitive treatments, etc. [38].
Despite concerns, lasers have been used safely to treat medical conditions in pregnant women. Laser and IPL are generally considered safe for patients with granulomatous conditions and warts. Limited studies indicate that Neodymium-doped Yttrium Aluminum Garnet (Nd:YAG) laser can be safely used to treat skin lesions during pregnancy. Genital warts have been successfully treated with the Nd:YAG laser without complications for the mother or fetus [39]. Other studies report the safe use of the Nd: YAG for severe inflammatory acne and pyogenic granulomas during pregnancy, with no observed side effects. In a recent study, a pulse dye laser (PDL) (585 nm) was used to treat pyogenic granulomas and warts during pregnancy, demonstrating it to be a safe treatment. Available studies indicate a good safety profile for PDL use in pregnancy, with minimal side effects such as mild erythema and pain. In conclusion, laser treatments appear relatively safe for medical conditions in pregnant women. However, laser and IPL are not recommended for cosmetic procedures during pregnancy due to a lack of safety studies [40].

4.3. Risks of Ingredients of Cosmetics

Cosmetic products are necessities in human’s daily life including pregnant women. Recent studies reported that 60–80% of pregnant women use cosmetic products, including facial cleansers, day cream, foundation, mascara, lipstick, eye pencil, eye shadow, and make-up remover. These products contain various chemical substances (e.g., parabens, formaldehyde, titanium dioxide, nitrosamine, phenol, and organic solvents) and heavy metals, which are either added purposely as efficacy components to enhance the skincare effect of cosmetic products or brought in through the raw materials, auxiliary materials, or technical problems during the production process [41].
Also, cosmetics are a significant tool for many professional aestheticians. Previous studies indicate that aestheticians who are constantly in contact with cosmetics have two to four times more exposure to toxins compared to those who use cosmetics intermittently. Over 10,000 chemicals are used in cosmetics, but many are not completely harmless [42].
Numerous synthetic chemical ingredients should be avoided due to their toxicity. Toxic substances are those capable of destroying life [43]. When toxic substances enter the body, they are metabolized in the liver, where they are inactivated and then excreted by the kidneys or bio accumulated [44]. The most common dangerous chemicals used in cosmetics include the following:
  • Acetone: This solvent, used in nail polish removers, can cause dry mouth, dizziness, nausea, difficulty speaking, and, in extreme cases, coma. It acts as a central nervous system (CNS) depressant [45].
  • Aluminum Compounds: Commonly found in deodorants and antiperspirants, aluminum compounds can block sweat glands and pores, preventing the body’s natural sweating process. There are concerns that these compounds may be linked to breast cancer, breast cysts, and Alzheimer’s disease. However, the dermal absorption of aluminum is not well understood, and it is not yet known whether aluminum can travel from the skin to the brain to cause Alzheimer’s disease. While aluminum may cause gene instability, alter gene expression, or enhance oxidative stress, its carcinogenicity has not been proven. Epidemiological research on aluminum exposure has been inconsistent and conflicting [46,47].
  • Ammonia: Found in many cosmetics, ammonia can cause allergic reactions and, with long-term exposure, may lead to coughing, respiratory arrest, and pulmonary edema, potentially resulting in death [48].
  • Titanium Dioxide: Commonly used in sunscreens and toothpastes, titanium dioxide can be absorbed through the skin or inhaled during manufacturing and use. Despite its extensive use, the biological effects and cellular response mechanisms of titanium dioxide nanoparticles (TiO2-NPs) are not fully understood. The toxicity of TiO2-NPs appears to involve reactive oxygen species (ROS) production, leading to oxidative stress, inflammation, genotoxicity, metabolic changes, and potential carcinogenesis. The extent and type of cell damage depend on the chemical and physical characteristics of TiO2-NPs, including size, crystal structure, and photo-activation [49].
  • Diethanolamines (DEA): Used mainly as surfactant foam boosters or viscosity increasing agents, DEA can cause allergic reactions and eye and skin irritation and is a potential carcinogen if used in the long term. Recent reports have raised concerns about an increase in allergic dermatitis associated with DEA [50]. Also, older studies in animals have found a link between maternal exposure to DEA and altered memory function in offspring [51].
  • Mineral Oil: Found in many creams for eyes, lips, and hydration, mineral oil forms a barrier on the skin that can prevent it from breathing, expelling toxins, hydrating, and producing healthy cells. Common reactions include premature skin aging, cardiac disorders, kidney and liver damage, and breathing difficulties [43].
  • Parabens: Parabens in cosmetics are very common and humans use them in daily life. The prenatal exposure to these chemicals is associated with poor birth outcomes. A recent study reported the association between prenatal exposure to parabens and birth outcomes with positive relationships between maternal exposure to methyl parabens and birth weight [52]. Parabens are used to inhibit microbial growth and extend the shelf life of products, but they have been associated with dermatitis and allergies. Many cosmetics also contain synthetic fragrances, which may include up to 600 different ingredients. The exact components are often not disclosed, only labeled as “Perfume” or “Fragrance”, leading to potential issues such as rashes, itching, cough, asthma, and vomiting, with some fragrances having a narcotic effect [53,54].
  • Formaldehyde: This is a toxic substance and is forbidden by the Cosmetics Regulation (EC) and is classified as a carcinogen (category 1B) and a skin sensitizer (Category 1). Some preservatives are allowed in cosmetic products fulfil their function since they are formaldehyde-releasers, preserving the final cosmetic product. Substances such as DMDM hydantoin, imidazolidinyl urea, and diazolidinyl urea, commonly used in cosmetic products, are known to release formaldehyde to fulfil a preserving function in the finished product. Formaldehyde is prohibited in cosmetic products and cannot be intentionally added, but formaldehyde-releasing substances are permitted; they are listed on Annex V of the Cosmetics Regulation (EC), No. 1223/2009, and have to be used within the restrictions given. According to the previous regulation, these products must be labelled with the warning ‘contains formaldehyde’ when the amount of released formaldehyde was more than 0.05% in the final product in order to communicate the presence of the substance and avoid allergic reactions to sensitized customers [55].
  • Aluminum (Al): Al is a known neurotoxin, and studies show that exposure can lead to neurological disorders. Aluminum is an element found in many items, including cosmetics and hygiene products like antiperspirants. The body usually excretes aluminum, but if levels exceed the body’s capacity, it can stay in tissues and organs. Studies indicate that Al is toxic in all developmental stages and may produce irreversible health effects even at low levels. Since Al is known to cross the placental barrier, pregnant women should be advised about this risk and should also be informed about avoiding the post-natal exposure of their children to Al. Recent findings show the need for further research on aluminum exposure and its associated interactions in vulnerable populations, e.g., pregnant women [56].
  • Toluene: Toluene is a solvent found in nail polishes and may be labeled Methylbenzene Toluol or Antisal 1a. Solvents increase the risk of miscarriage, stillbirth, preterm birth, low birth weight, and congenital disabilities. Those at greatest risk of exposure are those who work with solvents, such as cosmetologists, dry cleaners, artists, and printers [57].
  • Oxybenzone: Oxybenzone is a recognized endocrine-disrupting chemical (EDC) and is used as an ultraviolet (UV) absorber (70% of sunscreen products). Many studies have identified this chemical in the urine and blood of women in pregnancy and fetal and umbilical cord blood. A recent study demonstrated that women with medium to high levels of oxybenzone in their urine were associated with giving birth to neonates with Hirschsprung’s disease (HSCR) [58]. Oxybenzone is fat-soluble, meaning it enters into fat cells and can stay there for weeks, making it difficult for expecting women to know what their exposure level is. This is dangerous for both women in pregnancy and for women who are trying to conceive. Those who live in a sunny location and use sunscreen with oxybenzone daily all year round may have a higher risk factor than someone who uses it less frequently (e.g., on vacation). Also, it was reported that babies that are exposed to an endocrine disruptor like oxybenzone can face problems including poor sleep, adult attention-deficit/hyperactivity disorder (ADHD), and an increase in certain illnesses like bronchitis and sinusitis [59].
A study involving 9710 pregnant women in Zhuzhou City and Xiangtan City in Hunan province during the 2016–2017 period found no significant association between daily personal cosmetics use and the risk of preterm birth, low birth weight, macrosomia, or being large for gestational age. However, the study suggested that personal cosmetics use might increase the risk of small for gestational age (SGA), warranting further research to identify specific cosmetic products contributing to this risk [41].
Melasma is a common skin problem caused by brown to gray-brown patches on the face. Pregnancy is associated with increased melanocyte hormone secretion, elevated estrogen progestin levels, and sun exposure. As a result, pregnancy is a common cause of melasma. It can also be exacerbated by cosmetics, phototoxic drugs, or anticonvulsants. Melasma can be resolved partially or completely within 6 to 18 months postpartum [60]. Ingredients that can improve melasma include glycolic acid, lactic acid, TCA, and salicylic acid. Glycolic and lactic acid peels are considered safe during pregnancy, while TCA and salicylic acid peels should be avoided [61].
Acne, a common skin condition affecting adolescents and adults, may change unpredictably during pregnancy. High-quality guidelines for acne treatment during pregnancy are scarce, making management challenging. Acne should be treated during pregnancy to prevent the worsening, scarring, secondary infection, or psychological impairment of the mother. Safe products must be chosen. Systemic tetracycline, doxycycline, minocycline, or isotretinoin cannot be used [62]. Topical azelaic acid or benzoyl peroxide is recommended as baseline therapy. For inflammatory acne, a combination of topical erythromycin or clindamycin with benzoyl peroxide is advised. Oral erythromycin or cephalexin is generally safe for moderate to severe inflammatory acne when used short term. A brief course of oral prednisolone may be useful for treating severe nodular cystic acne after the first trimester. Topical and oral antibiotics should be used in combination with benzoyl peroxide to reduce bacterial resistance [63,64]. Oral retinoids are teratogenic and contraindicated during pregnancy. While some complementary therapies, including micronutrients and non-pharmacologic treatments, appear to be well tolerated, there is limited data on their safety and efficacy, and they are not currently recommended during pregnancy [7].

4.4. Breastfeeding Women

There are very few studies in the public literature on the safety of cosmetics for breastfeeding women. The main concern with using any cosmetic procedures during lactation is the potential systemic absorption of agents and their subsequent incorporation into breast milk, which could affect neonatal growth and development [64]. Most cosmetic procedures, such as BTX and chemical peels, are generally considered safe during lactation, as there is little concern about significant systemic absorption of the agents involved. However, procedures or surgeries that involve fat redistribution or removal, such as liposuction, are not recommended. Sclerotherapy should also be avoided during breastfeeding. Although hypertonic saline solutions used in sclerotherapy are generally considered safe, there are no studies on whether other sclerosing agents are excreted in breast milk. Therefore, it is recommended to avoid this treatment while breastfeeding [65].
Some women who have undergone sclerotherapy have continued breastfeeding by pumping and discarding breast milk for the first 48 h after treatment. However, there are no reported results, complications, or success rates associated with this approach [18].

5. Risks for Aestheticians and Dermatologists During Pregnancy

The combination of work and pregnancy in environments conducive to smooth functioning is a concern for many pregnant women. According to the National Perinatal Survey (ENP, 2016), 70.2% of women in the European Union (EU) worked during pregnancy in 2010. Additionally, the percentage of aesthetician workers exposed to certain occupational hazards is significantly higher than that of other professional groups. Specifically, 88.3% of aestheticians are exposed to chemical pollutants, compared to 33.2% of workers in other professions [66]. Numerous studies have examined the effects of exposure to occupational hazards, such as chemical agents (especially solvents), musculoskeletal disorders (MSDs), and noise, on pregnant women across various occupations. Some researchers have specifically focused on the cosmetics sector due to its unique occupational hazards and demographic characteristics, including the predominance of young women [18].
The reality is that all pregnant women are exposed to endocrine disruptors throughout gestation [58]. Endocrine disruptors are found in many everyday products, except cosmetics, food and beverage packaging, toys, carpets, and pesticides. Contact with these chemicals may occur through air, diet, skin, and water and therefore cannot be completely avoided or removed; however, women in pregnancy should make informed choices to reduce exposure and risk of any potential health effects. It is advisable to delay elective cosmetic procedures until the baby is born [66]. Also, another suggestion from studies is to recommend eating a diet high in fruits and vegetables (aim for nine to twelve cups daily). After discussing with the doctor, also consider taking a B complex supplement and extra folate which may help decrease the flow of toxins to the fetus [59].

6. Discussion

Skin changes during pregnancy, such as melasma, striae, varicose veins, hirsutism, skin growth (nevus (nevi) and ephelides), acne, etc., can negatively impact psychological well-being. When these skin changes are uncontrolled, they could become skin cancer [3,61]. So, it is important to be treated at an early stage.
However, women during pregnancy should be careful about what kind of cosmetics they use daily. It is important for them to use these cosmetics products after obtain a careful risk–benefit assessment by a aesthetician or dermatologist. Only those cosmetics and cosmetic procedures that are deemed safe and necessary should be performed on a pregnant woman. For example, dermatosurgical procedures, such as electrocautery, cryotherapy, and lasers (particularly genital warts), can be safely performed. Also, dermatological surgeries for skin cancer and other skin growths can be safely performed [28].
Caution is advised regarding chemical peels, botulinum toxin treatments, and biopsies for questionable lesions. Procedures that are contraindicated include fillers, sclerotherapy, and liposuction [54]. Aesthetic procedures should be conducted ethically, with specialized personnel adhering to current legislation [18].

7. Conclusions

There are many cosmetics and cosmetic procedures that treat aesthetic problems that appear during pregnancy. The lack of clinical studies prevents a clear determination of the effects of aesthetic applications and cosmetics products during pregnancy. Future research should focus on real-life scenarios involving long-term exposure to cosmetics ingredients and personal care products during pregnancy [62].
To sum up, cosmetic products, dermatosurgical, and aesthetic procedures (with biomedical technology, e.g., laser, ultrasound, radiofrequency, etc.), for pregnant women should be managed by qualified professionals to ensure safety. Furthermore, pregnant aestheticians or dermatologists should be treated with respect, considering the unique aspects of their pregnancy [67]. Further studies and new data on aesthetic applications and cosmetics should be added to better understand the safety and effects of pregnancy [62].

Author Contributions

Conceptualization: F.B. and E.R.; methodology: F.B. and V.K.; software: E.S. and E.A.; validation: F.B. and E.R.; formal analysis: F.B. and E.S.; investigation, F.B. and E.R.; resources, E.A.; data curation, F.B.; writing—original draft preparation, F.B.; writing—review and editing, E.R. and V.K.; visualization: N.T. and V.K.; supervision: E.R.; and project administration, F.B. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Snarskaya, E.S.; Olisova, Y.O.; Makatsariya, D.; Kochergin, N.G.; Radetskaya, L.; Bitsadze, V.; Khizroeva, J. Skin pathologies in pregnancy. J. Perinat. Med. 2019, 47, 371–380. [Google Scholar] [CrossRef] [PubMed]
  2. Amiard-Triquet, C. Pollution Tolerance in Aquatic Animals: From Fundamental Biological Mechanisms to Ecological Consequences. In Ecotoxicology: New Challenges and New Approaches; ISTE Press: London, UK; Elsevier: Kidlington, UK, 2019; pp. 33–91. [Google Scholar] [CrossRef]
  3. Putra, I.B.; Jusuf, N.K.; Dewi, N.K. Skin Changes and Safety Profile of Topical Products during Pregnancy. J. Clin. Aesthetic Dermatol. 2022, 15, 49–57. [Google Scholar] [PubMed] [PubMed Central]
  4. Kalra, A.; Lowe, A. Mechanical Behaviour of Skin. J. Mater. Sci. Eng. 2016, 5, 4. [Google Scholar] [CrossRef]
  5. Koumantaki-Mathioudaki, E.; Rallis, E. Dermatology and Pregnancy; Constantaras Publications: Athens, Greece, 2014; pp. 95–98. [Google Scholar]
  6. Borrelli, M.R.; Griffin, M.; Ngaage, L.M.; Longaker, M.T.; Lorenz, H.P. Striae Distensae: Scars without Wounds. Plast. Reconstr. Surg. 2021, 148, 77–87. [Google Scholar] [CrossRef]
  7. Chien, A.L.; Qi, J.; Rainer, B.; Sachs, D.L.; Helfrich, Y.R. Treatment of Acne in Pregnancy. J. Am. Board. Fam. Med. 2016, 29, 254–262. [Google Scholar] [CrossRef]
  8. Singal, A.; Arora, R. Nail as a window of systemic diseases. Indian Dermatol. Online J. 2015, 6, 67–74. [Google Scholar] [CrossRef]
  9. Biskanaki, F.; Kefala, V.; Kalofiri, P. The Latest in Non-Invasive Local Fat Treatment Method with Diode Laser (1060 nm). Rev. Clin. Pharmacol. Pharmacokinet. Int. Ed. 2019, 33, 35–38. Available online: https://www.researchgate.net/publication/335686929_The_latest_in_non-invasive_local_fat_treatment_method_with_diode_laser_1060nm (accessed on 10 September 2024).
  10. Kalofiri, P.; Biskanaki, F.; Kefala, V.; Tertipi, N.; Sfyri, E.; Rallis, E. Endocrine Disruptors in Cosmetic Products and the Regulatory Framework: Public Health Implications. Cosmetics 2023, 10, 160. [Google Scholar] [CrossRef]
  11. Califf, R.M.; McCall, J.; Mark, D.B. Cosmetics, Regulations, and the Public Health: Understanding the Safety of Medical and Other Products. JAMA Intern. Med. 2017, 177, 1080–1082. [Google Scholar] [CrossRef]
  12. Coulomb, B. Television at the Crossroads of the History of Consumption and Health: The Morhange Talc Affair (1972–1981). VIEW J. Eur. Telev. Hist. Cult. 2020, 9, 55. [Google Scholar] [CrossRef]
  13. Kroumpouzos, G. Cosmetic Procedures in Pregnancy: A Reappraisal. SKINmed 2017, 15, 93–96. [Google Scholar] [PubMed]
  14. Jones, J.; Toklu, H.Z. Cosmetovigilance: A New Concept for the Residency Curriculum. HCA Healthc. J. Med. 2020, 1, 181–183. [Google Scholar] [CrossRef] [PubMed]
  15. Toklu, H.Z.; Antigua, A.; Lewis, V.; Reynolds, M.; Jones, J. Cosmetovigilance: A review of the current literature. J. Fam. Med. Prim. Care 2019, 8, 1540–1545. [Google Scholar] [CrossRef]
  16. Altıokka, İ.; Üner, M. Safety in Cosmetics and Cosmetovigilance, Current Regulations in Türkiye. Turk. J. Pharm. Sci. 2022, 19, 610–617. [Google Scholar] [CrossRef]
  17. Biskanaki, F.; Kefala, V.; Lazaris, A.C.; Rallis, E. Aging and the Impact of Solar Ultraviolet Radiation on the Expression of Type I and Type VI Collagen. Cosmetics 2023, 10, 48. [Google Scholar] [CrossRef]
  18. Trivedi, M.K.; Kroumpouzos, G.; Murase, J.E. A review of the safety of cosmetic procedures during pregnancy and lactation. Int. J. Womens Dermatol. 2017, 3, 6–10. [Google Scholar] [CrossRef]
  19. Garg, A.M.; Mysore, V. Dermatologic and Cosmetic Procedures in Pregnancy. Indian J. Plast. Surg. 2022, 54, 507–513. [Google Scholar] [CrossRef]
  20. Katoch, S.; Mysore, V. Surgical Smoke in Dermatology: Its Hazards and Management. J. Cutan. Aesthetic Surg. 2019, 12, 1–7. [Google Scholar] [CrossRef]
  21. Fulgham, P.F.; Assimos, D.J.; Pearle, M.S.; Preminger, G.M. Clinical effectiveness protocols for imaging in the management of ureteral calculous disease: AUA technology assessment. J. Urol. 2013, 189, 1203–1213. [Google Scholar] [CrossRef]
  22. Laing, K.; Lam, T.B.L.; McClinton, S.; Cohen, N.P.; Traxer, O.; Somani, B.K. Outcomes of ureteroscopy for stone disease in pregnancy: Results from a systematic review of the literature. Urol. Int. 2012, 89, 380–386. [Google Scholar] [CrossRef]
  23. Rashid, A.O.; Attar, A.; Mohammed, K.S.; Fakhralddin, S.S.; Abdulla, L.N.; Buchholz, N. Direct Comparison of Pneumatic and Ho:YAG Laser Lithotripsy in the Management of Lower Ureteric Stones. Urol. Int. 2020, 104, 765–768. [Google Scholar] [CrossRef] [PubMed]
  24. Hendawy, A.F.; Aly, D.G.; Shokeir, H.A.; Samy, N.A. Comparative Study Between the efficacy of Long-Pulsed Neodymium- YAG Laser and Fractional CO2 Laser in the Treatment of Striae Distensae. J. Lasers Med. Sci. 2021, 12, e57. [Google Scholar] [CrossRef] [PubMed]
  25. Tan, M.; Kim, E.; Koren, G.; Bozzo, P. Botulinum toxin type A in pregnancy. Can. Fam. Physician 2013, 59, 1183–1184. [Google Scholar] [PubMed]
  26. Kroumpouzos, G.; Bercovitch, L. Ethics of esthetic procedures in pregnancy. Int. J. Womens Dermatol. 2018, 4, 194–197. [Google Scholar] [CrossRef]
  27. Oliveira Monteiro, E. Botulinum toxin and pregnancy. SKINmed 2006, 5, 308. [Google Scholar] [CrossRef]
  28. Wataganara, T.; Leelakusolvong, S.; Sunsaneevithayakul, P.; Vantanasiri, C. Treatment of severe achalasia during pregnancy with esophagoscopic injection of botulinum toxin A: A case report. J. Perinatol. 2009, 29, 637–639. [Google Scholar] [CrossRef]
  29. Robinson, A.Y.; Grogan, P.M. Onabotulinumtoxin A successfully used as migraine prophylaxis during pregnancy: A case report. Mil Med. 2014, 179, e703–e704. [Google Scholar] [CrossRef] [PubMed]
  30. Abdelkader, A.; Arslan, E.K.; Erol, H. Pregnancy outcomes following botulinum toxin type A exposure: A systematic review. Int. J. Sci. Res. Manag. 2018, 6, 89–100. [Google Scholar] [CrossRef]
  31. Moortgat, P.; Anthonissen, M.; Meirte, J.; Daele, U.V.; Maertens, K. The physical and physiological effects of vacuum massage on the different skin layers: A current status of the literature. Burn. Trauma 2016, 19, 34. [Google Scholar] [CrossRef]
  32. Andreou, E.; Biskanaki, F.; Sfyri, E.; Tertipi, N.; Kefala, V.; Rallis, E. The Lymphatic Massage and its results on the healthy body. Epith. Clin. Pharm. 2023, 41, 87–91. [Google Scholar]
  33. Pachtman Shetty, S.L.; Fogarty, S. Massage During Pregnancy and Postpartum. Clin. Obstet. Gynecol. 2021, 64, 648–660. [Google Scholar] [CrossRef] [PubMed]
  34. Biskanaki, F.; Kefala, V.; Skouras, G. Radio frequency innovation. New method of fat dissolving (contactless skin therapy). Ep. Klin. Farmakol. Kai Farmakokinet. 2018, 36, 91–96. Available online: https://www.researchgate.net/publication/328699402_Radio_frequency_innovation_New_method_of_fat_dissolving_contactless_skin_therapy (accessed on 10 September 2024).
  35. Kim, H.S.; Choi, H.D.; Pack, J.K.; Kim, N.; Ahn, Y.H. Biological Effects of Exposure to a Radiofrequency Electromagnetic Field on the Placental Barrier in Pregnant Rats. Bioelectromagnetics 2021, 42, 191–199. [Google Scholar] [CrossRef] [PubMed]
  36. Biskanaki, F.; Rallis, E.; Andreou, E.; Sfyri, E.; Tertipi, N.; Ninos, G.; Kefala, V. Laser Innovations in Aesthetics. Rev. Clin. Pharmacol. Pharmacokinet. 2024, 38, 17–21. [Google Scholar] [CrossRef]
  37. Kralik, J. Relaxing School Suncreen Restrictions. NCSL Legisbrief 2017, 25, 1–2. [Google Scholar] [PubMed]
  38. Ninos, G.; Kefala, V.; Biskanaki, F.; Dimitrios, D.; Tertipi, N.; Sfyri, E.; Andreou, E.; Rallis, E. Development of a proposed Laser Safety Protocol (LSP) for the prevention of eye and skin hazards in Biomedical Laser facilities. Rev. Clin. Pharmacol. Pharmacokinet. Int. Ed. 2024, 38, 51–56. [Google Scholar] [CrossRef]
  39. Thomas, M.M.; Houreld, N.N. The “in’s and outs” of laser hair removal: A mini review. J. Cosmet. Laser Ther. 2019, 21, 316–322. [Google Scholar] [CrossRef]
  40. Abedi, A.; Razzaghi, M.; Allameh, F.; Fallahkarkan, A.R. Pneumatic Lithotripsy Versus Laser Lithotripsy for Ureteral Stones. J. Lasers Med. Sci. 2018, 9, 233–236. [Google Scholar] [CrossRef]
  41. Li, H.; Zheng, J.; Wang, H.; Huang, G.; Huang, Q.; Feng, N.; Xiao, J. Maternal cosmetics use during pregnancy and risks of adverse outcomes: A prospective cohort study. Sci. Rep. 2019, 9, 8030. [Google Scholar] [CrossRef]
  42. Jones, A.L.; Kramer, R.S.S. Facial Cosmetics and Attractiveness: Comparing the Effect Sizes of Professionally-Applied Cosmetics and Identity. PLoS ONE 2016, 11, e0164218. [Google Scholar] [CrossRef]
  43. Sharmeen, J.B.; Mahomoodally, F.M.; Zengin, G.; Maggi, F. Essential Oils as Natural Sources of Fragrance Compounds for Cosmetics and Cosmeceuticals. Molecules 2021, 26, 666. [Google Scholar] [CrossRef] [PubMed]
  44. Kaličanin, B.; Velimirović, D. A Study of the Possible Harmful Effects of Cosmetic Beauty Products on Human Health. Biol. Trace Elem. Res. 2016, 170, 476–484. [Google Scholar] [CrossRef] [PubMed]
  45. Scheers, C.; Andre, J.; Richert, B. Nail cosmetology. Hand Surg. Rehabil. 2024, 43S, 101657. [Google Scholar] [CrossRef]
  46. Sanajou, S.; Şahin, G.; Baydar, T. Aluminium in cosmetics and personal care products. J. Appl. Toxicol. 2021, 41, 1704–1718. [Google Scholar] [CrossRef]
  47. Luo, L.; Yan, T.; Yang, L.; Zhao, M. Aluminum chloride and D-galactose induced a zebrafish model of Alzheimer’s disease with cognitive deficits and aging. Comput. Struct. Biotechnol. J. 2024, 23, 2230–2239. [Google Scholar] [CrossRef] [PubMed]
  48. Symanzik, C.; Weinert, P.; Babić, Z.; HalHOlmann, S.; Havmose, M.S.; Johansen, G.D.; Kezic, S.; Macan, M.; Macan, J.; Strahwald, J.; et al. Skin Toxicity of Selected Hair Cosmetic Ingredients: A Review Focusing on Hairdressers. Int. J. Environ. Res. Public Health 2022, 19, 7588. [Google Scholar] [CrossRef]
  49. Tucci, G.P. Titanium Dioxide Nanoparticles: A Risk for Human Health? Mini Rev. Med. Chem. 2016, 16, 762–769. [Google Scholar] [CrossRef]
  50. Fiume, M.M.; Heldreth, B.; Bergfeld, W.F.; Belsito, D.V.; Hill, R.A.; Klaassen, C.D.; Liebler, D.C.; Marks, J.G., Jr.; Shank, R.C.; Slaga, T.J.; et al. A Safety Assessment of Diethanolamides as Used in Cosmetics. Int. J. Toxicol. 2013, 32, 36S–58S. [Google Scholar] [CrossRef]
  51. Craciunescu, C.N.; Wu, R.; Zeisel, S.H. Diethanolamine alters neurogenesis and induces apoptosis in fetal mouse hippocampus. FASEB J. 2006, 20, 1635–1640. [Google Scholar] [CrossRef]
  52. Shin, B.; Kwon, J.A.; Park, E.K.; Kang, S.; Kim, S.; Park, E.; Kim, B. Prenatal Exposure to Parabens Affects Birth Outcomes through Maternal Glutathione S-Transferase (GST) Polymorphisms: From the Mothers and Kids Environmental Health (MAKE) Study. Int. J. Environ. Res. Public Health 2021, 18, 3012. [Google Scholar] [CrossRef]
  53. Amiri, A.; Pryor, E.; Rice, M.; Downs, C.A.; Turner-Henson, A.; Fanucchi, M.V. Formaldehyde exposure during pregnancy. MCN. Am. J. Matern. Child Nurs. 2015, 40, 180–185. [Google Scholar] [CrossRef] [PubMed]
  54. Fu, X.; He, J.; Zheng, D.; Yang, X.; Wang, P.; Tuo, F.; Wang, L.; Li, S.; Xu, J.; Yu, J. Association of endocrine disrupting chemicals levels in serum, environmental risk factors, and hepatic function among 5 to 14-year-old children. Toxicology 2022, 15, 153011. [Google Scholar] [CrossRef] [PubMed]
  55. Commission Regulation (EU) 2022/1181 Amending the Preamble of Annex V to Regulation (EC) No 1223/2009; European Union: Maastricht, The Netherlands, 2022.
  56. Röllin, H.B.; Nogueira, C.; Olutola, B.; Channa, K.; Odland, J. Prenatal Exposure to Aluminum and Status of Selected Essential Trace Elements in Rural South African Women at Delivery. Int. J. Environ. Res. Public Health 2018, 15, 1494. [Google Scholar] [CrossRef] [PubMed]
  57. Bowen, S.E.; Hannigan, J.H. Binge toluene exposure in pregnancy and pre-weaning developmental consequences in rats. Neurotoxicol. Teratol. 2013, 38, 29–35. [Google Scholar] [CrossRef]
  58. Gautam, K.; Seth, M.; Dwivedi, S.; Jain, V.; Vamadevan, B.; Singh, D.; Roy, S.K.; Downs, C.A.; Anbumani, S. Soil degradation kinetics of oxybenzone (Benzophenone-3) and toxicopathological assessment in the earthworm. Eisenia fetida. Environ. Res. 2022, 213, 113689. [Google Scholar] [CrossRef]
  59. DiNardo, J.C.; Downs, A.C. Can oxybenzone cause Hirschsprung’s disease? Reprod. Toxicol. 2019, 86, 98–100. [Google Scholar] [CrossRef] [PubMed]
  60. Basit, H.; Godse, K.V.; Al Aboud, A.M. Melasma; StatPearls Publishing: Treasure Island, FL, USA, 2024; Available online: https://www.ncbi.nlm.nih.gov/books/NBK459271/ (accessed on 10 September 2024).
  61. Lee, K.C.; Korgavkar, K.; Dufresne, R.G., Jr.; Higgins, H.W., 2nd. Safety of cosmetic dermatologic procedures during pregnancy. Dermatol. Surg. 2013, 39, 1573–1586. [Google Scholar] [CrossRef]
  62. Bayerl, C. Acne therapy in pregnancy. Hautarzt 2013, 64, 269–273. [Google Scholar] [CrossRef]
  63. Jakharia-Shah, N.; Chadha, P.; Watson, L. A review of the safety of common aesthetic procedures during pregnancy. J. Plast. Reconstr. Aesthetic Surg. 2018, 71, 1362–1380. [Google Scholar] [CrossRef]
  64. Vitale, M.; Gómez-Sánchez, M.J.; Vicente, M.H.; Colombo, F.; Milani, M. Efficacy, Tolerability, and Face Lipidomic Modification of New Regimen with Cleanser and Corrective Serum in Women with Acne-Prone. Skin Appl. Sci. 2024, 14, 7799. [Google Scholar] [CrossRef]
  65. Murase, J.E.; Heller, M.M.; Butler, D.C. Safety of dermatologic medications in pregnancy and lactation: Part I. Pregnancy. J. Am. Acad. Dermatol. 2014, 70, 401-e1. [Google Scholar] [CrossRef] [PubMed]
  66. Hassan, S.; Thacharodi, A.; Priya, A.; Meenatchi, R.; Hegde, T.A.; Thangamani, R.; Nguyen, H.T.; Pugazhendhi, A. Endocrine disruptors: Unravelling the link between chemical exposure and Women’s reproductive health. Environ. Res. 2024, 15, 117385. [Google Scholar] [CrossRef] [PubMed]
  67. Viotti, S.; Guidetti, G.; Loera, B.; Martini, M.; Sottimano, I.; Converso, D. Stress, work ability, and an aging workforce: A study among women aged 50 and over. Int. J. Stress Manag. 2016, 24, 98–121. [Google Scholar] [CrossRef]
Figure 1. A 32-year-old woman had various changes in her body due to pregnancy. (a) Changes in the vascular system. This figure is 3 months after childbirth. (b) Red streaks appeared in the 8th month only in the abdomen. This figure is one month after birth.
Figure 1. A 32-year-old woman had various changes in her body due to pregnancy. (a) Changes in the vascular system. This figure is 3 months after childbirth. (b) Red streaks appeared in the 8th month only in the abdomen. This figure is one month after birth.
Applsci 14 09885 g001
Table 1. Changes during pregnancy, childbirth, and lactation (modified by Dr. F. Biskanaki, 2024).
Table 1. Changes during pregnancy, childbirth, and lactation (modified by Dr. F. Biskanaki, 2024).
MelasmaThird month of pregnancy, in women with dark skin. It is located on the forehead, cheeks and chin. Melasma, or the mask of pregnancy, is the second most common complaint after striae and may resolve within 1 year of delivery in 70% women without any treatment [1].
ScarsDuring pregnancy, the level of active melanocytes is higher, leading to a higher concentration of melanin in a pregnant woman’s body. The scars look darker. The scars formed due to the extension of the skin.
Vascular systemTelangiectatic arteriole, telangiectasia, palmar erythema, varicose veins [4].
Linea NigraHyperpigmentation of the white abdomen line (1st trimester) affects 90% of pregnant women. After childbirth, it recedes enough or completely [5].
Stretch marks (striae)It affects a percentage of 50 to 90% of women, and appear after the 6th month of pregnancy. Stretch marks are characterized by thinner skin, but mainly a reduction in the density of the elastin fiber network. The collagen fibers break. At the striation level, skin appendages are absent. The appearance of the striae is mainly due to hormonal changes, hereditary factors, and significant weight gain or loss [5,6].
AcneAcne development is random. Indeed, it can worsen, improve, or remain unchanged [7].
NailsWhite milk spots on nails (leukonychia). Nails can change during pregnancy. Extra hormones can make them grow faster and become stronger. Some women, though, find that their nails split and break more easily during pregnancy, but nail changes are not permanent [8].
CelluliteThis is caused by high levels of estrogen and progesterone [9].
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Biskanaki, F.; Tertipi, N.; Andreou, E.; Sfyri, E.; Kefala, V.; Rallis, E. The Risk of Using Cosmetics and Cosmetic Procedures During Pregnancy. Appl. Sci. 2024, 14, 9885. https://doi.org/10.3390/app14219885

AMA Style

Biskanaki F, Tertipi N, Andreou E, Sfyri E, Kefala V, Rallis E. The Risk of Using Cosmetics and Cosmetic Procedures During Pregnancy. Applied Sciences. 2024; 14(21):9885. https://doi.org/10.3390/app14219885

Chicago/Turabian Style

Biskanaki, Foteini, Niki Tertipi, Eleni Andreou, Eleni Sfyri, Vasiliki Kefala, and Efstathios Rallis. 2024. "The Risk of Using Cosmetics and Cosmetic Procedures During Pregnancy" Applied Sciences 14, no. 21: 9885. https://doi.org/10.3390/app14219885

APA Style

Biskanaki, F., Tertipi, N., Andreou, E., Sfyri, E., Kefala, V., & Rallis, E. (2024). The Risk of Using Cosmetics and Cosmetic Procedures During Pregnancy. Applied Sciences, 14(21), 9885. https://doi.org/10.3390/app14219885

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