Despite years of research, the cause of infantile
colic is still shrouded in mystery. There is a growing body of evidence
to suggest that altered gut microbiota play a role in this distressing
though self-limited disorder. An increase of Proteobacteria and a
decline of Bifidobacteria have been noted in the stools of
colicky babies. It is hypothesized that the Proteobacteria cause
excessive fermentation of carbohydrates and proteins resulting in
excessive gas production. Bifidobacteria also change the levels of
immunomodulators like butyrate, beta defensive 2 and fecal calprotectin.
Butyrate has been shown to modulate intestinal transit times, and
visceral and central pain perception as well as produce an
anti-inflammatory effect in the gut.
A new randomized controlled study in 80 infants from
Italy has shown that Bifidobacterium animalis subsp. lactis when
given orally daily for 28 days was effective in reducing duration of
colic in 80% of the study group versus 31% of the placebo group.
There was also an increase in fecal butyrate and calprotectin, though
that could be tested only in a small number of patients. A previous
study with this probiotic along with low lactose, partially hydrolyzed
formula had shown good results in reducing colic. This study was done in
exclusively breast fed babies, and the intervention may becomea valuable
addition in the practicing pediatricians’armory against the frustrating
problem of the colicky infant.
(Aliment Pharmacol Ther. 2019 Dec 3)
The Surrogacy Regulation Bill
India has long been considered the surrogacy capital
of the world. Before 2008, commercial surrogacy was rampant in India.
There were no legal guidelines till the case of a Japanese baby
conceived by surrogacy in India hit the headlines in August 2008. The
Japanese parents came to India to conceive by surrogacy but got divorced
before the baby was born. In the ensuing confusion was born the seeds of
the Surrogacy Bill in India.
The Surrogacy Regulation Bill was finally passed by
the Lok Sabha in August 2019 and was then referred to the Rajya Sabha.
In this bill commercial surrogacy has been completely prohibited. All
foreign nationals, non-resident Indians or Persons of Indian Origin are
forbidden to avail commercial surrogacy in India.
It allows altruistic surrogacy to Indian married
couples who are childless. The surrogate mother and the couple who want
to have children must be close relatives. Homosexuals, single parents or
live-in couples are not allowed to have children by surrogacy. Couples
who already have children will also not be allowed to use surrogacy
services unless the child is severely physically or mentally challenged.
A lady can be a surrogate mother only once.
Commercial surrogacy has been considered as the root
cause of the prevalent exploitation, misdoings and irregularities, and
the Bill is an attempt to reduce this. However, many feel the Bill
seriously impinges on the rights of single parents, the LGBT community
and couples in a live-in relationship. The Rajya Sabha has now referred
it to a 23-member select committee for further refinements.
(The Times of India 2019 Nov 22)
VoxelotorReceives Approval for Sickle Cell Anemia
Voxelotor is a drug which aims to correct the root
cause of the problems in sickle cell anemia. The drug inhibits
polymerization of sickle hemoglobin. The FDA approved it after the phase
3 randomized controlled trial published this year. In the study, 274
patients were randomized to either Voxelotor or placebo. After 24 weeks,
there was significant improvement in hemoglobin,and reduction in
reticulocyte counts and indirect bilirubin - there were no serious
adverse effects. It is now approved for use in patients 12 years and
above.
The drug was discovered in 2017 and is an excellent
example of basic science research reaching the bedside in a relatively
short time. This was because it was granted fast track status and
accelerated approval in view of the huge impact it will make on the
lives of so many patients. However, caveats remain. Risk of delayed
oxygen delivery in the brain leading to silent infarcts needs to be
evaluated. Its use in variant SCDs such as sickle-thal and sickle cell
disease with hemoglobin below 7 g/dLhave also not been studied.
As with all new drugs, the initial blush of
enthusiasm may well fade with the reality of unanticipated side-effects,
if we are not vigilant.
(Medscape Medical News 2019 Nov 25)